4.7 Article

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

期刊

JOURNAL OF ELECTROANALYTICAL CHEMISTRY
卷 818, 期 -, 页码 223-230

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2018.04.043

关键词

Vitamin B9; RAM-MIP; Voltammetric sensor; Pharmaceutical formulations

资金

  1. Coordenacao de Aperfeicoamento de Nivel Superior (CAPES) [Pro-Forenses 3353/2014, 23038.007082/2014-03]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [481669/2013-2, 305552/2013-9, 472670/2012-3]
  3. Fundacao Araucaria do Parana [163/2014]
  4. SETI do Parana
  5. Instituto Nacional de Ciencia e Tecnologia de Bioanalitica (INCT) (FAPESP) [2014/50867-3]
  6. Instituto Nacional de Ciencia e Tecnologia de Bioanalitica (INCT) (CNPq) [465389/2014-7]
  7. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [14/50867-3] Funding Source: FAPESP

向作者/读者索取更多资源

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.

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