BSA Capped gold Nanoclusters Modulated by Copper ion for Sensitive and Selective Detection of Histidine in Biological Fluid

被引:9
|
作者
Al-mashriqi, Haitham Saad [1 ,2 ]
Cai, Muzi [1 ]
Qi, Shengda [1 ]
Zhai, Honglin [1 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
[2] Sanaa Univ, Dept Chem, Sanaa, Yemen
关键词
Gold nanocluster; Fluorescence probe; Copper ion; Detection; Histidine; TURN-ON DETECTION; FLUORESCENT-PROBE; AU NANOCLUSTERS; QUANTUM DOTS; METAL-IONS; COMBINATION; ENSEMBLE; CLUSTERS; CYSTEINE; SENSOR;
D O I
10.1007/s10895-022-03112-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This research proposed a sample and environmentally sustainable technique for the synthesis of bovine serum albumin capped gold nanoclusters (BSA-AuNCs) with outstanding fluorescence. The synthesized BSA-AuNCs were investigated using various ways before being combined with Cu2+ to produce a fluorescent switch probe (BSA-AuNCs-Cu2+) for histidine determination. After adding Cu2+, the fluorescence of the BSA-AuNCs was quenched, the fluorescence intensity was enhanced after adding histidine due to good coordination between Cu2+ and histidine. The significant chelation of histidine with Cu2+ demonstrated the viability of developing a selective "switch on " probe for histidine detecting over other amino acids. Unlike existing fluorescent nanomaterial-based approaches for detecting histidine, this study promises good selectivity, high efficiency, and the avoiding of chemical solvents. The designed BSA-AuNCs-Cu2+ fluorescent probe demonstrated an acceptable linear detection range of 0 to 240 mu M under optimum circumstances, with a detection limit of 0.9 mu M. The BSA-AuNCs-Cu2+ system was investigated in rat serum and human urine, with recoveries ranging from 97.2 to 108.2%, demonstrating its potential applicability for histidine detection with favorable results.
引用
收藏
页码:697 / 706
页数:10
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