Synthesis and enzymatic degradation of end-functionalized biodegradable polyesters

被引:12
作者
Zou, T [1 ]
Cheng, SX [1 ]
Zhuo, RX [1 ]
机构
[1] Wuhan Univ, Key Lab Biomed Polymers, Minist Educ, Dept Chem, Wuhan 430072, Peoples R China
关键词
biodegradable; functionalization; polyesters;
D O I
10.1007/s00396-004-1267-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
End-functionalization of biodegradable polymers/oligomers based on L-lactide and glycolide by cholesteryl moiety was investigated. We established the feasibility of preparing the functionalized polymers/oligomers, Chol-(LG)(m+n), through ring-opening copolymerization initiated by cholesterol bearing a hydroxyl group, without adding any catalyst. The functionalized polymers/oligomers of different molecular weights were obtained by controlling the feed ratio of the initiator cholesterol to the monomers. The chemical structure of end-functionalized polymers/oligomers was confirmed by FTIR and H-1 NMR. Incorporation of cholesteryl moiety into the polymer chains induces liquid crystallinity in the resultant oligomers when the molecular chains are not very long. The enzymatic degradation studies, for all the samples, were carried out using enzyme, proteinase K. Interestingly, the enzymatic degradation of cholesteryl end-functionalized polymers/oligomers resulted in a lamella-like porous structure on the sample surface, which is altogether different from the commonly reported spherical-pore structure formed during the degradation of conventional polyesters.
引用
收藏
页码:1091 / 1099
页数:9
相关论文
共 17 条
[1]   Biodegradable comb polyesters.: Part II.: Erosion and release properties of poly(vinyl alcohol)-g-poly(lactic-co-glycolic acid) [J].
Breitenbach, A ;
Pistel, KF ;
Kissel, T .
POLYMER, 2000, 41 (13) :4781-4792
[2]   Enzymatic degradation behavior and mechanism of poly(lactide-co-glycolide) foams by trypsin [J].
Cai, Q ;
Shi, GX ;
Bei, JZ ;
Wang, SG .
BIOMATERIALS, 2003, 24 (04) :629-638
[3]  
HWANG JJ, 2003, P NATL ACAD SCI USA, V99, P9662
[4]   In vitro biocompatibility of bioresorbable polymers: Poly(L,DL-lactide) and poly(L-lactide-co-glycolide) [J].
Ignatius, AA ;
Claes, LE .
BIOMATERIALS, 1996, 17 (08) :831-839
[5]   Microstructural analysis of poly[(L,L-lactide)-co-(glycolide)] by H-1 and C-13 nmr spectroscopy [J].
Kasperczyk, J .
POLYMER, 1996, 37 (02) :201-203
[6]   Self-assembling biomaterials:: L-lysine-dendron-substituted cholesteryl-(L-lactic acid)(n)over-bar [J].
Klok, HA ;
Hwang, JJ ;
Hartgerink, JD ;
Stupp, SI .
MACROMOLECULES, 2002, 35 (16) :6101-6111
[7]   Cholesteryl-(L-lactic acid)(n)over-bar building blocks for self-assembling biomaterials [J].
Klok, HA ;
Hwang, JJ ;
Iyer, SN ;
Stupp, SI .
MACROMOLECULES, 2002, 35 (03) :746-759
[8]   Effect of cholesteryl side chain and complexing with cholic acid on gene transfection by cationic poly(ethylene glycol) derivatives [J].
Koyama, Y ;
Ito, T ;
Kimura, T ;
Murakami, A ;
Yamaoka, T .
JOURNAL OF CONTROLLED RELEASE, 2001, 77 (03) :357-364
[9]   POLYLACTONES .30. VITAMINS, HORMONES AND DRUGS AS CO-INITIATORS OF ALET(3)-INITIATED POLYMERIZATIONS OF LACTIDE [J].
KRICHELDORF, HR ;
KREISERSAUNDERS, I .
POLYMER, 1994, 35 (19) :4175-4180
[10]  
Li SM, 2001, POLYM DEGRAD STABIL, V71, P61