Royal North Shore Hospital, Sydney, Australia
Melbourne University, Melbourne, Australia.
Antimicrob Agents Chemother. 2018 Nov 26;62(12). doi: 10.1128/AAC.01723-18. Print 2018 Dec.
To address the limited bioavailability and intolerance of the conventional itraconazole (ITZ) formulations, a new formulation labeled per iovailability (SUBA) itraconazole has been developed; however, the specific effects of food and gastric pH are unknown. This study evaluated the pharmacokinetic profile of SUBA itraconazole under fasting and fed conditions, as well as with the concomitant administration of a proton pump inhibitor. First, the effect of food was assessed in an open-label, randomized, crossover bioavailability study of 65-mg SUBA itraconazole capsules (2 65-mg capsules twice a day) in healthy adults ( = 20) under fasting and fed conditions to steady-state levels. Second, an open-label, two-treatment, fixed-sequence comparative bioavailability study in healthy adults ( = 28) under fasted conditions compared the pharmacokinetics of a single oral dose of SUBA itraconazole capsules (2 65-mg capsules/day) with and without coadministration of daily omeprazole delayed-release capsules (1 40-mg capsule/day) under steady-state conditions. In the fed and fasted states, SUBA itraconazole demonstrated similar concentrations at the end of the dosing interval, with modestly lower total and peak ITZ exposure being shown when it was administered under fed conditions than when it was administered in the fasted state, with fed state/fasted state ratios of 78.09% (90% confidence interval [CI], 74.49 to 81.86%) for the area under the concentration-time curve over the dosing interval (14,183.2 versus 18,479.8 ng · h/ml), 73.05% (90% CI, 69.01 to 77.33%) for the maximum concentration at steady state (1,519.1 versus 2,085.2 ng/ml), and 91.53% (90% CI, 86.41 to 96.96%) for the trough concentration (1,071.5 versus 1,218.5 ng/ml) being found. When dosed concomitantly with omeprazole, there was a 22% increase in the total plasma exposure of ITZ, as measured by the area under the concentration-time curve from time zero to infinity (P0.0069), and a 31% increase in the peak plasma exposure of ITZ, as measured by the maximum concentration (P0.0083).
为了解决传统伊曲康唑(ITZ)制剂生物利用度有限和不耐受的问题,开发了一种新的标记为生物利用度的伊曲康唑制剂(SUBA);然而,食物和胃内 pH 值的具体影响尚不清楚。本研究评估了空腹和进食条件下 SUBA 伊曲康唑的药代动力学特征,以及同时给予质子泵抑制剂的情况。首先,在健康成年人(n=20)中进行了一项开放标签、随机、交叉生物利用度研究,评估了 65 毫克 SUBA 伊曲康唑胶囊(每天两次服用 2 个 65 毫克胶囊)在空腹和进食条件下达到稳态水平时的药代动力学。其次,在健康成年人(n=28)中进行了一项开放标签、两治疗、固定序列比较生物利用度研究,比较了在空腹条件下单独口服 SUBA 伊曲康唑胶囊(每天 2 个 65 毫克胶囊)与同时给予每日奥美拉唑延迟释放胶囊(每天 1 个 40 毫克胶囊)的药代动力学,在稳态条件下。在进食和空腹状态下,SUBA 伊曲康唑在给药间隔结束时表现出相似的浓度,与空腹状态相比,进食状态下总暴露和峰暴露适度降低,进食状态/空腹状态比值分别为 78.09%(90%置信区间 [CI],74.49 至 81.86%)的浓度-时间曲线下面积(14,183.2 与 18,479.8 ng·h/ml)、73.05%(90%CI,69.01 至 77.33%)的稳态最大浓度(1,519.1 与 2,085.2 ng/ml)和 91.53%(90%CI,86.41 至 96.96%)的谷浓度(1,071.5 与 1,218.5 ng/ml)。当与奥美拉唑同时给药时,伊曲康唑的总血浆暴露量增加了 22%,这是通过浓度-时间曲线下从零时到无穷大的面积(P0.0069)来衡量的,伊曲康唑的峰血浆暴露量增加了 31%,这是通过最大浓度(P0.0083)来衡量的。