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具有抗氧化活性的含芹菜素微丸的控释口服给药

Controlled Release Oral Delivery of Apigenin Containing Pellets with Antioxidant Activity.

作者信息

Pápay Zsófia Edit, Kállai-Szabó Nikolett, Balogh Emese, Ludányi Krisztina, Klebovich Imre, Antal István

机构信息

Department of Pharmaceutics of the Semmelweis University, Hogyes Endre Str. 7, 1092 Budapest, Hungary.

出版信息

Curr Drug Deliv. 2017;14(1):145-154. doi: 10.2174/1567201813666160602193047.

Abstract

BACKGROUND

Drug delivery of phytochemicals has gained interest recently due to their remarkable health effects. Apigenin, a plant flavonoid, has antioxidant, anti-inflammatory and anticancer activities but its delivery is challenging. It could be absorbed through the whole intestine, however, it has poor bioavailability due to its low aqueous solubility. In Europe, the daily intake was estimated to be as low as 3 ± 1 mg. Pellets offer several advantages such as improved bioavailability and various resultant drug release profiles can be obtained by simply mixing pellets with different coatings.

OBJECTIVE

The objective of our study was to develop a carrier system containing 20 mg apigenin thus enhancing intake and to offer reduction of oxidative stress which can cause inflammation in the intestine.

METHOD

The apigenin powder was dispersed in aqueous solution of binding material and layered onto the inert cores in a fluidized bed apparatus. The layered cores were further coated with enteric polymers and the process parameters were optimized.

RESULTS

The prepared pellets met with the requirements and have good physical characteristic. 10% (w/w) Eudragit® L was suitable for enteric coating with a complete release at pH 6.8 within 1 hour. 15% (w/w) Eudragit® FS coating ensured acid resistance ability and colonic delivery. The therapeutic efficiency was confirmed with antioxidant activity measurement by using DPPH* assay.

CONCLUSION

Enteric coated spheres allow targeted delivery into the intestine and colon thus reaching the main absorption site. Pellets were proved to be an optimal delivery system for apigenin thus providing enhanced apigenin intake.

摘要

背景

由于植物化学物质具有显著的健康功效,其药物递送近来受到关注。芹菜素是一种植物黄酮类化合物,具有抗氧化、抗炎和抗癌活性,但其递送具有挑战性。它可通过整个肠道吸收,然而,由于其低水溶性,其生物利用度较差。在欧洲,估计每日摄入量低至3±1毫克。微丸具有多种优势,如提高生物利用度,并且通过简单地将微丸与不同包衣混合可获得各种药物释放曲线。

目的

我们研究的目的是开发一种含有20毫克芹菜素的载体系统,从而增加摄入量,并减轻可导致肠道炎症的氧化应激。

方法

将芹菜素粉末分散在粘合剂的水溶液中,并在流化床装置中分层到惰性核上。将分层的核进一步用肠溶聚合物包衣,并优化工艺参数。

结果

制备的微丸符合要求,具有良好的物理特性。10%(w/w)的尤特奇®L适用于肠溶包衣,在pH 6.8时1小时内完全释放。15%(w/w)的尤特奇®FS包衣确保了耐酸性和结肠递送。通过使用DPPH*测定法测量抗氧化活性来确认治疗效果。

结论

肠溶包衣微球可实现靶向递送至肠道和结肠,从而到达主要吸收部位。微丸被证明是芹菜素的最佳递送系统,从而提高了芹菜素摄入量。

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