检出限
鱼精蛋白
阳离子聚合
荧光
肝素
化学
赫普斯
线性范围
缓冲溶液
色谱法
核化学
生物化学
高分子化学
物理
量子力学
作者
Yu Lan,Yue Zhang,Changyao Liu,Ce Wang,Bin Xu,Li Zhao
标识
DOI:10.1016/j.saa.2023.123670
摘要
A highly sensitive detection platform for heparin was constructed via the utilization of a commercially available cationic fluorescent dye (cresyl violet acetate, CV) as a fluorescence probe. The electrostatic binding between CV and heparin quenched the fluorescence in 4-(2-hydroxyethyl)-1-piperazineethanesulfonic (HEPES) buffer solution (10 mM, pH 7.1). CV was highly selective towards heparin over other potential inferring substances. The detection limit of heparin detection was 5.19 ng/mL, and the linear working range was 0 ∼ 1 μg/mL in HEPES solution. In 1 % serum, the detection platform based on the fluorescence “turn-off” behavior of CV was also successfully constructed with a detection limit of 5.86 ng/mL in the linear range of 0 ∼ 0.8 μg/mL. Moreover, the CV-heparin complex was considered a potential sensor platform for the detection of protamine because of its stronger affinity for heparin and protamine.
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