In situ-forming hydrogels -: review of temperature-sensitive systems

被引:1049
作者
Ruel-Gariépy, E [1 ]
Leroux, JC [1 ]
机构
[1] Univ Montreal, Fac Pharm, Canada Res Chair Drug Delivery, Montreal, PQ H3C 3J7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
thermosensitivity; implants; in situ; injectables; drug delivery;
D O I
10.1016/j.ejpb.2004.03.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the past few years, an increasing number of in situ-forming systems have been reported in the literature for various biomedical applications, including drug delivery, cell encapsulation, and tissue repair. There are several possible mechanisms that lead to in situ gel formation: solvent exchange, UV-irradiation, ionic cross-linkage, pH change, and temperature modulation. The thermosensitive approach can be advantageous for particular applications as it does not require organic solvents, co-polymerization agents, or an externally applied trigger for gelation. In the last 2 decades, several thermosensitive formulations have been proposed. This manuscript focuses on aqueous polymeric solutions that form implants in situ in response to temperature change, generally from ambient to body temperature. It mainly reviews the characterization and use of polysaccharides, N-isopropylacrylamide copolymers, poly(ethylene oxide-b-propylene oxide-b-ethylene oxide) (poloxamer) and its copolymers, poly(ethylene oxide)/(D,L -lactic acid-co-glycolic acid) copolymers, and thermosensitive liposome-based systems. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:409 / 426
页数:18
相关论文
共 136 条
[1]   Intratumoral administration of paclitaxel in an in situ gelling poloxamer 407 formulation [J].
Amiji, MM ;
Lai, PK ;
Shenoy, DB ;
Rao, M .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2002, 7 (02) :195-202
[2]   Intraarterial protein delivery via intimally-adherent bilayer hydrogels [J].
An, YJ ;
Hubbell, JA .
JOURNAL OF CONTROLLED RELEASE, 2000, 64 (1-3) :205-215
[3]   X-RAY DIFFRACTION STUDIES OF POLYSACCHARIDE SULPHATES - DOUBLE HELIX MODELS FOR K-AND L-CARRAGEENANS [J].
ANDERSON, NS ;
CAMPBELL, JW ;
HARDING, MM ;
REES, DA ;
SAMUEL, JWB .
JOURNAL OF MOLECULAR BIOLOGY, 1969, 45 (01) :85-&
[4]   Extracellular matrix for a rechargeable cell delivery system [J].
Bae, YH ;
Vernon, B ;
Han, CK ;
Kim, SW .
JOURNAL OF CONTROLLED RELEASE, 1998, 53 (1-3) :249-258
[5]   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
[6]   Dose-dependent hyperlipidemia in rabbits following administration of poloxamer 407 gel [J].
Blonder, JM ;
Baird, L ;
Fulfs, JC ;
Rosenthal, GJ .
LIFE SCIENCES, 1999, 65 (21) :PL261-PL266
[7]   A study of the temperature-dependent micellization of pluronic F127 [J].
Bohorquez, M ;
Koch, C ;
Trygstad, T ;
Pandit, N .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1999, 216 (01) :34-40
[8]   Scaling of rheological properties of hydrogels from associating polymers [J].
Bromberg, L .
MACROMOLECULES, 1998, 31 (18) :6148-6156
[9]   Novel family of thermogelling materials via C-C bonding between poly(acrylic acid) and poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) [J].
Bromberg, L .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (11) :1956-1963
[10]   Properties of aqueous solutions and gels of poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide)-g-poly(acrylic acid) [J].
Bromberg, L .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (52) :10736-10744