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应用磁共振成像和动态胃肠道系统评估食物依赖的速释福沙那韦片剂的崩解情况。

Food-dependent disintegration of immediate release fosamprenavir tablets: in vitro evaluation using magnetic resonance imaging and a dynamic gastrointestinal system.

机构信息

Laboratory for Pharmacotechnology and Biopharmacy, Katholieke Universiteit Leuven, Leuven, Belgium.

出版信息

Eur J Pharm Biopharm. 2011 Feb;77(2):313-9. doi: 10.1016/j.ejpb.2010.10.009. Epub 2010 Nov 3.

Abstract

In the present study, we demonstrated the value of two advanced tools, the TNO gastric and small Intestinal Model (TIM-1) and magnetic resonance imaging (MRI), for the in vitro evaluation of food-dependent disintegration of immediate release fosamprenavir tablets. Upon introduction of a tablet with the nutritional drink Scandishake Mix® in the stomach compartment of TIM-1, simulating the fed state, disintegration and fosamprenavir dissolution were significantly postponed compared to the fasted state (lag time 80 ± 23 min). This resulted in a lag in the appearance of bioaccessible fosamprenavir (<5% during the first 2h), even though the nutritional state did not significantly alter the cumulative bioaccessibility after 5h. These results were in agreement with the previously observed postprandial delay in gastric fosamprenavir tablet disintegration and subsequent amprenavir absorption in healthy volunteers. Therefore, TIM-1 can be used in tablet development to identify food-induced disintegration issues causing unexpected clinical behavior. From a mechanistic perspective, we applied MRI to illustrate impaired water ingress in fosamprenavir tablets immersed in the nutritional drink compared to simulated gastric fluid. This effect may be attributed to both competition between nutritional components and the tablet for the available water (indicated by reduced rotational and translational diffusion) as well as the possible formation of a food-dependent precipitation layer on the HPMC-coated tablet.

摘要

在本研究中,我们展示了两种先进工具的价值,即 TNO 胃和小肠模型(TIM-1)和磁共振成像(MRI),用于体外评估食物依赖性即刻释放福沙那韦片剂的崩解。在 TIM-1 的胃腔部分引入含有营养饮料 Scandishake Mix®的片剂,模拟进食状态,与空腹状态相比,崩解和福沙那韦溶解明显延迟(滞后时间 80±23 分钟)。这导致生物可利用的福沙那韦出现时间延迟(在最初 2 小时内<5%),尽管营养状态在 5 小时后并没有显著改变累积生物可利用度。这些结果与之前在健康志愿者中观察到的餐后胃福沙那韦片剂崩解延迟以及随后的氨普那韦吸收相一致。因此,TIM-1 可用于片剂开发,以识别导致意外临床行为的食物诱导崩解问题。从机制角度来看,我们应用 MRI 来阐明在营养饮料中浸泡的福沙那韦片剂中水分进入的受损情况,与模拟胃液相比。这种效应可能归因于营养成分和片剂对可用水的竞争(由旋转和平移扩散减少表明)以及 HPMC 涂层片剂上可能形成的食物依赖性沉淀层。

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