Effects of one-time apple juice ingestion on the pharmacokinetics of fexofenadine enantiomers
pmid: 24903351
Effects of one-time apple juice ingestion on the pharmacokinetics of fexofenadine enantiomers
We examined the effect of a single apple juice intake on the pharmacokinetics of fexofenadine enantiomers in healthy Japanese subjects.In a randomized two phase, open-label crossover study, 14 subjects received 60 mg of racemic fexofenadine simultaneously with water or apple juice. For the uptake studies, oocytes expressing organic anion-transporting polypeptide 2B1 (OATP2B1) were incubated with 100 μM (R)- and (S)-fexofenadine in the presence or absence of 10 % apple juice.One-time ingestion of apple juice significantly decreased the area under the plasma concentration-time curve (AUC0-24) for (R)- and (S)-fexofenadine by 49 and 59 %, respectively, and prolonged the time to reach the maximum plasma concentration (t max) of both enantiomers (P < 0.001). Although apple juice greatly reduced the amount of (R)- and (S)-fexofenadine excretion into urine (Ae0-24) by 54 and 58 %, respectively, the renal clearances of both enantiomers were unchanged between the control and apple juice phases. For in vitro uptake studies, the uptake of both fexofenadine enantiomers into OATP2B1 complementary RNA (cRNA)-injected oocytes was significantly higher than that into water-injected oocytes, and this effect was greater for (R)-fexofenadine. In addition, apple juice significantly decreased the uptake of both enantiomers into OATP2B1 cRNA-injected oocytes.These results suggest that OATP2B1 plays an important role in the stereoselective pharmacokinetics of fexofenadine and that one-time apple juice ingestion probably inhibits intestinal OATP2B1-mediated transport of both enantiomers. In addition, this study demonstrates that the OATP2B1 inhibition effect does not require repeated ingestion or a large volume of apple juice.
- Kyushu University Japan
- University of Tokyo Japan
- University of the Ryukyus Japan
- Kanazawa University Japan
- Akita University Japan
Adult, Male, Histamine H1 Antagonists, Non-Sedating, Cross-Over Studies, Organic Anion Transporters, Stereoisomerism, RNA, Complementary, Beverages, Eating, Food-Drug Interactions, Intestinal Absorption, Area Under Curve, Fruit, Malus, Anti-Allergic Agents, Oocytes, Animals, Humans, Female, Terfenadine
Adult, Male, Histamine H1 Antagonists, Non-Sedating, Cross-Over Studies, Organic Anion Transporters, Stereoisomerism, RNA, Complementary, Beverages, Eating, Food-Drug Interactions, Intestinal Absorption, Area Under Curve, Fruit, Malus, Anti-Allergic Agents, Oocytes, Animals, Humans, Female, Terfenadine
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