Sm2O3 nanorod-modified graphite paste electrode for trace level voltammetric determination of acetaminophen and ciprofloxacin

被引:31
作者
Biswas, Sudip [1 ]
Naskar, Hemanta [2 ]
Pradhan, Susmita [3 ]
Chen, Yuling [1 ]
Wang, Yang [1 ]
Bandyopadhyay, Rajib [2 ,4 ]
Pramanik, Panchanan [5 ]
机构
[1] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
[2] Jadavpur Univ, Dept Instrumentat & Elect Engn, Salt Lake Campus, Kolkata 700098, India
[3] Jadavpur Univ, Dept Instrumentat Sci, Kolkata 700032, India
[4] ITMO Univ, Lab Artificial Sensory Syst, St Petersburg, Russia
[5] GLA Univ, Dept Chem & Nanosci, Mathura 281406, India
基金
中国国家自然科学基金;
关键词
ELECTROCATALYTIC OXIDATION; COMPOSITE FILM; ASCORBIC-ACID; METAL-OXIDE; CARBON; PARACETAMOL; GRAPHENE; NANOCOMPOSITE; TRANSPORT; SAFETY;
D O I
10.1039/c9nj04446a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Samarium oxide (Sm2O3) nanorods were synthesized through a sol-gel method in the presence of poly(ethylene glycol) as a structure-directing subagent. The transformation of the crystalline phase, crystallinity, bonding configurations, and morphology with calcination temperature was investigated by using powder X-ray diffraction, FESEM, XPS, and TEM. Furthermore, various spectroscopic analyses were done using FTIR, UV-Vis, and photoluminescence. A composite of Sm2O3 nanorods and graphite was used to prepare an electrochemical sensor for the detection of two different drug molecules in a binary mixture, namely acetaminophen (AC) and ciprofloxacin (CP). The effects of the crystalline phase on the electrocatalytic activity were analyzed. The modified electrode showed high sensitivity (93 mu A mu M-1 cm(-2) for AC and 6.5 mu A mu M-1 cm(-2) for CP) towards the drug molecules during the voltammetric determination. An optimized composition (3 : 7 Sm2O3 : graphite) of the modified electrode showed the best analytical performance. The strongest differential pulse voltammetric oxidation peaks for AC and CP were at around 533 +/- 3 mV and 976 +/- 043 mV, respectively. Anodic oxidation peaks were well-separated for effective analysis within a mixture. The sensor response was linear within the concentration range of 0.001-0.01-300 mu M and 0.05-1-170 mu M for AC and CP, respectively. The detection limits were 0.1 nM for AC and 5 nM for CP (S/N 3). The Sm2O3-9-3/GP electrode showed excellent analytical performance when analyzing spiked urine and pharmaceutical samples.
引用
收藏
页码:1921 / 1930
页数:10
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