首页> 外文期刊>Journal of Molecular Liquids >Mobilized lipase enzymatic biosensor for the determination of Chlorfenvinphos and Malathion in contaminated water samples: A voltammetric study
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Mobilized lipase enzymatic biosensor for the determination of Chlorfenvinphos and Malathion in contaminated water samples: A voltammetric study

机译:动员的脂肪酶酶生物传感器测定污染水样中的氯芬芬磷和马拉硫磷

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摘要

Concentration levels of organophosphorus pesticides like Chlorfenvinphos and Malathion were determined by lipase enzyme inhibition method. The developed enzymatic method was purely based on in situ generation of p-Nitrophenol by enzymatic hydrolysis of p-Nitrophenyl Acetate. The production of this in situ generated p-Nitrophenol concentration was depending on the effective hydrolysis of p-Nitrophenyl Acetate by the lipase enzyme. This electrochemically active p-Nitrophenol gave an anodic oxidation peak at a potential of+0.024 V versus SCE. The various parameters such as effective hydrolysis of substrate, substrate concentration and effect of pH were studied for lipase enzyme. A linear calibration for the Chlorfenvinphos and Malathion was obtained in the concentration ranges of 100-900 μM and 100-900 mM respectively with a correlation coefficient of 0.9894 and 0.9680 under the optimized conditions by following the incubation time of 25 min. The electrochemical experiments were performed in 0.1Mphosphate buffer solution (pH 7.0) at roomtemperature. The limit of detection and limit of quantification values were found to be 84.45 μM, 253.03 mM and 281.5 μM, 843.1 mM respectively for Chlorfenvinphos and Malathion under optimized conditions. The developed liquid state lipase enzyme sensor could be applied for the analysis of water samples contaminated with pesticides. The developed method gives the information about the intensity of toxicity of pesticides.
机译:通过脂肪酶抑制法测定了氯磷磷和马拉硫磷等有机磷农药的浓度。发达的酶促方法完全基于对硝基苯乙酸乙酸酯的酶促水解原位生成对硝基苯酚。原位产生的对硝基苯酚浓度的产生取决于脂肪酶对乙酸对硝基苯酯的有效水解。该电化学活性的对硝基苯酚在相对于SCE的电势为+0.024 V时给出了一个阳极氧化峰。研究了脂肪酶的各种参数,如底物的有效水解,底物浓度和pH值的影响。遵循25分钟的孵育时间,在最佳条件下,分别在100-900μM和100-900 mM的浓度范围内获得了对氯芬芬磷和马拉硫磷的线性校准,相关系数为0.9894和0.9680。在室温下在0.1M磷酸盐缓冲溶液(pH 7.0)中进行电化学实验。在优化条件下,氯芬芬磷和马拉硫磷的检出限和定量值分别为84.45μM,253.03 mM和281.5μM,843.1 mM。研制的液态脂肪酶传感器可用于分析农药污染的水样。所开发的方法可提供有关农药毒性强度的信息。

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