Injection-molded dosage form

Claim 2

A dosage form for delivering a therapeutic agent to an environment of use, the dosage form comprising: (a) an internal compartment; (b) a therapeutic composition comprising a therapeutic agent in the compartment; (c) an expandable composition comprising means for pushing the therapeutic composition from the dosage form in the compartment; (d) exit means in the dosage form that connects the therapeutic composition with the environment of use, and wherein the dosage form comprises: (e) an injection-molded membrane comprising a thermoplastic polycaprolactone, which injection-molded membrane is permeable to the passage of fluid and surrounds, defines and forms the internal compartment.

Claim 3

The dosage form for delivering the therapeutic agent according to claim 1; wherein the injection-molded membrane comprises a polycaprolactone copolymer with a member selected from the group consisting of dilactide, diglycolide, valerolactone and decalactone.

Claim 4

The dosage form for delivering the therapeutic agent according to claim 1, wherein the injection-molded membrane comprises a polycaprolactone and a polyalkylene oxide.

Claim 5

The dosage form for delivering the therapeutic agent according to claim 1, wherein the injection-molded membrane comprises polycaprolactone, polyalkylene oxide and poly(ethylene glycol-co-propylene glycol).

Claim 6

The dosage form for delivering the therapeutic agent according to claim 1, wherein the injection-molded membrane comprises a polycaprolactone and polyethylene glycol.

Claim 7

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) an osmotic composition in the second section; and wherein the dosage form comprises; (f) an injection-molded membrane, used for forming the first section and the second section, which membrane defines the first and second sections that form the internal lumen, the injection-molded membrane comprising a softening temperature of 40° C. to 180° C. and is permeable to the passage of fluid in the environment of use.

Claim 8

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) an osmotic composition in the second section; and wherein the dosage form comprises; (f) an injection-molded membrane, used for forming the first section and the second section, which membrane defines the first and second sections that form the internal lumen, the injection-molded membrane comprising a softening temperature of 40° C. to 180° C. and is permeable to the passage of fluid in the environment of use.

Claim 9

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) an osmotic composition in the second section comprises; (f) an injection-molded thermoplastic membrane forming the first section and the second section, the injection-molded membrane comprising a polycaprolactone that is permeable to the passage of fluid.

Claim 10

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) an osmotic composition in the second section comprises; (f) an injection-molded thermoplastic membrane forming the first section and the second section, the injection-molded membrane comprising a polycaprolactone that is permeable to the passage of fluid.

Claim 11

The dosage form for delivering the therapeutic agent according to claim 7, wherein the injection-molded membrane comprises a polycaprolactone copolymer selected from the group consisting of polycaprolactone dilactide copolymer, polycaprolactone diglycolide, polycaprolactone valerolactone, and polycaprolactone decalactone.

Claim 12

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) an osmotic composition in the second section; and wherein the dosage form comprises: (f) an injection-molded thermoplastic membrane forming the first section and the second section, the injection-molded membrane comprising a polycaprolactone and a polyalkylene oxide.

Claim 13

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) an osmotic composition in the second section; and wherein the dosage form comprises: (f) an injection-molded thermoplastic membrane forming the first section and the second section, the injection-molded membrane comprising a polycaprolactone and a polyalkylene oxide.

Claim 14

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) an osmotic composition in the second section and wherein the dosage form comprises: (f) an injection-molded thermoplastic membrane forming the first section and the second section, the injection-molded membrane comprising a polycaprolactone, polyalkylene oxide and poly(ethylene glycol-co-propylene glycol).

Claim 15

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) an osmotic composition in the second section and wherein the dosage form comprises: (f) an injection-molded thermoplastic membrane forming the first section and the second section, the injection-molded membrane comprising a polycaprolactone, polyalkylene oxide and poly(ethylene glycol-co-propylene glycol).

Claim 16

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) a composition comprising an osmopolymer in the second section comprises: (f) an injection-molded thermoplastic membrane forming the first section and the second section that comprises a polycaprolactone and a polyalkylene glycol.

Claim 17

A dosage form for delivering a therapeutic agent to an environment of use, wherein the dosage form comprises: (a) a first section; (b) a second section; (c) an internal lumen formed by the first section and the second section; (d) a therapeutic composition in the first section; (e) a composition comprising an osmopolymer in the second section comprises: (f) an injection-molded thermoplastic membrane forming the first section and the second section that comprises a polycaprolactone and a polyalkylene glycol.

Claim 18

A dosage form for delivering a therapeutic liquid formulation to an environment of use, wherein the dosage form comprises: (a) an internal compartment; (b) an exit in the dosage form that connects the internal compartment with the environment of use; (c) an osmotic composition in the internal compartment distant from the exit; and wherein the dosage form comprises: (d) a therapeutic liquid formulation in the internal compartment and adjacent to the exit; and, (e) an injection-molded thermoplastic membrane comprising a softening temperature of 40° C. and 180° C. that surrounds and forms the internal compartment, the injection-molded membrane permeable to the passage of fluid in the environment of use.

Claim 19

A dosage form for delivering a therapeutic liquid formulation to an environment of use, wherein the dosage form comprises: (a) an internal compartment; (b) an exit in the dosage form that connects the internal compartment with the environment of use; (c) an osmotic composition in the internal compartment distant from the exit; and wherein the dosage form comprises: (d) a therapeutic liquid formulation in the internal compartment and adjacent to the exit; and, (e) an injection-molded thermoplastic membrane comprising a softening temperature of 40° C. and 180° C. that surrounds and forms the internal compartment, the injection-molded membrane permeable to the passage of fluid in the environment of use.

Claim 20

A composition comprising 10% to 90% caprolactone-lactide copolymer and 10% to 80% of polyalkylene oxide with the composition equal to 100% and used for injection-molding a polymer membrane.

Claim 21

A composition comprising 10% to 90% caprolactone-lactide copolymer and 10% to 80% of polyalkylene oxide with the composition equal to 100% and used for injection-molding a polymer membrane.

Claim 22

A composition comprising 10% to 90% caprolactone-glycolide copolymer and 10% to 90% polyethylene oxide with the composition equal to 100% and used for injection-molding a polymer membrane.

Claim 23

A composition comprising 10% to 90% caprolactone-glycolide copolymer and 10% to 90% polyethylene oxide with the composition equal to 100% and used for injection-molding a polymer membrane.

Claim 24

A composition comprising 10% to 90% caprolactone-lactide copolymer, 10% to 50% polyethylene oxide and 10% to 50% poly(ethylene glycol-co-propylene glycol) with the composition equal to 100% and used for injection-molding a polymer membrane for manufacturing on oral dosage form.

Claim 25

A composition comprising 10% to 90% caprolactone-lactide copolymer, 10% to 50% polyethylene oxide and 10% to 50% poly(ethylene glycol-co-propylene glycol) with the composition equal to 100% and used for injection-molding a polymer membrane for manufacturing on oral dosage form.

Claim 26

A composition comprising 20% to 90% polycaprolactone and 10% to 80% ethylene-vinylacetate copolymer with the composition equal to 100% and the composition used for injection-molding a polymer membrane for manufacturing a therapeutic dosage form.

Claim 27

A composition comprising 20% to 90% polycaprolactone and 10% to 80% ethylene-vinylacetate copolymer with the composition equal to 100% and the composition used for injection-molding a polymer membrane for manufacturing a therapeutic dosage form.

Claim 28

A process for manufacturing a dosage form, wherein the process comprises: (a) injection molding a membrane into a shape that surrounds an internal space, which space comprises an opened end and a closed end; (b) placing in the space at the closed end a composition comprising fluid imbibing properties; (c) placing in the space at the opened end a composition comprising a drug; and (d) closing the opened end while maintaining an exit in the end for releasing drug from the dosage form.

Claim 29

A process for manufacturing a dosage form, wherein the process comprises: (a) injection molding a membrane into a shape that surrounds an internal space, which space comprises an opened end and a closed end; (b) placing in the space at the closed end a composition comprising fluid imbibing properties; (c) placing in the space at the opened end a composition comprising a drug; and (d) closing the opened end while maintaining an exit in the end for releasing drug from the dosage form.

Claim 30

A process for providing a dosage form, wherein the process comprises: (a) injection molding a composition comprising a polymer to provide a membrane which membrane surrounds an internal space with an opened end and a closed end; (b) depositing in the space at the closed end a composition that expands in the presence of aqueous fluids; (c) placing a composition comprising a drug in the space at the opened end; (d) crimping the membrane at the opened end to close the dosage form; and (e) maintaining an exit in the crimped end for delivering drug from the dosage form.

Claim 31

A process for providing a dosage form, wherein the process comprises: (a) injection molding a composition comprising a polymer to provide a membrane which membrane surrounds an internal space with an opened end and a closed end; (b) depositing in the space at the closed end a composition that expands in the presence of aqueous fluids; (c) placing a composition comprising a drug in the space at the opened end; (d) crimping the membrane at the opened end to close the dosage form; and (e) maintaining an exit in the crimped end for delivering drug from the dosage form.