IP Library Granted Patent US 9,301,919
Granted Patent B2
US 9,301,919 · App. 11/615,048 · Granted Apr 5, 2016

Sublimable sustained release delivery system and method of making same

Inventor: Richard Maskiewicz (Redlands, CA)
Assignee: OAKWOOD LABORATORIES, LLC
A61K9/0024A61K9/1617Y10S514/957
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Quick Facts
Patent No.
US 9,301,919
App. No.
11/615,048
Granted
Apr 5, 2016
Kind
B2
Abstract

The invention relates to compositions suitable for the delivery and/or stabilization of biologically active substances. The compositions comprise a sublimable matrix material and the biologically active agent to be delivered. The compositions can be used as drug delivery systems to treat a wide variety of diseases or as systems for the protection and stabilization of such substances. Also disclosed are methods for preparing compositions of the present invention.

Claims (22)

1. A matrix biological insert or implant which is a delivery system suitable for sustained release of a biologically active agent within a mammal, said delivery system comprising:

(a) at least one water insoluble sublimable matrix material that converts to vapor at a desired rate over a desired duration in the body of a mammal; and

(b) a biologically active agent dispersed within said sublimable matrix material in an amount of 0.05 to 40% by weight based on a weight of said delivery system sufficient for prolonged treatment of a disease or other pathological condition in said mammal,

wherein said sublimable matrix material has a sublimation enthalpy in a range of from 20 to 100 kJ/mole and is present in an amount of at least 60% by weight based on a weight of said delivery system effective to achieve a sustained release of said active agent in said mammal upon conversion of said sublimable matrix material to said vapor, and

wherein said sublimable matrix material is selected from the group consisting of adamantane, perfluoroadamantane, 1-methyladamantane, perfluoro-1-methyladamantane, tetraisopropylmethane, perfluorotetraisopropylmethane, 2,2,3,3-tetramethylbutane (hexamethylethane), perfluoro-2,2,3,3-tetramethylbutane, perfluoroneopentane, perfluoro-C60fullerene, cubane, perfluorocubane, octamethylcubane, perfluorooctamethylcubane, perfluoromethyladamantane, perfluorotri-tert-butylmethane, perfluorodimethyladamantane, perfluorohexamethylethane, perfluoro-1,3-dimethyladamantane, isocamphane, tricyclene, 1-ethyladamantane,1-methyldiadamantane, perfluorodimethylbicyclo[3.3.1]nonane, diadamantane, perfluorodiadamantane, tri-tert-butylmethane, norbornane, perfluoronorbornane, cyclododecane, perfluorocyclododecane, hexamethylcyclotrisiloxane, perfluoroundecane, perfluorododecane, bicyclo[3.3.1]nonane, tetracycloheptane, tricyclohexane, dimethyl-isopropyl-perhydrophenanthrene, hexamethylprismane, prismane, tetracyclododecane, bicyclo[3.3.3]undecane, 2-methyladamantane, pentacycloundecane, tricyclodecane, bicyclodecane, bicyclo[2.2.2]octane, perfluoro-1,3,5-trimethyladamantane, perfluoro-2,2-dimethyladamantane, perfluorotetracycloheptane, perfluorotricyclohexane, perfluorohexamethylprismane, perfluoroprismane, perfluorotetracyclododecane, perfluorobicyclo[3.3.3]undecane, perfluoro-2-methyladamantane, perfluoropentacycloundecane, perfluorotricyclodecane, perfluorobicyclodecane, perfluorobicyclo[3.3.1]nonane, perfluorobicyclo[2.2.2]octane, perfluorobicyclo[2.2.1]heptane, and mixtures thereof.

2. A matrix biological insert or implant which is a delivery system suitable for sustained release of a biologically active agent within a mammal, said delivery system comprising:

(a) at least one water insoluble sublimable matrix material that converts to vapor at a desired rate over a desired duration in the body of a mammal; and

(b) a biologically active agent dispersed within said sublimable matrix material in an amount of 0.05 to 40% by weight based on a weight of said delivery system sufficient for prolonged treatment of a disease or other pathological condition in said mammal,

wherein said sublimable matrix material has a sublimation enthalpy in a range of from 20 to 100 kJ/mole and is present in an amount of at least 60% by weight based on a weight of said delivery system effective to achieve a sustained release of said active agent in said mammal upon conversion of said sublimable matrix material to said vapor, and

wherein said sublimable matrix material is selected from the group consisting of hexamethylcyclotrisiloxane, cyclododecane, perfluorododecane, perfluorododecane or mixtures thereof.

3. A matrix biological insert or implant that delivers a biologically active agent within a mammal, said insert or implant comprising:

(a) at least one water insoluble sublimable matrix material that converts to vapor at a desired rate over a desired duration in the body of a mammal, wherein said sublimable matrix material is selected from the group consisting of adamantane, perfluoroadamantane, 1-methyladamantane, perfluoro-1-methyladamantane, tetraisopropylmethane, perfluorotetraisopropylmethane, 2,2,3,3-tetramethylbutane (hexamethylethane), perfluoro-2,2,3,3-tetramethylbutane, perfluoroneopentane, perfluoro-C60 fullerene, cubane, perfluorocubane, octamethylcubane, perfluorooctamethylcubane, perfluoromethyladamantane, perfluorotri-tert-butylmethane, perfluorodimethyladamantane, perfluorohexamethylethane, perfluoro-1,3-dimethyladamantane, isocamphane, tricyclene, 1-ethyladamantane, 1-methyldiadamantane, perfluorodimethylbicyclo[3.3.1]nonane, diadamantane, perfluorodiadamantane, tri-tert-butylmethane, norbornane, perfluoronorbornane, cyclododecane, perfluorocyclododecane, hexamethylcyclotrisiloxane, perfluoroundecane, perfluorododecane, bicyclo[3.3.1]nonane, tetracycloheptane, tricyclohexane, dimethyl-isopropyl-perhydrophenanthrene, hexamethylprismane, prismane, tetracyclododecane, bicyclo[3.3.3]undecane, 2-methyladamantane, pentacycloundecane, tricyclodecane, bicyclodecane, bicyclo[2.2.2]octane, perfluoro-1,3,5-trimethyladamantane, perfluoro-2,2-dimethyladamantane, perfluorotetracycloheptane, perfluorotricyclohexane, perfluorohexamethylprismane, perfluoroprismane, perfluorotetracyclododecane, perfluorobicyclo[3.3.3]undecane, perfluoro-2-methyladamantane, perfluoropentacycloundecane, perfluorotricyclodecane, perfluorobicyclodecane, perfluorobicyclo [3.3.1]nonane, perfluorobicyclo[2.2.2]octane, perfluorobicyclo[2.2.1]heptane, and mixtures thereof; and

(b) a biologically active agent dispersed in said sublimable matrix material in an amount of 0.05 to 40% by weight based on a weight of said delivery system sufficient for prolonged treatment of a disease or other pathological condition in a mammal,

wherein said sublimable matrix material has a sublimation enthalpy in a range of from 20 to 100 kJ/mole and is present in an amount of at least 60% by weight based on a weight of said insert or implant effective to achieve a sustained release of said active agent in said mammal upon conversion of said sublimable matrix material to said vapor,

wherein said insert or implant is compressed into a predetermined size and shape, is chemically inert, and is biocompatible.

4. The biological insert or implant of claim 3 wherein said sustained release of said active agent within said mammal occurs for a period of about 7 days.

5. The biological insert or implant of claim 3 further comprising a sublimation rate modifier selected from the group consisting of trimethylacetamide, 2,2-dimethyl-1,3-propanediol, neopentylpivalate, perfluorodecalin, tri-tert-butylmethanol, camphor, camphene, neo-pentyl alcohol, hexachloroethane, chlorobutanol, menthol, terpin hydrate, vanillin, ethyl vanillin, 1,3,5-trioxane, naphthalene, phenol, dextran, glycogen, tert-butanol, biodegradable polymers comprised of polylactic acid or copolymers of lactic and glycolic acids, polyorthoesters, or polyanhydrides, microparticles comprised of said biodegradable polymers, fatty acids, polyvinylpyrrolidone, polyethyleneglycol, polyvinyl alcohol, polyacrylic acid, cholesterol and microparticles thereof, triglycerides having a melting point above 37° C., collagen and microparticles thereof, gelatin and microparticles thereof, ethanol, propylene glycol, PEG 400, glycerol, polyglycerol, polysorbates, sucralose, sucralose pentahydrate, and mixtures thereof.

6. The biological insert or implant of claim 3 wherein said predetermined shape of said insert or implant is a disk, a cylinder, a rod, a ring or a pellet.

7. The biological insert or implant of claim 3 wherein said amount of said sublimable matrix material is at least 80% by weight based on the weight of said insert or implant.

8. The biological insert or implant of claim 3 wherein said sustained release of said active agent within said mammal occurs for a period of about 30 days.

9. The biological insert or implant of claim 3 wherein said sustained release of said active agent within said mammal occurs for a period of about 3 months.

10. The biological insert or implant of claim 3 which is a biological implant.

Assignments (2)
SECURITY INTEREST Recorded May 30, 2014
From: OAKWOOD LABORATORIES, L.L.C.
To: ALFERA PHARMACEUTICALS, LLC
Reel/Frame 033070/0329 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2006
From: MASKIEWICZ, RICHARD
To: OAKWOOD LABORATORIES, LLC
Reel/Frame 018671/0337 →
Continuity (2)
Provisional Application 60753114 · Dec 22, 2005
Related Publication 20070148098A1 · Jun 28, 2007