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地瑞那韦的肠道吸收部位依赖性及其与酮康唑的相互作用。

Site dependent intestinal absorption of darunavir and its interaction with ketoconazole.

作者信息

Stappaerts Jef, Annaert Pieter, Augustijns Patrick

机构信息

Laboratory of Drug Delivery and Disposition, KU Leuven, Leuven, Belgium.

Laboratory of Drug Delivery and Disposition, KU Leuven, Leuven, Belgium.

出版信息

Eur J Pharm Sci. 2013 Apr 11;49(1):51-6. doi: 10.1016/j.ejps.2013.01.015. Epub 2013 Feb 7.

Abstract

The expression of P-gp increases from proximal to distal parts of the small intestine, whereas for P450 enzymes the expression is reported to be highest in duodenum and jejunum, decreasing to more distal sites. To evaluate to what extent the regional differences in expression of P-gp and P450 enzymes affect the absorption of a dual substrate, we investigated the transport of darunavir across different small intestinal segments (duodenum, proximal jejunum and ileum). Moreover, the effect of ketoconazole on the intestinal absorption of darunavir was explored, since these drugs are commonly co-administered. Performing the rat in situ intestinal perfusion technique with mesenteric blood sampling, we found no significant differences in the transport of darunavir at the different intestinal segments. The involvement of P-gp in the absorption of darunavir was clearly shown by coperfusion of darunavir with the P-gp inhibitor zosuquidar. In presence of zosuquidar, a 2.2-, 4.2- and 5.7-fold increase in Papp values were measured for duodenum, proximal jejunum and ileum, respectively. Involvement of P450 mediated metabolism in the absorption of darunavir could not be demonstrated in this rat model. Upon studying the drug-drug interaction of darunavir with ketoconazole, data were indicative for an inhibitory effect of ketoconazole on P-gp as the main mechanism for the increased transport of darunavir across the small intestine.

摘要

P-糖蛋白的表达从小肠近端到远端逐渐增加,而对于细胞色素P450酶,据报道其在十二指肠和空肠中的表达最高,在更远端的部位则降低。为了评估P-糖蛋白和细胞色素P450酶表达的区域差异在多大程度上影响双重底物的吸收,我们研究了达芦那韦在不同小肠段(十二指肠、空肠近端和回肠)的转运情况。此外,还探讨了酮康唑对达芦那韦肠道吸收的影响,因为这些药物通常会联合使用。通过采用肠系膜采血的大鼠原位肠灌注技术,我们发现达芦那韦在不同肠段的转运没有显著差异。达芦那韦与P-糖蛋白抑制剂唑尼沙胺共同灌注清楚地表明了P-糖蛋白参与了达芦那韦的吸收。在唑尼沙胺存在的情况下,十二指肠、空肠近端和回肠的表观渗透系数(Papp)值分别增加了2.2倍、4.2倍和5.7倍。在该大鼠模型中未能证明细胞色素P450介导的代谢参与了达芦那韦的吸收。在研究达芦那韦与酮康唑的药物相互作用时,数据表明酮康唑对P-糖蛋白的抑制作用是达芦那韦在小肠中转运增加的主要机制。

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