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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Analysis of oxybutynin and N-desethyloxybutynin in human urine by dispersive liquid-liquid microextraction (DLLME) and capillary electrophoresis (CE)

Texto completo
Autor(es):
Moreira, B. J. [1] ; Borges, K. B. [2] ; de Oliveira, A. R. M. [3] ; de Gaitani, C. M. [1]
Número total de Autores: 4
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Dept Ciencias Farmaceut, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 Ribeirao Preto, SP - Brazil
[2] Univ Fed Sao Joao Del Rei, Dept Ciencias Nat, BR-36301160 Sao Joao Del Rei, MG - Brazil
[3] Univ Sao Paulo, Dept Quim, Fac Filosofia Ciencias & Letras Ribeirao Preto, BR-14040901 Ribeirao Preto, SP - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: ANALYTICAL METHODS; v. 7, n. 20, p. 8763-8770, 2015.
Citações Web of Science: 5
Resumo

A dispersive liquid-liquid microextraction (DLLME) procedure combined with capthary electrophoresis/diode array detection (CE/DAD) was developed and applied to the determination of oxybutynin (OXY) and N-desethyloxybutynin (DEO) in human urine. The electrophoretic analyses were performed using a 50 mu m i.d. fused silica uncoated capthary with an effective length of 36.5 cm and a 50 mmol L-1 solution of triethylamine, pH 3.0, as the background electrolyte. The temperature was set at 30 degrees C and a constant voltage of +30 kV was applied. Some experimental parameters that affect DLLME's extraction efficiency, such as the type and volume of the extraction and disperser solvents, extraction time and pH, were studied and optimized. The optimal DLLME conditions were found using the following method: 2.5% (w/v) NaCl was added to 5.0 mL of urine, the pH was adjusted to 11.0 and 140 mu L of carbon tetrachloride as the extraction solvent and 260 mu L of acetonitrile as the disperser solvent were quickly added. The performance criteria for linearity, sensitivity, precision, accuracy, recovery and stability have been assessed and they were within the Guidance for Industry: Bioanalytical Method Validation. The mean extraction recoveries for OXY and DEO were 71.4% (SD 6.4%) and 60.9% (SD 8.5%), respectively. The method showed linearity over the concentration range of 90-300 ng mL(-1) and 187.5-750 ng mL(-1), with correlation coefficients of 0.990 and 0.998 for OXY and DEO, respectively. Intra-day and inter-day precision and accuracy assays for these analytes were studied at three concentration levels and were lower than 15%. (AU)

Processo FAPESP: 10/17632-1 - Aplicações da eletroforese capilar nas áreas clínica, terapêutica e biotecnológica
Beneficiário:Cristiane Masetto de Gaitani
Linha de fomento: Auxílio à Pesquisa - Regular