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A novel surface modification technique for forming porous polymer monoliths in poly(dimethylsiloxane)

机译:在聚二甲基硅氧烷中形成多孔聚合物整料的新型表面改性技术

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摘要

A new method of surface modification is described for enabling the in situ formation of homogenous porous polymer monoliths (PPMs) within poly(dimethylsiloxane) (PDMS) microfluidic channels that uses 365 nm UV illumination for polymerization. Porous polymer monolith formation in PDMS can be challenging because PDMS readily absorbs the monomers and solvents, changing the final monolith morphology, and because PDMS absorbs oxygen, which inhibits free-radical polymerization. The new approach is based on sequentially absorbing a non-hydrogen-abstracting photoinitiator and the monomers methyl methacrylate and ethylene diacrylate within the walls of the microchannel, and then polymerizing the surface treatment polymer within the PDMS, entangled with it but not covalently bound. Four different monolith compositions were tested, all of which yielded monoliths that were securely anchored and could withstand pressures exceeding the bonding strength of PDMS (40 psi) without dislodging. One was a recipe that was optimized to give a larger average pore size, required for low back pressure. This monolith was used to concentrate and subsequently mechanical lyse B lymphocytes.
机译:描述了一种新的表面改性方法,该方法能够在使用365 nm紫外线照射进行聚合的聚二甲基硅氧烷(PDMS)微流体通道内原位形成均质的多孔聚合物整料(PPM)。 PDMS中多孔聚合物整料的形成可能具有挑战性,因为PDMS容易吸收单体和溶剂,从而改变了最终的整料形态,并且因为PDMS吸收了氧,从而抑制了自由基聚合。新方法是基于在微通道壁内顺序吸收非吸氢光引发剂和甲基丙烯酸甲酯和二丙烯酸乙二酯单体,然后在PDMS中聚合表面处理聚合物,使之纠缠但未共价键合。测试了四种不同的整体结构,所有这些整体结构都牢固固定并可以承受超过PDMS粘结强度(40 psi)的压力而不会脱落。一种是经过优化的配方,可提供较低的背压所需的更大的平均孔径。使用该整体物浓缩并随后机械裂解B淋巴细胞。

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