Self-assembled, thermosensitive PCL-g-P(NIPAAm-co-HEMA) micelles for drug delivery

被引:55
作者
Li, Yong-Yong
Zhang, Xian-Zheng [1 ]
Cheng, Han
Zhu, Jing-Ling
Cheng, Si-Xue
Zhuo, Ren-Xi
机构
[1] Wuhan Univ, Key Lab Biomed Polymers, Minist Educ, D-430072 Dresden, Germany
[2] Wuhan Univ, Dept Chem, D-430072 Dresden, Germany
关键词
controlled release; graft polymer; micelles; thermosensitivity;
D O I
10.1002/marc.200600521
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A novel thermosensitive amphiphilic copolymer (PCL-g-P(NIPAAm-co-HEMA)) comprised of hydrophobic PCL segments and hydrophilic P(NIPAAm-co-HEMA) segments was designed and synthesized. The structure of the copolymer was characterized by FT-IR, H-1 NMR and GPC analysis. The copolymer may self-assemble into micelles in water and the resulting micelles demonstrated temperature sensitivity with a lower critical solution temperature (LCST) of 33 degrees C. The critical micellar concentration (CMC) obtained from surface tension measurements and the fluorescence method was around 30 mg center dot L-1. Transmission electron microscopy (TEM) showed that the micelles exhibit a nanospheric morphology within a narrow size range of 150-160 nm. A cytotoxicity study showed that the PCL-g-P(NIPAAm-co-HEMA) copolymer exhibits good biocom- patibility. The controlled drug release of the resulting micelles was investigated and it was found that micelles loaded with prednisone acetate showed improved drug release behavior due to the special micellar structure.
引用
收藏
页码:1913 / 1919
页数:7
相关论文
共 22 条
[1]   Nano-engineering block copolymer aggregates for drug delivery [J].
Allen, C ;
Maysinger, D ;
Eisenberg, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :3-27
[2]   Biodegradable polymers [J].
Chandra, R ;
Rustgi, R .
PROGRESS IN POLYMER SCIENCE, 1998, 23 (07) :1273-1335
[3]   GRAFT-COPOLYMERS THAT EXHIBIT TEMPERATURE-INDUCED PHASE-TRANSITIONS OVER A WIDE-RANGE OF PH [J].
CHEN, GH ;
HOFFMAN, AS .
NATURE, 1995, 373 (6509) :49-52
[4]   Synthesis and characterization of poly(L-lysine)-g-poly(D,L-lactic-co-glycolic acid) biodegradable micelles [J].
Jeong, JH ;
Byun, Y ;
Park, TG .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2003, 14 (01) :1-11
[5]   Polymeric micelles - a new generation of colloidal drug carriers [J].
Jones, MC ;
Leroux, JC .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1999, 48 (02) :101-111
[6]  
JUN YJ, 2006, ANGEW CHEM INT EDIT, V45, P1
[7]   Pluronic® block copolymers in drug delivery:: From micellar nanocontainers to biological response modifiers [J].
Kabanov, AV ;
Alakhov, VY .
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS, 2002, 19 (01) :1-72
[8]   Block copolymer micelles for drug delivery: design, characterization and biological significance [J].
Kataoka, K ;
Harada, A ;
Nagasaki, Y .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 47 (01) :113-131
[9]   MICELLES BASED ON AB BLOCK COPOLYMERS OF POLY(ETHYLENE OXIDE) AND POLY(BETA-BENZYL L-ASPARTATE) [J].
KWON, G ;
NAITO, M ;
YOKOYAMA, M ;
OKANO, T ;
SAKURAI, Y ;
KATAOKA, K .
LANGMUIR, 1993, 9 (04) :945-949
[10]   Polymeric micelles for delivery of poorly water-soluble compounds [J].
Kwon, GS .
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS, 2003, 20 (05) :357-403