Validation of HPLC-UV methods for quantitatively determining landiolol and its major metabolite in human blood

Abstract

Landiolol is an ultra-short-acting β1-adrenergic receptor blocking agent that is used for both perioperative and postoperative patients with tachycardia during general anesthesia. Validated HPLC-UV methods that quantitatively determine landiolol and its major metabolite (M-1) in human blood were reported for clinical research of landiolol. These analytes were recovered from the same blood sample using a multi-step extraction process and determined with two different HPLC conditions. These methods were validated over concentration ranges of 0.05 to 10 μg/ml for landiolol and 0.1 to 20 μg/ml for M-1 and were found to have acceptable accuracy, precision, linearity, and selectivity. These methods are useful to the characterize of blood pharmacokinetics of landiolol and M-1 for clinical research. © 2009 Pharmaceutical Society of Japan.