BMC Pharmacology and Toxicology
Pharmacokinetic interaction between anlotinib and amlodipine besylate in rats
By Ruijie Xie, Yueling Huang, Zhiling Liu and 2 others.
Abstract
The aim of this study was to evaluate the pharmacokinetic interaction between anlotinib and amlodipine besylate after single and multiple administrations in rats. Sprague-Dawley (SD) rats were randomly divided into three groups: anlotinib group, amlodipine besylate group, and combination (anlotinib + amlodipine besylate) group. The anlotinib group received anlotinib at 6 mg/kg via oral gavage, the amlodipine besylate group received amlodipine besylate at 4 mg/kg via oral gavage, and the combination group received both anlotinib (6 mg/kg) and amlodipine besylate (4 mg/kg) simultaneously via oral gavage. Plasma concentrations of anlotinib and amlodipine were determined using a validated LC-MS/MS method. Mean plasma concentration-time curves were plotted, and pharmacokinetic parameters were calculated using non-compartmental modeling. Compared with the amlodipine group, Cmax and AUC0−t of amlodipine in the combination group increased to 2.34-fold and 2.01-fold, respectively, and CL decreased by 64.4% after single-dose administration (P < 0.05). After multiple-dose administration, AUC0−∞ and t1/2 increased to 3.30-fold and 2.73-fold, respectively, and clearance decreased by 64.9% (P < 0.05). The pharmacokinetic parameters of anlotinib were not significantly changed by co-administration with amlodipine (P > 0.05). Co-administration of anlotinib and amlodipine significantly increased the systemic exposure to amlodipine. Therefore, potential drug–drug interactions should be considered when these drugs are co-administered in clinical practice to ensure safe and rational medication use.



