Photosensitive controlled release with polyethylene glycol-anthracene modified alginate

被引:29
作者
Wells, L. A. [1 ]
Sheardown, H. [1 ]
机构
[1] McMaster Univ, Dept Chem Engn, Hamilton, ON L8S 4L8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Alginate; Photoresponsive; Anthracene; Drug delivery; Smart biomaterials; PROTEIN RELEASE; CROSS-LINKING; DRUG-RELEASE; HYDROGELS; BEADS; MICROPARTICLES; MICROSPHERES; STABILITY; DELIVERY;
D O I
10.1016/j.ejpb.2011.03.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Covalent modification of alginate with polyethylene glycol-conjugated anthracene molecules has the potential to both stabilize the alginate and act as a photosensitive crosslinker. Release studies with Coomassie Blue show lengthy release times from the alginate photogels that extend past 70 days with, for example, 17% versus 27% release at 1750 h (73 days) for photogels with and without 365-nm UV light treatment for 30 min at 10 mW/cm(2) in the initial release period. Photocrosslinking of the photogels after loading effectively "locks" in drug compounds to control their release. Effective crosslinking densities and controls of polyethylene glycol-crosslinked alginate and physically crosslinked calcium alginate gels suggest strong interactions between Coomassie Blue and both alginate and anthracene. Photogels containing anthracene-capped star-polyethylene glycol show increased photosensitivity with modified release profiles. Ultimately, the covalent modification of alginate with photoactive crosslinkers has the potential to produce a long-term, photosensitive, controlled release system. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:304 / 313
页数:10
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