Stimuli-responsive chitosan-graft-poly(N-vinylcaprolactam) as a promising material for controlled hydrophobic drug delivery

被引:121
作者
Prabaharan, Mani [1 ]
Grailer, Jamison J. [2 ]
Steeber, Douglas A. [2 ]
Gong, Shaoqin [1 ,3 ]
机构
[1] Univ Wisconsin, Dept Mech Engn, Milwaukee, WI 53211 USA
[2] Univ Wisconsin, Dept Biol Sci, Milwaukee, WI 53211 USA
[3] Univ Wisconsin, Dept Mat, Milwaukee, WI 53211 USA
基金
美国国家科学基金会;
关键词
chitosan; controlled release; cytotoxicity; poly(N-vinylcaprolactam); stimuli-responsive;
D O I
10.1002/mabi.200800010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A novel type of pH- and thermo-responsive copolymer, chitosan-graft-poly(N-vinylcaprolactam) (chitosan-g-PNVCL), was prepared by grafting carboxyl-terminated poly(N- vinylcaprolactam) (PNVCL-COOH) chains onto a chitosan backbone as a drug-delivery carrier. The formation of chitosan-g-PNVCL was confirmed by FT-IR and H-1 NMR techniques. Chitosan-g-PNVCL showed a definite phase transition at 32 degrees C as occurs in pure PNVCL. The swelling degree of the chitosan-g-PNVCL beads was found to be higher at pH 2.2 than at pH 7.4. Moreover, the swelling degree of the beads decreased with increased environmental temperature. Compared to the chitosan beads, the release profile of chitosan-g-PNVCL beads showed a slower and more controlled release of the entrapped ketoprofen. The release behavior of the chitosan-g-PNVCL beads was influenced by both the pH and temperature of the medium. The MTT assay showed no obvious cytotoxicity of chitosan-g-PNVCL against a human endothelial cell line over a concentration range of 0-400 mu g center dot mL(-1). These results suggest that chitosan-g-PNVCL could be a potential stimuli-responsive material for controlled drug delivery, and it may improve the bioavailability, efficacy, and compliance of the encapsulated drugs.
引用
收藏
页码:843 / 851
页数:9
相关论文
共 38 条
[1]   Reversible adsorption by a pH- and temperature-sensitive acrylic hydrogel [J].
Alvarez-Lorenzo, C ;
Concheiro, A .
JOURNAL OF CONTROLLED RELEASE, 2002, 80 (1-3) :247-257
[2]   TEMPERATURE-RESPONSIVE INTERPENETRATING POLYMER NETWORKS CONSTRUCTED WITH POLY(ACRYLIC ACID) AND POLY(N,N-DIMETHYLACRYLAMIDE) [J].
AOKI, T ;
KAWASHIMA, M ;
KATONO, H ;
SANUI, K ;
OGATA, N ;
OKANO, T ;
SAKURAI, Y .
MACROMOLECULES, 1994, 27 (04) :947-952
[3]  
Brannon-Peppas L., 1997, MED PLAST BIOMATER, V4, P34
[4]   Poly(N-isopropylacrylamide)-chitosan as thermosensitive in situ gel-forming system for ocular drug delivery [J].
Cao, Yanxia ;
Zhang, Can ;
Shen, Wenbin ;
Cheng, Zhihong ;
Yu, Liangli Lucy ;
Ping, Qineng .
JOURNAL OF CONTROLLED RELEASE, 2007, 120 (03) :186-194
[5]   Fluorescence investigations of the thermally induced conformational transition of poly(N-isopropylacrylamide) [J].
Chee, CK ;
Rimmer, S ;
Soutar, I ;
Swanson, L .
POLYMER, 2001, 42 (12) :5079-5087
[6]   Effect of molecular architecture of hydrophobically modified poly(N-isopropylacrylamide) on the formation of thermoresponsive core-shell micellar drug carriers [J].
Chung, JE ;
Yokoyama, M ;
Aoyagi, T ;
Sakurai, Y ;
Okano, T .
JOURNAL OF CONTROLLED RELEASE, 1998, 53 (1-3) :119-130
[7]   On the water swelling behaviour of poly(N-isopropylacrylamide) [P(N-iPAAm)], poly(methacrylic acid) [P(MAA)], their random copolymers and sequential interpenetrating polymer networks (IPNs) [J].
Díez-Peña, E ;
Quijada-Garrido, I ;
Barrales-Rienda, JM .
POLYMER, 2002, 43 (16) :4341-4348
[8]   Synthesis and characterization of AB-crosslinked graft copolymers based on maleilated chitosan and N-isopropylacrylamide [J].
Don, TM ;
Chen, HR .
CARBOHYDRATE POLYMERS, 2005, 61 (03) :334-347
[9]   'Smart' polymers and what they could do in biotechnology and medicine [J].
Galaev, IY ;
Mattiasson, B .
TRENDS IN BIOTECHNOLOGY, 1999, 17 (08) :335-340
[10]  
Gupta KC, 2000, POLYM INT, V49, P141, DOI 10.1002/(SICI)1097-0126(200002)49:2<141::AID-PI303>3.0.CO