Orbital - Vol. 10 No. 2 - January-March 2018
FULL PAPERS

Electroanalytical Determination of Fenthion in Passiflora alata Tincture Samples

Rafaela Ferreira França
University Camilo Castelo Branco, São José dos Campos, SP, Brazil
Thays de Souza Lima
Institute of Environmental, Chemical and Pharmaceutical Sciences, Department of Chemistry, DQ-UNIFESP, Diadema-SP, Brazil
Fábio Ruiz Simões
Institute of Environmental, Chemical and Pharmaceutical Sciences, Department of Chemistry, DQ-UNIFESP, Diadema-SP, Brazil
Lucia Codognoto
Institute of Environmental, Chemical and Pharmaceutical Sciences, Department of Chemistry, DQ-UNIFESP, Diadema-SP, Brazil
Published April 1, 2018
Keywords
  • fenthion,
  • boron-doped diamond electrode,
  • square wave voltammetry,
  • medicinal plants
How to Cite
(1)
França, R. F.; Lima, T. de S.; Simões, F. R.; Codognoto, L. Electroanalytical Determination of Fenthion in Passiflora Alata Tincture Samples. Orbital: Electron. J. Chem. 2018, 10, 92-97.

Abstract

In this work a direct, simple, fast and sensitive method to determine Fenthion was developed using a Boron-Doped Diamond Electrode and Square Wave Voltammetry. The method was applied into Passiflora alata herbal medicinal tinctures derivate from passion fruits. None previous treatment such as derivation or pre-concentration of the analyte was done. Cyclic Voltammetry results showed well defined irreversible oxidation peaks at around 1.27 V into the pH range of 2.0 to 8.0. Square Wave Voltammetry was used to analytical determination and the analysis parameters, such as frequency, amplitude and pH from support electrolyte were optimized. A calibration curve was obtained, and it was observed a sensitivity of 0.38 A/mol L-1 and linearity of 0.995. The limits of detection and quantification were 8.0x10-8 mol L-1 (21 mg L-1) and 2.5x10-7 mol L-1 (70 mg L-1), respectively. Recovery studies were applied using Passiflora alata samples fortified with Fenthion in concentrations of 2.5 µmol L-1and 4.0 µmol L-1, followed by the standard addition of the pesticide aliquots. It was observed that the complex matrix does not interferes in the method. The recovery results were about 98.4 and 112.0%, reinforcing that the method is suitable to determine the analyte in target complexes samples, such as Herbal Medicinal Plants.

DOI: http://dx.doi.org/10.17807/orbital.v10i2.1077