Thermosensitive Y-shaped micelles of poly(oleic acid-Y-N-isopropylacrylamide) for drug delivery

被引:85
作者
Li, Yong-Yong
Zhang, Xian-Zheng [1 ]
Kim, Gwang-Chol
Cheng, Han
Cheng, Si-Xue
Zhuo, Ren-Xi
机构
[1] Wuhan Univ, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
关键词
controlled release; copolymers; drug delivery; micelles; self-assembly;
D O I
10.1002/smll.200600041
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel thermosensitive amphiphilic copolymer comprised of two hydrophobic poly (oleic acid) (POA) segments and one hydrophilic poly (N-isopropylacrylamide) (PNIPAAm) segment was designed and synthesized. The structure of the copolymer was confirmed as Y-shaped by FTIR, H-1 NMR, and SEC-MALLS analysis. A cytotoxicity study shows that the P(OA-Y-NIPAAm) copolymer exhibits good biocompatibility. The copolymer may self-assemble into micelles in water, with the hydrophobic POA segments at the cores of micelles and the hydrophilic PNIPAAm segments as the outer shells. The resulting micelles demonstrate temperature sensitivity with a lower critical solution temperature (LCST) of 31.5 degrees C and a critical micelle concentration (CMC) of 12.6 mg L-1. Transmission electron microscopy (TEM) shows that the micelles exhibit a nanospheric morphology within a narrow size range of approximate to 10-30 nm. A study of controlled release reveals that the self-assembled micelles have great potential as drug carriers.
引用
收藏
页码:917 / 923
页数:7
相关论文
共 27 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]   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
[3]   Intelligent crew-cut aggregates formed by thermosensitive block copolymers and their multiple morphologies [J].
Chen, XR ;
Ding, XB ;
Zheng, ZH ;
Peng, YX .
MACROMOLECULAR BIOSCIENCE, 2005, 5 (02) :157-163
[4]   Thermo-responsive drug delivery from polymeric micelles constructed using block copolymers of poly(N-isopropylacrylamide) and poly(butylmethacrylate) [J].
Chung, JE ;
Yokoyama, M ;
Yamato, M ;
Aoyagi, T ;
Sakurai, Y ;
Okano, T .
JOURNAL OF CONTROLLED RELEASE, 1999, 62 (1-2) :115-127
[5]   Dispersion polymerization of styrene in ethanol-water mixture using polystyrene-b-poly(ethylene oxide) macromonomers as stabilizers [J].
Gibanel, S ;
Heroguez, V ;
Forcada, J ;
Gnanou, Y .
MACROMOLECULES, 2002, 35 (07) :2467-2473
[6]   Novel gemini-type reactive dispersants based on PS/PEO block copolymers: Synthesis and application [J].
Gibanel, S ;
Forcada, J ;
Heroguez, V ;
Schappacher, M ;
Gnanou, Y .
MACROMOLECULES, 2001, 34 (13) :4451-4458
[7]   VOLUME PHASE-TRANSITION IN A NONIONIC GEL [J].
HIROKAWA, Y ;
TANAKA, T .
JOURNAL OF CHEMICAL PHYSICS, 1984, 81 (12) :6379-6380
[8]   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
[9]   ENVIRONMENTAL EFFECTS ON VIBRONIC BAND INTENSITIES IN PYRENE MONOMER FLUORESCENCE AND THEIR APPLICATION IN STUDIES OF MICELLAR SYSTEMS [J].
KALYANASUNDARAM, K ;
THOMAS, JK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (07) :2039-2044
[10]   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