Molecular design of biodegradable polymeric micelles for temperature-responsive drug release

被引:294
作者
Nakayama, Masamichi
Okano, Teruo
Miyazaki, Takanari
Kohori, Fukashi
Sakai, Kiyotaka
Yokoyama, Masayuki
机构
[1] Kanagawa Acad Sci & Technol, Yokoyama Nano Med Ploymers Project, Takatsu Ku, Kawasaki, Kanagawa 2130012, Japan
[2] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, Shinjuku Ku, Tokyo 1628666, Japan
[3] Waseda Univ, Dept Appl Chem, Shinjuku Ku, Tokyo 1698555, Japan
基金
日本学术振兴会;
关键词
polymeric micelle; biodegradable polymer; thermo-response; temperature; targeting;
D O I
10.1016/j.jconrel.2006.07.007
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We designed thenno-responsive and biodegradable polymeric micelles for an ideal drug delivery system whose target sites are where external stimuli selectively release drugs from the polymeric micelles. The thermo-responsive micelles formed from block copolymers that were composed both of a hydrophobic block and a thermo-responsive block. Poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide) showing a lower critical solution temperature (LCST) around 40 degrees C was synthesized for the thermo-responsive block, while biodegradable poly(D,L-lactide), poly(epsilon-caprolactone), or poly(D,L-lactide-co-epsilon-caprolactone) was used for the hydrophobic block. By changing both the block lengths of the poly(D,L-lactide)-containing block copolymers, physical parameters such as micelle diameter and critical micelle concentration were varied. On the other hand, the choice of the hydrophobic block was revealed to be critical in relation to both on the thermo-responsive release of the incorporated anticancer drug, doxorubicin, and the temperature-dependent change of the hydrophobicity of the micelles' inner core. One polymeric micelle composition successfully exhibited rapid and thermo-responsive drug release while possessing a biodegradable character. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 56
页数:11
相关论文
共 46 条
[1]   Polycaprolactone-b-poly(ethylene oxide) copolymer micelles as a delivery vehicle for dihydrotestosterone [J].
Allen, C ;
Han, JN ;
Yu, YS ;
Maysinger, D ;
Eisenberg, A .
JOURNAL OF CONTROLLED RELEASE, 2000, 63 (03) :275-286
[2]  
Brown DM., 2004, DRUG DELIVERY SYSTEM
[3]   FLUORESCENCE STUDIES OF AMPHIPHILIC POLY(METHACRYLIC ACID)-BLOCK-POLYSTYRENE-BLOCK-POLY(METHACRYLIC ACID) MICELLES [J].
CAO, T ;
MUNK, P ;
RAMIREDDY, C ;
TUZAR, Z ;
WEBBER, SE .
MACROMOLECULES, 1991, 24 (23) :6300-6305
[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]   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
[6]   Inner core segment design for drug delivery control of thermo-responsive polymeric micelles [J].
Chung, JE ;
Yokoyama, M ;
Okano, T .
JOURNAL OF CONTROLLED RELEASE, 2000, 65 (1-2) :93-103
[7]   Reversibly thermo-responsive alkyl-terminated poly(N-isopropylacrylamide) core-shell micellar structures [J].
Chung, JE ;
Yokoyama, M ;
Suzuki, K ;
Aoyagi, T ;
Sakurai, Y ;
Okano, T .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1997, 9 (1-2) :37-48
[8]  
Duncan R, 1996, STP PHARMA SCI, V6, P237
[9]   Engineering polysaccharide-based polymeric micelles to enhance permeability of cyclosporin a across Caco-2 cells [J].
Francis, MF ;
Cristea, M ;
Yang, YL ;
Winnik, FM .
PHARMACEUTICAL RESEARCH, 2005, 22 (02) :209-219
[10]  
Hamann Philip R., 2002, P239