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Fabrication of Microfluidic Reactors and Mixing Studies for Luciferase Detection

机译:微流体反应器的制备和荧光素酶检测的混合研究

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We report the detection of luciferase by implementing a bioluminescent assay in microfluidic reactors. The reactors were fabricated in poly(methyl methacrylate) by hot embossing using a mold master with the reactor layouts made by high-precision micromilling. The overall fabrication process was simple to implement and had a quick turnaround time with low cost. Two reactors, one with smooth channels (called reactor I) and the other with staggered herringbone mixers (called reactor II), were studied for the bioluminescent assay. The assay was implemented by introducing a sample and an assay solution into the reactors and then mixing took place to achieve the enzymatic reactions. We found that the mixing efficiency in reactor II was 17.8 times higher than reactor I. Theoretical analysis of the experimental results indicated II. that the required channel length of mixing was linearly proportional to the flow rate. A calibration curve for luciferase was obtained for both reactors. We found that the detection sensitivity of reactor II was 3 times higher than reactor I. The limit of detection in reactor II was determined to be 0.14 (mu)g/mL luciferase. The device was further exploited to determine the concentration of luciferase samples obtained from in vitro protein expression.
机译:我们报告了通过在微流控反应堆中进行生物发光测定来检测荧光素酶。通过使用模具母版通过热压花在聚(甲基丙烯酸甲酯)中制造反应器,并通过高精度微铣削制造反应器布局。整个制造过程易于实施,并且周转时间短且成本低。研究了两个反应器,一个具有平滑通道(称为反应器I),另一个具有交错的人字形混合器(称为反应器II),用于生物发光测定。通过将样品和测定溶液引入反应器中,然后进行混合以实现酶促反应,来进行测定。我们发现反应器II中的混合效率比反应器I高17.8倍。对实验结果的理论分析表明,该反应器II。所需的混合通道长度与流速成线性比例关系。获得了两个反应器的萤光素酶的校准曲线。我们发现反应器II的检测灵敏度是反应器I的3倍。反应器II的检测极限被确定为0.14μg/ mL荧光素酶。该设备被进一步用来确定从体外蛋白质表达获得的萤光素酶样品的浓度。

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