Absorbable hemostatic composition

Claim 2

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) comprising either a biocompatible fatty acid salt alone, which comprises between 45% and 80% by weight based on the weight of the total composition; or a mixture of said fatty acid salt with a biocompatible in vivo absorption enhancing agent, in which said mixture comprises between 35% and 45% by weight of said fatty acid salt based on the weight of the total composition, and between 25% and 35% by weight of said absorption enhancing agent, based on the weight of the total composition; and (ii) a component (B) comprising a body absorbable biocompatible base selected from the group consisting of ethylene oxide/proplylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols, triglycerides and fatty acid esters, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain, said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 3

The composition of claim 1, in which component (A) comprises calcium stearate, calcium palmitate or calcium myristate.

Claim 4

The composition of claim 1, in which component (B) is selected from the group consisting of sesame oil, almond oil, castor oil, cottonseed oil, corn oil, olive oil, cod liver oil, safflower oil and soya oil.

Claim 5

The composition of claim 1, in which the absorption enhancing agent is selected from the group consisting of dextran, Carbowax, Pluronics, glycerine and propylene glycol.

Claim 6

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) consisting of a biocompatible fatty acid salt,

Claim 7

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) consisting of a biocompatible fatty acid salt,

Claim 8

(ii) at least 15% by weight of a component (B) comprising a body absorbable biocompatible base selected from the group consisting of ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols, triglycerides and fatty acid esters, and up to 40% by weight of water, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 9

(ii) at least 15% by weight of a component (B) comprising a body absorbable biocompatible base selected from the group consisting of ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols, triglycerides and fatty acid esters, and up to 40% by weight of water, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 10

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) comprising a mixture of a biocompatible fatty acid salt with a biocompatible in vivo absorption enhancing agent, in which said mixture comprises between 35% and 45% by weight of said fatty acid salt, based on the weight of the total composition, and between 25% and 35% by weight of said absorption enhancing agent, based on the weight of the total composition; (ii) at least 20% by weight of a component (B) comprising a body absorbable biocompatible base, selected from the group consisting of ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols, triglycerides and fatty acid esters, and up to 10% by weight of water, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 11

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) comprising a mixture of a biocompatible fatty acid salt with a biocompatible in vivo absorption enhancing agent, in which said mixture comprises between 35% and 45% by weight of said fatty acid salt, based on the weight of the total composition, and between 25% and 35% by weight of said absorption enhancing agent, based on the weight of the total composition; (ii) at least 20% by weight of a component (B) comprising a body absorbable biocompatible base, selected from the group consisting of ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols, triglycerides and fatty acid esters, and up to 10% by weight of water, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 12

The composition of claim 6, comprising about 38 weight % calcium stearate, about 28 weight % dextran, about 27 weight % castor oil and about 7 weight % water.

Claim 13

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) comprising a mixture of calcium stearate and dextran in which said mixture comprises between 35% and 45% by weight of said calcium stearate based on the weight of the total composition, and between 25% and 35% by weight of dextran, based on the weight of the total composition; and (ii) a component (B) comprising a biocompatible base consisting of a natural or synthetic oil or wax which is soluble in the body, said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 14

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) comprising a mixture of calcium stearate and dextran in which said mixture comprises between 35% and 45% by weight of said calcium stearate based on the weight of the total composition, and between 25% and 35% by weight of dextran, based on the weight of the total composition; and (ii) a component (B) comprising a biocompatible base consisting of a natural or synthetic oil or wax which is soluble in the body, said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 15

The composition of claim 8, in which component (B) is selected from the group consisting of sesame oil, almond oil, castor oil, cottonseed oil, olive oil, cod liver oil, safflower oil and soya oil.

Claim 16

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) comprising a mixture of a biocompatible fatty acid salt with a biocompatible in vivo absorption enhancing agent, in which said mixture comprises between 35% and 45% by weight of said fatty acid salt based on the weight of the total composition and between 25% and 35% by weight of said absorption enhancing agent based on the weight of the total composition; and (ii) a component (B) comprising a biocompatible base, consisting of a natural or synthetic oil or wax which is absorbable in the body, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 17

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) comprising a mixture of a biocompatible fatty acid salt with a biocompatible in vivo absorption enhancing agent, in which said mixture comprises between 35% and 45% by weight of said fatty acid salt based on the weight of the total composition and between 25% and 35% by weight of said absorption enhancing agent based on the weight of the total composition; and (ii) a component (B) comprising a biocompatible base, consisting of a natural or synthetic oil or wax which is absorbable in the body, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 18

The composition of claim 10, in which the absorption enhancing agent is selected from the group consisting of dextran, Carbowax, Pluronics, glycerine and propylene glycol.

Claim 19

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) consisting of a biocompatible fatty acid salt which comprises between 45% and 80% by weight based on the weight of the total composition; and (ii) a component (B) comprising a biocompatible base, consisting of a natural or synthetic oil or wax which is absorbable in the body, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 20

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising: (i) a component (A) consisting of a biocompatible fatty acid salt which comprises between 45% and 80% by weight based on the weight of the total composition; and (ii) a component (B) comprising a biocompatible base, consisting of a natural or synthetic oil or wax which is absorbable in the body, the cation of said fatty acid salt being selected from the group consisting of calcium, magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 21

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising between 35% and 45% by weight of calcium stearate, between 25% and 35% by weight of dextran, the remainder comprising castor oil.

Claim 22

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising between 35% and 45% by weight of calcium stearate, between 25% and 35% by weight of dextran, the remainder comprising castor oil.

Claim 23

The composition of claim 13, comprising about 41 weight percent calcium stearate, about 30 weight percent dextran and about 29 weight percent castor oil.

Claim 24

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising from 45% to 80% by weight of calcium stearate, and a body absorbable biocompatible base selected from the group consisting of isopropyl palmitate, sesame oil, almond oil, castor oil, ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols.

Claim 25

An absorbable hemostatic composition for use in the control of osseous hemorrhage, comprising from 45% to 80% by weight of calcium stearate, and a body absorbable biocompatible base selected from the group consisting of isopropyl palmitate, sesame oil, almond oil, castor oil, ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols.

Claim 26

The composition of claim 15, in which the calcium stearate comprises between 55% and 70% by weight of the composition.

Claim 27

The composition of claim 16, in which the calcium stearate comprises between about 59% and 61% by weight of the composition, and the base is castor oil.

Claim 28

A process for the control of bleeding from cut bone surfaces, which comprises applying to the cut bone surface a hemostatic composition comprising (i) a component (A) comprising either a biocompatible fatty acid salt alone which comprises between 45% to 80% by weight, based on the weight of the total composition; or a mixture of said fatty acid salt with a biocompatible in vivo absorption enhancing agent in which said mixture comprises between 35% and 45% by weight of said fatty acid salt based on the weight of the total composition, and between 25% and 35% by weight of said absorption enhancing agent based on the weight of the total composition; and (ii) a component (B) comprising a body absorbable biocompatible base, selected from the group consisting of ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols, triglycerides and fatty acid esters, the cation of said fatty acid salt being selected from the group consisting of calcium magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 29

A process for the control of bleeding from cut bone surfaces, which comprises applying to the cut bone surface a hemostatic composition comprising (i) a component (A) comprising either a biocompatible fatty acid salt alone which comprises between 45% to 80% by weight, based on the weight of the total composition; or a mixture of said fatty acid salt with a biocompatible in vivo absorption enhancing agent in which said mixture comprises between 35% and 45% by weight of said fatty acid salt based on the weight of the total composition, and between 25% and 35% by weight of said absorption enhancing agent based on the weight of the total composition; and (ii) a component (B) comprising a body absorbable biocompatible base, selected from the group consisting of ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols, triglycerides and fatty acid esters, the cation of said fatty acid salt being selected from the group consisting of calcium magnesium, zinc, aluminum, lithium and barium, the fatty acid anion being saturated or unsaturated and containing from 10 to 22 carbon atoms in the chain; said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 30

The process of claim 18, in which component (B) is selected from the group consisting of isopropyl palmitate, sesame oil, almond oil, castor oil, ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypolyethylene glycols.

Claim 31

A process for the control of bleeding from cut bone surfaces, which comprises applying to the cut bone surface a hemostatic composition comprising: (i) a component (A) comprising a mixture of calcium stearate and dextran in which said mixture comprises between 35% and 45% by weight of said calcium stearate based on the weight of the total composition and between 25% and 35% by weight of dextran based on the weight of the total composition; and (ii) a component (B) comprising a biocompatible base selected from the group consisting of ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypoly-ethylene glycols, triglycerides and fatty acid esters, said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 32

A process for the control of bleeding from cut bone surfaces, which comprises applying to the cut bone surface a hemostatic composition comprising: (i) a component (A) comprising a mixture of calcium stearate and dextran in which said mixture comprises between 35% and 45% by weight of said calcium stearate based on the weight of the total composition and between 25% and 35% by weight of dextran based on the weight of the total composition; and (ii) a component (B) comprising a biocompatible base selected from the group consisting of ethylene oxide/propylene oxide block copolymers, polyethylene glycols and methoxypoly-ethylene glycols, triglycerides and fatty acid esters, said composition having a putty-like consistency at room temperature, and a tackiness sufficient for it to adhere readily to a bloody bone surface.

Claim 33

The process of claim 20, in which component (B) is castor oil.

Claim 34

The process of claim 20, in which the composition includes up to 10 weight % of water based on the weight of the total composition, there being present at least 20 weight % of castor oil based on the weight of the total composition.