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使用Enterion胶囊评估依度沙班的区域胃肠道吸收情况。

Evaluation of regional gastrointestinal absorption of edoxaban using the enterion capsule.

作者信息

Parasrampuria Dolly A, Kanamaru Taro, Connor Alyson, Wilding Ian, Ogata Koichiro, Shimoto Yoshimasa, Kunitada Satoshi

机构信息

Daiichi Sankyo Pharma Development, Edison, NJ, USA.

Daiichi Sankyo Co., Ltd., Tokyo, Japan.

出版信息

J Clin Pharmacol. 2015 Nov;55(11):1286-92. doi: 10.1002/jcph.540. Epub 2015 Jun 26.

DOI:10.1002/jcph.540
PMID:25969414
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4755158/
Abstract

Two studies in healthy subjects assessed the absorption of edoxaban when delivered to specific locations within the gastrointestinal tract using Enterion capsules. In study 1 (single-dose, 4-way crossover), 8 participants received edoxaban 60 mg as immediate-release (IR) tablets (treatment A), as powder formulation delivered to the distal small bowel (treatment B) or ascending colon (treatment C), or as an aqueous suspension delivered to the ascending colon (treatment D). In study 2 (single-dose, 2-way crossover), 10 participants received edoxaban 30 mg as IR tablets (treatment E) or in granulate formulation with fumaric acid 50 mg, added to acidify the local gastrointestinal tract and enhance solubility, delivered to the ascending colon (treatment F). Peak and total exposure following targeted drug delivery to the distal gastrointestinal tract were significantly lower than with IR tablet delivery. In study 1, total exposure ratios of treatments B, C, and D compared with A were 14.9%, 7.9%, and 6.1%, respectively. In study 2, relative total exposure was 12.6% for treatment F despite the fumaric acid. Time to peak concentration was longer with higher variability for edoxaban delivered to the distal gastrointestinal tract compared with the IR tablet. These data indicate that edoxaban absorption occurs predominantly in the proximal small intestine.

摘要

两项针对健康受试者的研究评估了使用Enterion胶囊将依度沙班递送至胃肠道特定部位时的吸收情况。在研究1(单剂量、4交叉试验)中,8名参与者接受了60毫克依度沙班的速释(IR)片剂(治疗A)、递送至远端小肠的粉末制剂(治疗B)或升结肠的粉末制剂(治疗C),或递送至升结肠的水悬浮液(治疗D)。在研究2(单剂量、2交叉试验)中,10名参与者接受了30毫克依度沙班的IR片剂(治疗E)或添加了50毫克富马酸以酸化局部胃肠道并提高溶解度的颗粒制剂,递送至升结肠(治疗F)。将药物靶向递送至远端胃肠道后的峰值和总暴露量显著低于IR片剂给药。在研究1中,治疗B、C和D与A相比的总暴露率分别为14.9%、7.9%和6.1%。在研究2中,尽管使用了富马酸,治疗F的相对总暴露量仍为12.6%。与IR片剂相比,递送至远端胃肠道的依度沙班达到峰值浓度的时间更长,变异性更高。这些数据表明依度沙班的吸收主要发生在近端小肠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/4755158/9a561ee032b0/JCPH-55-1286-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/4755158/bd9d14f9c2be/JCPH-55-1286-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/4755158/9a561ee032b0/JCPH-55-1286-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/4755158/bd9d14f9c2be/JCPH-55-1286-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/4755158/9a561ee032b0/JCPH-55-1286-g002.jpg

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