Blend films were prepared from poly( L-lactide ) (PLLA) and poly( 1-caprolactone) (PCL) with different PLLA contents [X PLLA (w/w) Å PLLA/(PCL / PLLA)] by the solution-casting method and their hydrolysis behaviors were investigated up to 20 months in a phosphate-buffered solution of pH 7.4 at 37ЊC b
Blends of aliphatic polyesters. III. Biodegradation of solution-cast blends from poly(L-lactide) and poly(ε-caprolactone)
✍ Scribed by Hideto Tsuji; Akira Mizuno; Yoshito Ikada
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 346 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Phase-separated blend films were prepared with the solution casting method from poly(L-lactide) (PLLA) and poly(-caprolactone) (PCL) with different PLLA contents [X PLLA (w/w) ϭ PLLA/(PCL ϩ PLLA)] and their biodegradation was investigated in soil up to 20 months by gravimetry, gel permeation chromatography, tensile testing, differential scanning calorimetry, and scanning electron microscopy. The nonblended PCL film and the blend film with X PLLA ϭ 0.25 disappeared in 4 and 12 months, respectively, while most of the initial mass remained for the blend film of X PLLA ϭ 0.75 and the nonblended PLLA film. The decrease in weight remaining, molecular weight, tensile strength, and elongation-at-break was higher for blend films of low X PLLA . The melting temperature of PLLA in blend films of X PLLA ϭ 0.5 and 0.75, and of nonblended film, remained around 179°C upon biodegradation in soil for 20 months. The preferred biodegradation of PCL in blend films resulted in formation of microspheres of a PLLA-rich phase at the surface for the blend film of X PLLA ϭ 0.25 and the porous structure for blend films of X PLLA ϭ 0.5 and 0.75. Comparison of the weight loss of blend films in biodegradation in soil with that of the nonenzymatic hydrolysis in phosphate-buffered solution revealed preferred enzymatic degradation of PCL and insignificant attack to PLLA in the blends.
📜 SIMILAR VOLUMES
Hydrolysis of blend films prepared from amorphous poly(DL-lactide) (a-PLA) and isotactic crystalline poly(D-or L-lactide) (c-PLA) having different c-PLA contents [X Å c-PLA/(a-PLA / c-PLA)] was performed in phosphate buffered solution of pH 7.4 at 37ЊC. The blend films before and after hydrolysis we