Specific detection of cysteine and homocysteine in biological fluids by tuning the pH values of fluorosurfactant-stabilized gold colloidal solution

被引:75
作者
Xiao, Qunyan [1 ]
Shang, Fei [1 ]
Xu, Xuechen [1 ]
Li, Qianqian [1 ]
Lu, Chao [1 ]
Lin, Jin-Ming [2 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorosurfactant; Gold nanoparticles; Cysteine; Homocysteine; Biosensors; PERFORMANCE LIQUID-CHROMATOGRAPHY; SELECTIVE DETECTION; CAPILLARY-ELECTROPHORESIS; NANOPARTICLES; PLASMA; DERIVATIZATION; AMINOTHIOLS; GLUTATHIONE; MERCURY(II); SAMPLES;
D O I
10.1016/j.bios.2011.09.013
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This study describes the use of 14 nm nonionic fluorosurfactant-capped gold nanoparticles (FSN-capped AuNPs) for the simultaneous detection of cysteine (Cys) and homocysteine (Hcy) using colorimetric method, requiring no use of separation techniques. It was found that the kinetics of Cys/Hcy-induced aggregation of the 14 nm FSN-capped AuNPs strongly depends on the pH value of gold colloidal solution. At a pH of 6.5, the Cys-induced aggregation kinetics of the FSN-capped AuNPs was almost identical to that induced by Hcy, facilitating simultaneous detection of total Cys and Hcy up to a concentration as low as 0.15 mu M; while at pH 12.0, the kinetics of Cys-induced aggregation was much faster than that inducted by Hcy, leading to selective detection of Cys at concentration as low as 1.0 mu M in the presence of Hcy. The applicability of the method was validated by spiking known amount of Cys and Hcy in human urine and plasma samples, obtaining a recovery of 95.4-105.5%. The present approach is simple, high selective and provides high reproducibility, and has a great potentiality in disease diagnosis. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:211 / 215
页数:5
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