Hydrolytic Degradation of Amorphous Films of L-Lactide Copolymers with Glycolide and D-Lactide
✍ Scribed by Swapan K. Saha; Hideto Tsuji
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 551 KB
- Volume
- 291
- Category
- Article
- ISSN
- 1438-7492
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✦ Synopsis
Abstract
Summary: Films of poly(L‐lactic acid) (PLLA) and copolymers of L‐lactide (LLA) with either glycolide P(LLA‐GA) or D‐lactide P(LLA‐DLA) were prepared and an effect of comonomer type on the hydrolytic degradation of the films was studied in phosphate‐buffered solutions at 37 °C. The degraded films were investigated using gravimetry (weight loss and water absorption), gel permeation chromatography, DSC, X‐ray diffractometry, tensile testing and polarization optical microscopy. To exclude the effects of molecular weight and crystallinity on hydrolytic degradation, the films were prepared from polymers with similar molecular weights and were made amorphous by melt quenching. It was found that the hydrolytic degradation rate decreased in the order P(LLA‐GA) > P(LLA‐DLA) > PLLA. The hydrolytic degradation rate constant of PLLA and LLA copolymer films increased with increasing the water absorption (hydrophilicity), or with decreasing the initial glass transition temperature or the L‐lactyl unit sequence length, indicating that the hydrolytic degradation rate of the copolymers was closely related to these three parameters. The crystallization of P(LLA‐GA) film occurred within hydrolytic degradation for 20 weeks.
M~n~ of PLLA and LLA copolymer films as a function of hydrolytic degradation time.
magnified image__M__~n~ of PLLA and LLA copolymer films as a function of hydrolytic degradation time.
📜 SIMILAR VOLUMES
The i.r. and Raman spectra of glycolide, L-lactide and O,L-lactide in the solid state have been investigated in the 4000-100 cm -t range. An assignment of the fundamental vibrations is given. The Raman spectra of aqueous solutions of these cyclic diesters showed ring-opening and the beginning of pol
The e †ect of hydrolytic degradation on the microstructure of unoriented, random 50 : 50 poly(glycolic acid-co-D,L-lactic acid) was examined using simultaneous small and wide angle X-ray scattering (SAXS/WAXS) and di †erential scanning calorimetry (DSC). Samples were degraded in phosphatebu †ered sa