US20030027786A1 - Lipase inhibiting composition - Google Patents
Lipase inhibiting composition Download PDFInfo
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- US20030027786A1 US20030027786A1 US10/154,494 US15449402A US2003027786A1 US 20030027786 A1 US20030027786 A1 US 20030027786A1 US 15449402 A US15449402 A US 15449402A US 2003027786 A1 US2003027786 A1 US 2003027786A1
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- fatty acid
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- composition
- orlistat
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- XWZSWDUFMFPOPT-UHFFFAOYSA-N [H]C1(CO)OC(COCC2([H])OC([H])(COOC(=C)CCCCCCCCCCCCCCCC)C([H])(O)C([H])(O)C2([H])O)(C(O)O)C([H])(O)C1([H])O Chemical compound [H]C1(CO)OC(COCC2([H])OC([H])(COOC(=C)CCCCCCCCCCCCCCCC)C([H])(O)C([H])(O)C2([H])O)(C(O)O)C([H])(O)C1([H])O XWZSWDUFMFPOPT-UHFFFAOYSA-N 0.000 description 1
- AHLBNYSZXLDEJQ-TXVRJSAZSA-N [H][C@@]1(CCCCCC)C(=O)OC1C[C@@]([H])(CCCCCCCCCCC)OC(=O)[C@@]([H])(CC(C)C)NC=O Chemical compound [H][C@@]1(CCCCCC)C(=O)OC1C[C@@]([H])(CCCCCCCCCCC)OC(=O)[C@@]([H])(CC(C)C)NC=O AHLBNYSZXLDEJQ-TXVRJSAZSA-N 0.000 description 1
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- 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
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
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- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention relates to lipase inhibiting compositions having reduced food dependency and decreased formation of free oil.
- Lipase inhibitors are well known in the art and include lipstatin and orlistat. The latter is also known as tetrahydrolipstatin or THL and is derived from a natural product excreted by Streptomyces toxytricini. This class of compounds was found to exhibit in vitro as well as in vivo activity against various lipases, such as lingual lipase, pancreatic lipase, gastric lipase, and carboxylester lipase. Its use for the control or prevention of obesity and hyperlipidemia is described, for instance, in U.S. Pat. No. 4,598,089.
- Orlistat is currently administered at doses of 120 mg per meal and dosing is independent of the body mass of the human subject. Orlistat acts locally in the gastrointestinal (“GI”) tract and prevents lipase from digesting triglycerides and thus inhibits the formation of absorbable lipid degradation products. For this reason, systemic availability of the lipase inhibitors is not required and, instead, local residence in the GI tract is the preferred mode of delivery.
- GI gastrointestinal
- Lipase inhibitor compositions currently administered inhibit around 30% of fat absorption after consumption of a mixed meal; increasing the concentrations of lipase inhibitors in the pharmaceutical composition does not increase its clinical efficacy and/or potency while the intensity of local side effects increases.
- U.S. Pat. No. 5,447,953 discloses that by combining a lipase inhibitor with substantial amounts of water insoluble crude fibers, the inhibiting effect on fat absorption can be increased.
- Patent publication WO 00/09123 discloses that by combining a lipase inhibitor such as orlistat with low amounts of chitosan or a derivative or a salt thereof, the phenomenon of anal leakage of oil can be reduced.
- sucrose fatty acid ester subgroup can increase the activities of lipase inhibitors, decrease the food dependency and decreasing the formation of free oil.
- the subject invention provides a pharmaceutical composition
- a pharmaceutical composition comprising a lipase inhibitor having a melting point ⁇ 37° C., a sucrose fatty acid ester wherein the sucrose fatty acid ester is a mono-, di-, tri- or tetra-ester, and one or more pharmaceutically acceptable excipients.
- FIG. 2 is a bar graph that indicates the efficacy of Xenical in the less accessible meal was only 48.4% compared to the accessible, while the sucrose ester formulation 30 MG SUCROSEESTER P1670 reached 73.9% (double meal test in human volunteers).
- reference mixture soy oil/buffer
- FIG. 5 is a bar graph demonstrating the ability of certain sucrose esters to reduce production of free oil.
- the present invention relates to a pharmaceutical composition
- a pharmaceutical composition comprising a lipase inhibitor, preferably orlistat, having a melting point ⁇ 37° C., a sucrose fatty acid ester wherein the sucrose fatty acid ester is a mono-, di-, tri- or tetra-ester, and optionally one or more pharmaceutically acceptable excipients.
- Sucrose fatty acid esters are nonionic surfactants consisting of sucrose as hydrophilic moiety and one or more fatty acid moieties as lipophilic group(s). They are manufactured from purified sugar and vegetable oils. As sucrose has a total of 8 hydroxyl groups, compounds ranging from sucrose mono to octa fatty acid esters can be produced. The following formula shows as an example the chemical structure of sucrose monostearate:
- sucrose fatty acid ester comprises one single sucrose fatty acid ester as well as a mixture of two or more sucrose ester fatty acids as defined below.
- the substitution degree of sucrose ester varies between 1 and 4; e.g. mono-, di-, tri-, tetra-ester of fatty acids with sucrose.
- the term includes pure sucroseesters as well as mixtures of sucroseesters, wherein the sucroseester might be esterified by different fatty acids and might have several substitution degrees, e.g. mono-, di-, tri- or tetra-substituted.
- Sucrose fatty acid ester and mixtures thereof and there preparation are known in the art and commercially available [Mitsubishi-Kagaku Foods Corp., Montello Inc., Multi-Kem Corp., etc.; see also Garti et al., Sucrose Ester Microemulsions. J. Mol. Liq., 80(2,3), 253-296 (1999); and Allen et al., Carbohydrate-Alkyl Ester Derivatives as Biosurfactants, J. Surfactants Deterg., 2(3), 383-390 (1999)].
- lipase inhibitor refers to compounds which are capable of inhibiting the action of lipases, for example gastric and pancreatic lipases.
- orlistat and lipstatin as described in U.S. Pat. No. 4,598,089 are potent inhibitors of lipases.
- Lipstatin is a natural product of microbial origin, and orlistat is the result of a hydrogenation of lipstatin.
- Other lipase inhibitors include a class of compounds commonly referred to as panclicins. Panclicins are analogues of orlistat [Mutoh et al., J. Antibiot. 47(12), 1369-1375 (1994)].
- lipase inhibitor refers also to synthetic lipase inhibitors for example described in International Patent Application WO 99/34786 (Geltex Pharmaceuticals Inc.). These polymers are characterized in that they have been substituted with one or more groups that inhibit lipases.
- lipase inhibitor also comprises pharmaceutically acceptable salts of these compounds.
- lipase inhibitor also refers to 2-oxy-4H-3,1-benzoxazin-4-ones which have been described in International Patent Application WO00/40569 (Alizyme Therapeutics Ltd.), e.g.
- Orlistat is a known compound (formula I) useful for the control or prevention of obesity and hyperlipidemia.
- the sucroseester molecules are mono-, di- or tri-ester. More preferably, the sucrose ester molecules are a mono- or di-ester and most preferably the sucrose ester are a mono-ester.
- the fatty acid moieties may be identical or different (e.g. sucrosepalmitostearate), preferably identical.
- the preferred ratio (w/w) between the lipase inhibitor and the sucrose fatty acid ester is as follows:
- the composition may comprise 0.05 mg to 20 mg sucrose fatty acid ester per 1 mg lipase inhibitor, preferably 0.1 mg to 10 mg sucrose fatty acid ester per 1 mg lipase inhibitor, more preferably 0.1 to 2 mg sucrose fatty acid ester per 1 mg lipase inhibitor and most preferably 0.15 to 1 mg sucrose fatty acid ester per 1 mg lipase inhibitor.
- the lipase inhibitor is a lipophilic compound.
- the lipase inhibitor is orlistat.
- the fatty acid moiety of the sucrose fatty acid ester is a C 8 to C 24 saturated or partially non-saturated fatty acid.
- the fatty acid moiety of the sucrose fatty acid ester is a C 12 to C 18 saturated fatty acid, e.g. sucroselaurate, sucrosemyristate, sucrosepalmitate, sucrosestearate, sucrosearachidonate and sucrosebehanate, preferably sucroselaurate, sucrosemyristate, sucrosepalmitate, sucrosestearate, more preferably sucrosepalmitate or sucrosestearate.
- the fatty acid of the sucrose ester may be selected from C 8 to C 24 , preferably a C 12 to C 18 , mono- or polyunsaturated fatty acids, e.g. selected from the group consisting of palmitoleic acid, oleic acid, elaidic acid, erucic acid, linoleic acid, gamma-linolenic acid, alpha-linolenic acid and arachidonic acid, most preferably oleic acid, i.e. sucrose fatty acid esters may be sucroseoleate.
- mono- or polyunsaturated fatty acids e.g. selected from the group consisting of palmitoleic acid, oleic acid, elaidic acid, erucic acid, linoleic acid, gamma-linolenic acid, alpha-linolenic acid and arachidonic acid, most preferably oleic acid, i.e. sucrose fatty acid est
- the fatty acid moieties in a di-, tri-, or tetra-sucrose fatty acid ester may be a mixture of two or more fatty acid, e.g. sucrosepalmitostearate.
- compositions comprise 10 to 240 mg, more preferably 30 to 120 mg, e.g. 30, 40, 60, 80, 100, or 120 g.
- Especially preferred compositions comprise 60 to 120 mg orlistat and 20 mg to 100 mg sucrose fatty acid ester.
- compositions as defined above may comprise 120 mg orlistat and 60 mg sucrose ester or 120 mg orlistat and 30 mg sucrose fatty acid ester.
- Another composition may comprise 80 to 120 mg orlistat and 10 to 40 mg sucrose fatty acid ester or 20 to 60 mg orlistat and 5 to 15 mg sucrose fatty acid ester.
- Each dosage unit of the above pharmaceutical compositions can obtain the daily doses of the pharmaceutically active compound or may contain a fraction of the daily dose, such as one-third of the doses. Alternatively, each dosage unit may contain the entire dose of one of the compounds, and a fraction of the dose of the other compound. In such case the patient would daily take one of the combination dosage units, and one or more units containing only the other compound.
- Orlistat is preferably orally administered from 30 to 800 mg per day in divided doses two to three times per day (see above). Other preferred daily doses may range between 120 to 360 mg, more preferred are daily doses between 180 to 270 mg and most preferably are 180 mg. Daily doses are, preferably divided and administrated twice or, particularly, three times per day.
- the lipase inhibitor has to be administered within about one or two hours of ingestion of a meal containing fat.
- treatment be administered to a human who has a strong family history of obesity or has obtained a body mass index of 25 or greater.
- compositions of the present invention may be administered to humans in conventional oral compositions, such as, tablets, coated tablets, hard and soft gelatin capsules, emulsions, suspensions, sachets, bars or cracker.
- carriers which can be used for tablets, coated tablets, dragées, hard gelatin capsules and sachets are pharmaceutically acceptable excipients like lactose, other sugars and sugar alcohols like sorbitol, mannitol, maltodextrin, or other fillers; surfactants like sodium lauryl sulfate, Brij 96, Tween 80; disintegrants like sodium starch glycolate, maize starch or derivatives thereof; polymers like povidone, crospovidone; lubricants like talc; stearic acid or its salts and the like.
- the pharmaceutical preparations can contain preserving agents, solubilizers, stabilizing agents, wetting agents, binding agents, emulsifying agents, sweetening agents, coloring agents, flavoring agents, salts for varying the osmotic pressure, buffers, coating agents and antioxidants. They can also contain still other therapeutically valuable substances.
- the formulations may conveniently be presented in unit dosage form and may be prepared by any methods known in the pharmaceutical art.
- compositions may comprise one or more pharmaceutically acceptable excipients selected from the group consisting of mannitol, lactose, HPMC, lecthin, talcum, sorbitol, polyvinylpyrrolidone, polyethylenglycol, polysorbate, polyoxethylenstearate, and dimethicon, preferably lactose.
- Oral dosage forms are the preferred compositions for use in the present invention and these are the known pharmaceutical forms for such administration, for example tablets, capsules or sachets.
- the pharmaceutically acceptable excipients are known in the pharmacist's art. Tablets may be formed from a mixture of the active compounds with fillers, for example calcium phosphate; disintegrating agents, for example maize starch, lubricating agents, for example magnesium stearate; binders, for example microcrystalline cellulose or polyvinylpyrrolidone and other optional ingredients known in the art to permit tabletting the mixture by known methods.
- capsules for example hard or soft gelatin capsules, containing the active compound with or without added excipients, may be prepared by known methods.
- the contents of the capsule may be formulated using known methods so as to give sustained release of the active compound.
- the tablets and capsules may conveniently each contain the amounts of a pharmaceutically active compound and a sucrose ester as described above.
- the oral dosage form may be a chewable tablet comprising 10-240 mg of orlistat, 0.5-1000 mg of sucrose fatty acid ester and further excipients such as maltodextrin, lactose or cellulose, for example 120 mg orlistat, 30 mg sucrosepalmitate e.g. Sucrosepalmitate P1670, 960 mg maltodextrin, 360 mg Cellactose and 15 mg talcum.
- compositions of the present invention the active compounds may, if desired, be associated with other compatible pharmacologically active ingredients.
- vitamin supplements may be administered with the compounds of the present invention.
- the invention also refers to a process for preparing a composition as described above, comprising mixing a pharmaceutically active compound thereof with sucrose fatty acid ester and one or more pharmaceutically acceptable diluents and/or carriers.
- the invention also provides the use of the above combination of compounds in the manufacture of a medicament for the treatment and prevention of obesity. Additionally, it provides the above compositions for use in the treatment and prevention of obesity.
- the present invention refers to a method of treatment of obesity in a human in need of such treatment which comprises administration to the human of a pharmaceutically active compound as defined above and a sucrose fatty acid ester, and optionally additional pharmaceutical acceptable excipients.
- the invention also refers to the use of a composition as defined above for use in the treatment and prevention of obesity.
- Another embodiment of the present invention refers to a process for preparing a composition as defined above, comprising mixing a pharmaceutically active compound as defined in claim 1 with sucrose ester, and optionally, more pharmaceutically acceptable diluent and/or carrier.
- the invention refers to a kit for treatment of obesity, said kit comprising a first component which is a lipase inhibitor and a second component which is sucrose fatty acid ester unit dosage forms.
- Another embodiment relates to the use of a composition as defined above in the manufacture of medicaments useful for the treatment and prevention of obesity and to a method of treatment of obesity in a human in need of such treatment which comprises administration to the human of a therapeutically effective amount of a lipase inhibitor and a sucrose ester defined above.
- the invention also refers to a lipase inhibitor and sucrose ester as defined above for the treatment and prevention of obesity.
- EXAMPLE 1 Orlistat transfer into oil in vitro Transfer in Cream (%) Transfer in Oliveoil (%) Formulation after 10′ after 60′ after 10′ after 60′ Xenical 5 10 35 70 L-1695 55 65 55 80 P-1670 25 45 50 80 S-1670 10 25 60 90 O-1570 55 65 45 80
- Orlistat (4 mg) suspensions stabilized by sucroseesters (2 mg) were transferred into 5 ml of a 10% oil in water emulsion (pH value 4.5; oil components: olive oil and cream respectively).
- the dispersion underwent end-over end mixing for a desired period of time.
- the oil phase was separated by cold centrifugation and the orlistat content in the oil phase was determined by HPLC.
- an adequate experiment was also performed with a suspension of XENICAL® brand of orlistat-containing pharmaceutical composition.
- L-1695, P-1670, S-1670, 0-1570 are commercial sucroseesters (Sucroselaurate, Sucrosepalmitate, Sucrosestearate, Sucroseoleate respectively) from Mitsubishi-Kagaku Foods, Japan.
- sucroseester have a higher efficacy of the transfer orlistat transfer into oil compared to XENICAL®.
- orlistat is transferred into different kind of oils (cream: emulsified and casein covered oily droplets; olive oil: unprotected oil) at more comparable rates.
- cream emulsified and casein covered oily droplets; olive oil: unprotected oil
- the high food dependency of orlistat is reflected in the fact, that the transfer after 10 min into olive oil is 7 times more efficient than the transfer into cream.
- the sucrose ester show less food dependency. Therefore, a dose reduction and decreased side effects can be expected.
- composition 1 Orlistat 120 g Sucrosepalmitate P1670 30 g Maltodextrin 960 g Cellactose 360 g Talcum 15 g
- Orlistat, sucrosepalmitate and maltodextrin were homogeneously mixed and 350 g water were added stepwise under continuous mixing.
- composition 2 Orlistat 120 g Sucrosepalmitate P1670 240 g Maltodextrin 750 g Cellactose 375 g Talcum 15 g
- composition 3 Orlistat 60 g Sucrosepalmitate P1670 60 g Maltodextrin 750 g Cellactose 375 g Talcum 15 g
- composition 4 Orlistat 60 g Sucrosestearate S1811 60 g Maltodextrin 750 g Cellactose 375 g Talcum 15 g
- composition 5 Orlistat 60 g Sucrosemyristate M1695 60 g Maltodextrin 750 g Cellactose 375 g Talcum 15 g
- composition 6 Orlistat 60 g Sucrosestearate S1816 60 g Maltodextrin 750 g Cellactose 375 g Talcum 15 g
- composition 7 Orlistat 240 g Sucrosepalmitate P1670 60 g Avicel PH-105 35 g Sodium starch glycolate 60 g Povidone K30 30 g
- the ingredients are dry mixed together in a high speed mixer Diosna P50). 240 g water are added stepwise and the mixing process is continued for about 5 minutes. An extruder is fed with this material (NICA lab E-140; screen 0.8 mm mesh size, thickness 1.0 mm, screen surrounded by cooling device). The material is extruded to spaghettis of appropriate length. The temperature of the extrudate does not exceed 35° C. The extrudate is transferred to a spheronizer ((NICA lab S320) and spheronized for 0.5 to 3 minutes at 700 rpm. The wet pellets are dried in a fluidized bed dryer (Aeromatic, MP-1) at a temperature of below 35° C.
- a fluidized bed dryer Aeromatic, MP-1
- the dried pellets are sieved with sieve inserts of 0.5 and 1.25 mm mesh size, and under- and oversize fractions are discarded.
- the pellets are filled into a sachet at doses of 106 mg (corresponding to 60 mg orlistat).
- the above pellets are filled into Gelatin capsules size I at a dosage of 106 mg (corresponding to 60 mg orlistat).
- Magnesium stearate is added to the pellets described in Example 8 at a level of 1% (w/w) and homogeneously distributed by appropriate mixing. The mixture is compressed into 107 mg tablets which correspond to 60 mg orlistat.
- Table Reduced food-dependent efficacy of sucrose ester based orlistat formulations in an in vitro lipase inhibition assay with accessible and resistant fat.
- Xenical® pellets and Tablets from Example 2 and Example 3 were investigated. Water was added to a dispersed tablet to yield a orlistat concentration of 6.64 mg/ml. The sample was stirred for 15 min and a geometric dilution series was prepared. An aliquot from each dilution step was mixed with substrate and assessed for lipase inhibition. The final emulsion contained 2.5% (w/v) fat and 10 mg/ml USP pancreatin.
- the in vitro lipase test mimics the gastro-intestinal fat digestion and assesses formulation dependent inhibition of lipolysis.
- lipase substrate cream and grained hamburger/ french fries, representing resistant and accessible fat, respectively
- THL-formulation under simulated gastric conditions (i.e. at pH 4.5 in the presence of 20% human gastric fluid).
- the formulation can load fat droplets with THL.
- Lipolysis is then started by adding artificial intestinal fluid, containing bile salts, phospholipids and hydrolytic enzymes (pancreatin). After one hour organic solvent is added to stop the reaction and free fatty acids are quantified.
- the dose-response curve is dependent on the formulation as well as on the type of substrate employed.
- the IC50 value is the concentration which inhibits triglyceride cleavage by 50%.
- a high food dependency was observed for Xenical, the IC50 increased by a factor of 20.
- the in vitro food dependency of the sucrose ester based formulations was about 6-times less compared to Xenical®.
- Example 2 The 120 mg Orlistat tablet formulations described in Example 2 (30 mg Sucrosepalmitate) and Example 3 (240 mg Sucrosepalmitate), and Xenical® were tested on human volunteers by means of a double-meal test, which is composed of accessible fat (Lunch: Hamburger, French fries and a less accessible fat (Dinner: cheese meal). The nonabsorbed fat was determined after Bligh & Dyer [Bligh et al., Can. J. Biochem.Physiol., 37:911(1959)].
- Sucrose esters such as Surfhope SE Pharma D-1811 (Table 2) with a medium HLB value of 11 proofed to be slightly superior in their ability to stabilize an emulsion with respect to Surfhope SE Pharma D-1815 (Table 1) and Surfhope SE Pharma D-1805 (Table 3), respectively.
- reference mixture soy oil/buffer
- sucrose esters and hydrocolloids e.g., xanthan gum, gellan gum, carrageenan gum
- sphingomyelin e.g., xanthan gum, gellan gum, carrageenan gum
- aerosil derivatives e.g., calcium carboxymethylcellulose, chitosan, bentonites
- whey protein concentrates e.g., pectins, and poly(vinyl alcohol
- these studies showed that 1:1 combinations (w/w) of Surfhope SE Pharma D-1815 and Aerosil 200, carrageenan gum, and whey protein concentrates gave emulsions with clearly better stability than the single compounds alone, due to a yet unknown synergistic mechanism.
- the emulsions are stabilized with 1.0% (w/w) sucrose ester at different pH values.
- reference mixture soy oil/buffer
- Sucrose Fatty Acid Ester S-370F revealed very bad emulsification properties. Due to the high hydrophobicity of the compound solubility in the continuous aqueous phase was very low. However, the compound is very easily soluble in soy bean oil resulting in a significant increase in oil viscosity.
- sucrose esters such as Surfhope D-1811 or Surfhope D-1805 with a medium HLB value show the highest relative reduction in free oily excretion.
- sucrose esters on either end of the HLB scale which are either very hydrophilic (Surfhope D-1815) or very lipophilic (Surfhope D-1803) show less activity.
- Composition 8 Orlistat 240 g Sucrosepalmitate P1670 60 g Avicel PH-105 210 g Sodium starch glycolate 60 g Povidone K30 30 g Stearic acid 6 g
- the ingredients are dry mixed together in a high speed Aeromatic Fielder GP 1). 240 g water are added stepwise and the mixing process is continued for about 5 minutes. An extruder is fed with this material (NICA extruder; screen 0.8 mm mesh size, thickness 1.0 mm). The material is extruded to spaghettis of appropriate length. The temperature of the extrudate does not exceed 35° C. The extrudate is transferred to a spheronizer ((NICA spheronizer) and spheronized for 0.5 to 5 minutes. The wet pellets are dried in a fluidized bed dryer (Aeromatic, MP-1) at a temperature of below 35° C.
- the dried pellets are sieved with sieve inserts of 0.5 and 1.25 mm mesh size, and under- and oversize fractions are discarded.
- Stearic acid is added and homogeneously distributed by dry mixing.
- the resulting mixture is compressed to chewable tablets containing orlistat 120 mg, sucrosepalmitate 30 mg, Avicel 105 mg, sodium starch glycolate 30 mg, povidone 15 mg and stearic acid 3 mg.
- Composition 9 a) Orlistat 240 g b) Sucrosepalmitate P1670 60 g c) Avicel PH-105 210 g d) Sodium starch glycolate 60 g e) Povidone K30 30 g f) Stearic acid 6 g g) Lactose monohydrate (powder) 1460 g h) Avicel PH 102 200 g i) Maize starch 1500 100 g k) Sodium starch glycolate 100 g 1) Povidone 90F 60 g m) Glyceryl benehate 60 g n) Magnesium Stearate 20 g
- Layer 1 The ingredients a)-e) are dry mixed together in a high speedAeromatic Fielder GP 1). 240 g water are added stepwise and the mixing process is continued for about 5 minutes. An extruder is fed with this material (NICA extruder; screen 0.8 mm mesh size, thickness 1.0 mm). The material is extruded to spaghettis of appropriate length. The temperature of the extrudate does not exceed 35° C. The extrudate is transferred to a spheronizer ((NICA spheronizer) and spheronized for 0.5 to 5 minutes. The wet pellets are dried in a fluidized bed dryer (Aeromatic, MP-1) at a temperature of below 35° C.
- the dried pellets are sieved with sieve inserts of 0.5 and 1.25 mm mesh size, and under- and oversize fractions are discarded. Stearic acid is added and homogeneously distributed by dry mixing.
- Layer 2 The excipients g)-m) are mixed together in a high speed mixer (Aeromatic Fielder GP 1) for 5 minutes, 400 g water added for granulation.
- the wet granulate is sieved and dried in a fluidized bed dryer (Aeromatic, MP-1).
- the dried granulate is sieved, and homogeneously mixed with Magnesium stearate.
- the resulting mixtures of layer 1 and 2 are compressed to a two layer tablet (Kilian compressing equipment) containing orlistat 120 mg, sucrosepalmitate 30 mg, Avicel 105 mg, sodium starch glycolate 30 mg, povidone 15 mg and stearic acid 3 mg in layer 1 and containing Lactose 730 mg, Avicel 100 mg, maize starch 50 mg, sodium starch glycolate 50 mg, povidone 30 mg, glyceryl benehate 30 mg and magnesium stearate 10 mg in the second layer.
- a two layer tablet Korean compressing equipment
- composition 10 Orlistat 48 g Sucrosepalmitate P1670 12 g Sodium starch glycolate 48 g PEG 6000 72 g Xylit 122.4 g Mannit pulvis 122.4 g Myrj 52 12 g Plasdone S630 24 g Magnesium stearate 4.8 g Talc 24 g
- Composition 11 Orlistat 48 g Sucrosepalmitate P1670 12 g Sodium starch glycolate 48 g PEG 6000 72 g Xylit 98.4 g Mannit pulvis 98.4 g Myrj 52 12 g Alginic acid 32.64 g Plasdone S630 24 g Magnesium stearate 4.8 g Talc 14.4 g Calcium carbonate 15.36 g
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- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Zoology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
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Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/019,865 US8039508B2 (en) | 2001-06-06 | 2004-12-23 | Lipase inhibiting composition |
US13/213,379 US8343543B2 (en) | 2001-06-06 | 2011-08-19 | Lipase inhibiting composition |
US13/684,698 US20130079391A1 (en) | 2001-06-06 | 2012-11-26 | Lipase inhibiting composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01113793 | 2001-06-06 | ||
EP01113793.2 | 2001-06-06 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/019,865 Continuation US8039508B2 (en) | 2001-06-06 | 2004-12-23 | Lipase inhibiting composition |
Publications (1)
Publication Number | Publication Date |
---|---|
US20030027786A1 true US20030027786A1 (en) | 2003-02-06 |
Family
ID=8177654
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/154,494 Abandoned US20030027786A1 (en) | 2001-06-06 | 2002-05-23 | Lipase inhibiting composition |
US11/019,865 Expired - Lifetime US8039508B2 (en) | 2001-06-06 | 2004-12-23 | Lipase inhibiting composition |
US13/213,379 Expired - Lifetime US8343543B2 (en) | 2001-06-06 | 2011-08-19 | Lipase inhibiting composition |
US13/684,698 Abandoned US20130079391A1 (en) | 2001-06-06 | 2012-11-26 | Lipase inhibiting composition |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/019,865 Expired - Lifetime US8039508B2 (en) | 2001-06-06 | 2004-12-23 | Lipase inhibiting composition |
US13/213,379 Expired - Lifetime US8343543B2 (en) | 2001-06-06 | 2011-08-19 | Lipase inhibiting composition |
US13/684,698 Abandoned US20130079391A1 (en) | 2001-06-06 | 2012-11-26 | Lipase inhibiting composition |
Country Status (40)
Country | Link |
---|---|
US (4) | US20030027786A1 (el) |
EP (1) | EP1399152B1 (el) |
JP (2) | JP4261337B2 (el) |
KR (1) | KR100753729B1 (el) |
CN (1) | CN1514725B (el) |
AR (1) | AR034355A1 (el) |
AT (1) | ATE356622T1 (el) |
AU (1) | AU2002257817B2 (el) |
BG (1) | BG66346B1 (el) |
BR (1) | BRPI0210266B1 (el) |
CA (1) | CA2448030C (el) |
CO (1) | CO5540293A2 (el) |
CY (1) | CY1107641T1 (el) |
CZ (1) | CZ299948B6 (el) |
DE (1) | DE60218845T2 (el) |
DK (1) | DK1399152T3 (el) |
EC (1) | ECSP034871A (el) |
ES (1) | ES2282415T3 (el) |
GT (1) | GT200200106A (el) |
HK (1) | HK1067312A1 (el) |
HR (1) | HRP20030983B1 (el) |
HU (1) | HU230405B1 (el) |
IL (2) | IL158908A0 (el) |
JO (1) | JO2455B1 (el) |
MA (1) | MA27031A1 (el) |
ME (1) | ME00579B (el) |
MX (1) | MXPA03011191A (el) |
MY (1) | MY161871A (el) |
NO (1) | NO328006B1 (el) |
NZ (1) | NZ529630A (el) |
PA (1) | PA8546701A1 (el) |
PE (1) | PE20030230A1 (el) |
PL (1) | PL215266B1 (el) |
PT (1) | PT1399152E (el) |
RS (1) | RS50713B (el) |
RU (1) | RU2271808C2 (el) |
SI (1) | SI1399152T1 (el) |
SK (1) | SK287602B6 (el) |
WO (1) | WO2002098412A1 (el) |
ZA (1) | ZA200309007B (el) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005087025A1 (en) * | 2004-03-15 | 2005-09-22 | Bioferme Oy | Composition; use of a composition and a method for treating obesity |
US20070111914A1 (en) * | 2005-11-16 | 2007-05-17 | Conopco, Inc., D/B/A Unilever, A Corporation Of New York | Environmentally friendly laundry method and kit |
US20100087520A1 (en) * | 2008-10-06 | 2010-04-08 | Banner Pharmacaps, Inc. | Stable solutions of orlistat for pharmaceutical dosage forms |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030027786A1 (en) * | 2001-06-06 | 2003-02-06 | Karsten Maeder | Lipase inhibiting composition |
US8372430B2 (en) * | 2002-12-17 | 2013-02-12 | The Procter & Gamble Company | Compositions, methods, and kits useful for the alleviation of gastrointestinal effects |
KR100910000B1 (ko) * | 2005-05-13 | 2009-07-29 | 씨제이제일제당 (주) | 리파아제 저해제 함유 약학 조성물 |
WO2006132440A1 (ja) * | 2005-06-09 | 2006-12-14 | Takeda Pharmaceutical Company Limited | 固形製剤 |
KR101252635B1 (ko) * | 2006-04-20 | 2013-04-10 | (주)아모레퍼시픽 | 리파아제 저해제 및 친유성 오일흡수제를 포함하는 약학조성물 및 이로부터 제조된 경구 투여용 제제 |
EP1872777A1 (en) * | 2006-06-27 | 2008-01-02 | LEK Pharmaceuticals D.D. | Pharmaceutical composition comprising tetrahydrolipstatin |
GB0618725D0 (en) * | 2006-09-23 | 2006-11-01 | Jagotec Ag | Composition containing inhibitors of gastro-intestinal lipase |
PL216542B1 (pl) | 2008-03-20 | 2014-04-30 | Zakłady Farmaceutyczne POLPHARMA Spółka Akcyjna | Sposób wytwarzania stabilnej kompozycji orlistatu w postaci kapsułkowanego proszku |
FR2994386B1 (fr) * | 2012-08-07 | 2016-06-24 | Thorel Jean-Noel | Inhibition de l'adhesion de micro-organismes pathogenes par un ester de saccharose et/ou de sorbitan dans le traitement cosmetique de l'atopie cutanee |
US10743813B2 (en) | 2014-09-11 | 2020-08-18 | Rattan Nath | Diabetes control using postprandial feedback |
CN104546768B (zh) * | 2014-12-30 | 2017-06-16 | 重庆植恩药业有限公司 | 含有脂肪酶抑制剂的咀嚼片组合物及其制备方法 |
MA45430A (fr) | 2015-10-23 | 2019-05-01 | Erx Pharmaceuticals Inc | Analogues de célastrol |
CN113151373B (zh) * | 2021-03-09 | 2023-07-04 | 武汉臻治生物科技有限公司 | 一种具有抗菌及抗肿瘤活性的蔗糖单酯的制备方法及其应用 |
KR102637596B1 (ko) | 2022-03-18 | 2024-02-19 | (주)보노보씨 | 기능성 목공교구 |
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- 2002-05-23 US US10/154,494 patent/US20030027786A1/en not_active Abandoned
- 2002-05-29 HU HU0401208A patent/HU230405B1/hu unknown
- 2002-05-29 SK SK1609-2003A patent/SK287602B6/sk not_active IP Right Cessation
- 2002-05-29 CA CA002448030A patent/CA2448030C/en not_active Expired - Lifetime
- 2002-05-29 IL IL15890802A patent/IL158908A0/xx active IP Right Grant
- 2002-05-29 ME MEP-2008-904A patent/ME00579B/me unknown
- 2002-05-29 DE DE60218845T patent/DE60218845T2/de not_active Expired - Lifetime
- 2002-05-29 JP JP2003501451A patent/JP4261337B2/ja not_active Expired - Fee Related
- 2002-05-29 WO PCT/EP2002/005889 patent/WO2002098412A1/en active IP Right Grant
- 2002-05-29 KR KR1020037015985A patent/KR100753729B1/ko active IP Right Grant
- 2002-05-29 EP EP02727607A patent/EP1399152B1/en not_active Expired - Lifetime
- 2002-05-29 PL PL366890A patent/PL215266B1/pl unknown
- 2002-05-29 AT AT02727607T patent/ATE356622T1/de active
- 2002-05-29 SI SI200230524T patent/SI1399152T1/sl unknown
- 2002-05-29 BR BRPI0210266A patent/BRPI0210266B1/pt not_active IP Right Cessation
- 2002-05-29 PT PT02727607T patent/PT1399152E/pt unknown
- 2002-05-29 CZ CZ20033525A patent/CZ299948B6/cs not_active IP Right Cessation
- 2002-05-29 MX MXPA03011191A patent/MXPA03011191A/es active IP Right Grant
- 2002-05-29 RU RU2003136728/15A patent/RU2271808C2/ru active
- 2002-05-29 NZ NZ529630A patent/NZ529630A/en not_active IP Right Cessation
- 2002-05-29 CN CN028114957A patent/CN1514725B/zh not_active Expired - Lifetime
- 2002-05-29 AU AU2002257817A patent/AU2002257817B2/en not_active Expired
- 2002-05-29 RS YUP-960/03A patent/RS50713B/sr unknown
- 2002-05-29 DK DK02727607T patent/DK1399152T3/da active
- 2002-05-29 ES ES02727607T patent/ES2282415T3/es not_active Expired - Lifetime
- 2002-06-02 JO JO200254A patent/JO2455B1/en active
- 2002-06-04 PA PA20028546701A patent/PA8546701A1/es unknown
- 2002-06-04 AR ARP020102074A patent/AR034355A1/es not_active Application Discontinuation
- 2002-06-04 MY MYPI20022058A patent/MY161871A/en unknown
- 2002-06-05 GT GT200200106A patent/GT200200106A/es unknown
- 2002-06-05 PE PE2002000472A patent/PE20030230A1/es active IP Right Grant
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2003
- 2003-11-17 IL IL158908A patent/IL158908A/en unknown
- 2003-11-19 ZA ZA2003/09007A patent/ZA200309007B/en unknown
- 2003-11-26 HR HR20030983A patent/HRP20030983B1/xx not_active IP Right Cessation
- 2003-11-28 NO NO20035318A patent/NO328006B1/no not_active IP Right Cessation
- 2003-12-01 EC EC2003004871A patent/ECSP034871A/es unknown
- 2003-12-02 CO CO03106075A patent/CO5540293A2/es active IP Right Grant
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2004
- 2004-12-23 US US11/019,865 patent/US8039508B2/en not_active Expired - Lifetime
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2007
- 2007-05-29 CY CY20071100716T patent/CY1107641T1/el unknown
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2008
- 2008-11-12 JP JP2008289389A patent/JP2009108076A/ja active Pending
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2011
- 2011-08-19 US US13/213,379 patent/US8343543B2/en not_active Expired - Lifetime
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005087025A1 (en) * | 2004-03-15 | 2005-09-22 | Bioferme Oy | Composition; use of a composition and a method for treating obesity |
US20080038318A1 (en) * | 2004-03-15 | 2008-02-14 | Saska Tuomasjukka | Composition; Use Of A Composition And A Method For Treating Obesity |
AU2005220626B2 (en) * | 2004-03-15 | 2010-11-11 | Bioferme Oy | Composition; use of a composition and a method for treating obesity |
US20070111914A1 (en) * | 2005-11-16 | 2007-05-17 | Conopco, Inc., D/B/A Unilever, A Corporation Of New York | Environmentally friendly laundry method and kit |
US20100087520A1 (en) * | 2008-10-06 | 2010-04-08 | Banner Pharmacaps, Inc. | Stable solutions of orlistat for pharmaceutical dosage forms |
US8309107B2 (en) | 2008-10-06 | 2012-11-13 | Banner Pharmacaps, Inc. | Stable solutions of orlistat for pharmaceutical dosage forms |
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Owner name: F. HOFFMANN-LA ROCHE AG, SWITZERLAND Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:MAEDER, KARSTEN;MARTIN, RAINER EUGEN;RAAB, SUSANNE;AND OTHERS;REEL/FRAME:013499/0980;SIGNING DATES FROM 20020614 TO 20020619 |
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