Novel crosslinking methods to design hydrogels

被引:1947
作者
Hennink, W. E. [1 ]
van Nostrum, C. F. [1 ]
机构
[1] Univ Utrecht, Dept Pharmaceut, Utrecht Inst Pharmaceut Sci, NL-3508 TB Utrecht, Netherlands
关键词
Hydrogel; Crosslinking; Drug release; Tissue engineering; Degradation; ABA TRIBLOCK COPOLYMERS; LACTIC-ACID OLIGOMERS; AMPHIPHILIC MULTIBLOCK COPOLYMERS; IN-VIVO BIOCOMPATIBILITY; CONTROLLED-RELEASE SYSTEMS; DRUG-DELIVERY; STEREOCOMPLEX FORMATION; SWELLING BEHAVIOR; PROTEIN-DELIVERY; POLY(ETHYLENE GLYCOL);
D O I
10.1016/j.addr.2012.09.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hydrogels are presently under investigation as matrices for the controlled release of bioactive molecules, in particular pharmaceutical proteins, and for the encapsulation of living cells. For these applications, it is often required that the gels degrade under physiological conditions. This means that the originally three-dimensional structure has to disintegrate preferably in harmless products to ensure a good biocompatibility of the hydrogel. In this overview, different chemical and physical crosslinking methods used for the design of biodegradable hydrogels are summarized and discussed. Chemical crosslinking is a highly versatile method to create hydrogels with good mechanical stability. However, the crosslinking agents used are often toxic compounds, which have been extracted from the gels before they can be applied. Moreover, crosslinking agents can give unwanted reactions with the bioactive substances present in the hydrogel matrix. Such adverse effects are avoided with the use of physically crosslinked gels. (C) 2012 Published by Elsevier B.V.
引用
收藏
页码:223 / 236
页数:14
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