Synthesis and characterization of novel biodegradable block copolymer poly(ethylene glycol)-block-poly (L-lactide-co-2-methyl-2-carboxyl-propylene carbonate)

被引:38
作者
Guan, HL
Xie, ZG
Zhang, PB
Wang, X
Chen, XS
Wang, XH
Jing, XB [1 ]
机构
[1] Acad Sinica, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
关键词
biodegradable; carbonate; functionalization of polymers; polylactide; ring-opening polymerization;
D O I
10.1002/pola.20942
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
An amphiphilic block copolymer, poly(ethylene glycol)-block-poly(L-lactideco-2-methyl-2-benzoxycarbonyl-propylene carbonate) [PEG-b-P(LA-co-MBC)], was synthesized in bulk by the ring-opening polymerization Of L-lactide with 2-methyl-2-benzoxycarbonyl-propylene carbonate (MBC) in the presence of poly(ethylene glycol) as a macroinitiator with diethyl zinc as a catalyst. The subsequent catalytic hydrogenation of PEG-b-P(LA-co-MBC) with palladium hydroxide on activated charcoal (20%) as a catalyst was carried out to obtain the corresponding linear copolymer poly(ethyleneglycol)-block-poly(L-lactide-co-2-methyl-2-carboxyl-propylenecarbonate) [PEG-b-P(LA-co-MCC)] with pendant carboxyl groups. DSC analysis indicated that the glass-transition temperature (T-g) of PEG-b-MA-co-MBQ decreased with increasing MBC content in the copolymer, and T-g of PEG-b-P(LA-co-MCC) was higher than that of the corresponding PEG-b-P(LA-co-MBC). The in vitro degradation rate of PEG-b-P(LA-co-MCC) in the presence of proteinase K was faster than that of PEG-b-P(LA-co-MBC), and the cytotoxicity of PEG-b-P(LA-co-MCC) to chondrocytes from human fetal arthrosis was lower than that of poly (L-lactide). (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:4771 / 4780
页数:10
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