Control and prediction of gelation kinetics in enzymatically cross-linked poly(ethylene glycol) hydrogels

被引:60
|
作者
Sperinde, JJ
Griffith, LG [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, Div Bioengn & Environm Hlth, Cambridge, MA 02139 USA
关键词
D O I
10.1021/ma000459d
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We demonstrate control of gelation kinetics in formation of poly(ethylene glycol) (PEG) hydrogels by enzymatic cross-linking. A predictive model for gelation kinetics based on macromer structure and composition, stoichiometric ratios of reactants, cross-linking enzyme concentration, and the underlying kinetics of enzyme reaction was developed on the basis of classical Flory-Stockmayer theory. Experiments with substrate-functionalized multiarm comb PEG showed good agreement with theory upon variation of the enzyme concentration, with a slight overprediction in the time to gelation. Experiments with a substrate-functionalized difunctional PEG in conjunction with a polypeptide where macromer concentrations were varied were also consistent with theory, but with a slight underprediction of gelation time.
引用
收藏
页码:5476 / 5480
页数:5
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