Selective and sensitive voltammetric determination of folic acid using graphite/restricted access molecularly imprinted poly(methacrylic acid)/SiO2 composite

被引:27
作者
Kuceki, Michele [1 ]
de Oliveira, Fernanda Midori [1 ]
Segatelli, Mariana Gava [1 ]
Lombello Coelho, Malena Karla [2 ]
Pereira, Arnaldo Cesar [2 ]
da Rocha, Luana Rianne [1 ]
Mendonca, Jhessica de Cassia [1 ]
Teixeira Tarley, Cesar Ricardo [1 ,3 ]
机构
[1] Univ Estadual Londrina, Dept Quim, Rodovia Celso Garcia Cid,PR 445,Km 380, BR-86050482 Londrina, PR, Brazil
[2] Univ Fed Sao Joao Rei UFSJ, Dept Ciencias Nat, Campus Dom Bosco,Praca Dom Helvecio 74, BR-36301160 Sao Joao Del Rei, MG, Brazil
[3] Univ Estadual Campinas, UNICAMP, Inst Nacl Ciencia & Tecnol Bioanalit INCTBio, Inst Quim,Dept Quim Analit, Cidade Univ Zeferino Vaz Campus S-N, BR-13083861 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Vitamin B9; RAM-MIP; Voltammetric sensor; Pharmaceutical formulations; ELECTROCHEMICAL DETERMINATION; PERFORMANCE; ELECTRODE; WATER; NANOPARTICLES; TABLETS; SAMPLES;
D O I
10.1016/j.jelechem.2018.04.043
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The present study demonstrates the development of a voltammetric sensor based on graphite/restricted access molecularly imprinted poly(methacrylic acid)/SiO2 composite for folic acid determination in pharmaceutical formulation. The insertion of hybrid molecularly imprinted polymer with restricted access (RAM-MIP) into the graphite paste provided enhance in the cathodic peak current for FA. As the electric conductivity of RAM-MIP is very poor, the optimum content was found to be very low (3%, w/w) in the composite. Under optimized conditions (0.1 mol L-1 Britton-Robinson buffer and pH 4.5) using square wave voltammetry (frequency of 150 Hz, pulse amplitude of 90 mV and potential increment of 7 mV) a limit of detection of 0.72 mu g L-1 (1.63 nmol L-1) and a linear range from 5.0 to 100.0 mu g L-1 (0.01 to 0.23 mu mol L-1) were obtained. The method precision was assessed in terms of inter-day (n = 6) and infra-day precision (two consecutive days), whose relative standard deviations (RSD%) ranged from 3.56 to 5.01%. The developed method was applied for FA determination in pharmaceutical samples whose accuracy was attested by means of addition and recovery assays (97.7-105.0%) as well as by high performance liquid chromatography (HPLC) as a reference technique, thus indicating that RAM-MIP sensor might be successfully applied for quality control in the real samples.
引用
收藏
页码:223 / 230
页数:8
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