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A low temperature bonding of quartz microfluidic chip for serum lipoproteins analysis

机译:石英微流控芯片的低温键合,用于血清脂蛋白分析

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A low-temperature bonding method for microfab-rication of quartz microfluidic chips has been developed. The bonding process involved two steps: pre-bonding and post-annealing at low temperature. The bonding quality was evaluated by measuring the shear force at bonding interface and the electrical properties of the chips. Shear force of 5.66 MPa (566 N/cm~2) was obtained in a bonded chip after a post-annealing at 200℃ for 6 h. We owe the strong bonding strength to the formation of Si—O—Si bonds at the bonding interface during the post-annealing stage. The bonding procedures were not sensitive to surrounding and could be performed in a routine laboratory without clean room conditions. The performance of the fabricated microfluidic chips was tested by capillary zone electrophoresis (CZE) of serum lipoproteins with laser-induced fluorescence (LIF). The low-density (LDL) and high-density (HDL) lipoproteins in the serum was separated completely by using tricine buffer with methylglucamine.
机译:已经开发了用于石英微流体芯片的微制造的低温结合方法。粘合过程包括两个步骤:低温下的预粘合和后退火。通过测量键合界面处的剪切力和芯片的电性能来评估键合质量。在200℃下进行6h的退火后,粘合芯片的剪切力为5.66 MPa(566 N / cm〜2)。我们之所以具有强大的键合强度,是因为在后退火阶段在键合界面处形成了Si-O-Si键。粘接程序对周围环境不敏感,可以在没有洁净室条件下的常规实验室中进行。制备的微流控芯片的性能通过血清脂蛋白的毛细管区带电泳(CZE)和激光诱导荧光(LIF)进行测试。血清中的低密度脂蛋白(LDL)和高密度脂蛋白(HDL)通过使用带有甲基葡糖胺的Tricine缓冲液完全分离。

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