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A Simple Microfluidic Chip Design for Fundamental Bioseparation

机译:用于基本生物分离的简单微流控芯片设计

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A microchip pressure-driven liquid chromatographic system with a packed column has been designed and fabricated by using poly(dimethylsiloxane) (PDMS). The liquid chromatographic column was packed with mesoporous silica beads of Ia3d space group. Separation of dyes and biopolymers was carried out to verify the performance of the chip. A mixture of dyes (fluorescein and rhodamine B) and a biopolymer mixture (10 kDa Dextran and 66 kDa BSA) were separated and the fluorescence technique was employed to detect the movement of the molecules. Fluorescein molecule was a nonretained species and rhodamine B was attached onto silica surface when dye mixture in deionized water was injected into the microchannel. The retention times for dextran molecule and BSA molecule in biopolymer separation experiment were 45 s and 120 s, respectively. Retention factor was estimated to be 3.3 for dextran and 10.4 for BSA. The selectivity was 3.2 and resolution was 10.7. Good separation of dyes and biopolymers was achieved and the chip design was verified.
机译:通过使用聚(二甲基硅氧烷)(PDMS)设计和制造了带有填充柱的微芯片压力驱动液相色谱系统。液相色谱柱中装有Ia3d空间群的中孔二氧化硅微珠。进行染料和生物聚合物的分离以验证芯片的性能。分离染料(荧光素和若丹明B)的混合物和生物聚合物混合物(10 kDa葡聚糖和66 kDa BSA),并使用荧光技术检测分子的运动。当将去离子水中的染料混合物注入微通道时,荧光素分子是非保留物种,若丹明B附着在二氧化硅表面。生物聚合物分离实验中葡聚糖分子和BSA分子的保留时间分别为45 s和120 s。葡聚糖的保留因子估计为3.3,BSA的保留因子为10.4。选择性为3.2,分离度为10.7。实现了染料和生物聚合物的良好分离,并验证了芯片设计。

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