کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2480345 | 1556182 | 2015 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: High-dose short-term administration of naringin did not alter talinolol pharmacokinetics in humans High-dose short-term administration of naringin did not alter talinolol pharmacokinetics in humans](/preview/png/2480345.png)
Naringin is considered the major causative ingredient of the inhibition of intestinal drug uptake by grapefruit juice. Moreover, it is contained in highly dosed nutraceuticals available on the market. A controlled, open, randomized, crossover study was performed in 10 healthy volunteers to investigate the effect of high-dose naringin on the bioavailability of talinolol, a substrate of intestinal organic anion-transporting polypeptide (OATP)-mediated uptake. Following 6-day supplementation with 3 capsules of 350 mg naringin daily, 100 mg talinolol were administered orally with 3 capsules of the same dietary supplement (1050 mg naringin) on the seventh day. This test treatment was compared to 100 mg talinolol only (control). The results showed that short-term high-dose naringin supplementation did not significantly affect talinolol pharmacokinetics. Geometric mean ratios of test versus control ranged between 0.90 and 0.98 for talinolol cmax, AUC0−48h, AUC0−∞, t1/2 and Ae(0−48h). The high dose may provoke inhibition of the efflux transporter P-glycoprotein (P-gp) which counteracts the uptake inhibition. As disintegration and dissolution processes are required for the solid dosage form, dissolved naringin may arrive at the site of interaction after talinolol is already absorbed. In conclusion, the effect of nutraceuticals on drug pharmacokinetics can deviate from that observed when administered as food component due to the different dose and dosage form.
Mean plasma concentration–time profiles of talinolol (n = 10, arithmetic mean ± standard deviation) following a single oral dose of 100 mg talinolol alone (talinolol only) or with naringin (talinolol + naringin one-week treatment).Figure optionsDownload high-quality image (102 K)Download as PowerPoint slide
Journal: European Journal of Pharmaceutical Sciences - Volume 68, 20 February 2015, Pages 36–42