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首页> 外文期刊>RSC Advances >Fluorescence sensing of tyrosinase activity based on amine rich carbon dots through direct interaction in a homogeneous system: detection mechanism and application
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Fluorescence sensing of tyrosinase activity based on amine rich carbon dots through direct interaction in a homogeneous system: detection mechanism and application

机译:基于均匀系统直接相互作用的基于胺碳点的酪氨酸酶活性的荧光检测:检测机制及应用

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摘要

As a vital, copper-containing oxidase, tyrosinase (TYR) is useful as a biomarker for the screening of skin diseases. In this paper, a convenient and sensitive homogeneous fluorescence detection platform for the assay of TYR activity without any modified steps is described. Inspired by the fact that carbon dots (CDs) with excellent properties can be obtained through some surface modification, amine rich carbon dots (N-CDs) using a nitrogen doping process were developed as the fluorescent probe for this assay. The effect and the response mechanism of the degree of nitrogen doping in relation to the response of different CDs to the sensing of TYR activity using dopamine (DA) as a substrate were investigated. The DA was oxidized to o-dopaquinone with the catalyzation of TYR and quenched the fluorescence of the N-CDs by direct interaction. By using a set concentration of DA and other optimized reaction conditions, the fluorescence intensity of the N-CDs was directly applied to monitor the TYR activity. This assay for TYR activity showed a broad linear range from 0.05 to 6.0 U mL(-1) with a detection limit of 0.039 U mL(-1). The satisfactory recovery of the sensor for TYR activity in diluted human serum illustrated a potential clinical application.
机译:作为一种重要的含铜氧化酶,酪氨酸酶(Tyr)可用作筛查皮肤病的生物标志物。在本文中,描述了一种方便敏感的均匀荧光检测平台,用于无需任何修改的步骤的Tyr活性的测定。通过通过一些表面改性可以获得具有优异性能的碳点(CDS),使用氮掺杂工艺的胺碳点(N-CD)作为该测定的荧光探针而产生。研究了氮气掺杂程度与用多巴胺(DA)作为基材的不同CDS对Tyr活性的响应的影响和响应机理。通过直接相互作用催化Tyr并淬灭N-Cds的荧光,将DA氧化成O-多醌。通过使用DA和其他优化反应条件的设定浓度,直接施用N-CD的荧光强度以监测Tyr活性。 Tyr活性的该测定显示出的宽线性范围为0.05至6.0 U mL(-1),检测限为0.039uml(-1)。稀释的人血清中Tyr活性的传感器的令人满意的恢复说明了潜在的临床应用。

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  • 来源
    《RSC Advances》 |2019年第35期|共6页
  • 作者单位

    Fujian Med Univ Union Hosp Dept Gastr Surg Fuzhou 350001 Fujian Peoples R China;

    Fujian Med Univ Sch Pharm Higher Educ Key Lab Nano Biomed Technol Fujian Pr Dept Pharmaceut Anal Fuzhou 350122 Fujian Peoples R China;

    476 Hosp PLA Fuzhou 350002 Fujian Peoples R China;

    Fujian Med Univ Sch Pharm Higher Educ Key Lab Nano Biomed Technol Fujian Pr Dept Pharmaceut Anal Fuzhou 350122 Fujian Peoples R China;

    Fujian Med Univ Sch Pharm Higher Educ Key Lab Nano Biomed Technol Fujian Pr Dept Pharmaceut Anal Fuzhou 350122 Fujian Peoples R China;

    Fujian Med Univ Sch Pharm Higher Educ Key Lab Nano Biomed Technol Fujian Pr Dept Pharmaceut Anal Fuzhou 350122 Fujian Peoples R China;

    Fujian Med Univ Sch Pharm Higher Educ Key Lab Nano Biomed Technol Fujian Pr Dept Pharmaceut Anal Fuzhou 350122 Fujian Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学;
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