Topical drug delivery with thermo-irreversible gels

Claim 2

A hyperosmotic, isoosmotic, or hypoosmotic aqueous pharmaceutical composition having a osmolality and buffered pH, which is a liquid at room temperature or below and a thermo-reversible gel at mammalian body temperature, for administration to the skin of a mammal, said gel consisting essentially of water, an ionic polysaccharide,

Claim 3

A) a polyoxyalkylene block copolymer of the formula ##STR5## wherein A is a polyoxyalkylene moiety having an oxygen/carbon atom ratio of less than 0.5, x is at least 2, Y is derived from water or an organic compound containing x reactive hydrogen atoms, E is a polyoxyethylene moiety constituting at least 60% by weight of the copolymer, n has a value such that the average molecular weight is at least about 500 to about 900, as determined by the hydroxyl number of an intermediate, ##STR6## and the total average molecular weight of the copolymer is at least about 5000,

Claim 4

A) a polyoxyalkylene block copolymer of the formula ##STR5## wherein A is a polyoxyalkylene moiety having an oxygen/carbon atom ratio of less than 0.5, x is at least 2, Y is derived from water or an organic compound containing x reactive hydrogen atoms, E is a polyoxyethylene moiety constituting at least 60% by weight of the copolymer, n has a value such that the average molecular weight is at least about 500 to about 900, as determined by the hydroxyl number of an intermediate, ##STR6## and the total average molecular weight of the copolymer is at least about 5000,

Claim 5

B) a pharmacologically effective amount of a drug selected from the group consisting of antibacterials, antiinflammatories, antiparasitics, antivirals, anesthetics, antifungals, analgesics, and diagnostics, and

Claim 6

B) a pharmacologically effective amount of a drug selected from the group consisting of antibacterials, antiinflammatories, antiparasitics, antivirals, anesthetics, antifungals, analgesics, and diagnostics, and

Claim 7

C) a pharmaceutically acceptable buffer sufficient to maintain the pH of said aqueous composition at a desired level, and, optionally, a latent form of a counter-ion capable of thermo-irreversibly gelling the ionic polysaccharide.

Claim 8

C) a pharmaceutically acceptable buffer sufficient to maintain the pH of said aqueous composition at a desired level, and, optionally, a latent form of a counter-ion capable of thermo-irreversibly gelling the ionic polysaccharide.

Claim 9

The composition of claim 1, wherein said copolymer is prepared using a water soluble organic compound initiator (Y) having 1 to about 6 carbon atoms and wherein the pH is maintained at 7.4±0.2.

Claim 10

The composition of claim 2, wherein said polyoxyalkylene moiety is derived from an alkylene oxide selected from the group consisting of butylene oxide, propylene oxide, and mixtures thereof and Y is derived from an organic compound selected from the group consisting of propylene glycol, glycerin, pentaerythritol, trimethylolpropane, ethylenediamine and mixtures thereof.

Claim 11

The composition of claim 3, wherein said copolymer is a polyoxyethylene-polyoxypropylene block copolymer wherein said polyoxyethylene moiety constitutes at least about 70% by weight of the copolymer, the average molecular weight of A is at least about 1200, and the total molecular weight of the copolymer is at least about 10,000.

Claim 12

The composition of claim 4, wherein the intermediate of Formula II is prepared by initiation with propylene glycol and has a molecular weight of at least about 1500.

Claim 13

The composition of claim 5, wherein said copolymer has the formula: HO(C.sub.2 H.sub.4 O).sub.b (C.sub.4 H.sub.8 O).sub.a C.sub.2 H.sub.3 O).sub.b H (III) wherein in III, a and b are integers such that the hydrophobe base represented by (C 4 H 8 O) a has a molecular weight of at least about 500 as determined by hydroxyl number, the polyoxyethylene chain constituting at least about 70% by weight of the copolymer, and the copolymer having a total average molecular weight of at least 15,000, or HO(C.sub.2 H.sub.4 O).sub.b (C.sub.3 H.sub.6 O).sub.a (C.sub.2 H.sub.4 O)).sub.b H (IV) wherein in IV, a and b are integers such that the hydrophobe base represented by (C 3 H 6 O) a has a molecular weight of at least about 900 average molecular weight, as determined by hydroxyl number, the polyoxyethylene chain constitutes at least about 70% by weight of the copolymer, and the copolymer having a total average molecular weight of at least about 15,000,or ##STR7## wherein in V, a and b are integers such that the copolymer has a hydrophobe molecular weight of at least about 1500, a hydrophile content of at least about 70%, and a total average molecular weight of at least about 15,000.

Claim 14

The composition of claim 6, wherein said polyoxyalkylene block copolymer is ##STR8## present in the amount of about 10 to about 40% by weight of the total weight of said composition.

Claim 15

The composition of claim 7, wherein said polyoxyalkylene block copolymer is present in the amount of about 15 to about 30% by weight of said aqueous composition, said counter-ion is present as a microencapsulated component or incorporated with an ion exchange resin and is selected from the group consisting of at least one of calcium, strontium, and aluminum and said ionic polysaccharide is selected from the group consisting of an ammonium alginate, an alkali metal alginate, and mixtures thereof.

Claim 16

The composition of claim 7, wherein said polyoxyalkylene block copolymer is present in the amount of about 15 to about 30% by weight of said aqueous composition, the optional latent form of said counter-ion is present as a microencapsulated component or incorporated with an ion exchange resin and is selected from the group consisting of at least one of the metal phosphates, metaphosphates, pyrophosphates, and tripolyphosphates, and said ionic polysaccharide is chitosan.

Claim 17

A process for treating a condition requiring the application of a medicament, which comprises administering to the skin of a mammal a hyperosmotic, isoosmotic, or hypoosmotic buffered pH, which is at room temperature or below and a thermo-reversible gel at mammalian body temperature, said gel consisting essentially of water, an ionic polysaccharide, A) a polyoxyalkylene block copolymer of the formula ##STR9## wherein A is a polyoxyalkylene moiety having an oxygen/carbon atom ratio of less than 0.5, x is at least 1, Y is derived from water or an organic compound containing x reactive hydrogen atoms, E is a polyoxyethylene moiety, n has a value such that the average molecular weight of A is at least about 500 to about 900, as determined by the hydroxyl number of an intermediate, ##STR10## and wherein the total average molecular weight of the copolymer is at least about 5000, B) a pharmacologically effective amount of a drug selected from the group consisting of antibacterials, antiinflamatories, antiparasitics, antivirals, anesthetics, antifungals, analgesics, and diagnostics, and C) a pharmaceutically acceptable buffer sufficient to maintain the pH of said aqueous composition at a desired level and, optionally, a latent form of a counter-ion capable of thermo-irreversibly gelling the ionic polysaccharide.

Claim 18

A process for treating a condition requiring the application of a medicament, which comprises administering to the skin of a mammal a hyperosmotic, isoosmotic, or hypoosmotic buffered pH, which is at room temperature or below and a thermo-reversible gel at mammalian body temperature, said gel consisting essentially of water, an ionic polysaccharide, A) a polyoxyalkylene block copolymer of the formula ##STR9## wherein A is a polyoxyalkylene moiety having an oxygen/carbon atom ratio of less than 0.5, x is at least 1, Y is derived from water or an organic compound containing x reactive hydrogen atoms, E is a polyoxyethylene moiety, n has a value such that the average molecular weight of A is at least about 500 to about 900, as determined by the hydroxyl number of an intermediate, ##STR10## and wherein the total average molecular weight of the copolymer is at least about 5000, B) a pharmacologically effective amount of a drug selected from the group consisting of antibacterials, antiinflamatories, antiparasitics, antivirals, anesthetics, antifungals, analgesics, and diagnostics, and C) a pharmaceutically acceptable buffer sufficient to maintain the pH of said aqueous composition at a desired level and, optionally, a latent form of a counter-ion capable of thermo-irreversibly gelling the ionic polysaccharide.

Claim 19

The process of claim 10, wherein Y in said formulas I and II is a water soluble organic compound having 1-6 carbon atoms, and said copolymer is selected from the group consisting of a polyoxyethylene-polyoxybutylene block copolymer, a polyoxyethylene-polyoxypropylene block copolymer and mixtures thereof, and wherein the polyoxyethylene moiety constitutes at least 70% by weight of the polymer, and wherein the pH is maintained at about 7.4±0.2.

Claim 20

The process of claim 11, wherein said copolymer is selected from block copolymers which form aqueous gels at a concentration of about 10-50% by weight of the total weight of said composition.

Claim 21

The process of claim 12, wherein said Y is a compound selected from the group consisting of propylene glycol, glycerin, pentaerythritol, trimethylolpropane, ethylenediamine, and mixtures thereof.

Claim 22

The process of claim 13, wherein Y is derived from propylene glycol, A is the residue of propylene oxide, and the intermediate of Formula II has an average molecular weight of at least about 900.

Claim 23

The process of claim 14, wherein Y is derived from butylene glycol, A is the residue of butylene oxide, and the intermediate of Formula II has an average molecular weight of at least about 500.

Claim 24

The process of claim 15, wherein said copolymer has the formula HO(C.sub.2 H.sub.4 O).sub.b (C.sub.4 H.sub.8 O).sub.a (C.sub.2 H.sub.4 O).sub.b H (III) wherein in III, a and b are integers such that the hydrophobe base represented by (C 4 H 8 O) has a molecular weight of at least 1000, as determined by hydroxyl number, the polyoxyethylene chain constitutes at least about 60% by weight of the copolymer, and the copolymer has a total average molecular weight of at least 5,000, 10 or HO(C.sub.2 H.sub.4 O).sub.b (C.sub.3 H.sub.6 O).sub.a (C.sub.2 H.sub.4 O).sub.b H (IV) wherein in IV, a and b are integers such that the hydrophobe base represented by (C3H60) has a molecular weight of at least about 1500 average molecular weight, as determined by hydroxyl number, the polyoxyethylene chain constitutes at least about 60% by weight of the copolymer, and the copolymer has a total average molecular weight of at least 5,000, or ##STR11## wherein V, a and b are integers such that the copolymer has a hydrophobe molecular weight of at least 2000, a hydrophile content of at least about 60%, and a total average molecular weight of at least about 5,000.

Claim 25

The process of claim 16, wherein said copolymer is ##STR12##

Claim 26

The process of claim 17, wherein said counter-ion is derived from a compound selected from the group consisting of at least one of the metal phosphates, metaphosphates, pyrophosphates and tripolyphosphates and said ionic polysaccharide is chitosan, and said counter-ion is present as a microencapsulated component or incorporated with an ion exchange resin.

Claim 27

The process of claim 17 wherein said counter-ion is selected from the group consisting of at least one of calcium, strontium, and aluminum, said ionic polysaccharide is selected from the group consisting of an ammonium alginate, an alkali metal alginate, and mixtures thereof, and said counter-ion is present as a microencapsulated component or incorporated with an ion exchange resin.

Claim 28

A process for treating a condition requiring the application of a medicament which comprises administering to the skin of a mammal a hyperosmotic, isoosmotic, or hypoosmotic composition, having a buffered pH, consisting essentially of water, an ionic polysaccharide, a surfactant, a polyoxyalkylene polyether having a molecular weight of about 10,000 to about 100,000 which is selected from the group consisting of A) polyoxyalkylene polyethers prepared by reacting ethylene oxide and at least one lower alkylene oxide having 3 to 4 carbon atoms with at least one active hydrogen containing compound having from 3 to 10 carbon atoms and from 3 to 6 active hydrogens to prepare a heteric or block copolymer intermediate and further reacting said copolymer intermediate with at least one alpha-olefin oxide having an average carbon chain length of about 20 to about 45 aliphatic carbon atoms and wherein said alpha-olefin oxide is present in the amount of about 0.3 to 10 percent by weight based upon the total weight of said polyether,

Claim 29

A process for treating a condition requiring the application of a medicament which comprises administering to the skin of a mammal a hyperosmotic, isoosmotic, or hypoosmotic composition, having a buffered pH, consisting essentially of water, an ionic polysaccharide, a surfactant, a polyoxyalkylene polyether having a molecular weight of about 10,000 to about 100,000 which is selected from the group consisting of A) polyoxyalkylene polyethers prepared by reacting ethylene oxide and at least one lower alkylene oxide having 3 to 4 carbon atoms with at least one active hydrogen containing compound having from 3 to 10 carbon atoms and from 3 to 6 active hydrogens to prepare a heteric or block copolymer intermediate and further reacting said copolymer intermediate with at least one alpha-olefin oxide having an average carbon chain length of about 20 to about 45 aliphatic carbon atoms and wherein said alpha-olefin oxide is present in the amount of about 0.3 to 10 percent by weight based upon the total weight of said polyether,

Claim 30

B) polyoxyalkylene polyethers prepared by reacting ethylene oxide with at least one active hydrogen-containing compound having from 2 to 10 carbon atoms and from 2 to 6 active hydrogens to prepare a homopolymer intermediate and further reacting said homopolymer with at least one alpha-olefin oxide having an average carbon chain length of about 20 to 45 aliphatic carbon atoms and wherein said alpha-olefin oxide is present in the amount of about 0.3 to 10 percent by weight based on the total weight of said polyether, C) a pharmacologically effective amount of a drug selected from the group consisting of antibacterials, antiinflammatories, antiparasitics, antivirals, anesthetics, antifungals, analgesics, and diagnostics, and D) a pharmaceutically acceptable buffer sufficient to maintain the pH of said aqueous composition at a desired level, and, optionally, a latent form of a counter-ion capable of thermo-irreversibly gelling the ionic polysaccharide.

Claim 31

B) polyoxyalkylene polyethers prepared by reacting ethylene oxide with at least one active hydrogen-containing compound having from 2 to 10 carbon atoms and from 2 to 6 active hydrogens to prepare a homopolymer intermediate and further reacting said homopolymer with at least one alpha-olefin oxide having an average carbon chain length of about 20 to 45 aliphatic carbon atoms and wherein said alpha-olefin oxide is present in the amount of about 0.3 to 10 percent by weight based on the total weight of said polyether, C) a pharmacologically effective amount of a drug selected from the group consisting of antibacterials, antiinflammatories, antiparasitics, antivirals, anesthetics, antifungals, analgesics, and diagnostics, and D) a pharmaceutically acceptable buffer sufficient to maintain the pH of said aqueous composition at a desired level, and, optionally, a latent form of a counter-ion capable of thermo-irreversibly gelling the ionic polysaccharide.

Claim 32

The process of claim 20, wherein said polyether is prepared using a heteric copolymer intermediate and wherein the pH is maintained at about 7.4±0.2.

Claim 33

The process of claim 21, wherein said polyether is prepared using an alpha-olefin oxide having an average carbon chain length of about 20 to 30 carbon atoms, present in the amount of about 0.3 to 10 percent of the total weight of said polyether.

Claim 34

The process of claim 22, wherein said polyether contains a proportion of ethylene oxide residue to the residue of said lower alkylene oxide of about 70 to about 90 percent by weight of ethylene oxide residue to about 30 to about 10 percent by weight of said lower alkylene oxide residue.

Claim 35

The process of claim 23, wherein said polyether is prepared using propylene oxide as the lower alkylene oxide.

Claim 36

The process of claim 20, wherein said polyether is prepared using a block copolymer intermediate.

Claim 37

The process of claim 25, wherein said polyether is prepared using an alpha-olefin oxide having an average carbon chain length of about 20 to 30 carbon atoms, present in the amount of about 0.3 to 10 percent of the total weight of said polyether.

Claim 38

The process of claim 26, wherein said polyether is prepared using a proportion of ethylene oxide residue to the residue of said lower alkylene oxide of from about 70 to about 90 percent by weight of ethylene oxide residue to about 30 to about 10 percent by weight of said lower alkylene oxide residue.

Claim 39

The process of claim 27, wherein said polyether is prepared using propylene oxide as the alkylene oxide said

Claim 40

The process of claim 20, wherein polyether is polyether (B) of claim 19.

Claim 41

The process of claim 29, wherein said polyether is prepared using an alpha-olefin oxide having an average carbon chain length of about 20 to 30 carbon atoms, present in the amount of about 0.3 to 10 percent of the total weight of said polyether, said counter-ion is selected from the group consisting of at least one of the metal phosphates, metaphosphates, pyrophosphates, and tripolyphosphates, said ionic polysaccharide is chitosan, and said counter-ion is present as a microencapsulated component or incorporated with an ion exchange resin.

Claim 42

The process of claim 29, wherein said polyether is prepared using an alpha-olefin oxide having an average carbon chain length of about 20 to 30 carbon atoms, present in the amount of about 0.3 to I0 percent of the total weight of said polyether, said counter-ion is selected from the group consisting of at least one of calcium, strontium, and aluminum, said ionic polysaccharide is selected from the group consisting of an ammonium alginate, an alkali metal alginate, and mixtures thereof, and said counter-ion is present as a microencapsulated component or incorporated with an ion exchange resin.

Claim 43

A hyperosmotic, isoosmotic, or hypoosmotic aqueous pharmaceutical composition having a buffered pH for administration to the skin of a mammal to treat a condition requiring the application of a medicament, said composition consisting essentially of water, an ionic polysaccharide, a surfactant, a polyether having a molecular weight of about 10,000 to about 100,000 which is selected from the group consisting of A) polyethers prepared by reacting ethylene oxide and at least one lower alkylene oxide having 3 to 4 carbon atoms with at least one active hydrogen-containing compound having from 3 to I0 carbon atoms and from 3 to 6 active hydrogens to prepare a heteric or block copolymer intermediate and further reacting said copolymer intermediate with at least one alpha-olefin oxide having an average carbon chain length of about 20 to about 45 aliphatic carbon atoms and wherein said alpha-olefin oxide is present in the amount of about 0.3 to 10 percent by weight based upon the total weight of said polyether and B) polyethers prepared by reacting ethylene oxide with at least one active hydrogen containing compound having from 2 to 10 carbon atoms and from 2 to 6 active hydrogens to prepare a homopolymer intermediate and further reacting said homopolymer with at least one alpha-olefin oxide having an average carbon chain length of about 20 to 45 aliphatic carbon atoms, and wherein said alpha-olefin oxide is present in the amount of about 0.3 to I0 percent by weight based on the total weight of said polyether, C) a pharmacologically effective amount of a drug selected from the group consisting of antibacterials, antiinflammatories, antiparasitics, antivirals, anesthetics, antifungals, analgesics, and diagnostics, and D) a pharmaceutically acceptable buffer sufficient to maintain the pH of said aqueous composition at a desired level, and, optionally, a latent form of a counter-ion capable of thermo-irreversibly gelling the ionic polysaccharide.

Claim 44

A hyperosmotic, isoosmotic, or hypoosmotic aqueous pharmaceutical composition having a buffered pH for administration to the skin of a mammal to treat a condition requiring the application of a medicament, said composition consisting essentially of water, an ionic polysaccharide, a surfactant, a polyether having a molecular weight of about 10,000 to about 100,000 which is selected from the group consisting of A) polyethers prepared by reacting ethylene oxide and at least one lower alkylene oxide having 3 to 4 carbon atoms with at least one active hydrogen-containing compound having from 3 to I0 carbon atoms and from 3 to 6 active hydrogens to prepare a heteric or block copolymer intermediate and further reacting said copolymer intermediate with at least one alpha-olefin oxide having an average carbon chain length of about 20 to about 45 aliphatic carbon atoms and wherein said alpha-olefin oxide is present in the amount of about 0.3 to 10 percent by weight based upon the total weight of said polyether and B) polyethers prepared by reacting ethylene oxide with at least one active hydrogen containing compound having from 2 to 10 carbon atoms and from 2 to 6 active hydrogens to prepare a homopolymer intermediate and further reacting said homopolymer with at least one alpha-olefin oxide having an average carbon chain length of about 20 to 45 aliphatic carbon atoms, and wherein said alpha-olefin oxide is present in the amount of about 0.3 to I0 percent by weight based on the total weight of said polyether, C) a pharmacologically effective amount of a drug selected from the group consisting of antibacterials, antiinflammatories, antiparasitics, antivirals, anesthetics, antifungals, analgesics, and diagnostics, and D) a pharmaceutically acceptable buffer sufficient to maintain the pH of said aqueous composition at a desired level, and, optionally, a latent form of a counter-ion capable of thermo-irreversibly gelling the ionic polysaccharide.

Claim 45

The composition of claim 32, wherein .said polyether is prepared using a heteric copolymer intermediate and wherein the pH is maintained at 7.4 ±0.2.

Claim 46

The composition of claim 33, wherein said polyether is prepared using an alpha-olefin oxide having an average carbon chain length of about 20 to 30 carbon atoms, present in the amount of about 0.3 to 10 percent of the total weight of said polyether.

Claim 47

The composition of claim 34, wherein the polyether is prepared using a proportion of ethylene oxide residue to the residue of said lower alkylene oxide of about 70 to about 90 percent by weight of ethylene oxide residue to about 30 to about 10 percent by weight of said lower alkylene oxide residue.

Claim 48

The composition of claim 35, wherein said polyether is prepared using propylene oxide as the lower alkylene oxide.

Claim 49

The composition of claim 32, wherein said polyether is prepared using a block copolymer intermediate.

Claim 50

The composition of claim 37, wherein said polyether is prepared using an alpha-olefin oxide having an average carbon chain length of about 20 to 30 carbon atoms, present in the amount of about 0.3 to 10 percent of the total weight of said polyether.

Claim 51

The composition of claim 38, wherein the polyether is prepared using a proportion of ethylene oxide residue to the residue of said lower alkylene oxide of about 70 to about 90 percent by weight of ethylene oxide residue to about 30 to about 10 percent by weight of said lower alkylene oxide residue.

Claim 52

The composition of claim 39, wherein said polyether is prepared using propylene oxide as the lower alkylene oxide.

Claim 53

The composition of claim 32, wherein said polyether is polyether (B) of claim 32.

Claim 54

The composition of claim 41, wherein said polyether is prepared using an alpha-olefin oxide having an average carbon chain length of about 20 to 30 carbon atoms, present in the amount of about 0.3 to 10 percent of the total weight of said polyether, said counter-ion is selected from the group consisting of at least one of calcium, strontium, and aluminum, said ionic polysaccharide is selected from the group consisting of an ammonium alginate, an alkali metal alginate, and mixtures thereof and said counter-ion is present as a microencapsulated component or incorporated with an ion exchange resin.

Claim 55

The composition of claim 41, wherein said polyether is prepared using an alpha-olefin oxide having an average carbon chain length of about 20 to 30 carbon atoms, present in the amount of about 0.3 to 10 percent of the total weight of said polyether, said counter-ion is selected from the group consisting of at least one of the metal phosphates, metaphosphates, pyrophosphates, and tripolyphosphates, said ionic polysaccharide is chitosan and said counter-ion is present as a microencapsulated component or incorporated with an ion exchange resin.