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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >A novel fluorescence 'turn off - on' nanosensor for sensitivity detection acid phosphatase and inhibitor based on glutathione-functionalized graphene quantum dots
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A novel fluorescence 'turn off - on' nanosensor for sensitivity detection acid phosphatase and inhibitor based on glutathione-functionalized graphene quantum dots

机译:基于谷胱甘肽官能化石墨烯量子点的敏感性检测酸性磷酸酶和抑制剂的一种新型荧光“关闭”纳米传感器

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摘要

In this paper, we developed a label-free and sensitive fluorescence sensor for acid phosphatase (ACP) and its inhibitor parathion-methyl (PM) detection based on glutathione-functionalized graphene quantum dots (GQDs@GSH). Upon addition of MnO2 nanosheets, the fluorescence of GQDs@GSH could be efficiently quenched via a fluorescence resonance energy transfer. ACP could easily catalyze the hydrolysis of L-Ascorbic acid-2-phosphate (AAP) to ascorbic acid (AA), which could reduce MnO2 nanosheets to Mn2+ in acidic environment, leading to dramatically increase of the fluorescence intensity of GQDs@GSH. Quantitative detection of ACP in a broad range from 0.1 to 9 mU mL(-1) with a detection limit of 0.027 mU mL(-1) could be achieved. The feasibility of the proposed sensor in real samples analysis was also studied and satisfactory results were obtained. Furthermore, the fluorescence assay strategy could also be used for the detection of parathion-methyl (PM) as ACP inhibitor.
机译:本文基于谷胱甘肽官能化石墨烯量子点(GQDS @ GSH)开发了一种用于酸性磷酸酶(ACP)的无标记且敏感的荧光传感器及其抑制剂磷酸甲基(PM)检测。 加入MnO2纳米片后,可以通过荧光共振能量转移有效地淬灭GQDS @ GSH的荧光。 ACP可以容易地催化L-抗坏血酸-2-磷酸盐(AAP)的水解,以抗坏血酸(AA),其可以将MNO2纳米片减少到酸性环境中的MN2 +,导致GQDS @ GSH的荧光强度显着增加。 可以实现具有0.027μmL(-1)的0.1至9μmL(-1)的0.1至9μmL(-1)的宽范围的ACP的定量检测。 还研究了实际样品分析中所提出的传感器的可行性,并获得了令人满意的结果。 此外,荧光测定策略也可用于检测甲基甲基(PM)作为ACP抑制剂。

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