EP3648748A1 - Forme posologique solide à enrobage entérique comprenant des sels d'acides aminés d'acides gras oméga-3 - Google Patents

Forme posologique solide à enrobage entérique comprenant des sels d'acides aminés d'acides gras oméga-3

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Publication number
EP3648748A1
EP3648748A1 EP18735585.4A EP18735585A EP3648748A1 EP 3648748 A1 EP3648748 A1 EP 3648748A1 EP 18735585 A EP18735585 A EP 18735585A EP 3648748 A1 EP3648748 A1 EP 3648748A1
Authority
EP
European Patent Office
Prior art keywords
dosage form
omega
oral dosage
solid oral
enteric coated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP18735585.4A
Other languages
German (de)
English (en)
Inventor
Ashish Guha
Vishal KANERIA
Shraddha Joshi
Suraj BHOSALE
Smitha Shetty
Christine JARECKI
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Evonik Operations GmbH
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Evonik Operations GmbH
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Filing date
Publication date
Application filed by Evonik Operations GmbH filed Critical Evonik Operations GmbH
Publication of EP3648748A1 publication Critical patent/EP3648748A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806—Coating materials
    • A61K9/282—Organic compounds, e.g. fats
    • 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
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • A61K31/202—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having three or more double bonds, e.g. linolenic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2886—Dragees; Coated pills or tablets, e.g. with film or compression coating having two or more different drug-free coatings; Tablets of the type inert core-drug layer-inactive layer

Definitions

  • Enteric coated solid dosage form comprising omega-3 fatty acid amino acid salts
  • Omega-3 fatty acids particularly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)
  • EPA eicosapentaenoic acid
  • DHA docosahexaenoic acid
  • the EFSA European Food Safety Authority
  • EPA + DHA EFSA Panel on Dietetic Products, Nutrition and Allergies, EFSA Journal 2010, 8 (3), 1461
  • the AHA American Heart Association
  • omega-3 fatty acids especially from fish oil but also from other plant or microbial sources, are increasingly used as food supplements, food additives and medicaments.
  • DHA docosahexaenoic acid
  • omega- 3 fatty acid is eicosapentaenoic acid (EPA), which is referred to as "20:5 n-3" (all-cis-5,8, 1 1 , 14, 17- eicosapentaenoic acid).
  • EPA eicosapentaenoic acid
  • omega-3 fatty acid products introduced to the market are offered in the form of oils, starting from fish oil with a content of about 30% omega-3 fatty acids up to concentrates with over 90% content of EPA or DHA or mixtures of these two omega-3 fatty acids.
  • the formulations used are predominantly soft gelatine capsules.
  • numerous further product forms have been described, such as microencapsulations or powder preparations (C. J. Barrow, B. Wang, B.
  • the bioavailability of the different omega-3 derivatives for the human body is very diverse. Since omega-3 fatty acids as free fatty acids together with monoacyl glycerides are absorbed in the small intestine, the bioavailability of free omega-3 fatty acids is better than that of triglycerides or ethyl esters since these have firstly to be cleaved to the free fatty acids in the digestive tract (J. P. Schuchhardt, A. Hahn, Prostaglandins Leukotrienes Essent. Fatty Acids 2013, 89, 1 ). The stability to oxidation is also very different in different omega-3 derivatives.
  • Free omega-3 fatty acids are described as very sensitive to oxidation (J. P. Schuchhardt, A. Hahn, Prostaglandins Leukotrienes Essent. Fatty Acids 2013, 89, 1 ).
  • oxidation J. P. Schuchhardt, A. Hahn, Prostaglandins Leukotrienes Essent. Fatty Acids 2013, 89, 1 .
  • solid omega-3 form an increased stability compared to liquid products is assumed (J. A. Kralovec, H. S. Ewart, J. H. D. Wright, L. V. Watson, D. Dennis, C. J. Barrow, J. Functional Foods 2009, 1 , 217).
  • preparations of omega-3 fatty acids with diverse amino acids, such as lysine and arginine are known, either as mixtures (P. Literati Nagy, M. Boros, J.
  • omega-3 aminoalcohol salts by spray-drying is also mentioned (P. Rongved, J. Klaveness, US 2007/0213298 A1 ).
  • DHA amino acid salts is described by evaporation to dryness under high vacuum and low temperature or freeze-drying (T. Bruzzese, EP0734373 B1 und US 5750572).
  • the resulting products are described as very thick, transparent oils which transform at low temperature into solids of waxy appearance and consistency.
  • omega-3 fatty acid products are a fishy taste and smell. When the omega-3 fatty acid products are adsorbed in the stomach, further negative effects accrue, such as a fishy reflux and unpleasant fishy regurgitation, which shall be avoided.
  • Enteric film coatings are applied to oral dosage forms to delay the release of the active ingredients until the dosage form has passed through the acidic environment of the stomach (pH between 1.0 and 3.0) and has reached the less acidic environment of the proximal small intestine.
  • the physical chemical environment of the stomach and gastric physiology are highly variable, due to multiple factors such as disease state, medication, age, and eating.
  • the pH is less than 2.0 in healthy individuals, and gastric emptying occurs approximately every 30 minutes.
  • gastric emptying is delayed for 2 to 4 hours and gastric pH can be as high as pH 4.0.
  • enteric film coatings include methacrylic acid copolymers, polyvinyl acetate phthalate, cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate and hydroxypropyl methylcellulose acetylsuccinate.
  • shellac is a natural, food approved, resinous material, which is secreted by the female lac bug Kama lacca and is a complex mixture of materials.
  • the two main components with enteric properties being shelloic and aleuritic acid.
  • shellac is well known as a material with enteric-like properties, it has a number of drawbacks. Due to insolubility in water, shellac has traditionally been used in the form of organic solvent based solutions. Additionally, in its natural state, shellac is generally not soluble below a pH of 7.5 to 8.0.
  • shellac films simply soften and disintegrate after immersion in water for a number of hours. This is problematic as enteric coatings should generally be soluble or rupturable in the proximal intestinal environment. Lastly, shellac coatings have been reported to undergo esterification during aging, rendering the film completely water insoluble even in alkaline pH. Enteric coating using shellac for liquid omega-3 fatty acid compositions in food products has been described in the international patent application WO2012/168882A1. However, this publication refers to liquid components only.
  • solid omega-3 fatty acid preparations which can be readily and cost-effectively formulated as solid dosage forms, which have better bioavailability and in addition are also more stable than standard liquid formulations.
  • these solid dosage forms shall comprise an enteric coating, which allow a release of the omega-3 fatty acids in the small intestine at pH values below pH 7.0. To allow an optimal absorption of omega-3 fatty acids already in the upper intestine, it is desirable that those are released at a slight lower pH-value around pH 5.0.
  • enteric coated solid dosage forms according to the present invention comprising a core with one or more omega-3-fatty acid amino acid salts, and with a coating comprising shellac, which provides a delayed release of the omega-3 -fatty acid amino acid salts in the upper intestine.
  • the present invention accordingly relates in a first aspect to an enteric coated nutraceutical or pharmaceutical solid oral dosage form comprising a core with a nutraceutical or pharmaceutical active ingredient and an enteric coating wherein the enteric coating comprises shellac and wherein the nutraceutical or pharmaceutical active ingredient comprises one or more omega-3 fatty acid amino acid salts.
  • a food grade or pharma grade shellac it is preferred to use a food grade or pharma grade shellac. While not excluding other grades of shellac, a preferred type is dewaxed shellac, which is usually refined using a solvent extraction process. For production of light-colored grades, activated carbon is used followed by an additional filtration step to remove the activated carbon. The solvent is removed afterwards by evaporation in a thin film evaporator and recovered. The resin is then drawn to a thin film, which typically breaks into flakes after cooling.
  • Omega-3 fatty acids which may be present individually or in any preferred combination in a solid oral dosage form according to the invention, comprise for example a-linolenic acid (ALA) 18:3 (n-3) (cis,cis,cis-9, 12, 15-octadecatrienoic acid), stearidonic acid (SDA) 18:4 (n-3) (all-cis-6,9, 12, 15,- octadecatetraenoic acid), eicosatrienoic acid (ETE) 20:3 (n-3) (all-c; ' s-1 1 , 14, 17-eicosatrienoic acid), eicosatetraenoic acid (ETA) 20:4 (n-3) (all-cis-8, 1 1 ,14, 17-eicosatetraenoic acid),
  • ALA a-linolenic acid
  • SDA stearidonic acid
  • ETE eicosatrienoic acid
  • ETA eicosatetraeno
  • HPA heneicosapentaenoic acid
  • DPA docosapentaenoic acid
  • DPA docosapentaenoic acid
  • DPA docosapentaenoic acid
  • tetracosapentaenoic acid 24:5 (n-3) all-cis-9, 12, 15, 18,21- tetracosapentaenoic acid
  • tetracosahexaenoic acid nisinic acid) 24:6 (n-3) (all-cis- 6,9, 12, 15, 18,21-tetracosahexaenoic acid).
  • Polyunsaturated omega-3 fatty acids may be obtained from any suitable starting material, which may in addition be processed with any suitable method.
  • Typical starting materials include all parts of fish carcasses, vegetables and other plants, and material from microbial fermentation or fermentation of algae.
  • Typical processing methods for such starting materials are, inter alia, steps for crude oil extraction, such as extraction and separation of the starting materials and steps for refining crude oils, such as deposition and degumming, deacidification, bleaching and deodourizing (cf. e.g. "EFSA Scientific Opinion on Fish Oil for Human Consumption").
  • Further processing methods include, inter alia, steps for the at least partial conversion of omega-3 fatty acid esters to the corresponding free omega-3 fatty acids or inorganic salts thereof.
  • the source for omega-3 fatty acids is chosen from at least one of the following: fish oil, squid oil, krill oil, linseed oil, borage seed oil, algal oil, hemp seed oil, rapeseed oil, flaxseed oil, canola oil, soybean oil.
  • Omega-3 fatty acids may also be obtained by cleaving the omega-3 fatty acid esters and subsequent removal of the alcohols previously attached as part of the ester from compositions, which consist principally of omega-3 fatty acid esters.
  • the ester cleavage is preferably carried out under basic conditions. Methods for ester cleavage are well known from the prior art.
  • omega-3 fatty acids and amino acids are dissolved in the digestive tract, wherein the free omega-3 fatty acids are released which are suitable for direct absorption by the body, and prior chemical or enzymatic cleavage is no longer required, such as is the case in the omega-3 triglycerides in fish oil or the omega-3 fatty acid ethyl esters prepared therefrom.
  • the omega-3 fatty acids are only released in the small intestine, which demonstrably is the actual location in the body for the absorption of fatty acids from the digestive tract, such that the omega-3 fatty acids are available for immediate absorption in the preferred free form.
  • the effects such as reflux or unpleasant fishy regurgitation often usually linked with the absorption of omega-3 fatty acid oils by the too early release of the omega-3 fatty acid oils in the stomach is thus avoided.
  • the enteric coating further comprises an anionic polymer, preferably pectin or sodium alginate.
  • the use of pectin is preferred. It is further preferred that the ratio between shellac and the anionic polymer in the enteric coating is between more than 80:20 (more than 80% of shellac in the mixture of shellac and anionic polymer) and 100:0, preferably between 81 : 19 and 99: 1 , more preferably between 85: 15 and 95:5.. In a more preferred embodiment, the ratio between shellac and the anionic polymer in the enteric coating is between 90:10 and 95:5.
  • the enteric coating further comprises one or more plasticizers chosen from glycerol, mineral oil, triacetin, polyethylene glycol, glyceryl monostearate, mono- acetylated triglycerides and polysorbate.
  • Glycerol is the most preferred plasticizer due to its universal status as food plasticizer. Glycerol may be used in an amount ranging from 3% to 30% by weight (relating to the shellac-polymer).
  • the enteric coating further comprises one or more pigments such as titanium dioxide and talc.
  • the solid oral dosage form further comprises a subcoat, which is selected from the following: cellulose-derived polymers, selected from hydroxyl propyl methyl cellulose (HPMC), methyl hydroxyl ethyl cellulose (MHEC), ethyl cellulose (EC), hydroxyl propyl cellulose (HPC) and sodium carboxy methyl cellulose, polyvinylpyrrolidone (PVP), polyvinyl alcohol (PVA), polyethylene glycols (PEG), acrylate polymers, maize starch and mixtures thereof.
  • the subcoat builds an additional coating layer, which has additional taste- and/or odour-masking effects.
  • the solid oral dosage form further comprises an additional layer comprising one or more pigments, natural colours, flavours, sweeteners and/or cyclodextrins.
  • the amino acid(s) is/are selected from basic amino acids, preferably from lysine, arginine, ornithine and mixtures of the same.
  • the omega-3 fatty acid(s) is/are selected from eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), docosapentaenoic acid (DPA) and mixtures of the same.
  • EPA eicosapentaenoic acid
  • DHA docosahexaenoic acid
  • DPA docosapentaenoic acid
  • Omega-3 fatty acid amino acid salts are known in principle. As described at the outset, these may be obtained as fine, virtually colourless powders by precipitation from aqueous or aqueous alcoholic media or by spray-drying, which differ advantageously from the waxy consistency of these substances described hitherto. In a preferred configuration, the omega-3 fatty acid amino acid salts are obtained by precipitation from aqueous or alcoholic aqueous solution.
  • the enteric coated solid oral dosage form is characterized in that the release of the omega-3 fatty acid amino acid salts is less than 10% by weight of the content of omega-3 fatty acid amino acid salt when an in vitro dissolution testing for the solid dosage form is performed in 0.1 N hydrochloric acid for a period of 2 hours.
  • Dissolution testing is an in vitro method that characterizes how an active pharmaceutical ingredient (API) or an active food ingredient (AFI) is extracted out of a solid dosage form and indicates the efficiency of in vivo dissolution.
  • API active pharmaceutical ingredient
  • AFI active food ingredient
  • the specific dissolution technique employed was the industry standard dissolution testing methodology United States Pharmacopoeia (USP) Apparatus 1 basket.
  • USP United States Pharmacopoeia
  • the enteric coated solid oral dosage form is characterized in that the release of the omega-3 fatty acid amino acid salt is more than 60% by weight of the content of omega-3 fatty acid amino acid salt when an in vitro dissolution testing for the solid dosage form is performed in a solution with a pH between pH 4 and pH 6, preferably in a solution with a pH between pH 4 and pH 5 for a period of 3 hours.
  • the enteric coated solid dosage form comprises small particulates.
  • Small particulates also known as pellets in the pharmaceutical industry can be defined as small, free-flowing, spherical particulates with a relatively narrow size range usually between 0.1 and 2.0 mm and a low porosity (about 10%).
  • the multiparticulate dosage forms offers many important pharmacological and technological advantages over conventional single-unit dosage forms. They can be divided into desired dose strength without formulation or process changes and can be blended to deliver incompatible bioactive agents simultaneously and/or provide different release profiles at different sites in the gastrointestinal tract. When taken orally, pharmaceutical pellets disperse freely in the gastrointestinal tract and maximize drug absorption (due to the higher surface area) and minimize local irritation of the mucosa by certain irritating drugs. Thereby, versatile formulation designs are possible, which can easily be adapted to the different patient requirements.
  • the coating of the small particulates is at least 2.0 mg/cm 2 .
  • the weight gain I (mg/cm 2 ), which is achieved by coating of the pellets is calculated according to the following formula: wherein % Coating weight [w/w] corresponds to the percentage weight gain due to the coating layer (relating to the weight of the pellet core), W [mg] is the weight of the pellet core and A [mm 2 ] is the surface area of the pellet core.
  • the enteric coated solid oral dosage form is stable at a temperature of 40 °C and a relative humidity of 75% for at least 3 months. After storage under these conditions for three months, the dissolution profile is similar to the dissolution profile of a freshly prepared solid oral dosage form.
  • the present invention relates to a food supplement or pharmaceutical product comprising one or more enteric coated small particulates according to the present invention.
  • the dosage form of the food supplement or pharmaceutical product is selected from one of the following: Multiple-Unit Pellet System (MUPS) tablets, capsules, sachets, sprinkles, gummies and straw formulations.
  • MUPS Multiple-Unit Pellet System
  • the dosage form further comprises one or more additional active ingredients selected from anthocyanins, vitamins, minerals, fiber, fatty acids, amino acids and proteins. Further nutraceutically acceptable active ingredients may also be included in the dosage form.
  • the present invention relates to the use of a solid dosage form according to the invention as a food supplement or pharmaceutical product.
  • pharmaceutical products may comprise, in addition to the omega-3 fatty acids described here, both pharmaceutically acceptable auxiliaries and
  • statins such as statins, anti-hypertensive agents, antidiabetics, antidementia agents, antidepressants, anti-obesity agents, appetite suppressants and agents to improve memory and/or cognitive function.
  • Example 1 Preparation of omeqa-3 fatty acid lysine salt pellets for coating trials
  • the Hydroxypropyl Cellulose (HPC) was dissolved in the required quantity of purified water.
  • the omega-3 fatty acid lysine salt was added to the solution under high speed stirring.
  • the solution was then homogenized for 15-20 min until a lump free solution was formed.
  • the final solution was sprayed on sugar spheres to obtain the omega-3 fatty acid lysine pellets.
  • Metoprolol succinate and the microcrystalline celluloses Avicel PH 101 and CL 61 1 were sifted through a 40# sieve and mixed for 30 min in a rapid mixer granulator (RMG) at slow speed. Water was added under continuous mixing at slow speed and the wet mass was mixed further with chopper. The granulated mass was used for extrusion and the extrudates were obtained. 350-400 g of extrudate was added on a spheronization plate (Cross-Hatched type) for spheronization at 1700 rpm for 4 min to get pellets of optimum size and shape. The pellets were dried at 60°C for 2 hours in a fluid bed dryer granulator.
  • Example 3 Shellac coating on omeqa-3 fatty acid lysine salt pellets
  • Omega-3 fatty acid lysine salt pellets were prepared as described in Example 1 and used for the coating trials.
  • shellac SSB 55 Pharma shellac SSB 56 Pharma
  • shellac SSB 55 Astra all from SSB Stroever GmbH & Co. KG, Germany.
  • the characteristics referring to coating and dissolution of the different types of shellac were similar.
  • Ammonium hydrogen carbonate was dissolved in the required quantity of water and was heated up to a temperature of 80-90°C.
  • Shellac was added slowly to the solution under stirring, maintaining a constant temperature of 80-90°C to form a lump free solution.
  • Glycerol was added under stirring.
  • talc was added to the solution under stirring.
  • the final solution was then sprayed on omega-3 fatty acid lysine salt pellets (50 g of pellet material) until a weight gain of 3.5 mg/cm 2 was achieved.
  • the solid content of the coating dispersion was 10% (w/w).
  • the shellac-coated pellets were tested in dissolution studies in different buffer conditions with various pH-values.
  • the in vitro analysis was performed with 100 rpm and a bath temperature of 37°C ( ⁇ 0.5°C).
  • 900 ml of 0.1 N HCI was used as a media, followed by the buffer stage (of further 60 min) with 900 ml of phosphate buffer with the respective pH-value (pH 3.5, pH 4.5, pH 5.5 or pH 6.8).
  • the samples were analysed using RP-HPLC at 210nm.
  • the coated pellets showed enteric properties in 0.1 N HCI for 120 minutes (acceptance criteria is ⁇ 10%) followed by a release in pH 4.5 phosphate buffer and at higher pH-values (acceptance criteria > 60%).
  • Example 4 Shellac-pectin coating on omeqa-3 fatty acid lysine salt pellets
  • Omega-3 fatty acid lysine salt pellets were prepared as described in Example 1 and used for the coating trials.
  • Ammonium hydrogen carbonate was dissolved in half of the required quantity of water and was heated up to a temperature of 80-90°C.
  • Shellac was added slowly to the solution under stirring, maintaining a constant temperature of 80-90°C to form a lump free solution.
  • Glycerol followed by pectin was added slowly to the remaining half of water under stirring to form a lump free solution.
  • talc was added to the solution under stirring.
  • the final solution was then sprayed on omega-3 fatty acid lysine salt pellets (50 g of pellet material) until a weight gain of 4.3 mg/cm 2 was achieved.
  • the solid content of the coating dispersion was 10% (w/w).
  • the coated pellets showed enteric properties in 0.1 N HCI for 120 minutes followed by a release pH 4.5 phosphate buffer and at higher pH-values.
  • Omega-3 fatty acid lysine salt pellets were prepared as described in Example 1 and used for the coating trials.
  • the coating composition from Example 4 was used for the coating of the omega-3 fatty acid lysine salt pellets in which pectin was replaced by sodium alginate to get shellac-sodium alginate (ratio 95:5) until a weight gain of 4.3 mg/cm 2 was achieved.
  • the pellets coated with shellac-sodium alginate were tested in dissolution studies in different buffer conditions with various pH-values as described in Example 3.
  • the coated pellets showed enteric properties in 0.1 N HCI for 120 minutes followed by a release in pH 4.5 phosphate buffer and at higher pH-values.
  • Example 6 Shellac coating on Metoprolol succinate pellets Metoprolol succinate pellets were prepared as described in Example 2 and used for the coating trials. The shellac coating composition from Example 3 was used for the coating of the Metoprolol succinate pellets until a polymeric weight gain of 3.4 mg/cm 2 and 6.7 mg/cm 2 .
  • Metoprolol succinate pellets coated with shellac were tested in dissolution studies in different buffer conditions with various pH-values as described in Example 3.
  • Metoprolol succinate pellets were prepared as described in Example 2 and used for the coating trials.
  • the shellac-pectin coating composition from Example 4 was used for the coating of the Metoprolol succinate pellets until a polymeric weight gain of 2.7 mg/cm 2 and 1.1 mg/cm 2 .
  • the Metoprolol succinate pellets coated with shellac-pectin were tested in dissolution studies in different buffer conditions with various pH-values as described in Example 3.
  • Metoprolol succinate pellets only a very slight drug release could be observed at pH 6.8. This shows that the shellac-pectin coating does not work on Metoprolol succinate pellets.
  • Example 8 Preparation of Gummies containing omega-3 fatty acid lysine salt pellets coated with shellac-pectin
  • the shellac-pectin coated omega-3 fatty acid lysine salt pellets were prepared as described in Example 4. Gummies were prepared using the following materials:
  • Example 9 Preparation of MUPS tablets containing omeqa-3 fatty acid lysine salt pellets coated with shellac-pectin
  • the shellac-pectin coated omega-3 fatty acid lysine salt pellets were prepared as described in Example 4.
  • MUPS tablets were prepared using the following materials:
  • Microcrystalline cellulose (Avicel PH200, 802, 102) crosscarmellose sodium and colloidal silicon dioxide were sifted through a #30 mesh (600 microns).
  • the coated Omega-3 fatty acid lysine salt pellets were mixed with sifted ingredients in double cone blender for 15 minutes.
  • the sodium stearyl fumarate was sifted through #80 mesh (180 microns), added to the mixture and mixed further for 3 minutes.
  • the lubricated blend was finally compressed on a rotary tableting machine.
  • Example 10 Preparation of capsules containing omeqa-3 fatty acid lysine salt pellets coated with shellac-pectin
  • Example 1 1 Preparation of straws containing omeqa-3 fatty acid lysine salt pellets coated with shellac-pectin The shellac-pectin coated omega-3 fatty acid lysine salt pellets were prepared as described in Example 4 and filled in straws.
  • Example 12 Preparation of capsules containing omeqa-3 fatty acid lysine salt pellets coated with shellac-pectin and anthocyanins
  • the shellac-pectin coated omega-3 fatty acid lysine salt pellets were prepared as described in Example 4. 175 mg of shellac-pectin coated omega-3 fatty acid lysine salt pellets and 150 mg Healthberry® 865 (Evonik Nutrition and Care GmbH, Darmstadt, Germany) containing extracts of bilberries and blackcurrants with high concentrations in anthocyanins were filled in size 0 capsules.
  • Example 13 Preparation of flavoured omeqa-3 fatty acid lysine salt pellets coated with shellac- pectin
  • the shellac-pectin coated omega-3 fatty acid lysine salt pellets were prepared as described in Example 4.
  • Example 14 Preparation of shellac-pectin coated omeqa-3 fatty acid lysine salt pellets coated with ⁇ -cyclodextrin The shellac-pectin coated omega-3 fatty acid lysine salt pellets were prepared as described in Example 4. The coating dispersion was prepared with the following materials:
  • HPMC 6CPS was dissolved in water under stirring to form a lump free solution
  • ⁇ -cyclodextrin was added to the solution under stirring for 15 min.
  • the final dispersion was sprayed on the shellac- pectin coated omega-3 fatty acid lysine salt pellets to achieve a coat of ⁇ -cyclodextrin of 0.2 mg/cm 2 .
  • Example 15 Preparation of barrier coated omeqa-3 fatty acid lysine salt pellets coated with shellac-pectin Omega-3 fatty acid lysine salt pellets were prepared as described in Example 1 and used for the coating trials.
  • the coating dispersion was prepared with the following materials:
  • the amounts were calculated as % by weight with relation to the EUDRAGUARD® natural polym (w.r.t. polymer).
  • Glycerol was dissolved in the required quantity of purified water. The solution was heated up to 50- 60°C followed by slow addition of the EUDRAGUARD® natural polymer (a maize starch-based functional coating, Evonik Nutrition and Care GmbH, Darmstadt, Germany) under stirring.
  • talc was added to the solution under stirring. During the coating procedure the temperature of the coating dispersion was maintained between 40-50°C.
  • the omega-3 fatty acid lysine salt pellets were coated until a coating of 1.7 mg/cm 2 was achieved.
  • the barrier coated omega-3 fatty acid lysine salt pellets were further coated with shellac-pectin (95:5) under the same conditions as described in Example 4.
  • the barrier coated omega-3 fatty acid lysine salt pellets coated with shellac-pectin were tested in dissolution studies in different buffer conditions with various pH-values as described in Example 3:
  • the coated pellets showed enteric properties in 0.1 N HCI for 120 minutes followed by a release in pH 6.8 phosphate buffer and at higher pH-values.
  • Example 16 Stability studies of omeqa-3 fatty acid lysine salt pellets coated with shellac-pectin
  • the shellac-pectin coated omega-3 fatty acid lysine salt pellets were prepared as described in
  • Example 4 For analysing the stability of the shellac-pectin coated pellets, the pellets were filled in a HDPE container without silica and were stored at a temperature of 40 °C and a relative humidity (RH) of 75% for a period of 3 months. Dissolution studies were performed after different time points.
  • the dissolution characteristics of the shellac-pectin coated omega-3 fatty acid lysine salt pellets were found to be similar to the characteristics of the pellets before storage. This shows that the shellac-pectin coated pellets can be stored several months without negative effects on the stability of the pellets.

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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La présente invention concerne le domaine des formulations pharmaceutiques et nutraceutiques, et, plus spécifiquement, des formes posologiques orales solides à enrobages entériques, des compléments alimentaires, des produits pharmaceutiques et l'utilisation de ces formes posologiques. La forme posologique orale solide ou nutraceutique à enrobage entérique comprend un coeur avec un principe actif nutraceutique ou pharmaceutique et un enrobage entérique, le revêtement entérique comprenant de la gomme laque et le principe actif nutraceutique ou pharmaceutique comprenant un ou plusieurs sels d'acides aminés d'acides gras oméga-3.
EP18735585.4A 2017-07-06 2018-07-05 Forme posologique solide à enrobage entérique comprenant des sels d'acides aminés d'acides gras oméga-3 Withdrawn EP3648748A1 (fr)

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IN201731023754 2017-07-06
EP17186984 2017-08-21
PCT/EP2018/068261 WO2019008101A1 (fr) 2017-07-06 2018-07-05 Forme posologique solide à enrobage entérique comprenant des sels d'acides aminés d'acides gras oméga-3

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Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3962462A1 (fr) * 2019-04-30 2022-03-09 DSM IP Assets B.V. Nouveau système d'administration d'acides gras polyinsaturés
WO2020234221A1 (fr) * 2019-05-23 2020-11-26 Evonik Operations Gmbh Compositions prébiotiques
US20220312816A1 (en) * 2019-05-23 2022-10-06 Evonik Operations Gmbh Preparation for use in enhancing formation of short-chain fatty acids (scfas)
WO2021023849A1 (fr) * 2019-08-08 2021-02-11 Evonik Operations Gmbh Procédé de diffusion en continu pour la production de sels d'acides gras polyinsaturés
EP4125437A1 (fr) * 2020-04-01 2023-02-08 Evonik Operations GmbH Préparation destinée à être utilisée en tant que vasorelaxeur
WO2021197971A1 (fr) * 2020-04-01 2021-10-07 Evonik Operations Gmbh Préparation destinée à être utilisée en tant qu'antioxydant
WO2022078823A1 (fr) * 2020-10-16 2022-04-21 Evonik Operations Gmbh Composition nutraceutique ou pharmaceutique comprenant un amidon modifié

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU209973B (en) 1988-03-09 1995-01-30 Biorex Kutato Fejlesztoe Kft Process for production of antiviral and immunstimular pharmaceutical composition
IT1264987B1 (it) 1993-12-14 1996-10-17 Prospa Bv Sali di un acido grasso poliinsaturo e formulazioni farmaceutiche che li contengono
IT1274734B (it) 1994-08-25 1997-07-24 Prospa Bv Composizioni farmaceutiche contenenti acidi grassi poliinsaturi, loro esteri o sali, unitamente a vitamine o provitamine antiossidanti
ITMI20012384A1 (it) 2001-11-12 2003-05-12 Quatex Nv Uso di acidi grassi poliinsaturi per la prevenzione primaria di eventi cardiovascolari maggiori
US7098352B2 (en) 2001-11-16 2006-08-29 Virtus Nutrition Llc Calcium salt saponification of polyunsaturated oils
EP1996686A1 (fr) 2006-02-07 2008-12-03 Universitetet I Oslo Omega 3
WO2009032728A2 (fr) 2007-08-31 2009-03-12 Jh Biotech, Inc. Préparation d'acides gras sous forme solide
CA2705518A1 (fr) 2007-11-13 2009-05-22 Hercules Incorporated Formulation d'enrobage enterique dispersible dans l'eau pour des formes posologiques nutraceutiques et pharmaceutiques
US20100179089A1 (en) * 2009-01-13 2010-07-15 Deutz Nicolaas E P Compositions and Methods to Manage the Inflammatory Basis of Chronic Disease Conditions and Maintain an Optimal Immune Response in Elderly
EP3563842A1 (fr) 2009-04-29 2019-11-06 Amarin Pharmaceuticals Ireland Limited Compositions pharmaceutiques comprenant de l'epa et un agent cardiovasculaire et leurs procédés d'utilisation
US20110002986A1 (en) 2009-07-02 2011-01-06 Hercules Incorporated Stable Shellac Enteric Coating Formulation for Nutraceutical and Pharmaceutical Dosage Forms
EP2654463B1 (fr) 2010-12-21 2018-05-30 Omegatri AS Antioxydants dans la poudre et les comprimés à base d'huiles de poissons
US20120178813A1 (en) 2011-01-12 2012-07-12 Thetis Pharmaceuticals Llc Lipid-lowering antidiabetic agent
US20140051877A1 (en) 2011-04-28 2014-02-20 Nandakishore Jeevanrao Duragkar Eicosapentaenoic acid (epa) as polyunsaturated free fatty acid in its directly compressible powder form and process of isolation thereof
US20140018558A1 (en) 2011-04-28 2014-01-16 Nandakishore Jeevanrao Duragkar Docosahexaenoic acid (dha) as polyunsaturated free fatty acid in its directly compressible powder form and method of isolation thereof
RU2013156437A (ru) 2011-06-07 2015-07-20 СПАЙ Груп Лтд. Композиция и способы улучшения стабильности и продления срока хранения чувствительных пищевых добавок и пищевых продуктов из них
WO2013040507A1 (fr) 2011-09-15 2013-03-21 Omthera Pharmaceuticals, Inc. Méthodes et compositions pour traiter, inverser, inhiber ou prévenir la résistance à la thérapie antiplaquettaire
NZ626699A (en) 2012-01-06 2017-03-31 Omthera Pharmaceuticals Inc Dpa-enriched compositions of omega-3 polyunsaturated fatty acids in free acid form
US20140011814A1 (en) 2012-07-06 2014-01-09 Thetis Pharmaceuticals Llc Diamine and meglumine salt forms of fatty acids
WO2014011895A2 (fr) 2012-07-11 2014-01-16 Thetis Pharmaceuticals Llc Sels d'acides à solubilité élevée, formes posologiques intraveineuses, apport complémentaire nutritionnel et leurs procédés d'utilisation
US20140127299A1 (en) * 2012-11-07 2014-05-08 NaZura BioHealth, Inc. GRAS Enteric Coating Formulations and Methods of Making and Using Same

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