Document Detail


An enhanced strength retention poly(glycolic acid)-poly(L-lactic acid) copolymer for internal fixation: in vitro characterization of hydrolysis.
MedLine Citation:
PMID:  19816292     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In general, most bioabsorbable polymers used for internal fixation are composed of copolymers of glycolic acid and lactic acid (L and/or DL). Within this family of polymers resides the latitude to design materials with specific degradation properties to meet a variety of clinical needs. One material with an extensive clinical history is LactoSorb copolymer, which is composed of a molar ratio of 82:18 poly(L-lactic acid)-poly(glycolic acid). Fixation devices derived from this copolymer have been used in orthopedic and craniofacial surgeries. With a strength loss profile of approximately 12 weeks, it mirrors the profile of normal healing; however, in cases in which delayed healing is anticipated, a copolymer with a longer strength retention profile may be desirable. This study compared the hydrolytic degradation, in vitro, of the 82:18 copolymer with a related 85:15 poly(L-lactic acid)-poly(glycolic acid) copolymer. In addition to a difference in the copolymer ratio, the latter had a larger inherent viscosity (molecular weight) and a smaller polydispersity (molecular weight distribution). This copolymer had an equivalent initial tensile modulus as the 82:18 copolymer (0.8 GPa) but a strength retention profile that spanned 44 weeks. The activation energy of hydrolysis for the 85:15 copolymer was 38.8 kcal/mol, which was greater than the 23.8 kcal/mol historical value for the 82:18 copolymer. This suggests that hydrolysis of the 85:15 copolymer is more temperature-sensitive than that of the 82:18 copolymer. These results were interpreted in the context of the differences in the compositions of these 2 copolymers.
Authors:
William S Pietrzak; Mukesh Kumar
Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  The Journal of craniofacial surgery     Volume:  20     ISSN:  1536-3732     ISO Abbreviation:  J Craniofac Surg     Publication Date:  2009 Sep 
Date Detail:
Created Date:  2009-10-09     Completed Date:  2010-01-28     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9010410     Medline TA:  J Craniofac Surg     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1533-7     Citation Subset:  D    
Affiliation:
Biomet, Inc., 56 E Bell Drive, Warsaw, IN 46581, USA. bill.pietrzak@biomet.com
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MeSH Terms
Descriptor/Qualifier:
Absorbable Implants*
Biocompatible Materials / chemistry*
Elastic Modulus
Hot Temperature
Humans
Hydrolysis
Internal Fixators*
Lactic Acid / chemistry*
Materials Testing
Molecular Weight
Polyglycolic Acid / chemistry*
Prosthesis Design
Stress, Mechanical
Tensile Strength
Time Factors
Transition Temperature
Viscosity
Water / chemistry
Chemical
Reg. No./Substance:
0/Biocompatible Materials; 0/polylactic acid-polyglycolic acid copolymer; 26009-03-0/Polyglycolic Acid; 50-21-5/Lactic Acid; 7732-18-5/Water

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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