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A safer methylation procedure with boron trifluoride-methanol reagent for gas chromatographic analysis of ritalinic acid in urine.
Vu-Duc, T; Vernay, A.
Afiliación
  • Vu-Duc T; Unit of Drug Analysis, Institute of Occupational Health Sciences, Lausanne, Switzerland.
J Pharm Biomed Anal ; 10(2-3): 187-91, 1992.
Article en En | MEDLINE | ID: mdl-1391098
Ritalinic acid (RITA), the major metabolite of methylphenidate (Ritaline) is extracted with a solid-phase C8 column. Following elution, methylation of the carboxylic group is performed with boron trifluoride-methanol as a reagent. The methyl ester of RITA which structurally corresponds to the parent compound methylphenidate is reextracted at pH 9-11. Each step of the analytical method has been systematically studied, particularly the parameters governing the esterification reaction with BF3-methanol. The recovery from the overall method is 96%. The limit of detection is 0.05 micrograms ml-1 with GC-NPD for a 10-ml urine sample. The method has been successfully applied to the detection and quantitation of RITA in urine specimens. The specificity of the methylated RITA peak has been verified by GC-MS in scan mode. Use of diazomethane or sulphuric acid is thus replaced by the use of a less hazardous reagent.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Boranos / Metanol / Metilfenidato Límite: Humans Idioma: En Revista: J Pharm Biomed Anal Año: 1992 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Boranos / Metanol / Metilfenidato Límite: Humans Idioma: En Revista: J Pharm Biomed Anal Año: 1992 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Reino Unido