Biodegradable Hydrogels for Time-Controlled Release of Tethered Peptides or Proteins

被引:40
作者
Brandl, Ferdinand [1 ]
Hammer, Nadine [1 ]
Blunk, Torsten [1 ]
Tessmar, Joerg [1 ]
Goepferich, Achim [1 ]
机构
[1] Univ Regensburg, Dept Pharmaceut Technol, D-93040 Regensburg, Germany
关键词
SYSTEMS EMPLOYING 1,6-ELIMINATION; DRUG-DELIVERY; MODEL; HYDROLYSIS; DIFFUSION; ACYLATION; DESIGN;
D O I
10.1021/bm901235g
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tethering drug substances to it gel network is all effective way of controlling the release kinetics of hydrogel-based drug delivery systems Here, we report oil in situ forming, biodegradable hydrogels that allow for the covalent attachment of peptides or proteins. Hydrogels were prepared by step-growth polymerization of branched poly(ethylene glycol). The gel strength ranged from 1075 to 2435 Pit: the degradation time varied between 24 and 120 h. Fluorescence recovery after photobleaching showed that fluorescently labeled bovine serum albumin (FITC-BSA) was Successfully bound to the gel network during gel formation Within 168 h, the mobility of the tethered molecules gradually increased due to polymer degradation Using FITC-BSA and lysozyme as model proteins, we showed the potential of the developed hydrogels for time-controlled release. The obtained release profiles had a sigmoidal shape and matched the degradation profile very well. protein release wits complete after 96 h
引用
收藏
页码:496 / 504
页数:9
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