B12-Mediated, Long Wavelength Photopolymerization of Hydrogels

被引:41
作者
Rodgers, Zachary L. [1 ]
Hughes, Robert M. [2 ]
Doherty, Laura M. [1 ]
Shell, Jennifer R. [2 ]
Molesky, Brian P. [1 ]
Brugh, Alexander M. [1 ]
Forbes, Malcolm D. E. [1 ]
Moran, Andrew M. [1 ]
Lawrence, David S. [1 ,2 ,3 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Div Chem Biol & Med Chem, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
BLOCK-COPOLYMER HYDROGELS; CROSS-LINKED HYDROGELS; DESIGN; PHOTOINITIATORS; PHOTOCHEMISTRY; POLYMERIZATION; PHOTOLYSIS; ANALOGS;
D O I
10.1021/jacs.5b00182
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Medical hydrogel applications have expanded rapidly over the past decade. Implantation in patients by noninvasive injection is preferred, but this requires hydrogel solidification from a low viscosity solution to occur in vivo via an applied stimuli. Transdermal photo-cross-linking of acrylated biopolymers with photoinitiators and lights offers a mild, spatiotemporally controlled solidification trigger. However, the current short wavelength initiators limit curing depth and efficacy because they do not absorb within the optical window of tissue (600-900 nm). As a solution to the current wavelength limitations, we report the development of a red light responsive initiator capable of polymerizing a range of acrylated monomers. Photoactivation occurs within a range of skin type models containing high biochromophore concentrations.
引用
收藏
页码:3372 / 3378
页数:7
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