Photoregulated Hydrazone-Based Hydrogel Formation for Biochemically Patterning 3D Cellular Microenvironments

被引:59
作者
Azagarsamy, Malar A. [1 ,2 ]
Marozas, Ian A. [1 ,2 ]
Spans, Sergio [3 ]
Anseth, Kristi S. [1 ,2 ]
机构
[1] Univ Colorado, Howard Hughes Med Inst, Dept Chem & Biol Engn, 596 UCB, Boulder, CO 80303 USA
[2] Univ Colorado, BioFrontiers Inst, 596 UCB, Boulder, CO 80303 USA
[3] Eindhoven Univ Technol, Inst Complex Mol Syst, Dept Biomed Engn, POB 513, NL-5600 MB Eindhoven, Netherlands
基金
美国国家科学基金会;
关键词
CLICK CHEMISTRY; CULTURE; PH;
D O I
10.1021/acsmacrolett.5b00682
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Photodriven click reactions have emerged as versatile tools for biomaterial synthesis that can recapitulate critical spatial and temporal changes of extracellular matrix (ECM) microenvironments in vitro. In this article, we report on the synthesis of poly(ethylene glycol) (PEG) hydrogels using photodriven step -growth polymerization, where one of the reactive functionalities is formed by a photodeavage reaction. Upon photocleavage, an aldehyde functionality is generated that rapidly reacts with hydrazine-functionalized PEGs; the gelation kinetics and final material modulus are distinctly controlled by variations in the light intensity. This light-driven aldehyde generation is further exploited to install biochemical ligands in the hydrazone-based hydrogels with precise spatial control. We expect that user directed spatial and temporal control over both biophysical and biochemical gel properties through photochemical reactions and photopatterning, respectively, should provide newfound opportunities to probe and understand dynamic cell matrix interactions.
引用
收藏
页码:24 / 28
页数:5
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