Selective and sensitive colorimetric detection of the neurotransmitter serotonin based on the aggregation of bifunctionalised gold nanoparticles

被引:48
作者
Godoy-Reyes, Tania M. [1 ,2 ,4 ]
Llopis-Lorente, Antoni [1 ,2 ,4 ]
Costero, Ana M. [1 ,2 ,3 ]
Sancenon, Felix [1 ,2 ,4 ]
Gavina, Pablo [1 ,2 ,3 ]
Martinez-Manez, Ramon [1 ,2 ,4 ]
机构
[1] Univ Valencia, Univ Politecn Valencia, Inst Interuniv Invest Reconocimiento Mol & Desarr, Valencia, Spain
[2] CIBER BBN, Madrid, Spain
[3] Univ Valencia, Dept Quim Organ, Doctor Moliner 50, E-46100 Valencia, Spain
[4] Univ Politecn Valencia, Dept Quim, Camino Vera S-N, E-46022 Valencia, Spain
关键词
Serotonin (5-HT); Gold nanoparticles; Colorimetric detection; Aggregation; Neurotransmitters; GLASSY-CARBON ELECTRODE; PERFORMANCE LIQUID-CHROMATOGRAPHY; FLUOROMETRIC DETECTION; CARCINOID-TUMORS; ELECTROCHEMICAL DETECTION; PARKINSONS-DISEASE; RAT-BRAIN; DOPAMINE; CATECHOLAMINES; PLASMA;
D O I
10.1016/j.snb.2017.11.181
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We report a simple, sensitive and selective method for the colorimetric detection of serotonin (5-HT) in aqueous media using bifunctionalized gold nanoparticles (AuNPs). The probe (1) consisted of AuNPs functionalised with dithiobis(succinimidylpropionate) (DSP) and N-acetyl-l-cysteine (NALC). DSP was chosen to react with the amino group of 5-HT, whereas NALC was chosen to bind the hydroxyl group in 5-HT through hydrogen bonding and electrostatic interactions. A double interaction between nanoparticles and the hydroxyl and the amino group of serotonin led to interparticle-crosslinking aggregation. This, resulted in a colour change from red to blue that can be observed by the naked eye. The probe was selective to 5-HT and no colour modulation was observed in the presence of other neurotransmitters (i.e. dopamine, epinephrine, norepinephrine), selected biomolecules (i.e. L-tyrosine, gamma-aminobutyric acid, L-cysteine, uric acid, oxalic acid, aspartic acid and glutamic acid) and common inorganic species. A limit of detection as low as 0.1 mu M was determined in buffered water at pH 7 by UV-vis titrations. Similar response of the probe to 5-HT was observed in simulated blood serum, with a limit of detection of 0.12 mu M, and a linear response within the 0-3 mu M concentration range, which is within the range of the 5-HT concentrations of clinical interest. Finally, the performance of probe (1) in real human blood samples was evaluated, and showed a remarkable ability to distinguish between normal 5-HT levels and 5-HT levels indicative of disease. (c) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:829 / 835
页数:7
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