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US4529792A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for preparing synthetic absorbable poly(esteramides)

Assignee: 3M Co
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Filing: 1982-05-06
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Granted: 1985-07-16
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Expires: 2002-05-06
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Abstract

Abstract A body absorbable polymeric material for implantation which is a condensation product of reacting a diamine with lactic or glycolic acid to form a diamidediol which is then reacted with a bischloroformate or a compound selected from the group consisting of dicarboxylic acids, methyl and ethyl esters of dicarboxylic acids, diacidchlorides, and anhydrides of a dicarboxylic acid.

Inventors

  • 👤 Thomas H. Barrows

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 21:01
CPC Classifications
C; C08; C08G; C08G69/00; C08G69/44; A; A61; A61L; A61L17/00; A61L17/06; A61L17/10; A61L17/105

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 206 words
A process for making a body absorbable polymeric material having a plurality of units of the general formula: ##STR3## in which R 1 is hydrogen or methyl; R 3 and R 5 are identical or different and are groups selected from the class consisting of linear and branched alkylene, alkylene having 1 or 2 nonadjacent catenary oxygen or sulfur atoms, alkenylene, cycloalkylene and arylene; said groups having up to 25 carbon atoms in the cyclic compounds and from 2 to 25 carbon atoms in the non-cyclic compounds; R 2 and R 4 are hydrogen or alkyl having 1 to 4 carbon atoms or R 2 and R 4 together are linear or branched alkylene having one to four carbons forming with N--R 3 --N a heterocyclic group having 5 or 6 ring atoms; and a and b are independently zero or one said process comprising the steps of: reacting at least one diamine with lactic or glycolic acid to form at least one diamidediol; and reacting said at least one diamidediol with a bischloroformate or a compound selected from the group consisting of dicarboxylic acids, methyl and ethyl esters of dicarboxylic acids, diacidchlorides, and anhydrides of a dicarboxylic acid to provide said body adsorbable polymeric material.
Claim 2
Dependent Claim 206 words
A process for making a body absorbable polymeric material having a plurality of units of the general formula: ##STR3## in which R 1 is hydrogen or methyl; R 3 and R 5 are identical or different and are groups selected from the class consisting of linear and branched alkylene, alkylene having 1 or 2 nonadjacent catenary oxygen or sulfur atoms, alkenylene, cycloalkylene and arylene; said groups having up to 25 carbon atoms in the cyclic compounds and from 2 to 25 carbon atoms in the non-cyclic compounds; R 2 and R 4 are hydrogen or alkyl having 1 to 4 carbon atoms or R 2 and R 4 together are linear or branched alkylene having one to four carbons forming with N--R 3 --N a heterocyclic group having 5 or 6 ring atoms; and a and b are independently zero or one said process comprising the steps of: reacting at least one diamine with lactic or glycolic acid to form at least one diamidediol; and reacting said at least one diamidediol with a bischloroformate or a compound selected from the group consisting of dicarboxylic acids, methyl and ethyl esters of dicarboxylic acids, diacidchlorides, and anhydrides of a dicarboxylic acid to provide said body adsorbable polymeric material.
Claim 3
Dependent Claim 22 words
The process of claim 1 wherein said diamidediol is placed in a solvent prior to reacting with said compound or said bischloroformate.
Claim 4
Dependent Claim 11 words
The process of claim 1 wherein said compound is succinyl chloride.
Claim 5
Dependent Claim 19 words
The process of claim 2 wherein said solvent is selected from the group consisting of chlorobenzene, 1,1,2-trichloroethane and 1,4-dioxane.
Claim 6
Dependent Claim 22 words
The process of claim 2 which includes the additional step of removing said solvent after reacting with said compound or said bischloroformate.
Claim 7
Dependent Claim 16 words
The process of claim 1 wherein said diamidediol is a mixture comprised of 1,12-di(hydroxyacetamido)-4,9-dioxadodecane and 1,12-di(hydroxyacetamide)dodecane.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-07-15 1989-01-14 1989-07-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-07-15 1993-01-14 1993-07-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-07-15 1997-01-14 1997-07-16 $7700.00 Window Closed / Lapsed

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