Biomedical subjects

J Mauduit

Publications and source records attributed to J Mauduit.

4 recordsLinked to original sources

PubMed1996

Hydrolytic degradation of films prepared from blends of high and low molecular weight poly(DL-lactic acid)s.

Biodegradable films were prepared by casting acetone solutions of mixtures of a high molecular weight poly(DL-lactic acid) (HMW-PLA50) with 0, 10, and 30% w/w poly(DL-lactic acid) oligomers (LMW-PLA50), before drying. From size exclusion chromatography (SEC) it was shown that degradation occurred during film processing, in agreement with the acid-catalyzed degradation of polyesters. The higher the content of LMW-PLA50, the larger the decrease of the molar masses. The three selected film formulations were then allowed to age in isoosmolar 0.13M, pH 7.4 sodium phosphate buffer at 37 degrees C. The hydrolytic degradation was monitored by using various techniques, namely weighing to quantify water absorption and weight loss, SEC to evaluate molar mass changes, head space gas chromatography to assess the desorption of residual acetone, and enzymatic assay of the L-lactic acid released in the aging media. The presence of LMW-PLA50 clearly accelerated film degradation. Moreover, it was shown that the mechanism of degradation greatly depended on the content in the oligomers.

Absorption↗

PubMed1995

Hydrolytic degradation of benzylated poly(beta-malic acid): influence of sample size, sample shape, and polymer composition.

In order to investigate the effects of sample size, sample shape, and polymer composition on the hydrolytic degradation of water-insoluble benzylated poly(beta-malic acid) derivatives, three polymers were synthesized, namely PMLABe100, PMLABe90H10 and PMLABe80H20, containing 100, 90, and 80% of benzyl units respectively. For each polymer, 4-mm-thick compression molded pellets, 0.3-mm-thick casted films and 250-500 microns ground particles were made and allowed to age in 0.13 M, pH 7.4 sodium phosphate buffer at 37 degrees C. Degradation was monitored by measuring weight changes, variations of polymer composition, formation of benzyl alcohol, and molecular weight decreases. It was shown that degradation of particles and films depended initially on polymer composition due primarily to fast degradation of acid-rich segments present or formed by benzyl ester cleavages which led more or less rapidly to similar compositions for the three polymers. The higher the content in acid groups, the faster the degradation rate and the characteristic changes. It was also found that pellets made of PMLABe90H10 or PMLABe80H20 degraded heterogeneously and much faster than corresponding films and particles.

Benzene Derivatives↗

PubMed1994

Biodegradation of PLA/GA polymers: increasing complexity.

The degradation of aliphatic polyesters derived from lactic and glycolic acids (PLA/GA) depends on many factors. It has been found recently that the interior of large size devices degrades faster than the outer zone. A qualitative model has been proposed to account for this heterogeneous degradation. It is based on diffusion-reaction phenomena combined with the well-known autocatalytic effect of carboxylic chain ends. This contribution recalls the present understanding of the hydrolytic degradation of PLA/GA polymers and emphasizes its complexity on the basis of the influence of secondary factors such as the presence of a basic load, namely, gentamycin, in poly(lactic acid) matrices, and the presence of long stereoregular sequences in poly(DL-lactic acid) macromolecules.

Biocompatible Materials↗

PubMed1993

Biocompatibility and resorbability of a polylactic acid membrane for periodontal guided tissue regeneration.

The biocompatibility and degradation processes of biomembranes made of a mixture of a high molecular weight racemic polylactic acid (PLA50P) with 0, 10, 20 and 30% w/w racemic polylactic acid oligomers (PLA50p) were assessed for morphological changes in subcutaneous abdominal membrane implantations after 15, 21, 30 and 60 d in 45 Wistar rats. These membranes, prepared for periodontal guided tissue regeneration, showed excellent tissue tolerance without an inflammatory reaction. The higher the content in low molecular weight polylactic acid, the higher the degradation rate. At 60 d, the resorption process was almost complete. This process was initiated by outgrowths of short vascular septa, which developed into lobular networks infiltrating the membranes, which were progressively replaced by normal fibrous connective tissue.

Animals↗