Thermosensitive sol-gel reversible hydrogels

被引:1220
作者
Jeong, B
Kim, SW
Bae, YH [1 ]
机构
[1] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Ctr Controlled Chem Delivery, Salt Lake City, UT 84112 USA
[2] PNNL, Richland, WA 99352 USA
关键词
aqueous polymer solution; sol-gel transition; in situ hydrogel formation; temperature; drug delivery;
D O I
10.1016/S0169-409X(01)00242-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aqueous polymer solutions that are transformed into gels by changes in environmental conditions, such as temperature and pH, thus resulting in in situ hydrogel formation, have recently attracted the attention of many investigators for scientific interest and for practical biomedical or pharmaceutical applications. When the hydrogel is formed under physiological conditions and maintains its integrity for a desired period of time, the process may provide various advantages over conventional hydrogels. Because of the simplicity of pharmaceutical formulation by solution mixing, biocompatibility with biological systems, and convenient administration, the pharmaceutical and biomedical uses of the water-based sol-gel transition include solubilization of low-molecular-weight hydrophobic drugs, controlled release, labile biomacromolecule delivery, such as proteins and genes, cell immobilization, and tissue engineering. When the formed gel is proven to be biocompatible and biodegradable, producing non-toxic degradation products, it will provide further benefits for in vivo applications where degradation is desired. It is timely to summarize the polymeric systems that undergo sol-gel transitions, particularly due to temperature, with emphasis on the underlying transition mechanisms and potential delivery aspects. This review stresses the polymeric systems of natural or modified natural polymers, N-isopropylacrylamide copolymers, poly(ethylene oxide)/poly(propylene oxide) block copolymers, and poly(ethylene glycol)/poly(D,L-lactide-co-glycolide) block copolymers. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:37 / 51
页数:15
相关论文
共 97 条
[1]  
Ahn Y., 2001, US patent, Patent No. [US 6103528, 6103528]
[2]   MICELLIZATION OF POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE)-POLY(ETHYLENE OXIDE) TRIBLOCK COPOLYMERS IN AQUEOUS-SOLUTIONS - THERMODYNAMICS OF COPOLYMER ASSOCIATION [J].
ALEXANDRIDIS, P ;
HOLZWARTH, JF ;
HATTON, TA .
MACROMOLECULES, 1994, 27 (09) :2414-2425
[3]   POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE)-POLY(ETHYLENE OXIDE) BLOCK-COPOLYMER SURFACTANTS IN AQUEOUS-SOLUTIONS AND AT INTERFACES - THERMODYNAMICS, STRUCTURE, DYNAMICS, AND MODELING [J].
ALEXANDRIDIS, P ;
HATTON, TA .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1995, 96 (1-2) :1-46
[4]  
[Anonymous], 1992, THERMOREVERSIBLE GEL
[5]   AGAROSE DOUBLE HELIX AND ITS FUNCTION IN AGAROSE-GEL STRUCTURE [J].
ARNOTT, S ;
FULMER, A ;
SCOTT, WE ;
DEA, ICM ;
MOORHOUSE, R ;
REES, DA .
JOURNAL OF MOLECULAR BIOLOGY, 1974, 90 (02) :269-&
[6]   THE MICELLAR PROPERTIES OF THE POLY(OXYETHYLENE) POLY(OXYPROPYLENE) COPOLYMER PLURONIC-F127 IN WATER AND ELECTROLYTE SOLUTION [J].
ATTWOOD, D ;
COLLETT, JH ;
TAIT, CJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1985, 26 (1-2) :25-33
[7]   TEMPERATURE-DEPENDENCE OF SWELLING OF CROSS-LINKED POLY(N,N'-ALKYL SUBSTITUTED ACRYLAMIDES) IN WATER [J].
BAE, YH ;
OKANO, T ;
KIM, SW .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1990, 28 (06) :923-936
[8]   Absorption of insulin from Pluronic F-127 gels following subcutaneous administration in rats [J].
Barichello, JM ;
Morishita, M ;
Takayama, K ;
Nagai, T .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 184 (02) :189-198
[9]  
BEKTUROV EA, 1981, ADV POLYM SCI, V41, P99
[10]   Controlled-release delivery system for the alpha-MSH analog melanotan-I using poloxamer 407 [J].
Bhardwaj, R ;
Blanchard, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (09) :915-919