Solubility parameter based drug delivery system and method for altering drug saturation concentration

• US 5,474,783 A
• Filed: 06/27/1991
• Issued: 12/12/1995
• Est. Priority Date: 03/04/1988
• Status: Expired due to Term

• Current Assignee: Noven Pharmaceuticals Inc (Hisamitsu Pharmaceutical Company Incorporated)
• Original Assignee: Noven Pharmaceuticals Inc (Hisamitsu Pharmaceutical Company Incorporated)
• Inventors: Miranda, Jesus, Sablotsky, Steven
• Primary Examiner(s): VENKAT, JYOTHSNA A
• Application Number:
  US07/722,342
• Time in Patent Office: 1,629 Days
• Field of Search: 424/448, 424/449, 424/447, 524/506
• US Class Current: 424/448
• CPC Class Codes: A61F 13/0276 Apparatus or processes for manufacturing adhesive dressings or bandages
• CPC Class Codes: A61F 2013/00646 Medication patches, e.g. transcutaneous
• CPC Class Codes: A61K 9/7053 obtained by reactions only involving carbon to carbon unsaturated bonds, e.g. polyvinyl, polyisobutylene, polystyrene
• CPC Class Codes: A61K 9/7061 Polyacrylates
• CPC Class Codes: A61K 9/7069 obtained otherwise than by reactions only involving carbon to carbon unsaturated bonds, e.g. polysiloxane, polyesters, polyurethane, polyethylene oxide
• CPC Class Codes: A61L 15/18 containing inorganic materials
• CPC Class Codes: A61L 15/58 Adhesives
• CPC Class Codes: A61L 15/585 Mixtures of macromolecular compounds
• CPC Class Codes: A61P 11/06 Antiasthmatics
• CPC Class Codes: A61P 25/02 for peripheral neuropathies
• CPC Class Codes: A61P 27/06 Antiglaucoma agents or miotics
• CPC Class Codes: A61P 5/30 Oestrogens
• CPC Class Codes: A61P 9/10 for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
• CPC Class Codes: B26F 1/384 using rotating drums
• CPC Class Codes: C08L 31/04 Homopolymers or copolymers of vinyl acetate
• CPC Class Codes: C08L 33/00 Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
• CPC Class Codes: C08L 83/04 Polysiloxanes

Abstract

The method of adjusting the saturation concentration of a drug in a transdermal composition for application to the dermis, which comprises mixing polymers having differing solubility parameters, so as to modulate the delivery of the drug. This results in the ability to achieve a predetermined permeation rate of the drug into and through the dermis. In one embodiment, a dermal composition of the present invention comprises a drug, an acrylate polymer, and a polysiloxane. The dermal compositions can be produced by a variety of methods known in the preparation of drug-containing adhesive preparations, including the mixing of the polymers, drug, and additional ingredients in solution, followed by removal of the processing solvents. The method and composition of this invention permit selectable loading of the drug into the dermal formulation and adjustment of the delivery rate of the drug from the composition through the dermis, while maintaining acceptable shear, tack, and peel adhesive properties.

Claims

1. A pressure sensitive adhesive transdermal drug delivery system comprising:

(a) a blend consisting essentially of about 2% to about 96% by weight of a polyacrylate and about 98% to about 4% by weight of a polysiloxane, said blend being in an amount of about 99% to about 50% by weight of said system and wherein said ratio of polyacrylate to polysiloxane is from about 2;

98 to about 86;

14 by weight of said blend and wherein the permeation rate is controlled by varying the relative proportions of the polymers;

(b) a drug in the amount of about 0.3% to about 50% by weight of said system and wherein the drug is selected from the group consisting of nitroglycerin, isosorbide dinitrate, isosorbide mononitrates, quinidine sulfate, procainamide, bendroflumethiazide, chlorothiazide, nifedipine, nicardipine, timolol, propranolol, verapamil, diltiazem, captopril, clonidine, prazosin, testosterone, estropipate, 17β

-estradiol, 17β

-estradiol valerate, equilin, mestranol, estrone, estriol, 17β

-ethinyl estradiol, diethylstilbestrol, progesterone, 19-norprogesterone, norethindrone, norethindrone acetate, melengestrol, chloramdinone, ethisterone, medroxyprogesterone acetate, hydroxyprogesterone caproate, ethynodiol diacetate, norethynodrel, 17-alpha-hydroxyprogesterone, dydrogesterone, dimethisterone, ethinylestrenol, norgestrel, demegestone, promegestone, megestrol acetate, buprenorphine, naloxone, haloperidol, codeine, lidocaine, tetracaine, dyclonine, dibucaine, cocaine, procaine, mepivacaine, bupivacaine, etidocaine, prilocaine, benzocaine, fentanyl, hydrocortisone, cortisone, prednisolone, prednisone, halcinonide, betamethasone, ibuprophen, naproxen, fenoprofen, fenbufen, indoprofen, ketoprofen, suprofen, indomethacin, piroxicam, aspirin, salicylic acid, chlorpheniramine, theophilline, albuterol, terbutaline, metaproterenol, carbuterol, fenoterol, quinterenol, rimiterol, solmefamol, soterenol, tretoquinol, dopamine, phenylpropanolamine, epinephrine, pilocarpine, choline, acetylcholine, methacholine, carbachol, bethanechol, muscarine, arecoline, scopolamine, eucatropine, atropine, penicillin, tetracycline, papaverine, tamoxifen, dextroamphetamine, mazindol, alprazolam, chlordiazepoxide, clorazeptate, halazepam, oxazepam, prazepam, chlonazepam, flurazepam, triazolam, lorazepam, diazepam, thiopropazate, chlorpromazine, triflupromazine, mesoridazine, piperacetazine, thioridazine, acetophenazine, fluphenazine, perphenazine, trifluoperazine, chlorprothixene, thiothixene, bromperidol, loxapine, molindone, pyrimethamine, misoprostol, enprostil, levodopa, selegiline, baclofene, and mixtures thereof;

(c) optionally, an effective amount of a co-solvent for the drug, said amount being up to about 30% by weight of said system; and

(d) optionally, an effective amount of an enhancer, said amount being up to about 20% by weight of said system.

2. The transdermal drug delivery system of claim 1 further comprising fillers and excipients in an amount of about 1% to about 15% by weight of said transdermal drug delivery system.

3. The transdermal drug delivery system of claim 1, which is in the form of a sheet.

4. The transdermal drug delivery system of claim 1, wherein the drug is a β

₂ -adrenergic agonist selected from the group consisting of metaproterenol, terbutaline, albuterol, carbuterol, rimiterol, solmefamol, fenoterol, soterenol, tretoquinol, and quinterenol.

5. The transdermal drug delivery system of claim 4, wherein the β

₂ -adrenergic agonist is albuterol and the albuterol is present in the transdermal drug delivery system in an amount of about 0.3% to less than about 30% by weight.

6. The transdermal drug delivery system of claim 4, which comprises based on the weight of the transdermal drug delivery system, about 0.3 to about 50% by weight of albuterol, about 14 to about 97% by weight of polysiloxane, about 2 to about 85% by weight of polyacrylate, 0 to about 20% by weight of enhancers, and 0 to about 30% by weight of cosolvents.

7. The transdermal drug delivery system of claim 1, wherein the drug is a tranquilizer selected from the group consisting of alprazolam, chlordiazepoxide, clorazeptate, halazepam, oxazepam, prazepam, chlonazepam, flurazepam, triazolam, lorazepam and diazepam.

8. The transdermal drug delivery system of claim 7, wherein the tranquilizer is alprazolam.

9. The transdermal drug delivery system of claim 8, which comprises based on the weight of the transdermal drug delivery system, about 0.3 to about 50% by weight of alprazolam, about 14 to about 97% by weight of polysiloxane, about 2 to about 85% by weight of polyacrylate, 0 to about 20% by weight of enhancers, and 0 to about 30% by weight of cosolvents.

10. The transdermal drug delivery system of claim 1, which comprises based on the weight of the transdermal drug delivery system, about 0.3 to about 50% by weight of drug, about 14 to about 97% by weight of polysiloxane, about 2 to about 85% by weight of polyacrylate, 0 to about 20% by weight of enhancers, and 0 to about 30% by weight of cosolvents.

11. The transdermal drug delivery system of claim 1 which further comprises a hydrophilic filler.

12. The transdermal drug delivery system of claim 11, wherein the hydrophilic filler comprises aluminum silicate clay.

13. The transdermal drug delivery system of claim 1, wherein the polyacrylate of the blend is itself a pressure sensitive adhesive.

14. The transdermal drug delivery system of claim 13 further comprising a backing material superimposed on one surface of the pressure sensitive adhesive, said backing material being substantially impermeable to the drug contained therein.

15. The transdermal drug delivery system of claim 13 further comprising a release liner superimposed on a surface of the pressure sensitive adhesive opposite said backing material.

16. The transdermal drug delivery system of claim 1 wherein the drug is a progestional agent selected from the group consisting of progesterone, 19-norprogesterone, norethindrone, norethindrone acetate, melengestrol, chloramdinone, ethisterone, medroxyprogesterone acetate, hydroxyprogesterone caproate, ethynodiol diacetate, norethynodrel, 17a-hydroxyprogesterone, dydrogesterone, dimethisterone, ethinylesternol, norgestrel, demegestone, promegestone, and megestrol acetate.

17. The transdermal drug delivery system of claim 1, wherein the drug is a cardioactive agent selected from the group consisting of nitroglycerin, isosorbide dinitrate, isosorbide monitrates, quinidine sulfate, procainamide, bendroflumethiazide, chlorothiazide, nifedipine, nicardipine, verapamil, dilatiazem, timolol, propranolol, captopril, clonidine and prazosin.

18. The transdermal drug delivery system of claim 1, wherein the drug is a cholinergic agonist selected from the group consisting of choline, acetylcholine, methacholine, carbachol, bethanechol, pilocarpine, muscarine, and arecoline.

19. The transdermal drug delivery system of claim 1, wherein the drug is 17β

-estradiol and is present in the transdermal drug delivery system in an amount of from about 1% to about 5% by weight.

20. The transdermal drug delivery system of claim 16, wherein the progestational agent is norethindrone acetate and the norethindrone acetate is present in the transdermal drug delivery system in an amount of from about 1% to about 5% by weight.

21. The transdermal drug delivery system of claim 17, wherein the cardioactive agent is nitroglycerin and the nitroglycerin is present in the transdermal drug delivery system in an amount of about 0.3% to less than about 25% by weight.

22. The transdermal drug delivery system of claim 18, wherein the cholinergic agonist is pilocarpine and the pilocarpine is present in the transdermal drug delivery system in an amount of about 0.3% to less than about 30% by weight.

23. The transdermal drug delivery system of claim 1, wherein the drug is an antipsychotic selected from the group consisting of thiopropazate, chlorpromazine, triflupromazine, mesoridazine, piperacetazine, thioridazine, acetophenazine, fluphenazine, perphenazine, trifluoperazine, chlorprothixene, thiothixene, haloperidol, bromperidol, loxapine and molindone.

24. The transdermal drug delivery system of claim 23, wherein the antipsychotic is haloperidol.

25. The transdermal drug delivery system of claim 1, wherein the drug is an anesthetic selected from the group consisting of lidocaine, tetracaine, dyclonine, dibucaine, cocaine, procaine, mepivacaine, bupivacaine, etidocaine, prilocaine and benzocaine.

26. The transdermal drug delivery system of claim 25, wherein the anesthetic is lidocaine.

27. The transdermal drug delivery system of claim 1, wherein the drug is an analgesic selected from the group consisting of fentanyl, buprenorphine and codeine.

28. The transdermal drug delivery system of claim 1, wherein the drug is an estrogen selected from the group consisting of estropipate, 17β

-estradiol, equilin, mestranol, estrone, estriol, estradiol, and diethylstilbestrol.

29. The transdermal drug delivery system of claim 28, comprising a mixture of a progestational agent and an estrogen.

30. The transdermal drug delivery system of claim 29, wherein said progestational agent is selected from the group consisting of progesterone, 19-norprogesterone, norethindrone, norethindrone acetate, melengestrol, chloromadinone, ethisterone, medroxyprogesterone acetate, hydroxyprogesterone caproate, ethynodiol diacetate, norethynodrel, 17a-hydroxyprogesterone, dydrogesterone, dimethisterone, ethinylestrenol, norgestrel, demegestone, promegestone, and megestrol acetate.

31. The transdermal drug delivery system of claim 30, wherein said progestational agent is norethindrone acetate.

32. The transdermal drug delivery system of claim 29, wherein said estrogen is 17β

-estradiol.