首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Aripiprazole?Montmorillonite: A New Organic–Inorganic Nanohybrid Material for Biomedical Applications
Authors:Yeon‐Ji Oh  Goeun Choi  Prof Young Bin Choy  Dr Je Won Park  Jung Hyun Park  Prof Hwa Jeong Lee  Prof Yeo Joon Yoon  Hee Chul Chang  Prof Jin‐Ho Choy
Institution:1. Center for Intelligent Nano‐Bio Materials (CINBM), Department of Bioinspired Science and Department of Chemistry and Nano Science (Ewha Global Top?5 program), Ewha Womans University, Seoul 120‐750 (Korea), Fax: (+82)?2‐3277‐4340;2. Department of Biomedical Engineering, College of Medicine and Institute of Medical and Biological Engineering, Medical Research Center, Seoul National University, Seoul 110‐799 (Korea);3. Department of Chemistry and Nano Science, Ewha Womans University, Seoul 120‐750 (Korea);4. Division of Life and Pharmaceutical Sciences and College of Pharmacy, Ewha Womans University, Seoul 120‐750 (Korea);5. Global Strategy Center and Pharmaceutical Research Institute, Daewoong Pharmaceutical Co., LTD. 135‐090, Seoul (Korea)
Abstract:Poor aqueous solubility and the unpleasant taste of aripiprazole (APZ) have been recurring problems, owing to its low bioavailability and low patient tolerance, respectively. Herein, we prepared a nanohybrid system that was based on a bentonite clay material, montmorillonite (MMT), which could both mask the taste and enhance the solubility of APZ (i.e., APZ‐MMT). To further improve the efficacy of this taste masking and drug solubility, APZ‐MMT was also coated with a cationic polymer, polyvinylacetal diethylamino acetate (AEA). In vitro dissolution tests at neutral pH showed that the amount of drug that was released from the AEA‐coated APZ‐MMT was greatly suppressed (<1 %) for the first 3 min, thus suggesting that AEA‐coated APZ‐MMT has strong potential for the taste masking of APZ. Notably, in simulated gastric juice at pH 1.2, the total percentage of APZ that was released within the first 2 h increased up to 95 % for AEA‐coated APZ‐MMT. Furthermore, this in vitro release profile was also similar to that of Abilify®, a commercially available medication. In vivo experiments by using Sprague–Dawley rats were also performed to compare the pharmacokinetics of AEA‐coated APZ‐MMT and Abilify®. AEA‐coated APZ‐MMT exhibited about 20 % higher systemic exposure of APZ and its metabolite, dehydro‐APZ, compared with Abilify®. Therefore, a new MMT‐based nanovehicle, which is coated with a cationic polymer, can act as a promising delivery system for both taste masking and for enhancing the bioavailability of APZ.
Keywords:aripiprazole  clays  nanostructures  polymers  taste masking
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号