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自微乳化药物递送系统(SMEDDS)对决奈达隆肠道吸收的食物效应降低

Reduced Food-Effect on Intestinal Absorption of Dronedarone by Self-microemulsifying Drug Delivery System (SMEDDS).

作者信息

Han Sang Duk, Jung Sang Won, Jang Sun Woo, Son Miwon, Kim Byoung Moon, Kang Myung Joo

机构信息

Dong-A Pharmaceutical Co., Ltd.

出版信息

Biol Pharm Bull. 2015;38(7):1026-32. doi: 10.1248/bpb.b15-00110.

Abstract

The oral absorption of dronedarone (DRN), a benzofuran derivative with anti-arrhythmic activity, is significantly affected by food intake. The absolute bioavailability of the marketed product (Multaq, Sanofi, U.S.) was about 4% without food, but increased to 15% when administered with a high fat meal. Therefore, to reduce the food-effect on the intestinal absorption of DRN, a novel self-microemulsifying drug delivery system (SMEDDS) was formulated and the comparative in vivo absorption studies with the marketed product were carried out using male beagle dogs either in the fasted or fed state. The SMEDDS consisted of the drug, Labrafil M 1944CS, and Kolliphor EL in a weight ratio of 1 : 1 : 2, rapidly formed a fine oil-in-water emulsion with a droplet size less than 50 nm. An in vivo absorption study revealed that the area-under-curve (AUC0-24 h) and maximal plasma concentration (Cmax) were 10.4-fold (p<0.05) and 8.6-fold (p<0.05) higher, respectively, after the marketed product was orally administered to beagles in the fed state when compared to those in the fasted state. This food-effect were remarkably alleviated by SMEDDS formulation, with AUC0-24 h and Cmax 2.9-fold (p<0.05) and 2.6-fold (p<0.05) higher in the fed state when compared to the fasted state, by facilitating intestinal absorption of DRN in the fasted state. The results of this study suggest that SMEDDS may decrease the differences in oral absorption of DRN between the prandial states, improving therapeutic efficacy as well as patient compliance.

摘要

决奈达隆(DRN)是一种具有抗心律失常活性的苯并呋喃衍生物,其口服吸收受食物摄入的显著影响。市售产品(Multaq,赛诺菲,美国)在空腹时的绝对生物利用度约为4%,但与高脂餐同服时则增至15%。因此,为减少食物对DRN肠道吸收的影响,研发了一种新型自微乳化药物递送系统(SMEDDS),并使用雄性比格犬在禁食或进食状态下进行了与市售产品的体内吸收对比研究。该SMEDDS由药物、Labrafil M 1944CS和聚氧乙烯蓖麻油EL按重量比1∶1∶2组成,能迅速形成粒径小于50nm的精细水包油乳液。一项体内吸收研究显示,与禁食状态相比,市售产品在进食状态下口服给予比格犬后,曲线下面积(AUC0 - 24h)和最大血浆浓度(Cmax)分别高出10.4倍(p<0.05)和8.6倍(p<0.05)。通过促进DRN在禁食状态下的肠道吸收,SMEDDS制剂显著减轻了这种食物效应,进食状态下的AUC0 - 24h和Cmax与禁食状态相比分别高出2.9倍(p<0.05)和2.6倍(p<0.05)。本研究结果表明,SMEDDS可能会减少DRN在不同用餐状态下口服吸收的差异,提高治疗效果以及患者的依从性。

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