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Polydimethyl siloxane microfluidic channel protein functionalization techniques

机译:聚二甲基硅氧烷微流体通道蛋白功能化技术

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The most commonly used polymer in microfluidic device fabrication is polydimethylsiloxane (PDMS). Many applications require the functionalization of the surface of PDMS with proteins (e.g. antibodies) which prompted the evaluation of a variety of techniques that have been developed to bind proteins to the surface. such as non-specific binding, protein passive adsorption and activation with Glutaraldehyde cross-linking, or with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride) (EDC) cross linkers. It has been shown that using EDC crosslinker after APTES activation results in more than double the protein bonding strength to the PDMS surface than the bonding strength that results from passiveon-specific adsorption. The contribution of PDMS curing conditions on protein adsorption to its surface was also studied, and showed that increased curing time is the factor that reduces passive adsorption the most. Finally, we have shown that reaction time between the protein and surface has a direct relationship with bond strength and that initial protein concentration in solution was only an effective factor when the protein was at low concentrations.
机译:微流体装置制造中最常用的聚合物是聚二甲基硅氧烷(PDMS)。许多应用都需要用蛋白质(例如抗体)对PDMS表面进行功能化,这促使人们评估已开发出的各种使蛋白质与表面结合的技术。例如非特异性结合,通过戊二醛交联或通过1-乙基-3-(3-二甲基氨基丙基)碳二亚胺盐酸盐(EDC)交联剂进行的蛋白质被动吸附和活化。已经表明,在APTES活化后使用EDC交联剂会导致与PDMS表面的蛋白质结合强度比被动/非特异性吸附所产生的结合强度高一倍以上。还研究了PDMS固化条件对其表面蛋白质吸附的影响,结果表明固化时间的增加是最大程度降低被动吸附的因素。最后,我们证明了蛋白质与表面之间的反应时间与键合强度有直接关系,溶液中蛋白质的初始浓度仅在蛋白质处于低浓度时才是有效因素。

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