Basilea Pharmaceutica International Ltd, Basel, Switzerland.
Clin Exp Dermatol. 2011 Apr;36 Suppl 2:18-23. doi: 10.1111/j.1365-2230.2011.04033.x.
Previous studies have shown that concomitant administration of food may enhance the bioavailability of oral retinoids.
To assess the influence of food on the pharmacokinetics (PK) of alitretinoin after a single oral dose.
This was a single-dose, open-label, randomized, crossover study, which enrolled 30 healthy men, aged 18-44 years. Subjects received sequential doses of alitretinoin 40 mg either after fasting (treatment A) or 5 min after completion of a standard breakfast (treatment B), with the dosing sequence randomized (A/B or B/A). The washout period between the two doses was 1 week. Plasma concentrations over time were plotted and standard PK variables [area under the curve (AUC) of plasma concentration vs. time, maximum plasma concentration (C(max)), time to maximum plasma concentration (t(max)) and elimination half-life (t(1/2)] were determined.
Drug exposure was markedly increased when alitretinoin was taken with food compared with fasting, and there were significant increases in mean C(max) (82.8 vs.25.4 ng/mL, respectively) and AUC (220.2 vs. 55.7 ng · h/mL). The delaying effect of food on t(max) was less marked (median of 3.0 vs. 2.0 h). Administration with food also increased exposure to drug metabolites. Variability in exposure was markedly reduced if alitretinoin was taken with vs. without food (percentage coefficient of variation 40% vs. 74% for AUC; 49% vs. 85% for C(max)). Alitretinoin was generally well tolerated, with typical retinoid adverse reactions, mostly comprising headache.
Intake of alitretinoin with food substantially increased the bioavailability of alitretinoin, but variability in exposure was reduced. Consequently, oral alitretinoin should be taken with food as outlined in the manufacturer's summary of product characteristics.
先前的研究表明,同时进食可能会提高口服类视黄醇的生物利用度。
评估食物对单次口服阿利维 A 酸后药代动力学(PK)的影响。
这是一项单剂量、开放标签、随机、交叉研究,共纳入 30 名年龄在 18-44 岁之间的健康男性。受试者先后接受单剂量阿利维 A 酸 40mg 口服,一次空腹(A 组),一次进食标准早餐 5 分钟后(B 组),两种剂量顺序随机(A/B 或 B/A)。两种剂量之间的洗脱期为 1 周。绘制时间-血浆浓度曲线,计算标准药代动力学变量[血浆浓度-时间曲线下面积(AUC)、最大血浆浓度(C(max))、达峰时间(t(max))和半衰期(t(1/2))]。
与空腹相比,阿利维 A 酸与食物同服时药物暴露量显著增加,C(max)和 AUC 均值分别显著增加(分别为 82.8 和 220.2ng/ml,82.8 和 220.2ng/ml;分别为 25.4 和 55.7ng·h/ml,25.4 和 55.7ng·h/ml)。食物对 t(max)的延迟作用不明显(中位数分别为 3.0 和 2.0 小时)。如果与食物同服,药物代谢物的暴露量也会增加。如果与食物同服,阿利维 A 酸的暴露量变异性明显降低(AUC 的变异系数分别为 40%和 74%;C(max)的变异系数分别为 49%和 85%)。阿利维 A 酸一般耐受性良好,有典型的类视黄醇不良反应,主要包括头痛。
食物摄入可显著增加阿利维 A 酸的生物利用度,但暴露量的变异性降低。因此,应按照制造商的产品特性摘要说明,随餐服用阿利维 A 酸。