Wall coating for microchip capillary electrophoresis
Wall coating for microchip capillary electrophoresis
批准号:
6992241
负责人:
Vladislav Dolnik
金额:
$16.97万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-01 至 2006-08-31
中文摘要
描述(由申请人提供):本提案旨在开发用于由聚甲基丙烯酸甲酯(PMMA)和/或聚碳酸酯(PC)制成的塑料微芯片的亲水性、水解稳定的壁涂层。在过去十年的分析化学中,分析操作的微型化及其在微芯片上的集成已成为一个热门话题。毛细管电泳(CE)经常被置于这些努力的最前沿。然而,通道尺寸的小型化强调了通道表面的化学性质的影响。因此,表面固有存在的负电荷导致分析物吸附在通道壁上,并且还导致由这些功能驱动的电渗流,并损害高分辨率CE分离。到目前为止,只有少数涂层应用于玻璃和塑料微芯片。该项目将开发一种用于PMMA和/或PC制成的塑料微芯片的水解稳定的亲水性壁涂层。所提出的涂层将不携带任何电荷,因此将消除电渗流,并使分析物在通道壁上的吸附最小化。作为顶层,它将包含天然多糖刺槐豆胶或瓜尔胶,或通过热固定连接的合成聚合物聚(丙烯酰二乙醇胺)。我们将通过测量其电渗迁移率JIEEO(< 0.5 * 10-9 m2 V-1 s-1)和用NaOH溶液处理后的稳定性来表征该涂层。我们将通过模型蛋白的等电聚焦和M13 mp 18 DNA测序片段的CE来证明这种包被的实用性。
英文摘要
DESCRIPTION (provided by applicant): This proposal aims at the development of hydrophilic, hydrolytically stable wall coatings for plastic microchips made from poly (methyl methacrylate) (PMMA) and/or polycarbonate (PC). In analytical chemistry of the last decade, miniaturization of analytical operations and their integration on a microchip has become a hot topic. Capillary electrophoresis (CE) has been involved at the forefront of these efforts frequently. However, the miniaturization of the channel size emphasizes the influence of chemical properties of the channel surface. Therefore a negative charge that is inherently present at the surface results in adsorption of analytes on the channel wall and also in electroosmotic flow that is driven by these functionalities and compromises high-resolution CE separations. So far only a few coatings have been applied to glass and plastic microchips. This project will develop a hydrolytically stable, hydrophilic wall coating for plastic microchips made from PMMA and/or PC. The proposed coating will not carry any charge and will thus eliminate electroosmotic flow and minimize adsorption of analytes on the channel wall. As the top layer it will contain either natural polysaccharides locust bean gum or guaran, or a synthetic polymer poly (acryloyl diethanolamine) attached by thermal immobilization. We will characterize this coating by measuring its electroosmotic mobility JIEEO (< 0.5 * 10-9 m2V-1s-1) and stability after a treatment with NaOH solutions. We will demonstrate the utility of this coating by isoelectric focusing of model proteins and by CE of M13mp18 DMA sequencing fragments.
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