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一种基于氮掺杂石墨烯量子点的新型无标记荧光传感器,用于高灵敏度检测博莱霉素。

A novel label-free fluorescent sensor for highly sensitive detection of bleomycin based on nitrogen-doped graphene quantum dots.

机构信息

Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, China.

Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, China.

出版信息

Anal Chim Acta. 2018 Oct 22;1028:45-49. doi: 10.1016/j.aca.2018.04.038. Epub 2018 May 4.

Abstract

In this work, we presented a novel label-free biosensor for rapid detection of bleomycinsulphate (BLM). The biosensor was based on the fluorescent "turn off-on" of nitrogen-doped graphene quantum dots (N-GQDs), which was prepared in a green way from citric acid and ammonia. The richness of carboxyl groups on the N-GQDs enabled strong adsorption of ssDNA to the surface of N-GQDs through π-π stacking interactions, resulting in the effective fluorescence quenching of N-GQDs system. The ssDNA underwent an irreversible cleavage event via the oxidative effect of BLM with Fe(II) as a cofactor, thus a turn-on fluorescence signal was observed. Thereby, the concentration of BLM can be quantitatively determined in a broad range from 0.34 nmol/L to 1300 nmol/L with a detection limit of 0.34 nmol/L. The presented method was applied to the determination of BLM in human serum samples with satisfactory results.

摘要

在这项工作中,我们提出了一种新颖的无标记生物传感器,用于快速检测博莱霉素硫酸盐(BLM)。该生物传感器基于氮掺杂石墨烯量子点(N-GQDs)的荧光“关闭-开启”,其通过柠檬酸和氨以绿色方式制备。N-GQDs 上丰富的羧基基团通过π-π 堆积相互作用使 ssDNA 强烈吸附到 N-GQDs 的表面,从而有效猝灭 N-GQDs 体系的荧光。ssDNA 通过 BLM 与 Fe(II)作为共因子的氧化作用经历不可逆的切割事件,因此观察到开启的荧光信号。因此,可以在从 0.34 nmol/L 到 1300 nmol/L 的宽浓度范围内定量测定 BLM,检测限为 0.34 nmol/L。该方法已应用于人血清样品中 BLM 的测定,结果令人满意。

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