IP Library Granted Patent US 7,056,535
Granted Patent B2
US 7,056,535 · App. 10/027,441 · Granted Jun 6, 2006

Triggered release from proteinoid microspheres

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Quick Facts
Patent No.
US 7,056,535
App. No.
10/027,441
Granted
Jun 6, 2006
Kind
B2
Abstract

The invention provides proteinoid microsphere made up of a mixture of thermally condensed amino acids that are crosslinked with a bis dithiol crosslinker reagent. The proteinoid microspheres of the invention may be used to encapsulate a material or a compound and to provide slow, sustained or timed release of the material or compound. The proteinoid microspheres are stable in solution until exposed to a reducing agent. However, the in vivo environment provides a sufficient reduction potential to provide slow, sustained release of materials contained therein from the proteinoid microspheres of the present invention.

Claims (44)

1. A proteinoid microsphere comprising a mixture of amino acids that are thermally condensed and crosslinked with a crosslinker of any one of formulae I–VI.

COOH—S—S—(CH 2 ) n —S—S—COOH  I

COOH—S—S—X—S—S—COOH  II

NH 2 —S—S—(CH 2 ) n —S—S—NH 2   III

NH 2 —S—S—X—S—S—NH 2   IV

Aryl-S—S—(CH 2 ) n —S—S-Aryl  V

Aryl-S—S—X—S—S-Aryl  VI

wherein:

X is a spacer group of about approximately 3 to 100 angstroms by about 2 to 30 angstroms that comprises an alkane chain, an alkene chain, a cycloalkyl or aryl ring having five to fourteen carbon atoms, or a combination thereof;

n is an integer ranging from 1 to 18;

S is a sulfur atom; and

Aryl is a phenyl radical or an ortho-fused bicyclic radical having about nine to ten ring atoms wherein at least one ring is aromatic and wherein each Aryl moiety is substituted with at least one reactive group that can form a covalent linkage with an amino acid.

2. The proteinoid microsphere of claim 1 wherein the reactive group that can form a covalent linkage with an amino acid is carboxylate, nitro, amino or sulfhydryl.

3. The proteinoid microsphere of claim 1 wherein the reactive group that can form a covalent linkage with an amino acid is a carboxylate group.

4. A proteinoid microsphere comprising a mixture of amino acids that are thermally condensed and crosslinked with a crosslinker reagent of formula VII:

5. A therapeutic composition comprising a therapeutic agent encapsulated within a proteinoid microsphere that comprises a mixture of amino acids that are thermally condensed and crosslinked with a crosslinker of any one of formulae I–VI.

COOH—S—S—(CH 2 ) n —S—S—COOH  I

COOH—S—S—X—S—S—COOH  II

NH 2 —S—S—(CH 2 ) n —S—S—NH 2   III

NH 2 —S—S—X—S—S—NH 2   IV

Aryl-S—S—(CH 2 ) n —S—S-Aryl  V

Aryl-S—S—X—S—S-Aryl  VI

wherein:

X is a spacer group of about approximately 3 to 100 angstroms by about 2 to 30 angstroms that comprises an alkane chain, an alkene chain, a cycloalkyl or aryl ring having five to fourteen carbon atoms, or a combination thereof; n is an integer ranging from 1 to 18;

S is a sulfur atom; and

Aryl is a phenyl radical or an ortho-fused bicyclic radical having about nine to ten ring atoms wherein at least one ring is aromatic and wherein each Aryl moiety is substituted with at least one reactive group that can form a covalent linkage with an amino acid.

6. The therapeutic composition of claim 5 wherein the reactive group that can form a covalent linkage with an amino acid is carboxylate, nitro, amino or sulfhydryl.

7. The therapeutic composition of claim 5 wherein the reactive group that can form a covalent linkage with an amino acid is a carboxylate group.

8. A therapeutic composition comprising a therapeutic agent encapsulated within a mixture of amino acids that are thermally condensed and crosslinked with a crosslinker reagent of formula VII:

9. An article for wound treatment comprising a therapeutic agent encapsulated within a protenoid microsphere that comprises a mixture of amino acids that are thermally condensed and crosslinked with a crosslinker of any one of the formulae I–VI.

COOH—S—S—(CH 2 ) n —S—S—COOH  I

COOH—S—S—X—S—S—COOH  II

NH 2 —S—S—(CH 2 ) n —S—S—NH 2   III

NH 2 —S—S—X—S—S—NH 2   IV

Aryl-S—S—(CH 2 ) n —S—S-Aryl  V

Aryl-S—S—X—S—S-Aryl  VI

wherein:

X is a spacer group of about approximately 3 to 100 angstroms by about 2 to 30 angstroms that comprises an alkane chain, an alkene chain, a cycloalkyl or aryl ring having five to fourteen carbon atoms, or a combination thereof;

n is an integer ranging from 1 to 18;

S is a sulfur atom; and

Aryl is a phenyl radical or an ortho-fused bicyclic radical having about nine to ten ring atoms wherein at least one ring is aromatic and wherein each Aryl moiety is substituted with at least one reactive group that can form a covalent linkage with an amino acid.

10. The article of claim 9 wherein the reactive group that can form a covalent linkage with an amino acid is carboxylate, nitro, amino or sulfhydryl.

11. The article of claim 9 wherein the reactive group that can form a covalent linkage with an amino acid is a carboxylate group.

12. An article for wound treatment comprising a therapeutic agent encapsulated within a mixture of amino acids that are thermally condensed and crosslinked with a crosslinker reagent of formula VII:

Assignments (1)
NAME CHANGE Recorded Feb 3, 2015
From: KIMBERLY-CLARK WORLDWIDE, INC.
To: KIMBERLY-CLARK WORLDWIDE, INC.
Reel/Frame 034880/0742 →