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An alternating polarity switching assay for quantification of oxycodone and topiramate: An application of LC-MS/MS method in support to PK/PD study in rodents.

Authors :
Narayanasamy S
Pilli NR
Xu L
Chockalingam A
Shea KI
Stewart S
Patel V
Rouse R
Matta MK
Source :
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences [J Chromatogr B Analyt Technol Biomed Life Sci] 2019 Jun 15; Vol. 1118-1119, pp. 93-100. Date of Electronic Publication: 2019 Apr 22.
Publication Year :
2019

Abstract

In mass spectrometry, compounds that have different ionization properties experience challenges in simultaneous analysis. In the present paper, the authors proposed a polarity switching (+ve and -ve) LC-MS/MS method to analyze oxycodone and topiramate in a single run. The developed method was validated in the range of 5-1000 ng/mL for oxycodone and 20-5000 ng/mL for topiramate as per the US FDA guidelines. The mass spectrometer was operated in multiple reaction monitoring (MRM) mode to analyze oxycodone and topiramate simultaneously using oxycodone-d <subscript>6</subscript> and topiramate-d <subscript>12</subscript> as internal standards, respectively. Sample preparation was performed in 96-well protein precipitation plates using acetonitrile. Processed samples were analyzed using a C <subscript>18</subscript> column with a gradient mobile phase composed of 10 mm ammonium formate with 0.1% formic acid and acetonitrile. The method was validated for selectivity, specificity, linearity, precision and accuracy, dilution integrity and stability. After validation, this method was successfully applied to quantify oxycodone and topiramate in plasma of concomitantly treated Sprague Dawley (SD) rats.<br /> (Published by Elsevier B.V.)

Details

Language :
English
ISSN :
1873-376X
Volume :
1118-1119
Database :
MEDLINE
Journal :
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
Publication Type :
Academic Journal
Accession number :
31030106
Full Text :
https://doi.org/10.1016/j.jchromb.2019.04.044