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Molecular design of light-responsive hydrogels, for in-situ generation of fast and reversible valves for microfluidic applications

机译:光响应水凝胶的分子设计,用于原位生成用于微流控应用的快速和可逆阀门

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摘要

Light-responsive hydrogel valves with enhanced response characteristics compatible with microfluidics have been obtained by optimization of molecular design of spiropyran photoswitches and gel composition. Self-protonating gel formulations were exploited, wherein acrylic acid was copolymerized in the hydrogel network as an internal proton do-nor, to achieve a swollen state of the hydrogel in water at neutral pH. Light-responsive properties were endowed upon the hydrogels by copolymerization of spiropyran chromophores, using electron withdrawing and donating groups to tune the gel-swelling rate. Faster macroscopic swelling of the hydrogels was obtained by changing an ester to an ether at the 6’ position (factor of 4) or shifting the ether group to the 8’ position of the spiropyran (factor of 2.5) producing a 10 fold increase in total. The effect was also visible in the swelling behavior of the corresponding hydrogel valves, where the ob-served macroscopic changes were reversible and reproducible and in agreement with the molecular kinetics. Gel-valves integrated within microfluidic channels have been fabricated and allow reversible and repeatable operation, with opening of the valve effected in 1 minute, while closing takes around 5.5 minutes.
机译:通过优化螺吡喃光电开关的分子设计和凝胶组成,获得了具有与微流体兼容的增强响应特性的光响应水凝胶阀。利用了自质子化凝胶制剂,其中丙烯酸在水凝胶网络中作为内部质子配给体进行共聚,以在中性pH值下实现水凝胶在水中的溶胀状态。螺吡喃生色团的共聚赋予了水凝胶光响应特性,使用吸电子和供电基团来调节凝胶的溶胀速率。通过将酯转变为6'位置的醚(因子为4)或将醚基转移至螺吡喃的8'位置(因子为2.5),水凝胶的宏观膨胀更快,从而使总量增加了10倍。 。在相应的水凝胶阀的膨胀行为中也可以看到这种效果,其中观察到的宏观变化是可逆的和可再现的,并且与分子动力学一致。集成在微流体通道中的凝胶阀已经制造出来,可逆转且可重复操作,阀门的打开在1分钟内完成,而关闭大约需要5.5分钟。

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