共 38 条
Aluminum(III) triggered aggregation-induced emission of glutathione-capped copper nanoclusters as a fluorescent probe for creatinine
被引:73
作者:

Jalili, Roghayeh
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机构:
Univ Tabriz, Res Lab Adv Water & Wastewater Treatment Proc, Dept Appl Chem, Fac Chem, Tabriz 5166616471, Iran Univ Tabriz, Res Lab Adv Water & Wastewater Treatment Proc, Dept Appl Chem, Fac Chem, Tabriz 5166616471, Iran

Khataee, Alireza
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h-index: 0
机构:
Univ Tabriz, Res Lab Adv Water & Wastewater Treatment Proc, Dept Appl Chem, Fac Chem, Tabriz 5166616471, Iran
Iran Univ Med Sci, Hlth Promot Res Ctr, Tehran 1449614535, Iran
Near East Univ, Dept Mat Sci & Nanotechnol Engn, Fac Engn, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkey Univ Tabriz, Res Lab Adv Water & Wastewater Treatment Proc, Dept Appl Chem, Fac Chem, Tabriz 5166616471, Iran
机构:
[1] Univ Tabriz, Res Lab Adv Water & Wastewater Treatment Proc, Dept Appl Chem, Fac Chem, Tabriz 5166616471, Iran
[2] Iran Univ Med Sci, Hlth Promot Res Ctr, Tehran 1449614535, Iran
[3] Near East Univ, Dept Mat Sci & Nanotechnol Engn, Fac Engn, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkey
关键词:
Fluorescent nanomaterials;
Fluorometry;
Metal nanoclusters;
Nanosensor;
Nanoprobe;
Paired t-test;
Renal biomarker;
Real sample analysis;
Serum analysis;
MOLECULARLY IMPRINTED POLYMER;
SILVER NANOCLUSTERS;
QUANTUM DOTS;
CARBON DOTS;
SENSOR;
CHEMILUMINESCENCE;
NANOPARTICLES;
SERUM;
ASSAY;
D O I:
10.1007/s00604-018-3111-0
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Glutathione-capped copper nanoclusters (CuNCs) are presented that display aggregation-induced emission (AIE). This feature was exploited for selective and sensitive quantification of creatinine (CRN) which is an important diagnostic parameter. In the presence of Al3+ ions, suchCuNCs rapidly aggregate, and thisinduces enhanced a redemission. The AIE nature of CuNCs was proven via TEM and fluorimetry. On addition of CRN, the coordination between CRN and Al3+ ions led to the quenching of fluorescence due to weakening the AIE. The best fluorescence intensity was measured at excitation/emission peaks of 360/585nm. Quenched fluorescence intensity showed a linear dependence on the concentrations of CRN in the range of 2.5-34 gL(-1) with a detection limit of 0.63 gL(-1). The sensing mechanism of probe for CRN detection is discussed. The probe was applied to thedetermination of CRN in spikedhuman serum samples and gave satisfactory results.
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