A novel sensor for determination of naproxen based on change in localized surface plasmon peak of functionalized gold nanoparticles

被引:14
|
作者
Khodaveisi, Javad [1 ]
Shabani, Ali Mohammad Haji [1 ]
Dadfarnia, Shayessteh [1 ]
Saberi, Dariush [2 ]
机构
[1] Yazd Univ, Fac Sci, Dept Chem, Yazd 89195741, Iran
[2] Persian Gulf Univ, Fac Agr & Nat Resources, Fisheries & Aquaculture Dept, Bushehr 75169, Iran
关键词
Localized surface plasmon resonance; Naproxen; Thiolated beta-cyclodextrin; Gold nanoparticles; PERFORMANCE LIQUID-CHROMATOGRAPHY; ROOM-TEMPERATURE PHOSPHORESCENCE; SPECTROFLUOROMETRIC DETERMINATION; PHARMACEUTICAL-PREPARATIONS; BETA-CYCLODEXTRIN; DETECTION SYSTEM; TABLETS; ASSAY; NANOSTRUCTURES; AGGREGATION;
D O I
10.1016/j.saa.2017.02.008
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
A highly selective and sensitive colorimetric sensor for the determination of naproxen (NAP) based on the aggregation of the thiolated beta-cyclodextrin (T beta-CD) functionalized gold nanoparticles (T beta-CD-Au NPs) in the presence of NAP and Zn2+ is described. The hydrophobic end of NAP interacts with the immobilized T beta-CD on the Au NPs and forms the complex of T beta-CD:NAP while the Zn2+ ions form a 1:2 complex of (NAP)(2)Zn with the carboxyl groups of NAP resulting in the aggregation of functionalized gold nanoparticles. As a result of aggregation, the localized surface plasmon resonance (LSPR) band of functionalized gold nanoparticles around 520 nm decreases and a new red shifted band at 650 nm appears which increases gradually as the function of NAP concentration. The calibration graph derived from the intensity ratios of absorbance at 650 nm to 520 nm was linear in the concentration range of 4-180 mu g L-1 of NAP. At the optimum conditions, the limit of detection (LOD) and quantification (LOQ) were found to be 0.6 and 2.1 mu g L-1, respectively and the relative standard deviation at 20 mu g L-1 of NAP (n = 5) was 2.5%. The selectivity and applicability of the method was verified through analyzes of the synthetic samples containing the major interference compounds reported in literature as well as tablets, wastewater and urine samples. The accuracy of the method was evaluated by recovery experiments and analysis of pharmaceutical tablets. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:11 / 16
页数:6
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