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Enzymatic Strategies to Construct L-Lactate Biosensors Based on Polysulfone/Carbon Nanotubes Membranes

机译:基于聚砜/碳纳米管膜的L-乳酸生物传感器的酶促策略

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摘要

We present different strategies to construct amperometric L-lactate biosensors using the enzymes lactate dehydrogenase (LDH) and lactate oxidase (LOx). These biomolecules are incorporated into a polysulfone/carbon nanotubes composite matrix by means of an easy and rapid technique, i.e. inversion phase, and deposited onto carbon screen-printed electrodes. The use of redox mediators, Meldola's Blue and cobalt(II) phthalocyanine (CoPc) are necessary to reduce the working potential for the detection of NADH and H _2O _2 products. The working conditions for both biosensors have been optimized such as the pH, amount of immobilized enzyme and lifetime stability. LDH biosensor presents a linear interval range from 10 ~(-6) to 2×10 ~(-5)M L-lactate and a 3.7×10 ~(-7)M as limit of detection (LOD), and from 5×10 ~(-6) to 5×10 ~(-4)M and 3.4×10 ~(-6)M, in case of LOx, respectively.
机译:我们提出了使用乳酸脱氢酶(LDH)和乳酸氧化酶(LOx)来构建安培型L-乳酸生物传感器的不同策略。通过简单和快速的技术,即转化相,将这些生物分子掺入聚砜/碳纳米管复合基质中,并沉积到碳丝网印刷电极上。为了减少检测NADH和H _2O _2产品的工作潜力,必须使用氧化还原介体,Meldola蓝和钴(II)酞菁(CoPc)。两种生物传感器的工作条件均已优化,例如pH,固定化酶的量和使用寿命稳定性。 LDH生物传感器的线性间隔范围为10〜(-6)至2×10〜(-5)M L-乳酸盐和3.7×10〜(-7)M作为检测限(LOD),从5×在LOx的情况下,分别为10〜(-6)至5×10〜(-4)M和3.4×10〜(-6)M。

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