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Characterization and Optimization of Isotachophoresis Parameters for Pacific Blue Succinimidyl Ester Dye on a PDMS Microfluidic Chip

机译:PDMS微流体芯片上太平洋蓝琥珀酰亚胺酯染料同位集参数的表征与优化

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摘要

Isotachophoresis (ITP) for Pacific Blue (PB) dye using a polydimethylsiloxane (PDMS) microfluidic chip is developed and characterized by determining the types and concentrations of electrolytes, the ITP duration, and the electric field density. Among candidate buffers for the trailing electrolyte (TE) and leading electrolyte (LE), 40 mM borate buffer (pH 9) and 200 mM trisaminomethane hydrochloride (Tris-HCl) (pH 8) were selected to obtain the maximum preconcentration and resolution of the PB bands, respectively. With the selected TE and LE buffers, further optimization was performed to determine the electric field (EF) density and the ITP duration. These ITP parameters showed a 20–170,000 preconcentration ratio from initial PB concentrations of 10 nM–100 fM. Further demonstration was implemented to preconcentrate PB-conjugated lactate dehydrogenase (LDH) using the PDMS microfluidic chip. By utilizing the quenching nature of PB-LDH conjugation, we were able to identify concentrations of LDH as low as 10 ng/mL. This simple PDMS microfluidic chip-based ITP for PB preconcentration enables highly sensitive biological and chemical analyses by coupling with various downstream detection systems.
机译:使用聚二甲基硅氧烷(PDMS)微流体芯片的太平洋蓝色(PB)染料的同位孔(ITP)通过确定电解质的类型和浓度,ITP持续时间和电场密度来开发和表征。选择尾离电解质(TE)和前电解质(LE)的候选缓冲液中,选择40mM硼酸盐缓冲液(pH9)和200mM三氨基甲烷盐酸盐(Tris-HCl)(pH8)以获得最大的前浓缩和分辨率PB带分别。利用所选择的TE和Le缓冲器,进行了进一步的优化以确定电场(EF)密度和ITP持续时间。这些ITP参数显示了来自10nm-100 fm的初始PB浓度的20-170,000个前浓度。使用PDMS微流体芯片实施进一步证明以预先培育PB缀合的乳酸脱氢酶(LDH)。通过利用PB-LDH缀合的猝灭性质,我们能够将LDH的浓度识别为低至10ng / ml。这种简单的PDMS微流体芯片的ITP用于PB预浓度,通过与各种下游检测系统耦合来实现高度敏感的生物和化学分析。

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