Altered pharmacokinetics of paclitaxel by the concomitant use of morin in rats

The purpose of this study was to investigate the effect of morin on the pharmacokinetics of orally and intravenously administered paclitaxel in rats. Pharmacokinetic parameters of paclitaxel were determined in rats after an oral (30 mg kg−1) or intravenous (3 mg kg−1) administration of paclitaxel to rats in the presence and absence of morin (3.3 and 10 mg kg−1). Compared to the control given paclitaxel alone, pretreatment with morin 30 min prior to the oral administration of paclitaxel increased Cmax and AUC of paclitaxel by 70–90% and 30–70%, respectively, while there was no significant change in Tmax and terminal plasma half-life (T1/2) of paclitaxel. Consequently, absolute and relative bioavailability values of paclitaxel in the rats after the pretreatment with morin were significantly higher (p < 0.05) than those from the control. In contrast, following an intravenous administration of paclitaxel (3.3 mg kg−1), the pharmacokinetic profiles of paclitaxel were not altered significantly in the presence of morin. Those results suggest that the enhanced oral exposure of paclitaxel should be mainly due to the inhibition effect of morin on the gastrointestinal extraction of paclitaxel during the intestinal absorption. Therefore, the concurrent use of morin or morin-containing dietary supplement may provide a therapeutic benefit in the oral delivery of paclitaxel.