Poly(N-isopropylacrylamide) copolymers for constant temperature controlled drug delivery

被引:66
作者
Eeckman, F [1 ]
Moës, AJ [1 ]
Amighi, K [1 ]
机构
[1] Free Univ Brussels, Pharm Galen & Biopharm Lab, B-1050 Brussels, Belgium
关键词
poly(N-isopropylacrylamide); controlled drug release; thermosensitive copolymers; compression-coated tablets; salting out effect;
D O I
10.1016/j.ijpharm.2003.12.013
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
lnthecourseof the development of anew drug delivery concept, four thermosensitive copolymers of poly(N-isopropylacrylamide) (PNIPAAm), with phase transition temperature slightly higher than 37degreesC, were synthesised and used as time-controlled drug delivery agents. For this purpose, compression-coated tablets coated with the thermosensitive copolymers and containing Na2SO4 were prepared and in vitro dissolution tests were performed at constant physiological temperature, the lag time before drug release being controlled by the amount of Na2SO4 incorporated into the form. Due to the salting out effect, the lag time was increased by up to 80-90% for PNIPAAm-co-NVA and PNIPAAm-co-MVA coated tablets. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 119
页数:11
相关论文
共 22 条
[1]
BRASEL CS, 1996, J CONTROL RELEASE, V39, P57
[2]
Thermoassociative graft copolymers based on poly(N-isopropylacrylamide):: effect of added co-solutes on the rheological behaviour [J].
Durand, A ;
Hourdet, D .
POLYMER, 2000, 41 (02) :545-557
[3]
Evaluation of a new controlled-drug delivery concept based on the use of thermoresponsive polymers [J].
Eeckman, F ;
Moës, AJ ;
Amighi, K .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 241 (01) :113-125
[4]
Effect of some physiological and non-physiological compounds on the phase transition temperature of thermoresponsive polymers intended for oral controlled-drug delivery [J].
Eeckman, F ;
Amighi, K ;
Moës, AJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 222 (02) :259-270
[5]
EECKMAN F, 2004, IN PRESS EUR POLYM J
[6]
EFFECT OF COMONOMER HYDROPHILICITY AND IONIZATION ON THE LOWER CRITICAL SOLUTION TEMPERATURE OF N-ISOPROPYLACRYLAMIDE COPOLYMERS [J].
FEIL, H ;
BAE, YH ;
FEIJEN, J ;
KIM, SW .
MACROMOLECULES, 1993, 26 (10) :2496-2500
[7]
PHASE-TRANSITION OF AQUEOUS-SOLUTIONS OF POLY(N-ISOPROPYLACRYLAMIDE) AND POLY(N-ISOPROPYLMETHACRYLAMIDE) [J].
FUJISHIGE, S ;
KUBOTA, K ;
ANDO, I .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (08) :3311-3313
[8]
Synthesis and properties of ionically modified polymers with LCST behavior [J].
Hahn, M ;
Gornitz, E ;
Dautzenberg, H .
MACROMOLECULES, 1998, 31 (17) :5616-5623
[9]
Heskins M., 1968, J MACROMOL SCI CHEM, V2, P1441, DOI DOI 10.1080/10601326808051910
[10]
A novel positively thermosensitive controlled-release microcapsule with membrane of nano-sized poly(N-isopropylacrylamide) gel dispersed in ethylcellulose matrix [J].
Ichikawa, H ;
Fukumori, Y .
JOURNAL OF CONTROLLED RELEASE, 2000, 63 (1-2) :107-119