Mechanical Engineering Department, University of Maryland, College Park, Maryland 20742, USA.
Biomicrofluidics. 2012 Mar;6(1):16506-1650610. doi: 10.1063/1.3693589. Epub 2012 Mar 9.
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.
描述了一种新的表面改性方法,用于在聚二甲基硅氧烷(PDMS)微流道内原位形成均匀的多孔聚合物整体(PPM),该方法使用 365nmUV 光引发聚合。在 PDMS 中形成多孔聚合物整体具有挑战性,因为 PDMS 容易吸收单体和溶剂,从而改变最终的整体形态,并且 PDMS 吸收氧气,从而抑制自由基聚合。新方法基于顺序吸收非氢提取光引发剂和单体甲基丙烯酸甲酯和二乙烯基丙烯酸乙酯在微通道的壁内,然后聚合表面处理聚合物在 PDMS 中,与它缠结但不共价结合。测试了四种不同的整体组成,所有这些组成都产生了牢固固定的整体,并且能够承受超过 PDMS 结合强度(40psi)的压力而不会脱落。一种是优化配方以获得更大的平均孔径,以降低背压。该整体用于浓缩,随后通过机械裂解 B 淋巴细胞。