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表面活性剂诱导的微流控毛细管电渗流。

Surfactant-induced electroosmotic flow in microfluidic capillaries.

机构信息

Center for Biomedical Engineering, School of Engineering Brown University, Providence, RI, USA.

出版信息

Electrophoresis. 2012 Jul;33(14):2094-101. doi: 10.1002/elps.201100633.

Abstract

Control of EOF in microfluidic devices is essential in applications such as protein/DNA sizing and high-throughput drug screening. With the growing popularity of poly(methyl methacrylate) (PMMA) as the substrate for polymeric-based microfludics, it is important to understand the effect of surfactants on EOF in these devices. In this article, we present an extensive investigation exploring changes in EOF rate induced by SDS, polyoxyethylene lauryl ether (Brij35) and CTAB in PMMA microfluidic capillaries. In a standard protein buffer (Tris-Glycine), PMMA capillaries exhibited a cathodic EOF with measured mobility of 1.54 ± 0.1 (× 10⁻⁴ cm²/V.s). In the presence of surfactant below a critical concentration, EOF was independent of surfactant concentration. At high concentrations of surfactants, the electroosmotic mobility was found to linearly increase/decrease as the logarithm of concentration before reaching a constant value. With SDS, the EOF increased by 257% (compared to buffer), while it was decreased by 238% with CTAB. In the case of Brij35, the electroosmotic mobility was reduced by 70%. In a binary surfactant system of SDS/CTAB and SDS/Brij35, addition of oppositely charged CTAB reduced the SDS-induced EOF more effectively compared to nonionic Brij35. We propose possible mechanisms that explain the observed changes in EOF and zeta potential values. Use of neutral polymer coatings in combination with SDS resulted in 50% reduction in the electroosmotic mobility with 0.1% hydroxypropyl methyl cellulose (HPMC), while including 2% poly (N,N-dimethylacrylamide) (PDMA) had no effect. These results will potentially contribute to the development of PMMA-based microfluidic devices.

摘要

微流控设备中电渗流(EOF)的控制在蛋白质/DNA 大小测定和高通量药物筛选等应用中至关重要。随着聚甲基丙烯酸甲酯(PMMA)作为基于聚合物的微流控基板的日益普及,了解表面活性剂对这些设备中 EOF 的影响非常重要。在本文中,我们广泛研究了 SDS、聚氧乙烯月桂醚(Brij35)和 CTAB 在 PMMA 微流控毛细管中引起的 EOF 速率变化。在标准蛋白质缓冲液(Tris-Glycine)中,PMMA 毛细管表现出阴极 EOF,测得的迁移率为 1.54 ± 0.1(×10⁻⁴ cm²/V.s)。在低于临界浓度的表面活性剂存在下,EOF 与表面活性剂浓度无关。在表面活性剂浓度较高的情况下,电渗流迁移率被发现与浓度的对数呈线性增加/减少,直到达到恒定值。SDS 使 EOF 增加了 257%(与缓冲液相比),而 CTAB 则降低了 238%。Brij35 的情况下,电渗流迁移率降低了 70%。在 SDS/CTAB 和 SDS/Brij35 的二元表面活性剂体系中,添加带相反电荷的 CTAB 比非离子 Brij35 更有效地降低 SDS 诱导的 EOF。我们提出了可能的机制来解释观察到的 EOF 和 ζ 电位值的变化。使用中性聚合物涂层与 SDS 结合,使用 0.1%羟丙基甲基纤维素(HPMC)可使电渗流迁移率降低 50%,而包含 2%聚(N,N-二甲基丙烯酰胺)(PDMA)则没有影响。这些结果将有助于开发基于 PMMA 的微流控设备。

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