WO1999036099A1 - Compositions a liberation controlee, leur procede de fabrication et leur utilisation - Google Patents
Compositions a liberation controlee, leur procede de fabrication et leur utilisation Download PDFInfo
- Publication number
- WO1999036099A1 WO1999036099A1 PCT/JP1999/000086 JP9900086W WO9936099A1 WO 1999036099 A1 WO1999036099 A1 WO 1999036099A1 JP 9900086 W JP9900086 W JP 9900086W WO 9936099 A1 WO9936099 A1 WO 9936099A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- salt
- sustained
- acid
- release composition
- physiologically active
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/24—Follicle-stimulating hormone [FSH]; Chorionic gonadotropins, e.g. HCG; Luteinising hormone [LH]; Thyroid-stimulating hormone [TSH]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/08—Peptides having 5 to 11 amino acids
- A61K38/09—Luteinising hormone-releasing hormone [LHRH], i.e. Gonadotropin-releasing hormone [GnRH]; Related peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/542—Carboxylic acids, e.g. a fatty acid or an amino acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
- A61K9/1647—Polyesters, e.g. poly(lactide-co-glycolide)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/02—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/02—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
- A61P5/04—Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin for decreasing, blocking or antagonising the activity of the hypothalamic hormones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/06—Drugs for disorders of the endocrine system of the anterior pituitary hormones, e.g. TSH, ACTH, FSH, LH, PRL, GH
Definitions
- the present invention relates to a sustained-release preparation of a physiologically active substance and a method for producing the same.
- JP-A-7-97334 discloses a sustained-release preparation comprising a physiologically active peptide or a salt thereof, and a biodegradable polymer having a free lipoxyl group at a terminal, and a method for producing the same.
- GB2209937, GB2234169, GB2234896, GB2257909 and EP 62617 OA2 describe biodegradable polymers containing water-insoluble salts such as separately prepared peptides and pamoate salts of proteins.
- a composition based on or a method for producing the same is disclosed.
- W ⁇ 95Z 15767 discloses embonate (pamoate) of cetrorel ix (LH-RH angyo gonist) and a method for producing the same, and at the same time, converts the pamoate into a biodegradable polymer. It is described that the release of the peptide is the same as in the case of pamoate alone even if the peptide is encapsulated. Disclosure of the invention
- a novel composition containing a high content of a physiologically active substance, and capable of realizing a stable release rate over a long period by suppressing the initial excessive release.
- the present inventors have conducted intensive studies to solve the above-mentioned problems, and as a result, when forming a composition, a physiologically active substance and hydroxynaphthoic acid coexist to form a high content of a physiologically active substance.
- Into the biodegradable polymer When both are encapsulated, the bioactivity is released at a rate different from the release rate of the bioactive substance from the composition formed from the bioactive substance and hydroxynaphthoic acid prepared under the condition that no biodegradable polymer is present.
- the substance is released, and the release rate can be controlled by the properties of the biodegradable polymer ⁇ the amount of hydroxynaphthoic acid added.
- sustained-release composition comprising a physiologically active substance or a salt thereof, hydroxynaphthoic acid or a salt thereof, and a biodegradable polymer or a salt thereof,
- sustained-release composition according to (2) wherein the physiologically active substance is an LH-RH derivative.
- sustained-release composition according to (1) wherein the biodegradable polymer is a polymer of hydroxycarboxylic acid
- the ⁇ -hydroxycarponic acid polymer is a lactic acid-glycolic acid polymer.
- a method comprising mixing and dispersing a physiologically active substance or a salt thereof in an organic solvent solution containing a biodegradable polymer or a salt thereof and hydroxynaphthoic acid or a salt thereof, and then removing the organic solvent.
- (21) a medicament comprising the sustained-release composition according to (1), (22) Prostate cancer, benign prostatic hyperplasia, endometriosis, uterine fibroids, uterine fibroids, precocious puberty, dysmenorrhea or breast cancer containing the sustained-release composition described in paragraph (3).
- Prophylactic, therapeutic or contraceptive Prophylactic, therapeutic or contraceptive
- a sustained-release composition comprising a hydroxynaphthoic acid salt of a physiologically active substance and a biodegradable polymer or a salt thereof,
- (25) a method for improving the encapsulation efficiency of a physiologically active substance in a sustained-release composition characterized by using hydroxynaphthoic acid or a salt thereof,
- the present invention provides the method for producing a sustained-release composition according to any one of (30) to (32), wherein the method for removing the solvent is an in-water drying method.
- the physiologically active substance used in the present invention is not particularly limited as long as it is pharmacologically useful, and may be a non-peptide compound or a peptide compound. Examples of the non-peptide compound include agonists, antagonists, and compounds having an enzyme inhibitory action.
- the peptide compound for example, a physiologically active peptide is preferable, and the molecular weight is about 300 to about 400, 000, preferably about 400 to about 300, 000, more preferably about 4,000. Preferred are 500 to about 200,000 bioactive peptides
- bioactive peptide examples include luteinizing hormone-releasing hormone (LH-RH), insulin, somatosustin, growth hormone, growth hormone-releasing hormone (GH-RH), prolactin, erythropoietin, adrenocortical hormone, Melanocyte stimulating hormone, thyroid hormone releasing hormone, thyroid stimulating hormone, luteinizing hormone, follicle stimulating hormone, vasopressin, oxitocin, calcitonin, gastrin, secretin, pancreozymine, cholecystokinin, angiotensin, human placental lactogen , Human chorionic gonadotropin, enkephalin, endorphin, kyotorphin, tuftsin, thymopoietin, thymosin, thymothymulin, thymic factor, blood thymic factor, tumor necrosis factor, colony -Inducing factor, motilin, dinorphin, bombe
- the physiologically active substance used in the present invention may be itself or a pharmacologically acceptable salt.
- Such a salt examples include, when the physiologically active substance has a basic group such as an amino group, an inorganic acid (also referred to as an inorganic free acid) (eg, carbonic acid, bicarbonate, hydrochloric acid, sulfuric acid, nitric acid, boric acid) Acid), organic acids (also referred to as organic free acids) (eg, succinic acid, acetic acid, propionic acid, trifluoroacetic acid, etc.).
- an inorganic acid also referred to as an inorganic free acid
- organic acids also referred to as organic free acids
- succinic acid eg, succinic acid, acetic acid, propionic acid, trifluoroacetic acid, etc.
- an inorganic base also referred to as an inorganic free base
- an organic substance eg, organic amines such as triethylamine, basic amino acids such as arginine, etc.
- the physiologically active peptide may form a metal complex compound (eg, a copper complex, a zinc complex, etc.).
- LH-RH derivatives which are hormone-dependent diseases, especially sex hormone-dependent cancers (eg, prostate cancer, uterine cancer, breast cancer, pituitary tumor, etc.), benign prostatic hyperplasia , Endometriosis, uterine fibroids, precocious puberty, dysmenorrhea, amenorrhea, premenstrual syndrome, polyatrial ovary syndrome, and other sex hormone-dependent diseases and contraception (or When the rebound effect is used, an LH-RH derivative or a salt thereof that is effective for infertility) can be mentioned. Furthermore, an LH-RH derivative or a salt thereof that is effective for benign or malignant tumors that are sex hormone-independent but LH-RH sensitive is also included.
- sex hormone-dependent cancers eg, prostate cancer, uterine cancer, breast cancer, pituitary tumor, etc.
- benign prostatic hyperplasia e.g, Endometriosis, uterine fibroids
- LH-RH derivative or salt thereof include, for example, Treatment with GnRH analog: Treatment with GnRH analogs: Controversies and perspectives [Parillete Non-publishing Group Co., Ltd. (The Parthenon Publishing Group Ltd.) ) Published in 1996], JP-T3-503165, JP-A-3-101695, JP-A-7-97334, JP-A-8-259460, and the like.
- LH-RH derivative examples include an LH-RH agonist and an LH-RH antenna gonist.
- LH-RH antagonist examples include the general formula [I]
- B is a residue selected from NMeAph (Atz)
- B is a residue selected from DLys (Nic :), DCit, DLys (AzaglyNic), DLys (Azag Fur), DhArg (Et 2 ), DAph (Atz) and DhCi.
- C represents Lys (Nisp), Arg or hArg (Et 2 ), respectively.] Or a salt thereof or the like.
- Y represents a residue selected from DLeu, DAIa, DT ⁇ , DSer (tBu), D2Nal and DHis (ImBzl), and Z represents NH-C 2 H 5 or Gly-NH 2 , respectively
- the physiologically active peptide represented or a salt thereof is used.
- Table Y in is DLeu
- Z is a NH-C 2 H 5 base peptide (i.e., 5-0X0- Pro- His- by Trp-Ser-Tyr-DLeu- Leu-Arg- Pro- NH-C 2 Is preferred.
- peptides can be produced by the method described in the above-mentioned literature or gazette or a method analogous thereto.
- D2Nal D-3- (2-naphthyl) alanine residue
- D4ClPhe D-3- (4-black mouth) phenylalanine residue
- NMeAph (Atz): N-methyl-[5 '-(3, -amino- ⁇ ⁇ ⁇ - ⁇ , 2', 4'-triazolyl)] phenylalanine residue
- amino acids can have optical isomers, If it is not specified, it indicates L-form.
- the hydroxynaphthoic acid used in the present invention is one in which one hydroxyl group and one carboxyl group are bonded to different carbons of naphthylene. Therefore, calpoxy W
- soluble in alcohols eg, ethanol, methanol, etc.
- solvent in alcohols means, for example, 10 g / L or more with respect to methanol.
- 3-hydroxy-2-naphthoic acid 1-hydroxy-2-naphthoic acid and 3-hydroxy-2-naphthoic acid, in which a carbonyl group and a hydroxyl group are bonded to adjacent carbon atoms of the naphthylene ring, 2-Hydroxy-1-naphthoic acid is preferred.
- 3-hydroxy-2-naphthoic acid in which a hydroxyl group is bonded to the 3-position carbon of naphthalene and a carboxyl group is bonded to the 2-position carbon is preferable.
- Hydroxynaphthoic acid may be a salt.
- the salt examples include inorganic bases (eg, alkali metals such as sodium and potassium, alkaline earth metals such as calcium and magnesium) and organic bases (eg, organic amines such as triethylamine, basic amino acids such as arginine). And salts with transition metals (eg, zinc, iron, copper, etc.) and complex salts.
- inorganic bases eg, alkali metals such as sodium and potassium, alkaline earth metals such as calcium and magnesium
- organic bases eg, organic amines such as triethylamine, basic amino acids such as arginine
- salts with transition metals eg, zinc, iron, copper, etc.
- a solution of hydroxynaphthoic acid in water-containing organic solvent is applied to a weakly basic ion exchange column. Adsorb and then saturate. Next, after removing excess hydroxynaphthoic acid through a water-containing organic solvent, ion exchange is performed through a solution of a physiologically active substance or a salt thereof in a water-containing organic solvent, and the solvent may be removed from the obtained effluent.
- the organic solvent in the water-containing organic solvent alcohols (eg, methanol, ethanol, etc.), acetonitrile, tetrahydrofuran, dimethylformamide and the like are used.
- a method for removing the solvent for precipitating the salt a method known per se or a method analogous thereto is used. For example, there is a method of evaporating the solvent while adjusting the degree of vacuum using a liquid crystal display using a liquid crystal display.
- the hydroxynaphthoic acid salt of a physiologically active substance is slightly soluble in water, although it depends on the physiologically active substance to be used. And a sustained-release composition can be produced.
- biodegradable polymer used in the present invention examples include polyhydroxymonocarboxylic acids (eg, glycolic acid, lactic acid, etc.), ⁇ -hydroxydicarboxylic acids (eg, malic acid), ⁇ -hydroxytricarboxylic acids (eg, malic acid).
- polyhydroxymonocarboxylic acids eg, glycolic acid, lactic acid, etc.
- ⁇ -hydroxydicarboxylic acids eg, malic acid
- ⁇ -hydroxytricarboxylic acids eg, malic acid
- a polymer, a copolymer or a mixture thereof which is synthesized from one or more ⁇ -hydroxycarboxylic acids such as cunic acid, and has a free hydroxyl group; poly ( ⁇ -cyanoacrylate); poly Amino acids (eg, poly ( ⁇ -benzyl-L-glutamic acid), etc.); maleic anhydride copolymers (eg, styrene-maleic acid copolymer, etc.) are used.
- the bonding mode of the monomer may be any of random, block, and graft.
- the ⁇ -hydroxymonocarboxylic acids, monohydroxydicarboxylic acids, and ⁇ -hydroxytricarboxylic acids have an optically active center in the molecule
- any of the D-, L-, and DL-forms may be used.
- lactic acid-glycolic acid polymer hereinafter referred to as poly (lactide co-glycolide), poly (lactic acid-co-glycolic acid) or lactic acid-glycolic acid copolymer is also referred to.
- Lactic acid and glycolic acid homopolymers (polymers) and copolymers (copolymers) are collectively referred to as lactic acid homopolymers, such as lactic acid polymers, polylactic acid, and polylactide, and glycolic acid homopolymers are referred to as glycolic acid polymers, polydalicols. Acid, polyglycolide, etc.), poly (polycyanoacrylate) and the like are preferable. More preferably, it is a lactic acid-glycolic acid polymer, and more preferably, a lactic acid-monodalicholate polymer having a free carboxy group at a terminal.
- the biodegradable polymer may be a salt.
- the salt include inorganic bases (eg, alkali metals such as sodium and potassium, alkaline earth metals such as calcium and magnesium) and organic bases (eg, organic amines such as triethylamine, basic amino acids such as arginine) Etc.), or salts and complex salts with transition metals (eg, zinc, iron, copper, etc.).
- a lactic acid-glycolic acid polymer When a lactic acid-glycolic acid polymer is used as the biodegradable polymer, its composition ratio (mol%) is preferably about 100/0 to about 400, and about 100/0 to about 50 Z5. 0 is more preferred. Lactic acid homopolymer having a composition ratio of 100 to 100 is also preferably used.
- the optical isomer ratio of lactic acid which is one of the minimum repeating units of the “lactic acid-glycolic acid polymer” is about 75 Z 25 to about 25 Z for D-form ZL-form (mol Z mol%). Those in the range of 75 are preferred. As the D-form / L-form (mol / mol%), those having a range of about 60/40 to about 30Z70 are widely used.
- the weight average molecular weight of the “lactic acid-glycolic acid polymer” is usually about 3,000 to about 100,000, preferably about 3,000 to about 600,000, Preferably from about 3,000 to about 500,000, particularly preferably from about 20,000 to about 500,000. The one of 000 is used.
- the dispersity (weight average molecular weight, Z number average molecular weight) is usually preferably about 1.2 to about 4.0, more preferably about 1.5 to 3.5.
- the amount of free carboxyl groups of the “lactic acid-glycolic acid polymer” is usually preferably about 20 to about 1000 mol (micromol) per unit mass (gram) of the polymer, and more preferably about 40 to about 1000 mol. (Micromolar) is particularly preferred.
- the weight-average molecular weight, number-average molecular weight and dispersity in the present specification mean that the weight-average molecular weight is 1,110,000, 707,000, 455,645, 354,000, 189,000, 156,055, 98, Gel permeation chromatography using fifteen monodisperse polystyrenes of 900, 66, 437, 37, 200, 17, 100, 9, 830, 5, 870, 2,500, 1, 303, 504 The molecular weight in terms of polystyrene measured by GPC) and the calculated degree of dispersion.
- the measurement is performed using a high-speed GPC device (Tosoichi, HLC-8 120 GPC, detection method depends on the differential refractive index), GPC column KF 804LX 2 (Showa Denko), and chromatoform as the mobile phase.
- the flow rate is set at lm 1 / min.
- the amount of free carboxyl groups means a value obtained by a labeling method (hereinafter, referred to as “amount of carbonyl group by labeling method”).
- a labeling method a labeling method obtained by a labeling method.
- the free force of lipoxyl group Cmo 1 / L was determined by alkali titration, and the absorbance at 544 nm when DL-lactic acid hydrazide was used in the ONPH labeling method was calculated as B (/ cm )),
- the molar amount of free hydroxyl group per unit mass (gram) of the polymer can be obtained by the following equation.
- the “amount of lipoxyl group” is determined by dissolving a biodegradable polymer in a mixed solvent of toluene-aceton and methanol, and titrating the lipoxyl group with an alcoholic potassium hydroxide solution using phenolphthalein as an indicator. (Hereinafter, the value obtained by this method is referred to as “the amount of carboxyl groups by alkali titration”), but the end point of the titration is determined as a result of competing hydrolysis reactions of the polyester main chain during titration. It may be unclear and it is desirable to quantify using the labeling method described above.
- the rate of degradation and disappearance of the biodegradable polymer varies greatly depending on the copolymer composition, molecular weight, and the amount of free carboxyl groups.
- the release period can be prolonged by lowering the daricholic acid fraction or increasing the molecular weight and reducing the amount of free lipoxyl groups.
- the amount of free lipoxyl groups must be at least a certain value because it affects the rate of incorporation of the physiologically active substance into the drug product. Therefore, in order to obtain a biodegradable polymer for a long-term (for example, 6 months or more) type sustained-release preparation, in the case of a lactic acid-daricholic acid polymer, the above weight average molecular weight is about 20,000.
- the amount of free carboxyl groups is about 30 to about SS jumolZg, preferably about 40 to about 95 mol / g, more preferably about 50 to about 90 / mo1 / g.
- Polylactic acid eg, D_lactic acid, L—milk Acid, DL-lactic acid, etc., and particularly DL-lactic acid, etc. are preferred.
- the “lactic acid-glycolic acid polymer” is, for example, a non-catalytic dehydration polycondensation of lactic acid and glycolic acid (Japanese Patent Application Laid-Open No. 28521/1986) or a ring opening using a catalyst from a cyclic diester compound such as lactide and glycolide. It can be produced by polymerization (Encyclopedic Handbook of Biomaterials and Bioengineering Part A: Materials, Volume 2, Marcel Dekker, Inc. 1995).
- the polymer obtained by the above-mentioned known ring-opening polymerization method does not necessarily have a free hydroxyl group at the terminal of the obtained polymer, but is described, for example, in EP-A-0 0839525.
- the polymer can be modified into a polymer having a certain amount of carboxyl group per unit mass, and this can also be used.
- lactic acid-glycolic acid polymer having a free hydroxyl group at the terminal can be produced without problems by a known production method (for example, non-catalytic dehydration polycondensation method, see JP-A-61-28521), or It can also be manufactured by the following method.
- a carboxyl-protected hydroxymonocarboxylic acid derivative eg, D-lactic acid tert-butyl, L-benzyl lactate, etc.
- a carboxyl group-protected hydroxydicarboxylic acid derivative eg, dibenzyl tartronate
- 2-Hydroxyshetylmalonate e.g., 2-Hydroxyshetylmalonate, etc.
- hydroxylcarboxylic acid derivative having a protected oxyloxyl group or “hydroxydicarboxylic acid derivative having a protected oxyloxyl group” is, for example, a compound in which a carboxyl group (_C ⁇ H) is an amide (- Examples include hydroxycarboxylic acid derivatives that have been converted to CONH 2 ) or ester (—COOR), but among them, hydroxycarboxylic acid derivatives in which a carboxyl group (one COOH) is esterified (—COOR), etc. Is preferred.
- R in the ester is, for example, a C alkyl group such as methyl, ethyl, n-propyl, isopropyl, n-butyl, tert-butyl, etc.
- cyclopentyl, ⁇ 3 _ 8 cycloalkyl group such as cyclohexyl, for example, phenyl, ⁇ 6 such as a non _ naphthyl - 1 2 ⁇ Li Ichiru group, e.g., benzyl, phenylene Lou such Fuene Chill - 2
- Examples include an alkyl group or a C 7 _i 4 aralkyl group such as an ⁇ -naphthyl-C 2 aralkyl group such as an ⁇ -naphthylmethyl group.
- a tert-butyl group, a benzyl group and the like are preferable.
- cyclic ester compound refers to, for example, a cyclic compound having at least one ester bond in a ring. Specific examples include cyclic monoester compounds (lactones) and cyclic diester compounds (lactides).
- cyclic monoester compound examples include 4-membered lactones ( ⁇ -butane piolactone, 3-butyrolactone,] 3-isovalerolactone, 3-force prolactone, i3-isoforce prolactone, / 3- Methyl-3-valerolactone, etc., 5-membered lactones (such as aptyloractone, avalerolactone), 6-membered lactones (such as ⁇ -valerolactone), and 7-membered lactones (such as ⁇ -force prolactone) ), ⁇ -dioxanone, 1,5-dioxepan-2-one and the like.
- 4-membered lactones such as aptyloractone, avalerolactone
- 6-membered lactones such as ⁇ -valerolactone
- 7-membered lactones such as ⁇ -force prolactone
- R 1 and R 2 are the same or different and each represent a hydrogen atom or a 6- alkyl group such as methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, etc.
- R 2 is a methyl group
- R 1 is hydrogen atom, such as lactide
- R 1 and R 2 are each a hydrogen atom is preferred.
- glycolide, L-lactide, D-lactide, DL-lactide examples include meso-lactide and 3-methyl-1,4-dioxane-2,5-dione (including optically active forms).
- polymerization catalyst examples include organotin-based catalysts (eg, tin octylate, di-n-butyltin dilaurate, tetraphenyltin, etc.), aluminum-based catalysts (eg, triethylaluminum, etc.), zinc-based catalysts Catalysts (eg, getyl zinc, etc.);
- organotin-based catalysts eg, tin octylate, di-n-butyltin dilaurate, tetraphenyltin, etc.
- aluminum-based catalysts eg, triethylaluminum, etc.
- zinc-based catalysts eg, getyl zinc, etc.
- Aluminum-based catalysts and zinc-based catalysts are preferred from the viewpoint of ease of removal after the reaction, and zinc-based catalysts are more preferred from the viewpoint of safety when remaining.
- benzene, hexane, toluene and the like are used, among which hexane and toluene are preferable.
- the “polymerization method” may be a bulk polymerization method in which the reactants are melted or a solution polymerization method in which the reactants are dissolved in an appropriate solvent (for example, benzene, toluene, xylene, decalin, dimethylformamide, etc.). I just need. Preferred solvents include toluene and xylene.
- the polymerization temperature is not particularly limited.In the case of bulk polymerization, the temperature is not lower than the temperature at which the reactants are brought into a molten state at the start of the reaction, usually 100 to 300 ° C.
- the reaction may be carried out by refluxing with a condenser or in a pressure-resistant vessel.
- the polymerization time is appropriately determined in consideration of the polymerization temperature, other reaction conditions, physical properties of the target polymer, and the like, and is, for example, 10 minutes to 72 hours.
- the reaction mixture is dissolved in a suitable solvent (eg, acetone, dichloromethane, chloroform, etc.), and the polymerization is terminated with an acid (eg, hydrochloric acid, anhydrous acetic acid, trifluoroacetic acid, etc.).
- this is precipitated by mixing it in a solvent (eg, alcohol, water, ether, isopropyl ether, etc.) that does not dissolve the target substance by a conventional method, and the carboxyl group protected at the ⁇ end is precipitated.
- a solvent eg, alcohol, water, ether, isopropyl ether, etc.
- the polymer may be isolated.
- the polymerization method of the present application uses a so-called protic chain transfer agent such as a conventional methanol.
- a protic chain transfer agent such as a conventional methanol.
- hydroxycarboxylic acid derivatives with a protected carboxyl group eg, tert-butyl D-lactate, benzyl L-lactate
- hydroxydicarboxylic acid derivatives with a protected propyloxyl group eg, tartronic acid
- Dibenzyl, di-tert-butyl 2-hydroxyshetylmalonate, etc. are used.
- hydroxycarboxylic acid derivatives having a protected hydroxyl group eg, tert-butyl D-lactate, benzyl L-lactate
- hydroxydicarboxylic acid derivatives having a protected carboxyl group eg, dibenzyl tartronate,
- the polymer having a protected lipoxyl group at the ⁇ -terminal obtained by the polymerization reaction of the above (1) is subjected to a deprotection reaction to convert a free carboxyl group at the target ⁇ -terminal.
- a biodegradable polymer having the same can be obtained.
- the protecting group can be removed by a method known per se. As such a method, any method can be used as long as the protecting group can be removed without affecting the ester bond of poly (hydroxycarboxylic acid). For example, there are methods such as reduction and acid decomposition.
- Examples of the reduction method include catalytic reduction using a catalyst (eg, palladium carbon, palladium black, platinum oxide, etc.), reduction with sodium in liquid ammonia, reduction with dithiothreitol, and the like.
- a catalyst eg, palladium carbon, palladium black, platinum oxide, etc.
- reduction with sodium in liquid ammonia reduction with dithiothreitol, and the like.
- Examples of the acid decomposition method include inorganic acids (eg, hydrogen fluoride, hydrogen bromide, hydrogen chloride Acid decomposition with an organic acid (eg, trifluoroacetic acid, methanesulfonic acid, trifluoromethanesulfonic acid, etc.) or a mixture thereof. If necessary, a cation scavenger (eg, anisol, phenol, thioanisole, etc.) may be appropriately added during acid decomposition.
- inorganic acids eg, hydrogen fluoride, hydrogen bromide, hydrogen chloride
- an organic acid eg, trifluoroacetic acid, methanesulfonic acid, trifluoromethanesulfonic acid, etc.
- a cation scavenger eg, anisol, phenol, thioanisole, etc.
- an appropriate amount of trifluoroacetic acid is dissolved in a polymer dissolved in dichloromethane, xylene, toluene, etc.
- deprotection can be achieved by dissolving the polymer in trifluoroacetic acid and stirring for about 1 hour at room temperature.
- the acid decomposition method may be performed immediately after the polymerization reaction, in which case it can also serve as a polymerization termination reaction.
- the polymer obtained by the above deprotection reaction is subjected to an acid hydrolysis reaction to adjust the weight average molecular weight, the number average molecular weight or the amount of terminal carboxyl groups of the polymer according to the purpose. can do. Specifically, for example, it can be carried out by the method described in EP-A-0 839 525 or a method analogous thereto.
- the biodegradable polymer obtained as described above can be used as a base for producing a sustained-release preparation.
- a polymer having a free carboxylic acid group which is not specified at a terminal can be produced by a known production method (for example, see WO94 / 15787).
- a lactate-glycolic acid polymer whose terminal has been converted to a free hydroxyl group by a chemical treatment after ring-opening polymerization is, for example, Boehringer Ingelheim (Boehringer).
- Ingelheim KG may be used.
- the biodegradable polymer may be a salt (the salt of the biodegradable polymer includes, for example, the above-mentioned salts, etc.).
- the method for producing the biodegradable polymer includes, for example, (a) having the above-mentioned lipoxyl group Biodegradable polymers dissolved in organic solvents and inorganic bases (eg, alkali metals such as sodium and potassium, calcium, An aqueous solution containing ions of an alkaline earth metal such as gnesium, etc.) and an organic base (eg, organic amines such as triethylamine, basic amino acids such as arginine, etc.) is mixed and subjected to ion exchange reaction. To isolate the polymer that became
- a “lactic acid-glycolic acid polymer having a free terminal lipoxyl group at the terminal” manufactured by the above method is used. Is preferred.
- the weight ratio of the physiologically active substance in the composition of the present invention varies depending on the type of the physiologically active substance, the desired pharmacological effect and the duration of the effect, but the physiologically active substance or its salt and hydroxynaphthoic acid or its salt And a biodegradable polymer or a salt thereof in the case of a sustained release composition, the sum of the three being, for example, in the case of a bioactive peptide or a salt thereof, about 0.001 to About 50% by weight, preferably about 0.02 to about 40% by weight, more preferably about 0.1 to 30% by weight, most preferably about 14 to 24% by weight, In the case of a peptidic physiologically active substance or a salt thereof, the amount is about 0.01 to 80% by weight, preferably about 0.1 to 50% by weight.
- the same weight ratio is used when a hydroxynaphthoic acid salt of a physiologically active substance is contained.
- a sustained-release composition comprising a salt of a physiologically active peptide (provisionally referred to as (A)) and hydroxynaphthoic acid (provisionally referred to as (B))
- the salt of (A) and (B) (A) is usually about 5 to about 90% by weight, preferably about 10 to about 85% by weight, more preferably about 15 to about 80% by weight, and particularly preferably Is from about 30 to about 80% by weight.
- the amount of hydroxynaphthoic acid or a salt thereof is preferably Is about 1/2 to about 2 mol, about 3/4 to about 4/3 mol, particularly preferably about 4/5 to 1 mol of the hydroxynaphthoic acid or the salt thereof per 1 mol of the physiologically active substance or a salt thereof. About 6-5 moles.
- the composition of the present invention is designed by using, as an example, a sustained-release composition containing a bioactive substance, hydroxynaphthoic acid and a biodegradable polymer, where the bioactive substance is basic. This is described below.
- the composition coexists with a physiologically active substance as a base and hydroxynaphthoic acid as an acid, and when they are incorporated in the composition as a free form or a salt, the composition can be used.
- dissociation equilibrium is established in the presence of water or in the presence of trace amounts of water.
- the salt formed by the slightly water-soluble hydroxynaphthoic acid with the physiologically active substance is considered to be slightly water-soluble depending on the properties of the physiologically active substance. Therefore, the dissociation equilibrium is on the side of such a slightly water-soluble salt formation. Lean.
- compositions containing a high content of a basic physiologically active substance it is desirable to protonate most of the physiologically active substance into the above slightly water-soluble salt in view of the above dissociation equilibrium.
- the counter ion is mainly hydroxynaphthoic acid (preferably hydroxynaphthoic acid).
- Rigoma (lactic acid-glycolic acid oligomer) and monomer (lactic acid or dalicholic acid) always have one lipoxyl group, which is also a physiologically active substance.
- the movable counter ion species as described above, hydroxynaphthoic acid, lactic acid-glycolic acid oligomer (transfer) Possible molecular weight) and monomers (lactic or glycolic acid).
- a salt of a strong acid is generally generated preferentially depending on the composition ratio.
- the pKa of hydroxynaphthoic acid is, for example, that of 3-hydroxy-2-naphthoic acid 2.708 (Chemical Handbook Basic Edition II, The Chemical Society of Japan, issued September 25, 1969).
- the pKa of the lactoxyl group of the lactic acid-glycolic acid oligomer is determined by considering the contribution of the ester bond closest to the dissociation group.
- the salt of the bioactive substance is preferentially formed with the salt, and the properties of the salt are thought to determine the controlled release properties of the bioactive substance from the composition.
- the physiologically active substance include the aforementioned physiologically active substances.
- the fact that the salt formed by hydroxynaphthoic acid with the physiologically active substance is slightly water-soluble and not water-insoluble has a favorable effect on the sustained-release mechanism.
- water-insoluble as used herein means that when the substance is stirred in distilled water at a temperature of 40 ° C or lower for 4 hours, the mass of the substance dissolved in 1 L of the solution is 25 mg or less.
- the term “slightly water-soluble” as used herein refers to a case where the mass is greater than 25 mg and 5 g or less.
- the substance is a salt of a physiologically active substance
- the above definition is applied with the mass of the physiologically active substance dissolved in the above operation.
- the form of the sustained release composition in the present specification is not particularly limited, but is preferably in the form of fine particles, and particularly in the form of microspheres (in the case of a sustained release composition containing a biodegradable polymer, it is also referred to as microcapsules). preferable.
- microsphere refers to an injectable sphere that can be dispersed in a solution. Particles. The morphology can be confirmed by, for example, observation with a scanning electron microscope.
- a method for producing a sustained-release composition for example, a microcapsule, containing the physiologically active substance of the present invention or a salt thereof, hydroxynaphthoic acid or a salt thereof, and a biodegradable polymer or a salt thereof is exemplified.
- an organic solvent solution of hydroxynaphthoic acid or a salt thereof and a biodegradable polymer or a salt thereof is prepared.
- the organic solvent used for producing the sustained-release preparation of the present invention preferably has a boiling point of 120 ° C. or lower.
- organic solvent examples include halogenated hydrocarbons (eg, dichloromethane, chloroform, dichloroethane, trichloroethane, carbon tetrachloride, etc.), ethers (eg, ethyl ether, isopropyl ether, etc.), fatty acid esters (Eg, ethyl acetate, butyl acetate, etc.), aromatic hydrocarbons (eg, benzene, toluene, xylene, etc.), alcohols (eg, ethanol, methanol, etc.), and acetonitrile.
- dichloromethane is preferred as the organic solvent for the biodegradable polymer or its salt.
- Alcohols are preferable as the organic solvent of hydroxynaphthoic acid or a salt thereof. They may be mixed after being dissolved separately, or they may be used by dissolving the two in an organic solvent mixed at an appropriate ratio. Of these, a mixed solution of a halogenated hydrocarbon and an alcohol is preferred, and a mixed solution of dichloromethane and ethanol is particularly preferred.
- the content of ethanol in the mixed organic solvent of dichloromethane and ethanol is generally about 0.01 to about 50% (v / v ), More preferably about 0.05 to about 40% (v / v), And preferably from about 0.1 to about 30% (v / v).
- the concentration of the biodegradable polymer in the organic solvent solution varies depending on the molecular weight of the biodegradable polymer and the type of organic solvent.For example, when dichloromethane is used as the organic solvent, the concentration is generally about 0.5. From about 70% by weight, more preferably from about 1 to about 60% by weight, particularly preferably from about 2 to about 50% by weight.
- the concentration of hydroxynaphthoic acid or a salt thereof in an organic solvent is generally about 0.01 to about 10% by weight, more preferably about 10% by weight when a mixture of dichloromethane and ethanol is used as the organic solvent. 0.1 to about 5% by weight, particularly preferably about 0.5 to about 3% by weight.
- a physiologically active substance or a salt thereof is added to the thus-obtained solution of hydroxynaphthoic acid or a salt thereof and the biodegradable polymer in an organic solvent, and dissolved or dispersed.
- an organic solvent solution containing the obtained composition comprising a physiologically active substance or a salt thereof, hydroxysinaphthoic acid or a salt thereof and a biodegradable polymer or a salt thereof is added to an aqueous phase, and O (oil phase) (water Phase)
- O oil phase
- the solvent in the oil phase is volatilized or diffused in the aqueous phase to prepare a microcapsule.
- the volume of the aqueous phase at this time is generally about 1 to about 100,000 times the oil phase volume, more preferably about 5 to about 500,000 times, and particularly preferably about 1 to 100,000 times. It is selected from 0 times to about 2,000 times.
- An emulsifier may be added to the above external water phase.
- any emulsifier can be used as long as it can form a stable OZW emulsion.
- anionic surfactants sodium oleate, sodium stearate, sodium lauryl sulfate, etc.
- nonionic surfactants polyoxyethylene sorbitan fatty acid ester [Tween 80, Tween 60, Atra Powder Co., Ltd., polyoxyethylene castor oil derivatives [HC0-60, HC0-50, Nikko Chemicals, etc.)
- polyvinylpyrrolidone polyvinyl alcohol, carboxymethylcellulose, lecithin, gelatin, hyaluronic acid Etc. are used You. You may use one of these or a combination of several of them.
- the concentration in use is preferably in the range of about 0.01 to 10% by weight, more preferably in the range of about 0.05 to about 5% by weight.
- An osmotic pressure regulator may be added to the above external aqueous phase.
- the osmotic pressure adjusting agent may be any as long as it exhibits an osmotic pressure when used as an aqueous solution.
- osmotic pressure adjusting agent examples include polyhydric alcohols, monohydric alcohols, monosaccharides, disaccharides, oligosaccharides, amino acids, and derivatives thereof.
- polyhydric alcohols examples include trihydric alcohols such as glycerin, pentahydric alcohols such as arabitol, xylitol and aditol, and hexahydric alcohols such as mannitol, sorbitol and dulcyl. Are used. Of these, hexahydric alcohols are preferred, and mannitol is particularly preferred.
- monohydric alcohols include methanol, ethanol, isopropyl alcohol and the like, and among them, ethanol is preferable.
- Examples of the above monosaccharides include pentoses such as arabinose, xylose, lipose, and 2-deoxylipose, and hexoses such as glucose, fructose, galactose, mannose, sorbose, rhamnose, and fucose. Of these, hexoses are preferred.
- oligosaccharides for example, trisaccharides such as maltotriose, raffinose monosaccharide and the like, tetrasaccharides such as stachyose and the like are used, and among them, the trisaccharide is preferable.
- disaccharides and oligosaccharides for example, dalcosamine, galactosamine, glucuronic acid, galacturonic acid and the like are used. Any of the above amino acids can be used as long as it is L-integrated, and examples include glycine, leucine, and arginine. Of these, L-arginine is preferred.
- osmotic pressure regulators may be used alone or as a mixture. These osmotic pressure adjusting agents are used at a concentration such that the osmotic pressure of the external aqueous phase is about 1 Z50 to about 5 times, preferably about 1/25 to about 3 times the osmotic pressure of physiological saline.
- a method for removing the organic solvent a method known per se or a method analogous thereto is used. For example, a method in which an organic solvent is evaporated at normal pressure or gradually reduced pressure while stirring with a propeller-type stirrer or a magnetic stirrer or an ultrasonic generator, or the like, while adjusting the degree of vacuum using a rotary avaporator, etc. Examples include a method of evaporating the solvent and a method of gradually removing the organic solvent using a dialysis membrane.
- micro force cell obtained in this way is separated by centrifugation or filtration, and then, a free bioactive substance or a salt thereof, hydroxynaphthoic acid or a salt thereof, a drug attached to the surface of the microcapsule, and a drug Wash the retentate, emulsifier, etc. several times with distilled water, disperse it again in distilled water, etc., and freeze-dry.
- an anti-agglomeration agent may be added to prevent aggregation of the particles.
- the aggregation inhibitor include water-soluble polysaccharides such as mannitol, lactose, glucose, starches (eg, corn starch), amino acids such as glycine, and proteins such as fibrin and collagen. Of these, mannitol is preferred.
- the microcapsules may be heated under reduced pressure so that the microcapsules do not fuse with each other to remove water and the organic solvent in the microcapsules.
- the polymer is heated at a temperature slightly higher than the midpoint glass transition temperature of the biodegradable polymer determined by a differential scanning calorimeter under a condition of a heating rate of 10 to 20 ° C. per minute. More preferably, heating is performed within a temperature range about 30 ° C. higher than the midpoint glass transition temperature of the biodegradable polymer.
- the temperature range is preferably higher than the midpoint glass transition temperature and higher than the midpoint glass transition temperature by 10 ° C, more preferably, 5 ° C higher than the glass transition temperature above the midpoint glass transition temperature Heat in range.
- the heating time varies depending on the amount of micro force capsule, etc., but generally, about 12 hours to about 168 hours, preferably about 24 hours after the microcapsule itself reaches a predetermined temperature. Hours to about 120 hours, particularly preferably about 48 hours to about 96 hours.
- the heating method is not particularly limited as long as the method is capable of uniformly heating the microcapsules.
- heating and drying method for example, a method of heating and drying in a constant temperature bath, a fluidizing bath, a moving tank or a kiln, a method of heating and drying with a microwave, and the like are used. Of these, a method of heating and drying in a thermostat is preferred.
- an organic solvent solution of a biodegradable polymer or a salt thereof is prepared.
- concentrations of the organic solvent and the biodegradable polymer or a salt thereof in the organic solvent solution are the same as those described in the above item (I) ((ii).
- the ratio between the two is the same. Is the same as described in the above (I) (().
- a physiologically active substance or a salt thereof is added to an organic solvent solution of the biodegradable polymer or a salt thereof thus obtained and dissolved or dispersed. Then, a solution of hydroxynaphthoic acid or a salt thereof is added to an organic solvent solution (oil phase) containing the composition comprising the obtained physiologically active substance or a salt thereof and a biodegradable polymer or a salt thereof.
- An aqueous solution of alcohols eg, methanol, ethanol, etc.
- an aqueous solution of pyridine an aqueous solution of dimethylacetamide, etc.
- This mixture is emulsified by a known method such as a homogenizer or an ultrasonic wave to form a WZO emulsion.
- the obtained physiologically active substance or a salt thereof, hydroxynaphthoic acid or a salt thereof and a WZO emulsion composed of a biodegradable polymer or a salt thereof are added to an aqueous phase, and W (internal aqueous phase) / O (oil) is added.
- Phase) IW (outer water phase) forms emulsion
- the solvent in the oil phase is volatilized to prepare microcapsules.
- the volume of the external water phase is generally about 1 to about 10,000 times, more preferably about 5 to about 5,000 times, particularly preferably about 10 to about 2,000 times the oil phase volume. Choose from double.
- the emulsifiers and osmotic pressure regulators that may be added to the above external aqueous phase and the subsequent preparation method are the same as those described in the above (I) and (i).
- an organic solvent solution of hydroxynaphthoic acid or a salt thereof and a biodegradable polymer or a salt thereof is prepared, and the obtained organic solvent solution is referred to as an oil phase.
- the preparation method is the same as described in the above (I) (i).
- hydroxynaphthoic acid or a salt thereof and the biodegradable polymer may be separately prepared as organic solvent solutions, and then mixed.
- the concentration of the biodegradable polymer in the organic solvent solution depends on the molecular weight of the biodegradable polymer and the type of organic solvent.For example, when dichloromethane is used as the organic solvent, the concentration is generally about 0.5 to about 70% by weight, more preferably about 1 to about 60% by weight, particularly preferably about 2 to about 50% by weight.
- a solution or dispersion of a physiologically active substance or a salt thereof is prepared (for the solvent, water, a mixture of water and alcohols (eg, methanol, ethanol, etc.)).
- the concentration of the physiologically active substance or a salt thereof is generally 0.001 mg Zml to 10 g / m 1, more preferably 0.1 mg / m 1 to 5 g / m 1, and still more preferably 1 Omg / m 1 to 3 g / m1.
- dissolution aids and stabilizers may be used.
- heating, shaking, stirring and the like may be performed to such an extent that the activity is not lost, and the resulting aqueous solution is referred to as an internal aqueous phase.
- the inner water phase and the oil phase obtained as above are homogenized or known using ultrasonic waves or the like. W
- the volume of the oil phase to be mixed is about 1 to about 1000 times, preferably about 2 to 100 times, more preferably about 3 to 10 times the volume of the internal aqueous phase.
- the viscosity range of the obtained WZO emulsion is generally from about 15 to 20 ° C., from about 10 to 100,000 cp, preferably from about 100 to 5,000 cp. It is. More preferably, it is about 500-2, 000 cp.
- the obtained W / II emulsion comprising a physiologically active substance or a salt thereof, hydroxynaphthoic acid or a salt thereof and a biodegradable polymer or a salt thereof is added to an aqueous phase, and W (internal aqueous phase) / O ( Oil phase) IW (Outer water phase)
- W internal aqueous phase
- O Oil phase
- IW Outer water phase
- the solvent in the oil phase is volatilized or diffused into the outer water phase to prepare a microcapsule.
- the volume of the external water phase is generally about 1 to about 100,000 times the oil phase volume, more preferably about 5 to about 500,000 times, and particularly preferably about 1 to 100,000 times. It is selected from 0 times to about 2,000 times.
- the emulsifiers and osmotic pressure regulators that may be added to the above external aqueous phase, and the subsequent preparation method are the same as those described in the above (I) and (i).
- the bioactive substance or its salt, hydroxynaphthoic acid or its salt, and the biodegradable polymer mono- or its salt described in the above-mentioned (I) in-water drying method are used.
- the coacervation agent is gradually added to the organic solvent solution containing the composition consisting of under stirring to precipitate and solidify the microcapsules.
- the coacervation agent is selected from about 0.01 to 1, 000 times, preferably about 0.05 to 500 times, particularly preferably about 0.1 to 200 times the oil phase volume. Devour.
- the coacervation agent may be a high molecular weight compound, a mineral oil type or a vegetable oil type compound or the like that is miscible with an organic solvent, such as a physiologically active substance or a salt thereof, such as hydroxynaphthoic acid or a salt thereof, and a biodegradable polymer. Does not dissolve its salt complex It is not particularly limited as long as it is one. Specifically, for example, silicone oil, sesame oil, soybean oil, corn oil, cottonseed oil, coconut oil, linseed oil, mineral oil, n-hexane, n-heptane and the like are used. These may be used as a mixture of two or more.
- micro forceps obtained in this manner are collected, they are repeatedly washed with heptane or the like, and washed from a physiologically active substance or a salt thereof, hydroxynaphthoic acid or a salt thereof, and a biodegradable polymer or a salt thereof.
- the core cell base agent and the like other than the composition are removed and dried under reduced pressure. Alternatively, washing is carried out in the same manner as described in the underwater drying method (I) and (i), followed by freeze-drying and further heating and drying.
- the bioactive substance or its salt, hydroxynaphthoic acid or its salt, and the biodegradable polymer mono- or its salt described in the above-mentioned (I) in-water drying method are used. Is sprayed into the drying chamber of a spray drier using a nozzle, and the organic solvent in the atomized droplets is volatilized in a very short time to prepare microcapsules.
- the nozzle include a two-fluid nozzle type, a pressure nozzle type, and a rotating disk type. Thereafter, if necessary, washing may be carried out in the same manner as described in the underwater drying method (I), followed by freeze-drying and further heating and drying.
- the physiologically active substance or its salt, hydroxynaphthoic acid or its salt, and the biodegradable polymer or its salt described in the in-water drying method of (I) as a dosage form other than the aforementioned microcapsule An organic solvent solution containing, for example, using a rotary evaporator to adjust the degree of vacuum while evaporating the organic solvent and water to dryness, then pulverizing with a jet mill or the like to fine powder (also called microparticles) It may be.
- the pulverized fine powder may be washed in the same manner as described in the in-water drying method of the microcapsule production method (I), and then freeze-dried, and further heated and dried.
- microcapsules or fine powder obtained here can achieve drug release corresponding to the decomposition rate of the biodegradable polymer or lactic acid-glycolic acid polymer used.
- a method for producing a sustained-release composition containing the hydroxynaphthoate of the physiologically active substance of the present invention will be exemplified.
- a bioactive peptide is preferably used as the bioactive substance.
- a physiologically active substance or a salt thereof is added to an organic solvent solution of hydroxynaphthoic acid or a salt thereof so as to have a weight ratio shown in the definition of the amount of the physiologically active substance, and a hydroxynaphthoic acid salt of the physiologically active substance is added.
- an organic solvent solution containing The organic solvent is the same as described in the above (I) and (i).
- a mixed organic solvent is used, the ratio between the two is the same as described in the above section (I) (i).
- a method for removing an organic solvent for precipitating a composition containing a hydroxynaphthoic acid salt of a physiologically active substance a method known per se or a method analogous thereto is used. For example, there is a method of evaporating the organic solvent while adjusting the degree of vacuum by using a one-taleeve apole.
- composition containing the hydroxynaphthoate of the physiologically active substance thus obtained is prepared again to prepare a sustained-release composition (microspheres or fine particles).
- organic solvent examples include octogenated hydrocarbons (eg, dichloromethane, chloroform, dichloroethane, trichloroethane, carbon tetrachloride, etc.), ethers (eg, ethyl ether, isopropyl ether, etc.), fatty acid esters (eg, Examples include ethyl acetate, butyl acetate, etc.), and aromatic hydrocarbons (eg, benzene, toluene, xylene, etc.). These may be mixed and used at an appropriate ratio. Of these, halogenated hydrocarbons are preferred, and dichloromethane is particularly preferred.
- octogenated hydrocarbons eg, dichloromethane, chloroform, dichloroethane, trichloroethane, carbon tetrachloride, etc.
- ethers eg, ethyl ether, isopropyl ether, etc.
- a composition containing the obtained hydroxynaphthoate of a physiologically active substance An organic solvent solution containing is added to the aqueous phase to form an O (oil phase) ZW (aqueous phase) emulsion, and then the solvent in the oil phase is evaporated to prepare microspheres.
- the volume of the aqueous phase is generally about 1 to about 100,000 times the oil phase volume, more preferably about 5 to about 5,000 times, and particularly preferably. It is selected from about 10 times to about 2,000 times.
- the emulsifiers and osmotic pressure regulators that may be added to the above external aqueous phase and the subsequent preparation method are the same as those described in the above (I) and (i).
- a method for removing the organic solvent a method known per se or a method analogous thereto is used. For example, a method in which an organic solvent is evaporated at normal pressure or gradually reduced pressure while stirring with a propeller-type stirrer or a magnetic stirrer, or the like, and the organic solvent is removed while adjusting the degree of vacuum using a rotary evaporator. Examples of the method include evaporating.
- microspheres obtained in this way are separated by centrifugation or filtration, and the free bioactive substance, hydroxysinaphthoic acid, emulsifier, etc. attached to the surface of the microspheres are repeated several times with distilled water. Wash, disperse again in distilled water and freeze-dry.
- an anti-agglomeration agent may be added to prevent aggregation of the particles.
- the aggregation inhibitor include water-soluble polysaccharides such as mannitol, lactose, glucose, starches (eg, corn starch), amino acids such as glycine, and proteins such as fibrin and collagen. Of these, mannitol is preferred.
- the water and the organic solvent in the microspheres may be further removed by heating the microspheres under reduced pressure so that the microspheres do not fuse with each other.
- the heating time varies depending on the amount of microspheres, etc., but generally, about 12 hours to about 168 hours after the microspheres themselves reach a predetermined temperature. It is preferably about 24 hours to about 120 hours, particularly preferably about 48 hours to about 96 hours.
- the heating method is not particularly limited as long as the method is capable of uniformly heating the microsphere aggregate.
- the heating and drying method for example, a method of heating and drying in a constant temperature bath, a fluidizing bath, a moving tank or a kiln, a method of heating and drying with a microwave, and the like are used. Of these, a method of heating and drying in a thermostat is preferred.
- the resulting microspheres have a relatively uniform spherical morphology, have low resistance during injection administration, and are less prone to needle sticking. Also, since a thin needle can be used, the pain of the patient at the time of injection is reduced.
- a physiologically active substance or a salt thereof is added to an organic solvent solution of hydroxynaphthoic acid or a salt thereof so as to have a weight ratio as defined in the definition of the amount of the physiologically active substance.
- the organic solvent is the same as described in the above (I) and (i).
- the ratio between the two is the same as described in the above (I) and (i).
- an organic solvent solution containing a hydroxynaphthoate salt of a physiologically active substance is added to the aqueous phase to form an O (oil phase) / W (aqueous phase) emulsion, and then the solvent in the oil phase is evaporated.
- the volume of the aqueous phase at this time is generally about 1 to about 100,000 times the volume of the oil phase, more preferably about 5 to about 5,000 times, and particularly preferably about 10 to 100 times. Double to about 20000 times.
- the emulsifier and osmotic pressure regulator which may be added to the above external aqueous phase, and the subsequent preparation method are the same as those described in the above section (IV).
- the sustained-release composition of the present invention comprises microspheres, microcapsules, Particles), but when composed of two substances, a bioactive substance and hydroxynaphthoic acid, the microspheres are composed of a bioactive substance, hydroxynaphthoic acid and a biodegradable polymer. In the case of three members, a micro force cell is preferable.
- the sustained-release composition of the present invention can be formulated as it is or as a raw material into various dosage forms, and can be injected or implanted into intramuscular, subcutaneous, organs, etc., transmucosally into nasal cavity, rectum, uterus, etc.
- Drugs, oral preparations eg, capsules (eg, hard capsules, soft capsules, etc.), solid preparations such as granules and powders, syrups, emulsions, suspensions, etc.
- oral preparations eg, capsules (eg, hard capsules, soft capsules, etc.)
- solid preparations such as granules and powders, syrups, emulsions, suspensions, etc.
- a dispersant for example, a surfactant such as Tween 80 or HC0-60, sodium hyaluronate, lipoxymeter.
- a dispersant for example, a surfactant such as Tween 80 or HC0-60, sodium hyaluronate, lipoxymeter.
- Polysaccharides such as cellulose and sodium alginate, etc.
- preservatives eg, methylparaben, propylparaben, etc.
- tonicity agents eg, sodium chloride, mannitol, sorbitol, glucose, proline, etc.
- aqueous suspending agents eg, it can be dispersed with vegetable oils such as sesame oil and corn oil to give sustained-release injections that can be actually used as an oily suspension.
- the particle size of the sustained-release composition of the present invention may be within a range that satisfies the degree of dispersion and needle penetration.
- 0.1 to 300 m preferably in the range of about 0.5 to 150 m, more preferably in the range of about 1 to 100 m.
- a method of sterilizing the whole production process a method of sterilizing with gamma ray, a method of adding a preservative, and the like are mentioned, but are not particularly limited.
- the sustained-release composition of the present invention Since the sustained-release composition of the present invention has low toxicity, it can be used as a drug safe for mammals (eg, humans, cows, pigs, dogs, cats, mice, rats, rabbits, etc.). .
- the dose of the sustained-release composition of the present invention varies depending on the type and content of the physiologically active substance as the main drug, the dosage form, the duration of release of the physiologically active substance, the target disease, the target animal, and the like. Any effective amount of
- the sustained-release preparation is a 6-month preparation
- the dosage of the physiologically active substance as the main drug is preferably about 0.0 lmg to 1 Omg / kg body weight per adult. It can be appropriately selected from the range, more preferably from the range of about 0.05 mg to 5 mgZkg body weight.
- the dose of the sustained-release composition per dose is preferably selected from the range of about 0.05 mg to 5 OmgZkg body weight per adult, more preferably the range of about 0.1 mg to 30 mg / kg body weight. be able to.
- the frequency of administration may be once every few weeks, once a month, or once every few months (eg, 3 months, 4 months, 6 months, etc.). And the content, dosage form, duration of release of the bioactive substance, target disease, target animal, and the like.
- the sustained-release composition of the present invention can be used as a prophylactic / therapeutic agent for various diseases depending on the type of the physiologically active substance contained therein.
- the physiologically active substance is an LH-RH derivative.
- hormone-dependent diseases especially sex hormone-dependent cancers (eg, prostate, uterine, breast, pituitary, etc.), benign prostatic hyperplasia, endometriosis, uterine fibroids, precocious puberty, Prevention and treatment of sex hormone-dependent diseases such as dysmenorrhea, amenorrhea, premenstrual syndrome, and multilocular ovarian syndrome, and contraception (or use of the rebound effect after withdrawal from treatment) Can be used as an agent for the prevention and treatment of infertility.
- A peptide Acetate
- the solution was evacuated slowly using a rotary apparel and the organic solvent was evaporated. This residue was redissolved in 5.5 ml of dichloromethane and added to 400 ml of a 0.1 l% (w / w) polyvinyl alcohol (EG-40, manufactured by Nippon Synthetic Chemical) water solution that had been adjusted to 18 ° C in advance.
- the mixture was injected and stirred at 8, OOO rpm using a turbine type homomixer to obtain an O / W emulsion.
- the ⁇ / W emulsion was stirred at room temperature for 3 hours to volatilize dichloromethane, solidify the oil phase, sieved using a sieve with a mesh opening of 75 m, and centrifuged (05PR-22).
- microspheres were sedimented and collected at 2,000 ⁇ ⁇ ⁇ for 5 minutes using Hitachi, Ltd.). This was dispersed again in distilled water, and further centrifuged to wash free drug and the like, and microspheres were collected. The collected microspheres are redispersed by adding a small amount of distilled water, and freeze-dried. W
- l% (w / w) solution was poured into 900 ml of an aqueous solution of polyvinyl alcohol, and stirred at 7,000 ⁇ m using an evening bottle-type homomixer. And The ⁇ ZW emulsion is stirred at room temperature for 3 hours to diffuse the liquid and ethanol into the water phase or into the aqueous phase, and solidify the oil phase, and then sieve with a mesh opening of 75 m. Microcapsules at 2,000i "pm for 5 minutes using a centrifuge. Was settled and collected. This was dispersed again in distilled water, and further centrifuged to wash free drugs and the like, and microcapsules were collected.
- the collected microcapsules were redispersed by adding 250 mg of mannitol and a small amount of distilled water, and then freeze-dried to obtain a powder.
- the mass recovery of the microcapsules calculated by excluding the added mannitol was calculated to be 76%, and the peptide A content and the 3-hydroxy-2-naphthoic acid / peptide A molar ratio in the microcapsules were 34.7%, respectively. , 1.19.
- the encapsulation efficiency calculated by dividing the realized content by the charged content was 84.6%.
- Example 5 Subsequent operations were performed in the same manner as described in Example 3 to obtain a microphone-mouth capsule.
- the mass recovery of the microforce obtained by excluding the added mannitol was 85%, the peptide A content in the microcapsules and the molar ratio of 3-hydroxy-2-naphthoic acid nopeptide A were 3 respectively. 8.6%, 0.83.
- the encapsulation efficiency calculated by dividing the realized content by the charged content was 88.9%.
- This emulsion was poured into 800 ml of a 0.1% (w / w) aqueous solution of polyvinyl alcohol containing 5% mannitol, which had been adjusted to 18 ° C in advance, and stirred at 7, OOO rpm using a turbine-type homomixer to obtain a WZO ZW emulsion. And This WZO / W emulsion is stirred at room temperature for 3 hours to volatilize dichloromethane and ethanol or diffuse into the aqueous phase to solidify the oil phase, and then sieve using a sieve with a mesh opening of 75 // m. The microcapsules were collected by sedimentation using a centrifuge at 2, OOO rpm for 5 minutes.
- each microsphere obtained in Examples 1 and 2 or about 60 mg of each microcapsule obtained in Examples 3 to 5 was added to 0.5 ml of a dispersion medium (0.25 mg of carboxymethylcellulose, 5 mg of polysorbate 80 and 25 mg of mannitol in distilled water), and administered subcutaneously to the back of an 8- to 10-week-old male SD rat with a 22 G needle.
- a dispersion medium (0.25 mg of carboxymethylcellulose, 5 mg of polysorbate 80 and 25 mg of mannitol in distilled water
- the rats were sacrificed, and the microspheres or microcapsules remaining at the administration site were taken out.
- Peptide A in this was quantified and divided by the initial content, and the survival rate obtained is shown in Table 1.
- Example 5 81% 44% 25% 17% 13% From the experimental results of Examples 1 and 2, the release of peptide A from microspheres consisting of peptide A and 3-hydroxy-2-naphthoic acid was Depending on the difference in the ratio between the two, the release of peptide A was faster when the ratio of 3-hydroxy-2-naphthoic acid was higher. Also, according to the experimental results of Examples 3, 4 and 5, the microcapsules composed of three members to which the lactic acid-glycolic acid copolymer was added showed different results from the release of peptide A from the microspheres composed of only two members. It was clarified that the release behavior could be controlled by combining lactic acid-glycolic acid copolymers having different compositions, weight average molecular weights and terminal carboxyl groups. Example 7.
- peptide B 5-oxo-Pro-His-Trp-Ser-Tyr-DLeu-Leu-Arg-Pro-NH-C 2 H 5 (hereinafter abbreviated as peptide B; manufactured by Takeda Pharmaceutical)
- a solution dissolved in 0.8 ml of distilled water was added to a DL-lactic acid polymer (weight average molecular weight: 36,000, number average molecular weight: 18,000, lipoxyl group content by labeling assay 70.4 amol / g) 3.08 g and 0.12 g of 3-hydroxy-2-naphthoic acid were mixed with a solution of 5 ml of dichloromethane and 0.3 ml of ethanol in a mixed organic solvent and emulsified with a homogenizer to form a WZO emulsion.
- this WZO emulsion was poured into 800 ml of a 0.1% (w / w) aqueous solution of polyvinyl alcohol (EG-40, manufactured by Nippon Synthetic Chemical Industry) previously adjusted to 15 ° C. The mixture was stirred at 7, ⁇ to obtain a WZOZW emulsion.
- This WZOZW emulsion is stirred at room temperature for 3 hours to evaporate dichloromethane and ethanol or diffuse into the external aqueous phase, solidify the oil phase, sieve through a 75 m sieve, and then centrifuge Using a separator (05PR-22, Hitachi, Ltd.), the microcapsules were sedimented and collected at 1, OOOrpm for 5 minutes.
- a solution of 1. g of peptide B acetate in 1.2 ml of distilled water was added to a DL-lactic acid polymer (weight-average molecular weight 25,200, number-average molecular weight 12,800, and the amount of carboxyl group by labeling assay).
- 62.5 mol / g) 4.62 g and 0.18 g of 3-hydroxy-2-naphthoic acid were mixed with a solution of 7.5 ml of dichloromethane and 0.45 ml of ethanol in a mixed organic solvent, and emulsified with a homogenizer.
- a WZO emulsion was formed.
- this WZO emulsion was injected into 1200 ml of a 0.1% (w / w) aqueous solution of polyvinyl alcohol (EG-40, manufactured by Nippon Synthetic Chemical Industry) which had been adjusted to 15 ° C in advance.
- the mixture was stirred at 7,000 ⁇ ⁇ ⁇ using a mixer to obtain a WZOZW emulsion.
- This WZOZW emulsion was stirred at room temperature for 3 hours to evaporate dichloromethane and ethanol or diffuse into the external aqueous phase, solidify the oil phase, and then sieved using an Hm opening sieve.
- microcapsules were sedimented and collected at 2,000 rpm for 5 minutes using a centrifuge (05PR-22, Hitachi, Ltd.). This was dispersed again in distilled water, followed by further centrifugation to wash free drug and the like, and to collect a microcapsule.
- the collected microcapsules were redispersed in a small amount of distilled water, dissolved by adding 0.3 g of mannitol, and freeze-dried to obtain a powder.
- the mass recovery of the microcapsules calculated by excluding the added mannitol was 55.2%
- the content of peptide B in the microcapsules was 21.3%
- the content of 3-hydroxy-2-naphthoic acid was 2.96. %Met.
- the encapsulation efficiency determined by dividing these realized contents by the charged contents was 99.7% for peptide B and 102.2% for 3-hydroxy-2-naphthoic acid.
- Example 8 The DL-lactic acid polymer described in Example 8 was converted to a DL-lactic acid polymer (weight-average molecular weight: 28,800, number-average molecular weight: 14,500, lipoxyl group content by labeling determination method: 78.1 mol / g)
- Microcapsule powder was prepared in the same manner as described in Example 8 except that Obtained.
- the mass recovery of the microcapsules calculated by excluding the added mannitol was 50.2, the content of peptide B in the microcapsules was 20.8%, and the content of 3-hydroxy-2-naphthoic acid was 2.7. 8%.
- the encapsulation efficiencies determined by dividing these realized contents by the charged contents were 103.4% for peptide B and 92.7% for 3-hydroxy_2-naphthoic acid. Comparative Example 1
- a solution prepared by dissolving 1.g of peptide B acetate in 1.2 ml of distilled water was mixed with a solution of 4.8 g of DL-lactic acid polymer dissolved in 7.8 ml of dichloromethane as in Example 9 and homogenized.
- To form a W / O emulsion was formed.
- the W / ⁇ emulsion was poured into 1200 ml of a 0.1% (w / w) aqueous solution of polyvinyl alcohol (EG-40, manufactured by Nippon Synthetic Chemical Industry) previously adjusted to 15 ° C, and a turbine-type homomixer was added.
- EG-40 polyvinyl alcohol
- Example 10 Thereafter, the same operation as in Example 8 was performed to obtain a microcapsule powder.
- the mass recovery of the microcapsules calculated by excluding the added mannitol was 53.6%, and the peptide content in the microcapsules was 12.1%.
- the encapsulation rate of peptide ⁇ determined by dividing the realized content by the charged content was 60.6%, which is much lower than in Example 9. Therefore, it is clear that the encapsulation efficiency of the peptide was increased by the addition of 3-hydroxy-2-naphthoic acid.
- Example 10 Example 10
- a solution obtained by dissolving 1.00 g of peptide acetate in 1.00 ml of distilled water was added to a DL-lactic acid polymer (weight average molecular weight 49, 500, number average molecular weight 17,500, (45.9 amol / g) 3.85 g and 0.15 g of 3-hydroxy-2-naphthoic acid were mixed with a solution of 7.5 ml of dichloromethane and 0.4 ml of ethanol in a mixed organic solvent and mixed with a homogenizer. Emulsified to form a WZO emulsion.
- microcapsule powder was obtained in the same manner as described in Example 8, except that the amount of the aqueous solution of polyvinyl alcohol (w / w) was 1000 ml, and the amount of mannitol added was 0.257 g. .
- the mass recovery of the microcapsules calculated by excluding the added mannitol was 53.8%, the content of peptide B in the microcapsules was 18.02%, and the content of 3-hydroxy-2-naphthoic acid was 2.70%. there were.
- the encapsulation efficiency determined by dividing these realized contents by the charged contents was 90.1% for peptide B and 90.1% for 3-hydroxy-2-naphthoic acid.
- a solution of 202 g dissolved in 1.20 ml of distilled water was added to DL-lactic acid polymer (weight average molecular weight 19,900, number average molecular weight 10,700, (Amount of 104.6 mol / g) 4.
- a W / O emulsion was formed.
- a microcapsule powder was obtained in the same manner as in Example 8, except that the amount of mannitol added was 0.303 g.
- a solution prepared by dissolving 1.00 g of peptide B acetate in 1.000 ml of distilled water was added to a DL-lactic acid polymer (weight average molecular weight 25,900, number average molecular weight 7,100, terminal carboxyl group 98.2 mol / g) 3.85 g and 0.15 g of 3-hydroxy-12-naphthoic acid were mixed with a solution of 5.5 ml of dichloromethan and 0.35 ml of ethanol in a mixed organic solvent and homogenized.
- W weight average molecular weight 25,900, number average molecular weight 7,100, terminal carboxyl group 98.2 mol / g
- Example 7 The mixture was emulsified with a 45-genizer to form a WZO emulsion. Subsequent operations were performed in the same manner as described in Example 7 to obtain microcapsule powder. The mass recovery of the microcapsules was 48.8%, the content of peptide B in the microcapsules was 21.31%, and the content of 3-hydroxy-2-naphthoic acid was 2.96. Encapsulation efficiencies determined by dividing these realized contents by the charged contents were 106.5% for peptide B and 98.7% for 3-hydroxy-21-naphthoic acid. Comparative Example 2
- a solution obtained by dissolving 1.00 g of the acetate salt of peptide B in 1.00 ml of distilled water was mixed with a solution of 4.00 g of DL-lactic acid polymer dissolved in 5 ml of dichloromethane as in Example 12 and emulsified with a homogenizer. , Formed a W / ⁇ emulsion. Subsequent operations were performed in the same manner as described in Example 7 to obtain microcapsule powder. The mass recovery of the microcapsules was 48.7%, and the content of peptide B in the microcapsules was 11.41%.
- DL-lactic acid polymer (Weight average molecular weight 30,600, Number average molecular weight 14,400, Amount of lipoxyl group by labeling quantitative method 63.0 niol / g) 89.2 g dissolved in 11.3 g dichloromethane
- the obtained solution was mixed with a solution obtained by dissolving 3.45 g of 3-hydroxy-2-naphthoic acid in a mixed organic solvent of 38.8 g of dichloromethane and 6.27 g of ethanol, and the mixture was adjusted to 28.5 ° C.
- microcapsules were continuously sedimented at 2, OOO rpm using a centrifuge (H-600S, manufactured by Domestic Centrifuge) and collected.
- the collected microcapsules were re-dispersed in a small amount of distilled water, sieved using a 90-m mesh sieve, added with 9.98 g of mannitol, dissolved, and freeze-dried to obtain a powder.
- the mass recovery of the microcapsules calculated by excluding the added mannitol was 66.53 ⁇ 4, the content of peptide B in the microcapsules was 22.3%, and the content of 3-hydroxy_2-naphthoic acid was 2.99%.
- Met The encapsulation rates determined by dividing these realized contents by the charged contents were 104.5% for peptide B and 102.1% for 3-hydroxy-2-naphthoic acid.
- Example 8 About 45 mg of the microcapsules described in Example 8 was added to 0.3 ml of a dispersing medium (0.15 mg of rupoxymethylcellulose, 0.3 mg of polysorbate 80, and 15 mg of mannitol) in distilled water. They were dispersed and administered subcutaneously to the back of 7-week-old male SD rats with a 22G needle. After a predetermined time from the administration, the rats were sacrificed, and the microcapsules remaining at the administration site were removed. Peptide B and 3-hydroxy-2-naphthoic acid in this were quantified and determined by dividing by the respective initial contents. Table 2 shows the residual ratio and the characteristics of the DL-lactic acid polymer used. Table 2 Characteristics of DL-lactic acid polymer of microcapsules described in Example 8
- the microforce peptide described in Example 8 can be kept for one day after administration, despite having a high bioactive substance content.
- the survival rate of bioactive substances is dramatically higher at 90% or more. Therefore, 3-hydroxy-2-naphthoic acid not only has the effect of incorporating a high amount of a bioactive substance into a sustained-release preparation, but also has the effect of very effectively inhibiting the initial excessive release of the bioactive substance. It is obvious.
- These microcapsules have been able to release bioactive substances at a constant rate for a very long time.
- Example 7 Example 9 Example 1 0 Example 1 1 Example 1 2 Comparative Example 1
- Example 7 The microcapsules obtained in Example 7 were subcutaneously administered to rats by the method described in Experimental Example 2, and the blood was collected. The results of measuring the concentrations of peptide B and testosterone in the serum obtained in Table 4 are shown in Table 4. Show. Table 4
- the sustained-release composition of the present invention contains a high amount of a physiologically active substance, and can suppress the initial excessive release to realize a long-term stable release rate.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Endocrinology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Organic Chemistry (AREA)
- Reproductive Health (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Gastroenterology & Hepatology (AREA)
- Inorganic Chemistry (AREA)
- Zoology (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Description
Claims
Priority Applications (14)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SK1027-2000A SK10272000A3 (sk) | 1998-01-16 | 1999-01-13 | Prostriedok s trvalým uvoľňovaním, spôsob jeho výroby a jeho použitia |
AU18897/99A AU758596B2 (en) | 1998-01-16 | 1999-01-13 | Sustained release compositions, process for producing the same and utilization thereof |
EP99900300A EP1048301A4 (en) | 1998-01-16 | 1999-01-13 | COMPOSITIONS WITH DELAYED ACTIVE INGREDIENTS, PROCESS FOR THEIR PREPARATION AND THEIR USE |
CA002316273A CA2316273A1 (en) | 1998-01-16 | 1999-01-13 | Sustained-release composition, method of its production and use thereof |
HU0100221A HUP0100221A3 (en) | 1998-01-16 | 1999-01-13 | Sustained release compositions, process for producing the same and utilization thereof |
BR9906903-2A BR9906903A (pt) | 1998-01-16 | 1999-01-13 | Composição com liberação sustentada, processos para produzir a mesma, para suprimir a brusca liberação inicial da susbtância bioativa de uma composição com liberação sustentada e para aumentar a eficiência da inclusão da substância bioativa em uma composição com liberação sustentada, produto farmacêutico, agente para prevenir ou tratar câncer prostático, hipertrofia prostática, endometriose, histeromioma, metrofibroma, puberdade precoce, dismenorréia, ou câncer do seio, ou um contraceptivo, e, composto |
PL99341733A PL341733A1 (en) | 1998-01-16 | 1999-01-13 | Prolonged release composition, method of obtaining same and application thereof |
IL13695199A IL136951A0 (en) | 1998-01-16 | 1999-01-13 | Sustained-release composition, method of its production and use thereof |
NZ505651A NZ505651A (en) | 1998-01-16 | 1999-01-13 | Sustained release composition comprising biologically active substance, hydroxynaphthoic acid and biodegradable polymer |
US09/582,926 US6740634B1 (en) | 1998-01-16 | 1999-01-13 | Sustained release compositions, process for producing the same and utilization thereof |
NO20003530A NO20003530L (no) | 1998-01-16 | 2000-07-07 | Vedvarende frigivelsessammensetning, metode for dets produksjon og anvendelse derav |
IS5560A IS5560A (is) | 1998-01-16 | 2000-07-11 | Efnablanda með tafða losun, aðferð til að framleiða hana og notkun hennar |
HR20000471A HRP20000471A2 (en) | 1998-01-16 | 2000-07-13 | Sustained-release composition, method of its production and the use thereof |
US10/799,320 US7388032B2 (en) | 1998-01-16 | 2004-03-12 | Sustained release compositions, process for producing the same and utilization thereof |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10/6412 | 1998-01-16 | ||
JP641298 | 1998-01-16 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09582926 A-371-Of-International | 1999-01-13 | ||
US10/799,320 Division US7388032B2 (en) | 1998-01-16 | 2004-03-12 | Sustained release compositions, process for producing the same and utilization thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1999036099A1 true WO1999036099A1 (fr) | 1999-07-22 |
WO1999036099A8 WO1999036099A8 (fr) | 1999-11-18 |
Family
ID=11637664
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1999/000086 WO1999036099A1 (fr) | 1998-01-16 | 1999-01-13 | Compositions a liberation controlee, leur procede de fabrication et leur utilisation |
Country Status (19)
Country | Link |
---|---|
US (2) | US6740634B1 (ja) |
EP (1) | EP1048301A4 (ja) |
KR (1) | KR100577877B1 (ja) |
CN (1) | CN1199686C (ja) |
AU (1) | AU758596B2 (ja) |
BR (1) | BR9906903A (ja) |
CA (1) | CA2316273A1 (ja) |
HR (1) | HRP20000471A2 (ja) |
HU (1) | HUP0100221A3 (ja) |
IL (1) | IL136951A0 (ja) |
IS (1) | IS5560A (ja) |
NO (1) | NO20003530L (ja) |
NZ (1) | NZ505651A (ja) |
OA (1) | OA11446A (ja) |
PL (1) | PL341733A1 (ja) |
RU (1) | RU2230550C2 (ja) |
SK (1) | SK10272000A3 (ja) |
TR (1) | TR200002059T2 (ja) |
WO (1) | WO1999036099A1 (ja) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001005380A1 (fr) * | 1999-07-15 | 2001-01-25 | Takeda Chemical Industries, Ltd. | Compositions a liberation lente, techniques de production et methodes d'utilisation |
WO2002002144A1 (en) | 2000-07-05 | 2002-01-10 | Takeda Chemical Industries, Ltd. | Medicinal preparations for treating sex hormone-dependent diseases |
WO2002014347A2 (de) * | 2000-08-17 | 2002-02-21 | Zentaris Ag | Verfahren zur herstellung von peptidsalzen, deren verwendung und die peptidsalze enthaltende pharmazeutische zubereitungen |
WO2002043766A1 (fr) * | 2000-11-29 | 2002-06-06 | Takeda Chemical Industries, Ltd. | Compositions medicinales et leur procede de preparation |
WO2002047722A1 (fr) * | 2000-12-15 | 2002-06-20 | Takeda Chemical Industries, Ltd. | Compositions medicinales agoniste ou antagoniste de la gonadoliberine non peptidyl, methode de production et utilisation desdites compositions |
WO2002087616A1 (fr) * | 2001-04-25 | 2002-11-07 | Takeda Chemical Industries, Ltd. | Remedes contre la recurrence postoperative du cancer du sein chez les femmes en premenopause |
EP1158014A4 (en) * | 1998-12-15 | 2003-01-22 | Takeda Chemical Industries Ltd | METHOD FOR PRODUCING POLYMERS |
WO2003041739A1 (en) | 2001-11-13 | 2003-05-22 | Takeda Chemical Industries, Ltd. | Anticaner agents |
US7019106B2 (en) | 2000-08-07 | 2006-03-28 | Wako Pure Chemical Industries, Ltd. | Lactic acid polymer and process for producing the same |
US20060228414A1 (en) * | 2003-07-15 | 2006-10-12 | Pr Phamaceuticals, Inc | Method for the preparation of controlled release formulations |
JP2010513225A (ja) * | 2006-12-18 | 2010-04-30 | 武田薬品工業株式会社 | 徐放性組成物およびその製造法 |
US8088726B2 (en) * | 2002-06-25 | 2012-01-03 | Takeda Pharmaceutical Company Limited | Process for producing sustained-release composition |
US8815801B2 (en) * | 2001-06-29 | 2014-08-26 | Takeda Pharmaceutical Company Limited | Controlled release composition and method of producing the same |
US8900636B2 (en) | 2003-07-23 | 2014-12-02 | Evonik Corporation | Controlled release compositions |
US8916196B2 (en) | 2003-04-10 | 2014-12-23 | Evonik Corporation | Method for the production of emulsion-based microparticles |
Families Citing this family (105)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6828415B2 (en) * | 1993-02-19 | 2004-12-07 | Zentaris Gmbh | Oligopeptide lyophilisate, their preparation and use |
EP1374855A1 (en) * | 2001-03-30 | 2004-01-02 | Takeda Chemical Industries, Ltd. | Medicinal solutions |
US7344507B2 (en) | 2002-04-19 | 2008-03-18 | Pelikan Technologies, Inc. | Method and apparatus for lancet actuation |
TWI225416B (en) * | 2001-06-29 | 2004-12-21 | Takeda Chemical Industries Ltd | Sustained-release composition and process for producing the same |
WO2003015820A1 (fr) * | 2001-08-10 | 2003-02-27 | Takeda Chemical Industries, Ltd. | Medicaments combines d'agoniste de la gnrh |
AU2002358831B2 (en) | 2001-10-10 | 2007-09-06 | Pierre Fabre Medicament | Prolonged release biodegradable microspheres and method for preparing same |
WO2003055470A1 (fr) * | 2001-12-26 | 2003-07-10 | Takeda Chemical Industries, Ltd. | Nouvelle microsphere et son procede de production |
US7674232B2 (en) | 2002-04-19 | 2010-03-09 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
WO2004029129A1 (ja) * | 2002-09-24 | 2004-04-08 | Asahi Kasei Chemicals Corporation | グリコール酸共重合体及びその製造方法 |
US20070207211A1 (en) * | 2003-04-10 | 2007-09-06 | Pr Pharmaceuticals, Inc. | Emulsion-based microparticles and methods for the production thereof |
CA2544733A1 (en) * | 2003-10-09 | 2005-04-21 | Inverseon, Inc. | Methods for treating diseases and conditions with inverse agonists and for screening for agents acting as inverse agonists |
US20070276024A1 (en) * | 2003-10-09 | 2007-11-29 | Inverseon , Inc. | Methods for Treating Diseases and Conditions with Inverse Agonists and for Screening for Agents Acting as Inverse Agonists |
TW200529890A (en) * | 2004-02-10 | 2005-09-16 | Takeda Pharmaceutical | Sustained-release preparations |
TW200613012A (en) * | 2004-07-02 | 2006-05-01 | Takeda Pharmaceuticals Co | Sustained-release composition, process for producing the same and use of the same |
US7528175B2 (en) * | 2004-10-08 | 2009-05-05 | Inverseon, Inc. | Method of treating airway diseases with beta-adrenergic inverse agonists |
US20060222716A1 (en) * | 2005-04-01 | 2006-10-05 | Joseph Schwarz | Colloidal solid lipid vehicle for pharmaceutical use |
EP1866319B1 (en) | 2005-04-01 | 2011-11-23 | The Regents of The University of California | Phosphono-pent-2-en-1-yl nucleosides and analogs |
US20090156545A1 (en) * | 2005-04-01 | 2009-06-18 | Hostetler Karl Y | Substituted Phosphate Esters of Nucleoside Phosphonates |
EP1716847B1 (en) * | 2005-04-28 | 2008-01-02 | Nipro Corporation | Bioabsorbable pharmaceutical formulation comprising a PLGA copolymer |
US20070027107A1 (en) * | 2005-07-29 | 2007-02-01 | Curt Hendrix | Compositions and methods for treating estrogen-dependent diseases and conditions |
EP3363455A1 (en) | 2005-12-30 | 2018-08-22 | Zensun (Shanghai) Science & Technology, Co., Ltd. | Extended release of neuregulin for improved cardiac function |
PL2383271T3 (pl) * | 2006-03-13 | 2013-12-31 | Kyorin Seiyaku Kk | Aminochinolony jako inhibitory GSK-3 |
JP2009530280A (ja) * | 2006-03-13 | 2009-08-27 | エンサイシブ・ファーマシューティカルズ・インコーポレイテッド | シタクスセンタンナトリウムの配合物 |
JP2009530284A (ja) * | 2006-03-13 | 2009-08-27 | エンサイシブ・ファーマシューティカルズ・インコーポレイテッド | 拡張期心不全を治療するための方法と組成物 |
US20080026061A1 (en) * | 2006-06-22 | 2008-01-31 | Reichwein John F | Crystalline N-(4-chloro-3-methyl-5-isoxazolyl)-2-[2-methyl-4.5-(methylenedioxy)phenylacetyl]-thiophene-3-sulfonamide |
EP2066662B1 (en) | 2006-09-21 | 2012-12-05 | Kyorin Pharmaceutical Co., Ltd. | Serine hydrolase inhibitors |
WO2008057604A2 (en) * | 2006-11-08 | 2008-05-15 | The Regents Of The University Of California | Small molecule therapeutics, syntheses of analogues and derivatives and methods of use |
US7892776B2 (en) | 2007-05-04 | 2011-02-22 | The Regents Of The University Of California | Screening assay to identify modulators of protein kinase A |
RU2343908C1 (ru) * | 2007-09-05 | 2009-01-20 | Руслан Дмитриевич Илюк | Средство для профилактики и лечения алкоголизма и способ его применения |
MX2010002667A (es) * | 2007-09-11 | 2010-04-01 | Activx Biosciences Inc | Cianoaminoquinolonas y tetrazoloaminoquinolonas como inhibidores de gsk-3. |
BRPI0816814B1 (pt) | 2007-09-12 | 2021-08-31 | Kyorin Pharmaceutical Co. Ltd | Composto, composição farmacêutica e uso de um composto |
WO2009139880A1 (en) * | 2008-05-13 | 2009-11-19 | Celgene Corporation | Thioxoisoindoline compounds and compositions and methods of using the same |
CN102395576A (zh) * | 2009-02-27 | 2012-03-28 | 埃姆比特生物科学公司 | 调控jak激酶的喹唑啉衍生物和其使用方法 |
AU2010221990B2 (en) | 2009-03-11 | 2015-06-04 | Kyorin Pharmaceutical Co., Ltd. | 7-cycloalkylaminoquinolones as GSK-3 inhibitors |
CA2770454A1 (en) | 2009-08-19 | 2011-02-24 | Ambit Biosciences Corporation | Biaryl compounds and methods of use thereof |
US20110301235A1 (en) | 2009-12-02 | 2011-12-08 | Alquest Therapeutics, Inc. | Organoselenium compounds and uses thereof |
IN2012DN04858A (ja) * | 2009-12-23 | 2015-09-25 | Map Pharmaceuticals Inc | |
WO2011150201A2 (en) | 2010-05-27 | 2011-12-01 | Ambit Biosciences Corporation | Azolyl amide compounds and methods of use thereof |
US9296722B2 (en) | 2010-05-27 | 2016-03-29 | Ambit Biosciences Corporation | Azolyl urea compounds and methods of use thereof |
US8633207B2 (en) | 2010-09-01 | 2014-01-21 | Ambit Biosciences Corporation | Quinazoline compounds and methods of use thereof |
MX2013006166A (es) * | 2010-12-15 | 2013-08-01 | 3M Innovative Properties Co | Fibras degradables. |
EP3513787A1 (en) | 2011-01-10 | 2019-07-24 | Invion, Inc | Use of beta-adrenergic inverse agonists for smoking cessation |
AR082266A1 (es) * | 2011-05-13 | 2012-11-28 | Univ Nac Del Litoral | Microparticula inyectable de liberacion controlada |
MX2013015373A (es) | 2011-06-23 | 2014-02-11 | Map Pharmaceuticals Inc | Nuevos analogos de fluoroergolina. |
JP6162130B2 (ja) | 2011-10-14 | 2017-07-12 | アムビト ビオスシエンセス コルポラチオン | Iii型受容体チロシンキナーゼの調節因子としての複素環式化合物及びその使用 |
CA2859173A1 (en) | 2011-12-19 | 2013-06-27 | Map Pharmaceuticals, Inc. | Novel iso-ergoline derivatives |
US8946420B2 (en) | 2011-12-21 | 2015-02-03 | Map Pharmaceuticals, Inc. | Neuromodulatory compounds |
US9012640B2 (en) | 2012-06-22 | 2015-04-21 | Map Pharmaceuticals, Inc. | Cabergoline derivatives |
US8895743B2 (en) | 2012-12-21 | 2014-11-25 | Map Pharmaceuticals, Inc. | Methysergide derivatives |
CN105683182A (zh) | 2013-08-30 | 2016-06-15 | 埃姆比特生物科学公司 | 联芳基乙酰胺化合物及其使用方法 |
US9499514B2 (en) | 2014-07-11 | 2016-11-22 | Celgene Corporation | Antiproliferative compounds and methods of use thereof |
TW201618783A (zh) | 2014-08-07 | 2016-06-01 | 艾森塔製藥公司 | 以布魯頓(Bruton)氏酪胺酸激酶(BTK)佔據和BTK再合成速率為基礎之治療癌症、免疫和自體免疫疾病及發炎性疾病之方法 |
US20170319548A1 (en) | 2014-09-12 | 2017-11-09 | Tobira Therapeutics, Inc. | Cenicriviroc combination therapy for the treatment of fibrosis |
EP3209658A1 (en) | 2014-10-24 | 2017-08-30 | Biogen MA Inc. | Diterpenoid derivatives and methods of use thereof |
EP3253753A4 (en) | 2015-01-20 | 2018-06-27 | Xoc Pharmaceuticals, Inc | Ergoline compounds and uses thereof |
AU2016209490B2 (en) | 2015-01-20 | 2020-09-03 | Xoc Pharmaceuticals, Inc. | Isoergoline compounds and uses thereof |
PT3640345T (pt) | 2015-08-17 | 2021-12-29 | Kura Oncology Inc | Métodos de tratamento de doentes com cancro usando inibidores da farnesiltransferase |
US10112924B2 (en) | 2015-12-02 | 2018-10-30 | Astraea Therapeutics, Inc. | Piperdinyl nociceptin receptor compounds |
MX367669B (es) | 2016-01-08 | 2019-08-30 | Celgene Corp | Compuestos antiproliferativos y sus composiciones farmacéuticas y usos. |
TWI733734B (zh) | 2016-01-08 | 2021-07-21 | 美商西建公司 | 2-(4-氯苯基)-n-((2-(2,6-二氧六氫吡啶-3-基)-1-氧基異吲哚啉-5-基)甲基)-2,2-二氟乙醯胺之固體型式,及其醫藥組合物及用途 |
US10047077B2 (en) | 2016-04-13 | 2018-08-14 | Skyline Antiinfectives, Inc. | Deuterated O-sulfated beta-lactam hydroxamic acids and deuterated N-sulfated beta-lactams |
US20190119758A1 (en) | 2016-04-22 | 2019-04-25 | Kura Oncology, Inc. | Methods of selecting cancer patients for treatment with farnesyltransferase inhibitors |
DK3534885T3 (da) | 2016-11-03 | 2021-04-12 | Kura Oncology Inc | Farnesyltransferase-inhibitorer til anvendelse i behandling af kræft |
WO2018089692A1 (en) | 2016-11-09 | 2018-05-17 | Phloronol, Inc. | Eckol derivatives, methods of synthesis and uses thereof |
EP3432883B1 (en) | 2017-02-21 | 2021-07-28 | Kura Oncology, Inc. | Methods of treating cancer with farnesyltransferase inhibitors |
US10137121B2 (en) | 2017-02-21 | 2018-11-27 | Kura Oncology, Inc. | Methods of treating cancer with farnesyltransferase inhibitors |
US10085999B1 (en) | 2017-05-10 | 2018-10-02 | Arixa Pharmaceuticals, Inc. | Beta-lactamase inhibitors and uses thereof |
JP2020522504A (ja) | 2017-06-01 | 2020-07-30 | エックスオーシー ファーマシューティカルズ インコーポレイテッドXoc Pharmaceuticals, Inc | 多環式化合物およびそれらの用途 |
MY200746A (en) | 2017-08-07 | 2024-01-13 | Kura Oncology Inc | Methods of treating cancer with farnesyltransferase inhibitors |
US10806730B2 (en) | 2017-08-07 | 2020-10-20 | Kura Oncology, Inc. | Methods of treating cancer with farnesyltransferase inhibitors |
WO2019113269A1 (en) | 2017-12-08 | 2019-06-13 | Kura Oncology, Inc. | Methods of treating cancer patients with farnesyltransferase inhibitors |
CA3117968A1 (en) | 2018-11-01 | 2020-05-07 | Kura Oncology, Inc. | Methods of treating cancer with farnesyltransferase inhibitors |
JP7407461B2 (ja) | 2018-12-19 | 2024-01-04 | シャイ・セラピューティクス・エルエルシー | がん、炎症性疾患、ras病、及び線維性疾患の処置のためのrasスーパーファミリーと相互作用する化合物 |
CA3124616A1 (en) | 2018-12-21 | 2020-06-25 | Kura Oncology, Inc. | Therapies for squamous cell carcinomas |
WO2020163554A1 (en) | 2019-02-06 | 2020-08-13 | Dice Alpha, Inc. | Il-17a modulators and uses thereof |
US20220142983A1 (en) | 2019-03-01 | 2022-05-12 | Kura Oncology, Inc. | Methods of treating cancer with farnesyltransferase inhibitors |
WO2020190604A1 (en) | 2019-03-15 | 2020-09-24 | Kura Oncology, Inc. | Methods of treating cancer patients with farnesyltransferase inhibitors |
CN113795253A (zh) | 2019-03-29 | 2021-12-14 | 库拉肿瘤学公司 | 用法呢基转移酶抑制剂治疗鳞状细胞癌的方法 |
TW202102218A (zh) | 2019-04-01 | 2021-01-16 | 美商庫拉腫瘤技術股份有限公司 | 以法呢基(farnesyl)轉移酶抑制劑治療癌症的方法 |
US20220305001A1 (en) | 2019-05-02 | 2022-09-29 | Kura Oncology, Inc. | Methods of treating acute myeloid leukemia with farnesyltransferase inhibitors |
KR20220101075A (ko) | 2019-09-16 | 2022-07-19 | 다이스 알파, 인크. | Il-17a 조절인자 및 이의 용도 |
US11529331B2 (en) | 2020-05-29 | 2022-12-20 | Boulder Bioscience Llc | Methods for improved endovascular thrombectomy using 3,3′-diindolylmethane |
WO2021257828A1 (en) | 2020-06-18 | 2021-12-23 | Shy Therapeutics, Llc | Substituted thienopyrimidines that interact with the ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease |
WO2022006228A1 (en) | 2020-06-30 | 2022-01-06 | Prosetta Biosciences, Inc. | Isoquinoline derivatives, methods of synthesis and uses thereof |
WO2022165000A1 (en) | 2021-01-27 | 2022-08-04 | Shy Therapeutics, Llc | Methods for the treatment of fibrotic disease |
WO2022164997A1 (en) | 2021-01-27 | 2022-08-04 | Shy Therapeutics, Llc | Methods for the treatment of fibrotic disease |
CR20230472A (es) | 2021-03-10 | 2024-03-21 | Dice Molecules Sv Inc | Inhibidores de integrina alpha v beta 6 y alpha v beta 1 y sus usos |
EP4326721A1 (en) | 2021-04-22 | 2024-02-28 | Protego Biopharma, Inc. | Spirocyclic imidazolidinones and imidazolidinediones for treatment of light chain amyloidosis |
EP4347568A1 (en) | 2021-05-27 | 2024-04-10 | Protego Biopharma, Inc. | Heteroaryl diamide ire1/xbp1s activators |
WO2023069770A1 (en) | 2021-10-22 | 2023-04-27 | Prosetta Biosciences, Inc. | Novel host-targeted pan-respiratory antiviral small molecule therapeutics |
WO2023102378A1 (en) | 2021-11-30 | 2023-06-08 | Kura Oncology, Inc. | Macrocyclic compounds having farnesyltransferase inhibitory activity |
WO2023129576A2 (en) | 2022-01-03 | 2023-07-06 | Lilac Therapeutics, Inc. | Acyclic thiol prodrugs |
US11932665B2 (en) | 2022-01-03 | 2024-03-19 | Lilac Therapeutics, Inc. | Cyclic thiol prodrugs |
WO2023192904A1 (en) | 2022-03-30 | 2023-10-05 | Biomarin Pharmaceutical Inc. | Dystrophin exon skipping oligonucleotides |
GB2619907A (en) | 2022-04-01 | 2023-12-27 | Kanna Health Ltd | Novel crystalline salt forms of mesembrine |
WO2023201282A1 (en) | 2022-04-14 | 2023-10-19 | Bristol-Myers Squibb Company | Novel gspt1 compounds and methods of use of the novel compounds |
WO2023201348A1 (en) | 2022-04-15 | 2023-10-19 | Celgene Corporation | Methods for predicting responsiveness of lymphoma to drug and methods for treating lymphoma |
WO2023215781A1 (en) | 2022-05-05 | 2023-11-09 | Biomarin Pharmaceutical Inc. | Method of treating duchenne muscular dystrophy |
WO2024054832A1 (en) | 2022-09-09 | 2024-03-14 | Innovo Therapeutics, Inc. | CK1α AND DUAL CK1α / GSPT1 DEGRADING COMPOUNDS |
US20240131005A1 (en) | 2022-09-30 | 2024-04-25 | Boulder Bioscience Llc | Compositions and methods for treating non-hemorrhagic closed head injury |
US20240174672A1 (en) | 2022-10-26 | 2024-05-30 | Protego Biopharma, Inc. | Spirocycle Containing Pyridone Compounds |
WO2024092040A1 (en) | 2022-10-26 | 2024-05-02 | Protego Biopharma, Inc. | Spirocycle containing bicyclic heteroaryl compounds |
WO2024092043A1 (en) | 2022-10-26 | 2024-05-02 | Protego Biopharma, Inc. | Spirocycle containing pyridine compounds |
WO2024118801A1 (en) | 2022-11-30 | 2024-06-06 | Protego Biopharma, Inc. | Linear heteroaryl diamide ire1/xbp1s activators |
WO2024118810A1 (en) | 2022-11-30 | 2024-06-06 | Protego Biopharma, Inc. | Cyclic pyrazole diamide ire1/xbp1s activators |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0515997A (ja) * | 1990-08-10 | 1993-01-26 | Yoshitsuka Seiki:Kk | 粉末成形プレス |
JPH08259460A (ja) * | 1995-01-23 | 1996-10-08 | Takeda Chem Ind Ltd | 徐放性製剤の製造法 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4049640A (en) * | 1975-12-12 | 1977-09-20 | American Cyanamid Company | Substituted bisnaphthylazo diphenyl ureido complement inhibitors |
US4211769A (en) * | 1977-08-24 | 1980-07-08 | Takeda Chemical Industries, Ltd. | Preparations for vaginal administration |
US4272398A (en) * | 1978-08-17 | 1981-06-09 | The United States Of America As Represented By The Secretary Of Agriculture | Microencapsulation process |
US5270305A (en) * | 1989-09-08 | 1993-12-14 | Glaxo Group Limited | Medicaments |
US5869097A (en) * | 1992-11-02 | 1999-02-09 | Alza Corporation | Method of therapy comprising an osmotic caplet |
WO1996022786A1 (en) | 1995-01-23 | 1996-08-01 | Takeda Chemical Industries, Ltd. | Sustained-release preparation and use |
US5565188A (en) * | 1995-02-24 | 1996-10-15 | Nanosystems L.L.C. | Polyalkylene block copolymers as surface modifiers for nanoparticles |
US6132768A (en) * | 1995-07-05 | 2000-10-17 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Oral pharmaceutical composition with delayed release of active ingredient for reversible proton pump inhibitors |
US5840835A (en) * | 1995-10-30 | 1998-11-24 | Merck & Co., Inc. | Inhibitors of peptide binding to MHC class II proteins |
US5635765A (en) * | 1996-02-26 | 1997-06-03 | Cypress Semiconductor Corporation | Multi-layer gate structure |
DK0889722T3 (da) | 1996-03-28 | 2003-02-10 | Takeda Chemical Industries Ltd | Præparat med forsinket frigivelse og fremstilling deraf |
GB9611194D0 (en) * | 1996-05-29 | 1996-07-31 | Smithkline Beecham Plc | Container |
AU730546B2 (en) * | 1996-11-15 | 2001-03-08 | Pathogenesis Corporation | Pure biologically active colistin, its components and a colistin formulation for treatment of pulmonary infections |
WO1998032423A1 (en) | 1997-01-29 | 1998-07-30 | Takeda Chemical Industries, Ltd. | Sustained-release microspheres, their production and use |
SK342002A3 (en) * | 1999-07-15 | 2002-05-09 | Takeda Chemical Industries Ltd | Sustained release compositions, process for producing the same and use thereof |
AR034641A1 (es) | 2001-06-29 | 2004-03-03 | Takeda Pharmaceutical | Composicion de liberacion controlada y metodo para producirla |
-
1999
- 1999-01-13 RU RU2000121545/15A patent/RU2230550C2/ru not_active IP Right Cessation
- 1999-01-13 BR BR9906903-2A patent/BR9906903A/pt not_active IP Right Cessation
- 1999-01-13 CA CA002316273A patent/CA2316273A1/en not_active Abandoned
- 1999-01-13 SK SK1027-2000A patent/SK10272000A3/sk unknown
- 1999-01-13 IL IL13695199A patent/IL136951A0/xx not_active IP Right Cessation
- 1999-01-13 EP EP99900300A patent/EP1048301A4/en not_active Withdrawn
- 1999-01-13 TR TR2000/02059T patent/TR200002059T2/xx unknown
- 1999-01-13 HU HU0100221A patent/HUP0100221A3/hu unknown
- 1999-01-13 AU AU18897/99A patent/AU758596B2/en not_active Ceased
- 1999-01-13 WO PCT/JP1999/000086 patent/WO1999036099A1/ja not_active Application Discontinuation
- 1999-01-13 US US09/582,926 patent/US6740634B1/en not_active Expired - Fee Related
- 1999-01-13 NZ NZ505651A patent/NZ505651A/en unknown
- 1999-01-13 CN CNB998021148A patent/CN1199686C/zh not_active Expired - Fee Related
- 1999-01-13 PL PL99341733A patent/PL341733A1/xx unknown
- 1999-01-13 KR KR1020007007533A patent/KR100577877B1/ko not_active IP Right Cessation
-
2000
- 2000-07-07 NO NO20003530A patent/NO20003530L/no not_active Application Discontinuation
- 2000-07-11 IS IS5560A patent/IS5560A/is unknown
- 2000-07-13 HR HR20000471A patent/HRP20000471A2/hr not_active Application Discontinuation
- 2000-07-14 OA OA1200000208A patent/OA11446A/en unknown
-
2004
- 2004-03-12 US US10/799,320 patent/US7388032B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0515997A (ja) * | 1990-08-10 | 1993-01-26 | Yoshitsuka Seiki:Kk | 粉末成形プレス |
JPH08259460A (ja) * | 1995-01-23 | 1996-10-08 | Takeda Chem Ind Ltd | 徐放性製剤の製造法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP1048301A4 * |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1158014A4 (en) * | 1998-12-15 | 2003-01-22 | Takeda Chemical Industries Ltd | METHOD FOR PRODUCING POLYMERS |
US6756472B1 (en) | 1998-12-15 | 2004-06-29 | Takeda Chemical Industries, Ltd. | Process for producing polymer |
US7265157B1 (en) | 1999-07-15 | 2007-09-04 | Takeda Pharmaceutical Company Limited | Sustained release compositions, process for producing the same and use thereof |
WO2001005380A1 (fr) * | 1999-07-15 | 2001-01-25 | Takeda Chemical Industries, Ltd. | Compositions a liberation lente, techniques de production et methodes d'utilisation |
WO2002002144A1 (en) | 2000-07-05 | 2002-01-10 | Takeda Chemical Industries, Ltd. | Medicinal preparations for treating sex hormone-dependent diseases |
US8092830B2 (en) | 2000-08-07 | 2012-01-10 | Wako Pure Chemical Industries, Ltd. | Lactic acid polymer and process for producing the same |
US7019106B2 (en) | 2000-08-07 | 2006-03-28 | Wako Pure Chemical Industries, Ltd. | Lactic acid polymer and process for producing the same |
WO2002014347A2 (de) * | 2000-08-17 | 2002-02-21 | Zentaris Ag | Verfahren zur herstellung von peptidsalzen, deren verwendung und die peptidsalze enthaltende pharmazeutische zubereitungen |
WO2002014347A3 (de) * | 2000-08-17 | 2002-08-08 | Zentaris Ag | Verfahren zur herstellung von peptidsalzen, deren verwendung und die peptidsalze enthaltende pharmazeutische zubereitungen |
US6780972B2 (en) | 2000-08-17 | 2004-08-24 | Zentaris Gmbh | Method for the synthesis of peptide salts, their use and the pharmaceutical preparations, containing peptide salts |
WO2002043766A1 (fr) * | 2000-11-29 | 2002-06-06 | Takeda Chemical Industries, Ltd. | Compositions medicinales et leur procede de preparation |
WO2002047722A1 (fr) * | 2000-12-15 | 2002-06-20 | Takeda Chemical Industries, Ltd. | Compositions medicinales agoniste ou antagoniste de la gonadoliberine non peptidyl, methode de production et utilisation desdites compositions |
WO2002087616A1 (fr) * | 2001-04-25 | 2002-11-07 | Takeda Chemical Industries, Ltd. | Remedes contre la recurrence postoperative du cancer du sein chez les femmes en premenopause |
US20060160745A1 (en) * | 2001-04-25 | 2006-07-20 | Yasutaka Igari | Agents for preventing postoperative recurrence of premenopausal breast cancer |
US8815801B2 (en) * | 2001-06-29 | 2014-08-26 | Takeda Pharmaceutical Company Limited | Controlled release composition and method of producing the same |
WO2003041739A1 (en) | 2001-11-13 | 2003-05-22 | Takeda Chemical Industries, Ltd. | Anticaner agents |
US8088726B2 (en) * | 2002-06-25 | 2012-01-03 | Takeda Pharmaceutical Company Limited | Process for producing sustained-release composition |
US8916196B2 (en) | 2003-04-10 | 2014-12-23 | Evonik Corporation | Method for the production of emulsion-based microparticles |
US10272044B2 (en) | 2003-04-10 | 2019-04-30 | Evonik Corporation | Method for the production of emulsion-based microparticles |
US20060228414A1 (en) * | 2003-07-15 | 2006-10-12 | Pr Phamaceuticals, Inc | Method for the preparation of controlled release formulations |
US8871269B2 (en) * | 2003-07-15 | 2014-10-28 | Evonik Corporation | Method for the preparation of controlled release formulations |
US8900636B2 (en) | 2003-07-23 | 2014-12-02 | Evonik Corporation | Controlled release compositions |
JP2010513225A (ja) * | 2006-12-18 | 2010-04-30 | 武田薬品工業株式会社 | 徐放性組成物およびその製造法 |
JP2010222371A (ja) * | 2006-12-18 | 2010-10-07 | Takeda Chem Ind Ltd | 徐放性組成物およびその製造法 |
Also Published As
Publication number | Publication date |
---|---|
WO1999036099A8 (fr) | 1999-11-18 |
PL341733A1 (en) | 2001-05-07 |
CA2316273A1 (en) | 1999-07-22 |
AU1889799A (en) | 1999-08-02 |
CN1288387A (zh) | 2001-03-21 |
HUP0100221A3 (en) | 2002-11-28 |
US20050025826A1 (en) | 2005-02-03 |
NZ505651A (en) | 2003-08-29 |
EP1048301A4 (en) | 2005-03-09 |
AU758596B2 (en) | 2003-03-27 |
BR9906903A (pt) | 2000-12-12 |
IS5560A (is) | 2000-07-11 |
RU2230550C2 (ru) | 2004-06-20 |
KR20010033949A (ko) | 2001-04-25 |
NO20003530D0 (no) | 2000-07-07 |
CN1199686C (zh) | 2005-05-04 |
OA11446A (en) | 2004-04-30 |
SK10272000A3 (sk) | 2001-01-18 |
US6740634B1 (en) | 2004-05-25 |
IL136951A0 (en) | 2001-06-14 |
HRP20000471A2 (en) | 2000-12-31 |
EP1048301A1 (en) | 2000-11-02 |
US7388032B2 (en) | 2008-06-17 |
KR100577877B1 (ko) | 2006-05-09 |
NO20003530L (no) | 2000-09-14 |
TR200002059T2 (tr) | 2001-01-22 |
HUP0100221A2 (hu) | 2001-06-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO1999036099A1 (fr) | Compositions a liberation controlee, leur procede de fabrication et leur utilisation | |
JP4819172B2 (ja) | 徐放性組成物およびその製造法 | |
JP5622760B2 (ja) | 乳酸重合体及びその製造方法 | |
US20080014237A1 (en) | Sustained release compositions, process for producing the same and use thereof | |
US20040241229A1 (en) | Sustained-release composition and process for producing the same | |
CA2355186C (en) | Process for producing polymer | |
JPH11269094A (ja) | 徐放性組成物、その製造法および用途 | |
JP3716146B2 (ja) | ポリマーの製造方法 | |
JP2003206243A (ja) | 徐放性組成物およびその製造法 | |
JP2001081043A (ja) | 徐放性組成物、その製造法および用途 | |
JP2004256546A (ja) | 徐放性組成物およびその製造法 | |
JP2004155792A (ja) | 徐放性組成物およびその製造法 | |
MXPA00006641A (en) | Sustained release compositions, process for producing the same and utilization thereof | |
CZ20002470A3 (cs) | Prostředek s trvalým uvolňováním, způsob jeho výroby a jeho použití |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 136951 Country of ref document: IL Ref document number: 1200000712 Country of ref document: VN Ref document number: 99802114.8 Country of ref document: CN |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AL AM AU AZ BA BB BG BR BY CA CN CU CZ EE GD GE HR HU ID IL IN IS JP KE KG KR KZ LC LK LR LT LV MD MG MK MN MX NO NZ PL RO RU SG SI SK SL TJ TM TR TT UA US UZ VN YU |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW SD SZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
AK | Designated states |
Kind code of ref document: C1 Designated state(s): AL AM AU AZ BA BB BG BR BY CA CN CU CZ EE GD GE HR HU ID IL IN IS JP KE KG KR KZ LC LK LR LT LV MD MG MK MN MX NO NZ PL RO RU SG SI SK SL TJ TM TR TT UA US UZ VN YU |
|
AL | Designated countries for regional patents |
Kind code of ref document: C1 Designated state(s): GH GM KE LS MW SD SZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
WR | Later publication of a revised version of an international search report | ||
ENP | Entry into the national phase |
Ref document number: 2316273 Country of ref document: CA Ref document number: 2316273 Country of ref document: CA Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: IN/PCT/2000/96/KOL Country of ref document: IN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 18897/99 Country of ref document: AU |
|
WWE | Wipo information: entry into national phase |
Ref document number: PV2000-2470 Country of ref document: CZ |
|
WWE | Wipo information: entry into national phase |
Ref document number: 09582926 Country of ref document: US Ref document number: PA/a/2000/006641 Country of ref document: MX |
|
WWE | Wipo information: entry into national phase |
Ref document number: 10272000 Country of ref document: SK |
|
WWE | Wipo information: entry into national phase |
Ref document number: 505651 Country of ref document: NZ Ref document number: 1020007007533 Country of ref document: KR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1999900300 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: P20000471A Country of ref document: HR Ref document number: 2000/02059 Country of ref document: TR |
|
WWP | Wipo information: published in national office |
Ref document number: PV2000-2470 Country of ref document: CZ |
|
WWP | Wipo information: published in national office |
Ref document number: 1999900300 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 1020007007533 Country of ref document: KR |
|
NENP | Non-entry into the national phase |
Ref document number: 2000539871 Country of ref document: JP |
|
WWG | Wipo information: grant in national office |
Ref document number: 18897/99 Country of ref document: AU |
|
WWG | Wipo information: grant in national office |
Ref document number: 1020007007533 Country of ref document: KR |
|
WWR | Wipo information: refused in national office |
Ref document number: PV2000-2470 Country of ref document: CZ |