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Quick and simple LC-MS/MS method for the determination of simvastatin in human plasma: application to pharmacokinetics and bioequivalence studies BJPS
Silva,Suéllen Cristina Rennó; Rezende,Gustavo Rodrigues de; Boralli,Vanessa Bergamin.
A simple, rapid, and sensitive method based on liquid chromatography-tandem mass spectrometry for the quantitative determination of simvastatin in human plasma was developed and validated. After a simple extraction with methyl tert-butyl ether, the analyte and internal standard (lovastatin) were analyzed using reverse-phase liquid chromatography, on a Kinetex C18column (100 × 4.6 mm, 2.6 μm) using acetonitrile: ammonium acetate (2 mM + 0.025 % formic acid) (70: 30, v/v) as a mobile phase in a run time of 3.5 min. Detection was carried out using electrospray positive ionization mass spectrometry in the multiple-reaction monitoring mode. The method was linear over 0.04-40.0 ng/mL concentration range. The mean extraction recovery of simvastatin was 82% (RSD...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Simvastatin/determination; Liquid chromatography/quantitative analysis; Tandem mass spectrometry/quantitative analysis; Human plasma/determination of simvastatin; Simvastatin/bioequivalence; Simvastatin/pharmacokinetics.
Ano: 2014 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502014000300543
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Liquid-liquid extraction combined with high performance liquid chromatography-diode array-ultra-violet for simultaneous determination of antineoplastic drugs in plasma BJPS
Sanson,Ananda Lima; Silva,Suéllen Cristina Rennó; Martins,Matheus Coutinho Gonçalves; Giusti-Paiva,Alexandre; Maia,Patrícia Penido; Martins,Isarita.
A liquid-liquid extraction (LLE) combined with high-performance liquid chromatography-diode array detection method for simultaneous analysis of four chemically and structurally different antineoplastic drugs (cyclophosphamide, doxorubicin, 5-fluorouracil and ifosfamide) was developed. The assay was performed by isocratic elution, with a C18 column (5 µm, 250 x 4.6 mm) and mobile phase constituted by water pH 4.0- acetonitrile-methanol (68:19:13, v/v/v), which allowed satisfactory separation of the compounds of interest. LLE, with ethyl acetate, was used for sample clean-up with recoveries ranging from 60 to 98%. The linear ranges were from 0.5 to 100 µg mL-1, for doxorubicin and 1 to 100 µg mL-1, for the other compounds. The relative standard deviations...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Antineoplastic drugs/simultaneous determination in plasma; Liquid-liquid extraction; High-performance liquid chromatography/diode array detector.
Ano: 2011 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502011000200017
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