B. Ramesha, N. Manjulaa, S.R. Bijargib, V.U.M. Sarmaa, P. Sita Devia. Comparison of conventional and supported liquid extraction methods for the determination of sitagliptin and simvastatin in rat plasma by LC-ESI-MS/MS[J]. Journal of Pharmaceutical Analysis, 2015, (3): 161-168.
Citation:
B. Ramesha, N. Manjulaa, S.R. Bijargib, V.U.M. Sarmaa, P. Sita Devia. Comparison of conventional and supported liquid extraction methods for the determination of sitagliptin and simvastatin in rat plasma by LC-ESI-MS/MS[J]. Journal of Pharmaceutical Analysis, 2015, (3): 161-168.
B. Ramesha, N. Manjulaa, S.R. Bijargib, V.U.M. Sarmaa, P. Sita Devia. Comparison of conventional and supported liquid extraction methods for the determination of sitagliptin and simvastatin in rat plasma by LC-ESI-MS/MS[J]. Journal of Pharmaceutical Analysis, 2015, (3): 161-168.
Citation:
B. Ramesha, N. Manjulaa, S.R. Bijargib, V.U.M. Sarmaa, P. Sita Devia. Comparison of conventional and supported liquid extraction methods for the determination of sitagliptin and simvastatin in rat plasma by LC-ESI-MS/MS[J]. Journal of Pharmaceutical Analysis, 2015, (3): 161-168.
aNatural Products Chemistry Division, Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500607, India bMedicinal Chemistry & Pharmacology Division, Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500607, India
Three extraction methods were compared for their efficiency to analyze sitagliptin and simvastatin in rat plasma by LC–MS/MS, including (1) liquid–liquid extraction (LLE), (2) solid phase extraction (SPE) and (3) supported liquid extraction (SLE). Comparison of recoveries of analytes with different extraction methods revealed that SLE was the best extraction method. The detection was facilitated with ion trap-mass spectrometer by multiple reactions monitoring (MRM) in a positive ion mode with ESI. The transitions monitored were m/z 441.1→325.2 for simvastatin, 408.2→235.1 for sitagliptin and 278.1→260.1 for the IS. The lower limit of quantification (LLOQ) was 0.2 ng/mL for sitagliptin and 0.1 ng/mL for simvastatin. The effective SLE offers enhanced chromatographic selectivity, thus facilitating the potential utility of the method for routine analysis of biological samples along with pharmacokinetic studies.