Shah S S, Zhu K J, Pitt C G
Amgen Inc., Thousand Oaks, CA 91320.
J Biomater Sci Polym Ed. 1994;5(5):421-31. doi: 10.1163/156856294x00121.
ABA block copolymers of polyethylene glycol and poly-DL-lactic acid were prepared by ring-opening polymerization of DL-dilactide with alpha,omega-dihydroxy polyethylene glycol, Mn 1000 or 2000. The morphology of the resulting copolymers, with PEG:PLA ratios(mol/mol) of 1:2, 1:3 and 1:4, was characterized by DSC and ESR spectroscopy. The rate of water uptake was biphasic, reflecting the contribution of two processes: rapid diffusion of water into the initially miscible PEG and PLA blocks; then a slower rate of hydration possibly due to phase separation and hydrolytic cleavage of the PLA blocks. The rate of hydrolytic degradation of the block copolymers in DI water at 37 degrees C was measured by two methods: weight loss and colorimetric analysis of the carboxy end group concentration resulting from chain scission of PLA blocks. As a result of phase separation, the rate of scission of PLA blocks in the copolymers was similar to that of the PLA homopolymer. The more rapid onset of weight loss of the copolymers, relative to PLA, is attributed to the greater water solubility of PEG-PLA oligomers and their greater diffusivity in the more highly hydrated copolymers.
聚乙二醇与聚-DL-乳酸的ABA嵌段共聚物是通过DL-丙交酯与α,ω-二羟基聚乙二醇(Mn为1000或2000)的开环聚合反应制备的。通过差示扫描量热法(DSC)和电子自旋共振光谱(ESR)对所得共聚物进行表征,其聚乙二醇与聚乳酸(PEG:PLA)的摩尔比分别为1:2、1:3和1:4。吸水率呈双相性,反映了两个过程的作用:水快速扩散到最初互溶的聚乙二醇和聚乳酸嵌段中;然后由于相分离和聚乳酸嵌段的水解裂解,水合速率变慢。通过两种方法测量了嵌段共聚物在37℃去离子水中的水解降解速率:失重法和对聚乳酸嵌段链断裂产生的羧基端基浓度进行比色分析。由于相分离,共聚物中聚乳酸嵌段的断裂速率与聚乳酸均聚物的断裂速率相似。相对于聚乳酸,共聚物失重更快的起始阶段归因于聚乙二醇-聚乳酸低聚物更高的水溶性及其在水合程度更高的共聚物中更大的扩散性。