Specific time-delayed burst profile delivery system

• US 20060280795A1
• Filed: 06/08/2005
• Published: 12/14/2006
• Est. Priority Date: 06/08/2005
• Status: Abandoned Application

• Current Assignee: Dexcel Pharma Technologies (Dexcel Limited)
• Original Assignee: Dexcel Pharma Technologies (Dexcel Limited)
• Inventors: Gomberg, Maxim, Penhasi, Adel, Gomberg, Mila
• Application Number:
  US11/147,388
• Publication Number:
  US 20060280795A1
• Time in Patent Office: Days
• US Class Current: 424/472
• CPC Class Codes: A61K 9/2886 having two or more different drug-free coatings; Tablets of the type inert core-drug layer-inactive layer of the type active core-drug layer-inactive layer A61K9/209
• CPC Class Codes: A61K 9/4891 Coated capsules; Multilayered drug free capsule shells with drug coating for immediate release A61K9/4808; osmotic devices A61K9/0004

Abstract

The invention provides a delivery device for the delayed release of an active agent in the gastrointestinal tract comprising a core, comprising an active agent; a first outer coating, comprising a relatively hydrophobic substantially water insoluble polymer having substantially water insoluble hydrophilic particles embedded therein; and a first inner coating layer, comprising an agent that can cause the dissolution of at least one of the water insoluble components of the outer coating, and optionally a water soluble polymer, such that the insoluble particles in the outer coating, upon absorption of liquid, form channels leading to the inner coating layer, thus enabling the dissolution thereof, whereby the agents contained therein are released to cause the dissolution and/or degradation (destruction) of the outer coating, and the release of the pharmaceutically acceptable active agent from the core of the device.

Claims

1. A delivery device for the delayed release of an active agent in the gastrointestinal tract comprising:

a) a core, comprising an active agent;

b) a first outer coating, comprising a relatively hydrophobic substantially water insoluble polymer having substantially water insoluble hydrophilic particles embedded therein; and

c) a first inner coating layer, comprising an agent that can cause the dissolution of at least one of said water insoluble components of said outer coating, and optionally a water soluble polymer, such that said insoluble particles in said outer coating, upon absorption of liquid, form channels leading to said inner coating layer, thus enabling the dissolution thereof, whereby the agents contained therein are released to cause at least the dissolution, degradation or destruction of said outer coating, and the release of the active agent from the core of said device.

2. The device of claim 1 for the delayed release of a physiologically acceptable active agent in the gastro-intestinal tract having a physiologically acceptable active agent incorporated therein.

3. The device of claim 1 for the delayed release of a pharmaceutically acceptable active agent in the gastrointestinal tract having a pharmaceutically acceptable active agent incorporated therein.

4. The device of claim 1 wherein it is further coated with an enteric coating.

5. The device according to claim 4 wherein the enteric coating is more preferably selected from the group consisting of hydroxypropylmethyl cellulose phthalate, polyvinyl acetate phthalate, cellulose a cetate phthalate, hydroxypropylmethyl cellulose acetate succinate, poly(methacrylic acid, methyl methacrylate)1:

1, poly(methacrylic acid, ethyl acrylate)1;

1, alginic acid, and sodium alginate.

6. The device according to claim 4 wherein, the outer enteric coating further comprises a plasticizer.

7. The device according to claim 6 wherein, the plasticizer preferably includes at least one of dibutyl sebacate, polyethylene glycol and polypropylene glycol, dibutyl phthalate, diethyl phthalate, triethyl citrate, tributyl citrate, acetylated monoglyceride, acetyl tributyl citrate, triacetin, dimethyl phthalate, benzyl benzoate, butyl and/or glycol esters of fatty acids, refined mineral oils, oleic acid, castor oil, corn oil, camphor, glycerol and sorbitol or a combination thereof.

8. The device of claim 1 wherein the relatively hydrophobic polymer of the first outer coating is selected from the group consisting of dimethylaminoethylacrylate/ethylmethacrylate copolymer, the copolymer being based on acrylic and methacrylic acid esters with a low content of quaternary ammonium groups, wherein the molar ratio of the ammonium groups to the remaining neutral (meth)acrylic acid esters is approximately 1:

20, said polymer corresponding to USP/NF “

Ammonio Methacrylate Copolymer Type A”

, an ethylmethacrylate/chlorotrimethylammoniumethyl methacrylate copolymer, the copolymer based on acrylic and methacrylic acid esters with a low content of quaternary ammonium groups wherein the molar ratio of the ammonium groups to the remaining neutral (meth)acrylic acid esters is 1;

40, the polymer corresponding to USP/NF “

Ammonio Methacrylate Copolymer Type B”

, a dimethylaminoethylmethacrylate/methylmethacrylate and butylmethacrylate copolymer, a copolymer based on neutral methacrylic acid esters and dimethylaminoethyl methacrylate esters wherein the polymer is cationic in the presence of acids, an ethylacrylate and methylacrylate/ethylmethacrylate and methyl methylacrylate copolymer, the copolymer being a neutral copolymer based on neutral methacrylic acid and acrylic acid esters, ethylcellulose, shellac, and waxes.

9. The device of claim 8 wherein the relatively hydrophobic polymer is ethylcellulose, Eudragit E, Eudragit RL, Eudragit RS, and Eudragit NE.

10. The device of claim 1 wherein the substantially water insoluble hydrophilic particles are selected from the group consisting of water insoluble cross-linked polysaccharide, a water insoluble cross-linked protein, a water insoluble cross-linked peptide, water insoluble cross-linked gelatin, water insoluble cross-linked hydrolyzed gelatin, water insoluble cross-linked collagen, water insoluble cross linked polyacrylic acid, water insoluble cross-linked cellulose derivatives, water insoluble cross-linked polyvinyl pyrrolidone, micro crystalline cellulose, insoluble starch, micro crystalline starch and a combination thereof.

11. The device of claim 10 wherein the water insoluble cross-linked polysaccharide is selected from the group consisting of insoluble metal salts or cross-linked derivatives of alginate, pectin, xantham gum, guar gum, tragacanth gum, locust bean gum, carrageenan, modified cellulose and covalently cross-linked derivatives thereof.

12. The device of claim 10 wherein the substantially water insoluble hydrophilic particles are chosen from insoluble metal salts of a polysaccharide.

13. The device of claim 10 wherein the insoluble metal salts of said polysaccharide are chosen from the group consisting of calcium pectinate and calcium alginate.

14. The device of claim 10 wherein the water insoluble cross-linked cellulose derivatives is selected from the group consisting of cross-linked derivatives of hydroxypropylcellulose, hydroxypropylmethylcellulose, hydroxyethylcellulose, methylcellulose, carboxymethylcellulose, and metal salts of carboxymethylcellulose.

15. The device of claim 10 wherein the substantially water insoluble hydrophilic particle is microcrystalline cellulose.

16. The device according to claim 1 wherein said first inner coating layer comprising pharmaceutically acceptable water soluble polymer.

17. A device according to claim 16 wherein said water soluble polymer is selected from the group consisting of Povidone (PVP:

polyvinyl pyrrolidone), polyvinyl alcohol, copolymer of PVP and polyvinyl acetate, HPC (hydroxypropyl cellulose) (more preferably a low molecular weight), HPMC (hydroxypropyl methylcelluloseY (more preferably a low molecular weight), carboxy methyl cellulose (more preferably a low molecular weight), ethylcellulose, hydroxyethyl cellulose, gelatin, polyethylene oxide, acacia, dextrin, magnesium aluminum silicate, starch, polyacrylic acid, polyhydroxyethylmethacrylate (PHEMA), polymethacrylates and their copolymers, gum, water soluble gum, polysaccharide, hydroxypropylmethyl cellulose phthalate, polyvinyl acetate phthalate, cellulose acetate phthalate, hydroxypropylmethyl cellulose acetate succinate, poly(methacrylic acid, methyl methacrylate)1;

1 and poly(methacrylic acid, ethyl acrylate)1;

1, alginic acid, and sodium alginate, and any other pharmaceutically acceptable water soluble polymer and a mixture thereof.

18. A device according to claim 16 wherein said water soluble polymer is a pharmaceutically acceptable polymer that dissolves in aqueous medium with pH >

4.

19. A device according to claim 1 wherein said dissolution agent of said first inner coating layer is a non-volatile organic acid.

20. A device according to claim 19 wherein said non-volatile organic acid selected from the group consisting of citric acid, fumaric acid, malic acid, ascorbic acid (Vitamin C), lactic acid, oxalic acid, maleic acid, malonic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebasic acid, tartaric acid, acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, succinic acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, palmatic acid, and the like, and amino acids selected from the group consisting of aspartic acid and glutamic acid, and any other pharmaceutically acceptable organic acids and a mixture thereof.

21. A device according to claim 1 wherein said dissolution agent of said first inner coating layer is a chelating agent.

22. A device according to claim 21 wherein said chelating agent is selected from the group consisting but not limited to antioxidants, the mono-, di-, tri- and tetrapotassium salt of ethylenediaminetetraacetic acid (EDTA, edetic acid), mono-, di-, tr-i and tetrasodium salt of EDTA, disodium calcium salt of EDTA, other EDTA salts, ethylenediaminetetraacetic acid, fumaric acid, malic acid, oxalic acid, maltol, and salts of any pharmaceutically acceptable organic acid.

23. A device according to claim 21 wherein said outer coating comprises an insoluble metal salt of a polysaccharide in amount of at least 30% of said first outer film coating weight.

24. A device according to claim 1 further comprising a further water soluble, inner coating layer which separates between said first inner coating and said core.

25. A device according to claim 24 wherein said water soluble, inner coating layer comprises a buffering agent.

26. A device according to claim 24 wherein said water soluble inner layer coating comprises a water soluble polymer selected from the group, listed in claim 15.

27. A device according to claim 1 wherein said core comprising a gelatin capsule.

28. A device according to claim 1, wherein the active agents are selected from the group consisting of compounds that act on:

the peripheral nerves, adrenergic receptors, cholinergic receptors, nervous system, skeletal muscles, cardiovascular system, smooth muscles, blood circulatory system, blood coagulation system, synaptic sites, neuroeffector junctional sites, endocrine and hormone systems, immunological system, reproductive system, skeletal systems, autocoid systems, alimentary and excretory systems, inhibitory and histamine systems and the central nervous system.

29. A device according to claim 1, wherein the active agent is selected from the group consisting of anti-hypertensives, diuretics, anti-arrthrytics cholesterol lowering drugs, immunosuppressants, steroidals, anti-inflammatories, hormonals, anti-psoriatics hypoglycemics, analgesics, antiviral drugs, antimicrobials anti-parasitics, anti-cancer drugs, antiepileptics, CNS stimulants, CNS depressants, antidepressants, 5 HT inhibitors, anti-schizophrenics, anti-Alzheimer drugs, anti-ulcer drugs, proton pump inhibitors, anti-asthmatics, anticoagulation drugs and vitamins.

30. A device according to claim 3 wherein said pharmaceutically acceptable active agent is selected from a group of drugs of poor bioavailability, said drugs being selected from the group consisting of anti-hypertensives, immunosuppressants, anti-inflammatories, diuretics, antiepileptics, cholesterol lowering drugs, hormonals hypoglycemics, antiviral drugs, nasal decongestants, antimicrobials, anti-arthritics, analgesics, anti-cancer drugs, anti-parasitics, proteins, peptides, polypeptides, CNS stimulants, CNS depressants, 5 HT inhibitors, anti-schizophrenics, anti-Alzheimer drugs, anti-psoriatics, steroidals, oligonucleotides, anti-ulcer drugs, proton pump inhibitors, anti-asthmatics, thrombolyitics and vitamins.

31. A device according to claim 3 wherein said pharmaceutically acceptable active agent is a compound metabolized by Cytochrome P450 3A enzymes, said compound being selected from the group including but not limited to Alprazolam, Amiodarone, Amitriptyline, Astemizole, Atrovastatin, Budesonide, Bupropion, Buspirone, Caffeine, Carbamazepime, Cerivastatin, Cisapride, Claritromycin, Clomipramin, Clonazepam, Codeine, Cyclosporine, Dexametazone, Dextrometorphan, DHEA, Diazepam, Diltiazem, Disopiramide, Donepezil, Doxycicline, Erytromycin, Estradiol, Ethylestradiol, Felodipine, Fluoxetine, Imipramine, Lanzoprazole, Lidocaine, Loratidine, Lovastatin, Midazolam, Nefazodone, Nicardipine, Nifedipine, Nizoldipine, Norethindrone, Omeprazole, Ondansetron, Orphenadrine, Paroxetine, Progesterone, Pro[afenone, Quethiapine, Quinidine, Rifampin, Sertraline, Sibutramine, Sildenafil, Simvastatin, Tacrolimus, Tamoxifen, Terfenadine, Testosterone, Theophyline, Trazodone, Triazolam, Venlafaxine, Verapamyl, Vinblastine, (R)-Warfarin, Zolpidem.

32. A device according to claim 1, wherein the active agent is active agent is selected from the group consisiting of peptides, proteins, polypeptides, oligonucleotides or polysaccharides.

33. A device according to claim 32 wherein said polypeptides are selected from the group consisting of, therapeutical agents, nutritional products, steroids, hormones, insulin, growth hormone (GH), growth hormone releasing hormone (GHRH), epithelial growth factor, vascular endothelial growth and permeability factor (VEGPF), nerve growth factor, cytokines, interleukins, interferons, GMCSF, hormone-like products, neurological factor, neurotropic factor, neurotransmitter, neuromodulator, enzyme, antibody, peptide, proteic fragment, vaccine, adjuvant, an antigene, immune stimulating or inhibiting factor, heomatopoietic factor, anti-cancer product, anti-inflammatory agent, anti-parasitic compound, anti-microbial agent, cell proliferation inhibitor or activator, cell differentiating factor, blood coagulation factor, immunoglobulin, anti-angiogenic product, negative selective markers or “

suicide”

agent, toxic compound, anti-angiogenic agent, and the like, and structurally similar bioactive equivalents thereof.