WO2018051020A1 - Nouveaux polymères de glucose pour dialyse péritonéale - Google Patents
Nouveaux polymères de glucose pour dialyse péritonéale Download PDFInfo
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- WO2018051020A1 WO2018051020A1 PCT/FR2017/052446 FR2017052446W WO2018051020A1 WO 2018051020 A1 WO2018051020 A1 WO 2018051020A1 FR 2017052446 W FR2017052446 W FR 2017052446W WO 2018051020 A1 WO2018051020 A1 WO 2018051020A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H3/00—Compounds containing only hydrogen atoms and saccharide radicals having only carbon, hydrogen, and oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
- C08L3/12—Amylose; Amylopectin; Degradation products thereof
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L13/00—Meat products; Meat meal; Preparation or treatment thereof
- A23L13/40—Meat products; Meat meal; Preparation or treatment thereof containing additives
- A23L13/42—Additives other than enzymes or microorganisms in meat products or meat meals
- A23L13/426—Addition of proteins, carbohydrates or fibrous material from vegetable origin other than sugars or sugar alcohols
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/30—Foods or foodstuffs containing additives; Preparation or treatment thereof containing carbohydrate syrups; containing sugars; containing sugar alcohols, e.g. xylitol; containing starch hydrolysates, e.g. dextrin
- A23L29/35—Degradation products of starch, e.g. hydrolysates, dextrins; Enzymatically modified starches
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/125—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives containing carbohydrate syrups; containing sugars; containing sugar alcohols; containing starch hydrolysates
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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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
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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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
- A61K31/718—Starch or degraded starch, e.g. amylose, amylopectin
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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
- A61P3/02—Nutrients, e.g. vitamins, minerals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/08—Plasma substitutes; Perfusion solutions; Dialytics or haemodialytics; Drugs for electrolytic or acid-base disorders, e.g. hypovolemic shock
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B33/00—Preparation of derivatives of amylose
Definitions
- the present invention relates to a novel glucose polymer particularly useful for parenteral administration, as well as to its method of preparation.
- the invention also relates to compositions comprising such a glucose polymer, as well as to their methods of preparation.
- the invention finally relates to its use as a medicament, for example as an osmotic agent for peritoneal dialysis. Context of the invention
- Dialysis is a procedure to supplement or replace kidney function in some patients.
- the methods mainly used today are hemodialysis and peritoneal dialysis.
- hemodialysis the patient's blood passes through a kidney dialysis machine that includes a membrane that acts as an artificial kidney, to filter and purify the blood. Because it is an extracorporeal treatment that requires special equipment, hemodialysis inevitably faces some drawbacks such as the availability of dialysis machines and the possibility of infections and contaminations.
- Peritoneal dialysis does not require such equipment, since it advantageously uses the peritoneum of the patient as a filter membrane.
- the peritoneum is a membranous abdominopelvic wall covering of the body walls that is able to act as a natural semi-permeable membrane, due to its large number of blood vessels and capillaries.
- the treatment involves introducing via a catheter a peritoneal dialysis solution into the peritoneal cavity. During a given exposure period, fluid and solute exchange occurs between the solution and the blood until it reaches equilibrium. The dialysis solution or dialysate is then removed from the body by a catheter.
- Peritoneal dialysis solutions are sterile and typically include water, electrolytes (Na +, Cl-, Ca2 +, Mg2 +), a buffer (lactate and / or carbonate), and an osmotic agent.
- the role of the osmotic agent is to make the dialysis solution slightly hypertonic. By gradient effect, movements of fluids and solutes are thus effected, from the blood to the dialysate.
- Conventional solutions use glucose as the osmotic agent, which is an inexpensive compound, and has the advantage of producing high ultrafiltration levels.
- the GDPs are molecules of low molecular weight, among which are mainly 5-hydroxymethyl furaldehyde (5-HMF), and also for example furaldehyde and 3,4-didesoxyglucosone-3-ene (3,4-DGE) .
- the GDPs cause abdominal pain, discomfort during infusion, and are cytotoxic. They inhibit cell proliferation and impair the functions of inflammatory cells.
- 3,4-DGE for example, is lethal to leucocytes and mesothelial cells at the concentrations usually found in peritoneal dialysis solutions. GDPs also favor the production of advanced glycation end products (AGEs), which cause dysfunctions of proteins and cellular functions.
- AGEs advanced glycation end products
- the first approach is based on a method using two separate solutions, conventionally contained in two- or three-compartmented bags.
- a first solution comprises glucose, which is sterilized separately under very acidic conditions, in order to minimize the formation of GDPs.
- a second solution comprises the buffer at a high pH. These two solutions are then mixed in order to obtain a solution having reduced amounts of GDPs and a pH approaching physiological pH.
- a major disadvantage of this approach is that this mixing step, in addition to complicating the process, increases the risk of contamination.
- the second approach is based on the development of new osmotic agents that can be considered more biocompatible.
- glucose polymers such as icodextrin are an attractive alternative to glucose.
- these compounds allow for more sustainable and linear ultrafiltration.
- their effectiveness is independent of the peritoneal permeability to small solutes, so that it is possible to maintain ultrafiltration during episodes of peritonitis.
- icodextrin can not be strictly considered biocompatible because of its glucosidic nature. Although to a lesser extent, its heat sterilization also leads to the production of toxic GDPs, and the pH of dialysis solutions containing it remains low (5-6).
- the object of the present invention is to provide osmotic agents which make it possible to overcome the disadvantages discussed above, related to the use of glucose or glucose polymers of the prior art.
- the present invention in particular aims to provide glucose polymers that allow the preparation of solutions for parenteral administration with extremely low levels of GDPs.
- the present invention also aims to provide glucose polymers that allow the preparation of solutions at a pH close to physiological pH, without recourse to the use of two-or three-compartment pockets.
- the present invention aims to address these problems by providing osmotic agents which also have good pharmacokinetic properties.
- the novel glucose polymer proposed by the Applicant is a modified glucose polymer, in particular obtained from starch, characterized in that it is obtained by branching and reduction of a starch having an amylose content of from minus 10%, said polymer having an ⁇ -1,6 bonding ratio of less than 20%.
- the new glucose polymers of the invention allow the preparation of solutions in which after sterilization, the GDPs are not detectable, and this, despite the high pH of the solution; This makes it possible to envisage the preparation of solutions having a pH close to physiological pH, without having recourse to methods using two- or three-compartmented bags.
- glucose polymers of the invention have good pharmacokinetic properties, especially better than that obtained with starches poor in amylose and / or with starches having too high branching rates.
- the invention thus firstly relates to a glucose polymer characterized in that it is obtained by branching and reduction of a starch having an amylose content of at least 10%, and in that said glucose polymer has a ⁇ -1,6 bond ratio less than 20%.
- the invention also relates to a process for preparing such a glucose polymer.
- the subject of the invention is also a composition comprising such a glucose polymer, in particular a pharmaceutical composition such as, for example, a peritoneal dialysis solution.
- a pharmaceutical composition such as, for example, a peritoneal dialysis solution.
- the invention also relates to a process for preparing such a composition.
- the subject of the invention is also the use of such a glucose polymer or of such a composition as a medicament and / or in peritoneal dialysis, and / or in parenteral nutrition, and / or in plasma filling, and / or in as an osmotic agent, and / or as a plasma expander, and / or in vaccinology, and / or as an adjuvant, and / or as a protein stabilizer, and / or as a protein carrier.
- a glucose polymer or of such a composition as a medicament and / or in peritoneal dialysis, and / or in parenteral nutrition, and / or in plasma filling, and / or in as an osmotic agent, and / or as a plasma expander, and / or in vaccinology, and / or as an adjuvant, and / or as a protein stabilizer, and / or as a protein carrier.
- the invention firstly relates to a glucose polymer characterized in that it is obtained by branching and reduction of a starch having an amylose content of at least 10%, and in that it has a degree of a-1, 6 less than 20%.
- the glucose polymer of the invention is thus characterized firstly that it is derived from a starch having an amylose content of at least 10%, this percentage being expressed as the dry weight of amylose relative to the dry weight. total starch.
- starch is conventionally understood to mean a starch isolated from any suitable source, for example from plants chosen from cereals, tuberose and legumes. This starch is preferably a pea starch, or a corn starch.
- amylose content of a starch can conventionally be determined by those skilled in the art by potentiometric determination of the iodine absorbed by the amylose to form a complex.
- this amylose content is at least 20%, preferably at least 30%, preferably at least 35%, preferably at least 40%, preferably at least 45%. preferably at least 50%, preferably at least 55%, preferably at least 60%. It is generally at most equal to 85% or 80%.
- This amylose content is for example chosen from a range of from 20 to 85%, preferably from 30 to 80%, preferably from 50 to 75%.
- the glucose polymer of the invention is also characterized in that it is obtained by reduction of a starch. This reduction typically leads to the conversion of carbonyl groups into hydroxyl groups.
- the glucose polymer of the invention may be defined in that it comprises carbonyl groups converted into hydroxyls.
- the glucose polymer of the invention is also characterized in that it is obtained by branching of the starch, and in that it has a content of ⁇ -1,6 bonds of less than 20%.
- branching is conventionally meant the fact of subjecting the starch to branching enzymes forming ⁇ -1-6 bonds, for example chosen from the glycogen branching enzymes, starch branching enzymes, or a mixture thereof.
- this connection rate does not exceed 20% in the context of the present invention.
- This level of glucosidic linkages a-1, 6 may be conventionally determined by those skilled in the art by proton NMR. For example, it will be possible to refer to the method described in the Example in point B. below.
- this level of glucosidic linkages a-1, 6 is at least 8%, preferably at least 9%, preferably at least 10%, preferably at least 1%, of preferably at least 12%.
- This glucoside bonding ratio a-1, 6 is for example chosen in a range ranging from 8 to 19%, from 9 to 19%, from 10 to 19%, from 10 to 18%, from 10 to 17%, from 10 to at 16%, or from 1 to 16%, preferably from 12 to 16%, preferably from 13 to 15%.
- the glucose polymer according to the invention has an average molecular weight (M w) chosen in the range from 20 000 to 200 000 daltons (Da), especially for use in peritoneal dialysis; this M w being determined by liquid chromatography and detection by differential refractometry, preferably using pullulans for calibration.
- M w average molecular weight chosen in the range from 20 000 to 200 000 daltons (Da), especially for use in peritoneal dialysis; this M w being determined by liquid chromatography and detection by differential refractometry, preferably using pullulans for calibration.
- this M w is less than 100,000 Da, in particular for use in peritoneal dialysis, more preferably less than 50,000 Da. It is preferably greater than 25,000 Da. It is for example chosen in the range of 25,000 to 50,000 Da, preferably 30,000 to 40,000 Da.
- the glucose polymer of the invention can be defined by its M w as determined by liquid chromatography with detection by light scattering.
- the glucose polymer according to the invention preferably has an Mw of at least 30,000 Da, in particular for use in peritoneal dialysis.
- This M w is preferably at least 40,000 Da, preferably at least 50,000 Da, preferably at least 50,000 Da, preferably at least 60,000 Da, preferably at least 70,000 Da, preferably at least 80,000 Da, preferably at least 90,000 Da, preferably at least 100,000 Da. It does not generally exceed 1 500 000 Da, or even 1 000 000 Da, even 800 000 Da, even 700 000 Da, even 600 000 Da or 500 000 Da or 400 000 Da or 300 000 Da.
- this Mw in particular for use in peritoneal dialysis, is chosen from a range of from 30,000 to 600,000 Da, preferably from 40,000 to 500,000 Da, preferably from 50,000 to 400,000 Da, preferably from 60,000 to 300,000 Da, for example from 100,000 to 200,000 Da.
- the polydispersity index (polyD) of the glucose polymer according to the invention is less than 3.0, preferably less than 2.5, more preferably less than 2.0. It is generally greater than 0.5, for example between 1.0 and 3.0, preferably between 1.5 and 2.5.
- This polyD corresponds to the ratio between the weight average molecular weight M w and the number average molecular weight MN of the glucose polymer.
- M w and M N may in the present invention be determined by two methods as defined before. For example, we can refer to methods 1 and 2 described in the Example in point B. below.
- the polymer is a maltodextrin, particularly an icodextrin.
- the glucose polymer according to the invention can also be defined by its pH after sterilization at 121 ° C. for 45 minutes, which is in a range from 6 to 8, preferably from 7 to 8; said pH being measured on the basis of a 5% aqueous solution of said glucose polymer.
- the glucose polymer of the invention has, in particular after heat sterilization, in particular at 121 ° C. for 15 minutes:
- 5-HMF 5-hydroxymethyl furaldehyde
- 3,4-DGE 3,4-didesoxyglucosone-3-ene
- the contents of 5-HMF and furaldehyde can be determined by those skilled in the art by liquid chromatography and detection by UV spectrophotometry at 280 nm.
- the 3,4-DGE content can be determined by those skilled in the art by liquid chromatography, preferably using pyrazine carboxamide for calibration, and detection by UV spectrophotometry at 230 nm.
- the glucose polymer according to the invention has an osmolality of between 200 and 300 mOsm / kg; said osmolality being determined on the basis of a 0.4% solution of said glucose polymer.
- This osmolality is for example between 230 and 280 mOsm / kg, or between 230 and 250 mOsm / kg.
- This osmolality can conventionally be determined by those skilled in the art by means of an osmometer. For example, it will be possible to refer to the method described in the Example in point B. below.
- the glucose polymer according to the invention has a reducing sugar content of less than 3.5%, this percentage being expressed as the dry weight of reducing sugars relative to the total dry weight of the glucose polymer.
- This content is preferably less than 2.5%, preferably less than 1.0%, preferably less than 0.5%, preferably less than 0.1%, more preferably less than 0.05%. It is generally greater than 0.001%, or even greater than 0.005%.
- This reducing sugar content can conventionally be determined by those skilled in the art by means of the Bertrand method. For example, it will be possible to refer to the method described in the Example in point B. below.
- the glucose polymer according to the invention is soluble to very soluble in water at ambient temperature (25 ° C.).
- soluble to very soluble in water is conventionally meant that a maximum volume of water of 30 ml is required to dissolve 1 dry gram of said compound (see for example the European Pharmacopoeia reference “1 .4. , 07/2014: 10000 ").
- the glucose polymer of the invention may comprise other modifications, as long as it does not contravene the properties sought in the present invention, especially in terms of efficacy and safety. These modifications can be physical and / or chemical.
- the glucose polymer may for example be substituted. However, generally and advantageously, the glucose polymer of the invention is not substituted, that is to say in particular that it is not esterified, and / or etherified.
- the present invention also relates to a method, particularly useful for the preparation of a glucose polymer according to the invention, comprising subjecting a starch having an amylose content of at least 10% to:
- the branching step may be performed by means of a branching enzyme, for example selected from glycogen branching enzymes, starch branching enzymes, or a mixture thereof.
- a branching enzyme for example selected from glycogen branching enzymes, starch branching enzymes, or a mixture thereof.
- Such enzymes are commercially available.
- the product BRANCHZYME® Novozyme
- the reduction can be carried out by any technique known to those skilled in the art, for example by means of the use of sodium tetrahydoborate or dihydrogen, optionally in the presence of a catalyst such as Raney nickel.
- the branching step takes place before the reduction step.
- the operating conditions for the reduction are such that they allow the conversion of the reducing functions to hydroxyls without altering the hyperbranched structure of the polymer of glucose.
- the pH is adjusted during the reduction step to ensure that it does not damage the hyperbranched structure of the product, that is to say so as not to oxidize or hydrolyze the product.
- the reaction can be carried out at a temperature of about 40 ° C. for a reaction time making it possible to obtain a reducing sugar content as low as possible while maintaining the hyperbranched structure of starch, for example about 20 h.
- the reaction can for example be carried out at about 120 ° C for about 2-4 h.
- the method further comprises a hydrolysis step, preferably by means of an enzymatic treatment, preferably by means of a ⁇ -amylase and / or an amyloglucosidase.
- this hydrolysis step is subsequent to the branching step. It is preferably prior to the reduction step.
- the process of the invention comprises a prior step of solubilizing the starch, preferably by heating (also commonly known as "starch cooking").
- the method may further comprise an additional chromatography step, in particular so as to reduce the polyD of the glucose polymer to be obtained.
- the starch can then be purified and / or dried by any technique known to those skilled in the art.
- Examples of treatment useful for the purification (total or partial) of the glucose polymer of the invention are filtration, ultrafiltration, activated carbon treatment, these treatments can be combined with each other.
- the present invention also relates to a composition comprising the glucose polymer of the invention, in particular a pharmaceutical composition.
- the composition may comprise a pharmaceutically acceptable carrier or excipient. It may be a solution ready to be administered, especially parenterally, for example a preferably aqueous and sterile solution. It may also be a composition useful for the preparation of a solution to be administered. In the latter case for example, it can act a ready-to-use powdery composition, which can be reconstituted by a simple addition of water, before being sterilized and / or administered.
- the solution to be administered is chosen from a solution of peritoneal dialysis, parenteral nutrition, and plasma filling. It is most preferably a peritoneal dialysis solution.
- the glucose polymer concentration of the invention is selected in a range of from 1 to 20%, preferably from 1 to 15%, preferably from 1 to 10%. This concentration is preferably at least 2%, preferably at least 3%, preferably at least 4%. It is for example chosen in the range of 4 to 10%, preferably 5 to 9%, preferably 6 to 9%, for example 7 to 8%.
- this composition when this composition is a peritoneal dialysis solution, it is hypertonic. It thus preferably has an osmolality of greater than 280 mOsm / kg, preferably greater than 320 mOsm / kg.
- this composition when this composition is a solution for parenteral nutrition, or for plasma filling, it is isotonic. It thus preferably has an osmolality chosen in a range from 260 to 340 mOsm / kg, ideally in a range from 280 mOsm / kg to 320 mOsm / kg.
- the composition according to the invention has a pH chosen in a range from 6.00 to 9.00, preferably from 7.00 to 8.00, in particular from 7.30 to 7.50, for example from 7.35 to 7.45.
- the composition of the invention in particular the solution intended to be administered, in particular after sterilization with heat, presents: a content of 5-hydroxymethyl furaldehyde (5-HMF) of less than 135 ppb, preferably less than 100 ppb, preferably less than 50 ppb, preferably less than 30 ppb, preferably less than 20 ppb, preferably less than 10 ppb; ppb, preferably less than 8 ppb, preferably less than 6 ppb, preferably less than 4 ppb, preferably less than 2 ppb; and or,
- 5-HMF 5-hydroxymethyl furaldehyde
- 3,4-DGE 3,4-didesoxyglucosone-3-ene
- composition of the invention comprises other substances, as long as it does not contravene the properties sought in the present invention, especially as regards safety and efficacy.
- these other substances are typically chosen from:
- - active agents for example (i) osmotic agents, and / or plasma expander and / or parenteral nutrition agents other than the glucose polymer of the invention, for example icodextrin, glucose, dextrans , hydroxyethyl starch, (ii) therapeutic proteins, for example vaccines, antibodies;
- buffers for example lactate or citrate buffers
- the substance of the invention represents at least 50% by dry weight of the osmotic agents, and / or plasma expander and / or parenteral nutrition agents of the composition, preferably at least 60%, preferably at least 70%, preferably at least 80%, preferably at least 90%.
- the substance of the invention is the only osmotic agent and / or plasma expander and / or parenteral nutrition agent of the composition of the invention.
- the present invention also relates to the use of a glucose polymer according to the present invention for the preparation of a composition for peritoneal dialysis, and / or of a parenteral nutrition composition, and / or a plasma filling composition, and / or as an osmotic agent, and / or as a plasma expander, and / or for the preparation of a vaccine, in particular as an adjuvant, and / or for stabilizing proteins, and / or as a protein carrier.
- the subject of the invention is also a method for preparing a composition according to the invention, in particular a peritoneal dialysis solution, comprising mixing the polymer of the invention with at least one other substance, in particular as defined. before for the composition of the invention, and / or with a solvent, preferably water.
- this process comprises a step of sterilizing said composition, preferably heat sterilization.
- the invention also relates to the use of a glucose polymer or a composition according to the invention as a medicament.
- the present invention also relates to a method of treatment, comprising administering a glucose polymer or composition according to the invention, to a patient in need thereof.
- the glucose polymer or composition of the invention is for parenteral use.
- the glucose polymer is particularly suitable for use in peritoneal dialysis, especially as an osmotic agent.
- the present invention relates to a glucose polymer according to the present invention for its use in peritoneal dialysis, in particular in a peritoneal dialysis solution, in particular as an osmotic agent. It also relates to the use of a glucose polymer according to the present invention for the manufacture of a peritoneal dialysis solution, in particular for the treatment of chronic renal failure.
- the present invention also relates to a method for treating chronic renal failure by peritoneal dialysis in a subject, comprising administering a dialysis solution comprising the glucose polymer according to the present invention to said subject, in particular by injection in the peritoneal cavity.
- glucose polymer of the invention can also be used in other applications where parenteral administration is desired, for example for use in parenteral nutrition, plasma filling, especially as a plasma expander, or in vaccinology , especially as an adjuvant, or as a protein stabilizer, or as a protein carrier.
- the medicament of the invention is typically intended for a patient suffering from renal insufficiency, that is to say having a partial or total loss of renal function, consecutive for example to a diabetes or an infection.
- the present invention relates to a glucose polymer according to the present invention for use in a peritoneal dialysis solution. It also relates to the use of a glucose polymer according to the present invention for the manufacture of a peritoneal dialysis solution, in particular for the treatment of renal failure.
- the present invention also relates to a method of treating renal failure, comprising administering a peritoneal dialysis solution comprising the glucose polymer according to the present invention to said subject.
- the drug of the invention is typically intended for a patient suffering from hypovolemia, typically caused by rupture of the continuity of the vascular compartment, for example following trauma, surgery, burn.
- the present invention relates to a glucose polymer according to the present invention for use in a plasma filling solution. It also relates to the use of a glucose polymer according to the present invention for the manufacture of a plasma filling solution, in particular for the treatment of hypovolemia.
- the present invention also relates to a method of treating hypovolemia in a subject, comprising administering a plasma filling solution comprising the glucose polymer of the present invention to said subject.
- the drug of the invention is typically intended for a patient in whom enteral or oral nutrition is not possible, for example a patient suffering from intestinal insufficiency or food intolerance with vomiting.
- the present invention relates to a glucose polymer according to the present invention for use in a parenteral nutrition solution. It also relates to the use of a glucose polymer according to the present invention for the manufacture of a parenteral nutrition solution, in particular for the treatment of intestinal insufficiency or food intolerance with vomiting.
- the present invention also relates to a method of parenteral nutrition in a subject, comprising administering a parenteral nutrition solution comprising the glucose polymer according to the present invention to said subject, said subject being able to suffer from intestinal insufficiency or to food intolerance with vomiting.
- this concentration expresses well the number of grams of said substance per 100 ml of said solution.
- This mass in grams is indeed a dry mass, that is to say it excludes in particular the mass of water possibly present in the substance in its powder form, before solubilization.
- Figure 1 Influence of sterilization on the pH of solutions using different polymers of glucose or glucose (positive control), the pH being measured after sterilization at 121 ° C for 15 or 45 minutes.
- Figure 2 Influence of sterilization on the production of GDPs, namely 5-hydroxymethyl furaldehyde (5H-MF), furaldehyde, and 3,4-didesoxyglucosone-3-ene (3,4-DGE), solutions using different polymers of glucose or glucose (positive control).
- GDPs namely 5-hydroxymethyl furaldehyde (5H-MF), furaldehyde, and 3,4-didesoxyglucosone-3-ene (3,4-DGE)
- Figure 3 Influence of sterilization on protein reactivity, solutions using different glucose polymers or glucose (positive control) by measuring the absorbance at 284 nm.
- the starch used had a 65% amylose content (EURLYON® 7, Roquette).
- a starch milk starch (suspension) at 10% solids and pH 7.5 was baked at 160 ° C. The resulting glue was cooled to 75 ° C, and the pH was adjusted to 7.0.
- the starch was then subjected to a branching step by means of a branching enzyme (BRANCHZYME®, Novozymes), used at a rate of 625 to 1000 U / g dry starchy material, for 22 hours at 65 ° C. and at pH 7.0.
- BRANCHZYME® branching enzyme
- the reaction medium was then cooled to 48 ° C., and the pH was adjusted to 5.5.
- the branched starch thus obtained was subjected to a hydrolysis step using a ⁇ -amylase (OPTIMALT® BBA, Genencor International), used at a rate of 1 to 4 U / g dry starchy material, for 2 hours. at 48 ° C and a pH of 5.5. The enzyme was then quenched by heating for 1 hour at 85 ° C. The reaction mixture was cooled to 50 ° C and the pH was adjusted to 3.5. The reaction product was centrifuged at 5,000 rpm, and the supernatant was collected.
- a ⁇ -amylase OPTIMALT® BBA, Genencor International
- a solution of 30% branched starch thus obtained was prepared. Solubilization was favored by heating at 90 ° C, then the temperature was lowered to 40 ° C. The pH was adjusted to 10.5 with sodium hydroxide (3% NaOH).
- the starch in solution was subjected to a reduction step by means of 200 mol% of NaBH 4 with respect to the reducing functions.
- the pH was adjusted to 6.5. 18% H 2 SO 4 was added to the reaction product.
- the solution was dialyzed on 1000 Da membrane overnight. The product thus obtained was rotavapor dried and milled with a knife mill.
- the product [ICO] corresponds to an unmodified, i.e. unreduced, icodextrin.
- a reduced prior icodextrin according to US Pat. No. 6,770,148 has been prepared by reducing an icodextrin. For reduction, the procedure was as described in point 1. above.
- the product [HBS] corresponds to a product obtained by branching the starch, but having not undergone a reduction.
- the glucose polymer was connected by means of a branching enzyme and subjected to a hydrolysis step by means of a ⁇ -amylase.
- the glucose used was anhydrous dextrose (ROQUETTE).
- glucose polymers [HBS-red] according to the invention, and glucose polymers [ICO-red], [ICO], [HBS] were determined according to the following methods.
- the ratio of bonds a-1, 6. The ratio of ⁇ -1, 6 bonds was determined by proton NMR.
- the level of glucosidic linkages a-1, 6, expressed in percentages, corresponds to the amount of signal of the proton carried by the C1 of an anhydroglucose unit which binds another anhydroglucose unit by an ⁇ -1, 6 bond, when the a value of 100 has been given to all the glucoside proton signals carried by all C1 of the glucose residues of said glucose polymers.
- the osmolality was determined on the basis of an aqueous solution made of osmosis water comprising 0.4% of glucose polymer.
- the osmolality measurement of this solution was performed using an osmometer (FISKE® ASSOCIATES MARK 3), following the manufacturer's instructions. 3. Determination of the weight average molecular weight (Mw) and number (MN), and calculation of the polydolarity index (polyD). The average molecular weights M w and MN were determined according to two methods.
- Method 1 liquid chromatography (using pullulans of different M w for calibration) and detection by differential refractometry.
- a set of columns (Shodex OH pak SB - 800 QH) composed of the following columns was used:
- Stallions pullulan used had the next M w (Da): 78,000; 40,400; 21,000; 12,000; 47,300; 22,800; 1,800; 5,900.
- the elution solvent was an aqueous 0.2 M sodium nitrate solution containing 0.02% sodium azide filtered through a 0.02 ⁇ filter.
- the flow rate of the mobile phase for chromatography was 0.5 mL / min.
- Method 2 Liquid chromatography with light scattering detection (RI Detector and DAWN-HELEOS II Light Diffusion Detector).
- the elution solvent was an aqueous 0.1 M sodium nitrate solution containing 0.02% sodium azide filtered through a 0.02 ⁇ filter, and the dilution solvent was dimethylsulfoxide (DMSO) containing 0.1 M sodium nitrate.
- DMSO dimethylsulfoxide
- the flow rate of the mobile phase for chromatography was 0.5 mL / min.
- the calibration was performed with a pullulan (Pullulan P50, Shodex). 4. Determination of the reducing sugar content. The reducing sugar content was determined by the Bertrand method.
- the inventors have studied the influence of sterilization on the pH of solutions using different polymers of glucose or glucose (positive control).
- the glucose polymer according to the invention [HBS-red] is the one which has the pH closest to that of the physiological pH after sterilization. This is not the case for the comparative polymers [ICO-red], [ICO] and [HBS], which have acidic pH after sterilization, lower than 6.5, or even lower than 6.0; or deviations of more than one pH unit from the physiological pH.
- the inventors have studied the influence of sterilization on the production of GDPs, namely 5-hydroxymethyl furaldehyde (5-HMF), furaldehyde, and 3,4-didesoxyglucosone-3-ene (3, 4-DGE), solutions using different glucose polymers or glucose. 20 ml to 4% solutions of each of the test substances were prepared in osmosis water. The GDPs content was measured after sterilization at 121 ° C for 15 minutes.
- GDPs 5-hydroxymethyl furaldehyde
- furaldehyde furaldehyde
- 3, 4-DGE 3,4-didesoxyglucosone-3-ene
- the content of 5-HMF and furaldehyde was determined by liquid chromatography (using standards of 5-HMF (Merck - Ref.8.206.78.001) or furaldehyde for calibration respectively), and detection by UV spectrophotometry at 280 nm .
- chromatography a column with a particle size of 9 ⁇ , 8% crosslinking, an internal diameter of 7.8 mm and a length of 300 mm (HPX 87H column - Biorad - Ref.125.0140) was used.
- the conditions were as follows: eluent H2SO4 5mN (1 N sulfuric acid), flow rate 0.8 mL / min.
- the 3,4-DGE content was determined by liquid chromatography (using pyrazinecarboxamide (Sigma - Ref P7136) for calibration), and detection by UV spectrophotometry at 230 nm.
- chromatography a column with a particle size of 5 ⁇ , a pore size of 120 ⁇ , an internal diameter of 4.6 mm and a length of 15 cm (Supelcosil LC-18 - Supelco - Ref 58230) has been used.
- the conditions were as follows: Elution solvent H 2 O / MeOH, flow rate 1.0 mL / min.
- the glucose polymer according to the invention [HBS-red] is the only one for which, after sterilization, the GDPs are not detectable.
- the inventors have studied the influence of sterilization on the reactivity towards proteins, solutions using different glucose polymers or glucose. 0.5% solutions of each of the substances to be tested were prepared in a phosphate buffer (pH 7, 200 mM), in the absence or in the presence of 0.5% of L-lysine.
- the absorbance of the solutions at 284 nm was measured before and after sterilization at 121 ° C for 45 minutes.
- the phosphate buffer used for the realization of the solutions was used as a negative control.
- the difference in absorbance observed between the substance to be tested alone before and after sterilization can be attributed to the production of degradation products.
- the difference in absorbance observed between the substance to be tested in the presence and absence of lysine after sterilization can be attributed to the reactions that occur between the test substance and lysine, thus reflecting the reactivity of these substances. against proteins (Maillard reaction).
- the greater the difference in absorbance the more the substance can be judged to be reactive with respect to proteins.
- the results indicate that the glucose polymer [HBS-red] according to the invention is the least reactive substance vis-à-vis proteins. This very low reactivity suggests an excellent tolerance of the glucose polymer of the invention.
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JP2019514226A JP7058263B2 (ja) | 2016-09-15 | 2017-09-14 | 腹膜透析用の新規グルコースポリマー |
EP17780810.2A EP3512911A1 (fr) | 2016-09-15 | 2017-09-14 | Nouveaux polymères de glucose pour dialyse péritonéale |
US16/332,169 US11498939B2 (en) | 2016-09-15 | 2017-09-14 | Glucose polymers for peritoneal dialysis |
CN202211461871.4A CN115746408A (zh) | 2016-09-15 | 2017-09-14 | 用于腹膜透析的新颖的葡萄糖聚合物 |
CN201780056120.5A CN109689762A (zh) | 2016-09-15 | 2017-09-14 | 用于腹膜透析的新颖的葡萄糖聚合物 |
CA3036439A CA3036439C (fr) | 2016-09-15 | 2017-09-14 | Polymeres de glucose pour dialyse peritoneale |
MX2019002994A MX2019002994A (es) | 2016-09-15 | 2017-09-14 | Nuevos polimeros de glucosa para la dialisis peritoneal. |
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FR1658648A FR3055898B1 (fr) | 2016-09-15 | 2016-09-15 | Nouveaux polymeres de glucose pour dialyse peritoneale |
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EP (1) | EP3512911A1 (fr) |
JP (1) | JP7058263B2 (fr) |
CN (2) | CN109689762A (fr) |
CA (1) | CA3036439C (fr) |
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CN114460202A (zh) * | 2022-02-11 | 2022-05-10 | 山东威高肾科医疗器械有限公司 | 一种血液透析液中葡萄糖浓度的检测方法 |
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US3928135A (en) * | 1972-05-02 | 1975-12-23 | Jeremiah Milner | Process for the production of glucose polymers |
US20020065410A1 (en) * | 1999-12-02 | 2002-05-30 | Antrim Richard L. | Branched starches and branched starch hydrolyzates |
EP1369432A2 (fr) * | 2002-06-06 | 2003-12-10 | Roquette FrÀ¨res | Polymères solubles de glucose hautement branchés et leur procédé d'obtention |
US6770148B1 (en) | 1998-12-04 | 2004-08-03 | Baxter International Inc. | Peritoneal dialysis solution containing modified icodextrins |
EP1548033A2 (fr) * | 2003-12-19 | 2005-06-29 | Roquette FrÀ¨res | Polymères solubles de Glucose hautement branchés |
JP2008095117A (ja) * | 2004-09-30 | 2008-04-24 | Ezaki Glico Co Ltd | 高分岐かつ高分子量のグリコーゲン |
US20080241904A1 (en) * | 2001-04-27 | 2008-10-02 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | Process for producing isomaltose and uses thereof |
WO2011095736A1 (fr) * | 2010-02-02 | 2011-08-11 | Roquette Freres | Polymeres solubles de glucose branches pour la dialyse peritoneale |
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JP3811008B2 (ja) | 1998-08-24 | 2006-08-16 | 黒川 清 | カルボニルストレス状態改善剤、および腹膜透析液 |
TW520501B (en) | 2000-12-29 | 2003-02-11 | Amic Technology Taiwan Inc | Bias device for a magneto-resistive random access memory |
DE10237442B4 (de) | 2002-08-16 | 2004-08-19 | Fresenius Kabi Deutschland Gmbh | Hochverzweigte, niedrig substituierte Stärkeprodukte |
US20040121982A1 (en) * | 2002-12-20 | 2004-06-24 | Leo Martis | Biocompatible dialysis fluids containing icodextrins |
FR2897869B1 (fr) * | 2006-02-28 | 2011-05-06 | Roquette Freres | Polymeres solubles de glucose hautement branches pour la nutrition enterale, parenterale et pour la dialyse peritoneale |
JP4397965B1 (ja) | 2008-09-18 | 2010-01-13 | 日本食品化工株式会社 | 新規分岐グルカン並びにその製造方法および用途 |
FR2945043B1 (fr) * | 2009-04-30 | 2019-07-26 | Roquette Freres | Procede de purification de polymeres de glucose destines aux solutions de dialyse peritoneale |
-
2016
- 2016-09-15 FR FR1658648A patent/FR3055898B1/fr active Active
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2017
- 2017-09-14 EP EP17780810.2A patent/EP3512911A1/fr active Pending
- 2017-09-14 CN CN201780056120.5A patent/CN109689762A/zh active Pending
- 2017-09-14 CN CN202211461871.4A patent/CN115746408A/zh active Pending
- 2017-09-14 JP JP2019514226A patent/JP7058263B2/ja active Active
- 2017-09-14 MX MX2019002994A patent/MX2019002994A/es unknown
- 2017-09-14 WO PCT/FR2017/052446 patent/WO2018051020A1/fr unknown
- 2017-09-14 US US16/332,169 patent/US11498939B2/en active Active
- 2017-09-14 CA CA3036439A patent/CA3036439C/fr active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
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US3928135A (en) * | 1972-05-02 | 1975-12-23 | Jeremiah Milner | Process for the production of glucose polymers |
US6770148B1 (en) | 1998-12-04 | 2004-08-03 | Baxter International Inc. | Peritoneal dialysis solution containing modified icodextrins |
US20020065410A1 (en) * | 1999-12-02 | 2002-05-30 | Antrim Richard L. | Branched starches and branched starch hydrolyzates |
US20080241904A1 (en) * | 2001-04-27 | 2008-10-02 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | Process for producing isomaltose and uses thereof |
EP1369432A2 (fr) * | 2002-06-06 | 2003-12-10 | Roquette FrÀ¨res | Polymères solubles de glucose hautement branchés et leur procédé d'obtention |
EP1548033A2 (fr) * | 2003-12-19 | 2005-06-29 | Roquette FrÀ¨res | Polymères solubles de Glucose hautement branchés |
JP2008095117A (ja) * | 2004-09-30 | 2008-04-24 | Ezaki Glico Co Ltd | 高分岐かつ高分子量のグリコーゲン |
WO2011095736A1 (fr) * | 2010-02-02 | 2011-08-11 | Roquette Freres | Polymeres solubles de glucose branches pour la dialyse peritoneale |
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CA3036439C (fr) | 2024-02-13 |
CA3036439A1 (fr) | 2018-03-22 |
JP7058263B2 (ja) | 2022-04-21 |
FR3055898B1 (fr) | 2018-11-02 |
FR3055898A1 (fr) | 2018-03-16 |
EP3512911A1 (fr) | 2019-07-24 |
CN109689762A (zh) | 2019-04-26 |
MX2019002994A (es) | 2019-07-01 |
JP2019529641A (ja) | 2019-10-17 |
CN115746408A (zh) | 2023-03-07 |
US20190300558A1 (en) | 2019-10-03 |
US11498939B2 (en) | 2022-11-15 |
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