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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.)

Coupling DLLME-CE for the Stereoselective Analysis of Venlafaxine and Its Main Metabolites after Biotransformation by Fungi

Texto completo
Autor(es):
Bortoleto, Marcela A. [1] ; Bocato, Mariana Z. [2] ; Pupo, Monica T. [2] ; Gaitani, Cristiane M. [2] ; Oliveira, Anderson R. M. [1]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Fac Filosofia Ciencias & Letras Ribeirao Preto, Dept Quim, BR-14040901 Ribeirao Preto, SP - Brazil
[2] Univ Sao Paulo, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 Ribeirao Preto, SP - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Journal of the Brazilian Chemical Society; v. 26, n. 9, p. 1956-1966, SEP 2015.
Citações Web of Science: 3
Resumo

Fungal biotransformations have become very important in the study of chiral drugs because the reactions performed by these microorganisms may be enantioselective. However, analyses of analytes present in liquid culture medium have proved to be very difficult due to the complexity of this matrix. The aim of this work was to couple dispersive liquid-liquid microextraction (DLLME) with capillary electrophoresis to evaluate the biotransformation of the antidepressant drug venlafaxine (Vx) into its chiral metabolites, N-desmethylvenlafaxine (NDV) and O-desmethylvenlafaxine (ODV) by fungi. The chiral separation was carried out in 50 mmol L-1 sodium phosphate buffer pH 2.0 containing 8 mmol L-1 alpha-cyclodextrin and 1.0% (m/v) carboxymethyl-beta-cyclodextrin. The temperature of the capillary was set at 20 degrees C. A voltage of + 20 kV was applied during analysis. The DLLME was accomplished using 300 mu L of isopropanol (disperser solvent) and 200 mu L of chloroform (extraction solvent). The method was completely validated and showed to be linear over the concentration range of 75-938 ng mL(-1) for ODV and NDV enantiomers and of 500-15000 ng mL(-1) for venlafaxine enantiomers with a correlation coefficient higher than 0.99. The selectivity of the method was evaluated and no interference peaks were detected in the migration time of the analytes. The limit of quantification was 75 ng mL(-1) for metabolite enantiomers and 500 ng mL(-1) for venlafaxine enantiomers. The study showed a stereoselective biotransformation of venlafaxine into (+)-(S)-N-desmethylvenlafaxine by the fungus Cunninghamella elegans ATCC 10028B with an enantiomeric excess of 100%. (AU)

Processo FAPESP: 13/17658-9 - Desenvolvimento e validação de métodos cromatográficos e eletroforéticos para posterior aplicação em estudos de biotransformação e metabolismo in vitro - fase 2
Beneficiário:Anderson Rodrigo Moraes de Oliveira
Linha de fomento: Auxílio à Pesquisa - Regular
Processo FAPESP: 11/17508-1 - Desenvolvimento e validação de métodos cromatográficos e eletroforéticos para posterior aplicação em estudos de biotransformação e metabolismo in vitro
Beneficiário:Anderson Rodrigo Moraes de Oliveira
Linha de fomento: Auxílio à Pesquisa - Regular