Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, China.
Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, China.
Anal Chim Acta. 2018 Oct 22;1028:45-49. doi: 10.1016/j.aca.2018.04.038. Epub 2018 May 4.
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.
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。