DEVELOPMENT AND VALIDATION OF A LIQUID CHROMATOGRAPHY – MASS SPECTROMETRY METHOD FOR ESTIMATION OF PRAZIQUANTEL IN HUMAN PLASMA

Purchase PDF

Published: 2015-09-10

Page: 1-9


SRINIVASA REDDY

Norwich Clinical Services Pvt. Ltd., 147/F, 8th Main, 3rd Block, Koramangala, Bangalore– 560034, India

LOKESH RAMANNA

Norwich Clinical Services Pvt. Ltd., 147/F, 8th Main, 3rd Block, Koramangala, Bangalore– 560034, India

JIBIN JOSEPH

Norwich Clinical Services Pvt. Ltd., 147/F, 8th Main, 3rd Block, Koramangala, Bangalore– 560034, India

LICTO THOMAS

Norwich Clinical Services Pvt. Ltd., 147/F, 8th Main, 3rd Block, Koramangala, Bangalore– 560034, India

ARINDAM MUKHOPADHYAY *

Norwich Clinical Services Pvt. Ltd., 147/F, 8th Main, 3rd Block, Koramangala, Bangalore– 560034, India

SARAL THANGAM

Norwich Clinical Services Pvt. Ltd., 147/F, 8th Main, 3rd Block, Koramangala, Bangalore– 560034, India

*Author to whom correspondence should be addressed.


Abstract

Schistosomiasis is one of the most frequently occurring tropical diseases in the world. Praziquantel is the drug of choice worldwide for treatment and control of schistosomiasis. A highly sensitive LC-MS/MS for quantification of praziquantel was developed and validated. Chromatographic separations were achieved using an isocratic binary mobile phase [2 mM ammonium acetate (containing 0.05% formic acid): Acetonitrile: 45:55v/v] at a flow rate of 1.0 mL/min on a C18 column (100 x 4.6 mm i.d) maintained at 50°C and estimated in API 4000 Mass spectrometer in the positive atmospheric pressure ionization mode by following multiple reactions monitoring (MRM) transitions for parent and daughter ions. Deuterated praziquantel was used as an internal standard. A linear calibration plot was achieved for in the concentration ranges of 1.012 ng/ml to 751.552 ng/ml. The mean percentage of recovery was 87.34 with mean % CV of 5.19. It is a fully validated method and can successfully be applied for estimation of praziquantel during biostudies.

 

 

Keywords: Praziquantel, liquid chromatogrphy – mass spectrometry (LC-MS/MS), reverse phase (C18) column, human plasma, schistosomiasis


How to Cite

REDDY, S., RAMANNA, L., JOSEPH, J., THOMAS, L., MUKHOPADHYAY, A., & THANGAM, S. (2015). DEVELOPMENT AND VALIDATION OF A LIQUID CHROMATOGRAPHY – MASS SPECTROMETRY METHOD FOR ESTIMATION OF PRAZIQUANTEL IN HUMAN PLASMA. Journal of International Research in Medical and Pharmaceutical Sciences, 6(1), 1–9. Retrieved from https://ikprress.org/index.php/JIRMEPS/article/view/1506