A sensitive and selective high performance liquid chromatographic (HPLC) method was developed and validated for the rapid quantification of rivastigmine (CAS 123441-03-2) in micro quantity in rat plasma samples. The chromatographic separation was achieved with a reverse phase monomeric column C 18 (4.6 x 250 mm, 5 μm) and the mobile phase consisted of acetonitrile and 20 mmol/L phosphate buffer pH 3.0 (25:75) with a flow rate of 1 mL/min. The effluents were measured by fluorimetric detection with excitation and emission wavelengths at 220 nm and 293 nm, respectively. The calibration curve was linear (r 2 >0.99) ranging from 25-3000 ng/mL and the lower limit of quantification was 25 ng/mL. The method was validated with excellent sensitivity, selectivity, accuracy, precision, recovery and stability. The method has been successfully applied in a pharmacokinetic study of rivastigmine in rats. © ECV Editio Cantor Verlag.
|Number of pages||6|
|Publication status||Published - 2008|
Karthik, A., Subramanian, G. S., Surulivelrajan, M., Ranjithkumar, A., & Kamat, S. B. (2008). Fluorimetric determination of rivastigmine in rat plasma by a reverse phase - High performance liquid chromatographic method: Application to a pharmacokinetic study. Arzneimittel-Forschung/Drug Research, 58(5), 205-210. https://www.scopus.com/inward/record.uri?eid=2-s2.0-44849134863&partnerID=40&md5=8492d87239ba7d8129e712091efe2871