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Online restricted-access material combined with high-performance liquid chromatography and tandem mass spectrometry for the simultaneous determination of vanillin and its vanillic acid metabolite in human plasma.
Li, De-Qiang; Zhang, Zhi-Qing; Yang, Xiu-Ling; Zhou, Chun-Hua; Qi, Jin-Long.
Afiliação
  • Li DQ; Department of Pharmacy, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
  • Zhang ZQ; Department of Pharmacy, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
  • Yang XL; Department of Pharmacy, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
  • Zhou CH; Department of Pharmacy, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China. zhouchunhua80@126.com, 13383662009@163.com.
  • Qi JL; Department of Pharmacology, Hebei Medical University, Shijiazhuang, Hebei, China.
J Sep Sci ; 39(17): 3318-26, 2016 Sep.
Article em En | MEDLINE | ID: mdl-27384745
ABSTRACT
An automated online solid-phase extraction with restricted-access material combined with high-performance liquid chromatography and tandem mass spectrometry was developed and validated for the simultaneous quantification of vanillin and its vanillic acid metabolite in human plasma. After protein precipitation by methanol, which contained the internal standards, the supernatant of plasma samples was injected to the system, the endogenous large molecules were flushed out, and target analytes were trapped and enriched on the adsorbent, resulting in a minimization of sample complexity and ion suppression effects. Calibration curves were linear over the concentrations of 5-1000 ng/mL for vanillin and 10-5000 ng/mL for vanillic acid with a coefficient of determination >0.999 for the determined compounds. The lower limits of quantification of vanillin and vanillic acid were 5.0 and 10.0 ng/mL, respectively. The intra- and inter-run precisions expressed as the relative standard deviation were 2.6-8.6 and 3.2-10.2%, respectively, and the accuracies expressed as the relative error were in the range of -6.1 to 7.3%. Extraction recoveries of analytes were between 89.5 and 97.4%. There was no notable matrix effect for any analyte concentration. The developed method was proved to be sensitive, repeatable, and accurate for the quantification of vanillin and its vanillic acid metabolite in human plasma.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasma / Automação / Ácido Vanílico / Benzaldeídos / Cromatografia Líquida de Alta Pressão / Espectrometria de Massas em Tandem Tipo de estudo: Evaluation_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasma / Automação / Ácido Vanílico / Benzaldeídos / Cromatografia Líquida de Alta Pressão / Espectrometria de Massas em Tandem Tipo de estudo: Evaluation_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article