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Drug Res (Stuttg) 2014; 64(08): 399-405
DOI: 10.1055/s-0033-1358739
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Bioanalytical LC-MS/MS Method Development and Validation of Novel Antidiabetic Candidate S007-1261 in Rat Plasma and its Application to Pharmacokinetic and Oral Bioavailability Studies

A. Misra
1   Pharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow, India
,
H. N. Kushwaha
1   Pharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow, India
,
N. Gautam
1   Pharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow, India
,
B. Singh
1   Pharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow, India
,
P. C. Verma
2   Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow, India
,
R. Pratap
2   Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow, India
,
S. K. Singh
1   Pharmacokinetics and Metabolism Division, CSIR-Central Drug Research Institute, Lucknow, India
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received 12. September 2013

accepted 24. Oktober 2013

Publikationsdatum:
20. November 2013 (online)

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Abstract

A sensitive and selective LC-MS/MS method has been developed and validated for CDRI antidiabetic candidate S007-1261 in rat plasma using 16-dehydropregnenolone as an internal standard. The API 4000 triple quadrupole LC-MS/MS system was operated under multiple reaction monitoring mode using electrospray ionization technique in positive mode. The sample processing method involves 2-step liquid-liquid extraction using n-hexane as an extracting solvent. The analyte was chromatographed on RP 18, waters column (3.5 µm, 2.1 mm i.d.×30 mm) with guard using acetonitrile and ammonium acetate buffer (pH 5.0, 10 mM) in 90:10 (v/v) composition at a flow rate of 0.40 mL min−1. The chromatographic run time was 5.30 min. Calibration curve shows linearity over concentration range 1.56–200 ng mL−1. The lower limit of detection was 0.39 ng mL−1 and lower limit of quantitation was 1.56 ng mL−1. The inter- and intra-day accuracy and precision were found to be within the assay variability limits as per US FDA guidelines. The absolute recovery of S007-1261 was found to be >90%. S007-1261 does not show any stability problems as it was stable at room temperature for 8 h. S007-1261 was also stable up to 3 freeze-thaw cycles and can be stored up to 30 days at −60°C. The assay was successfully applied to both oral (40 mg kg−1) and intravenous (10 mg kg−1) pharmacokinetic studies in male Sprague-Dawley rats. The oral bioavailability of S007-1261 was found to be 33.61%.

Key words

antidiabetic - LC-MS/MS - S007-1261 - pharmacokinetics - rat plasma
 

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