涂层
乙基纤维素
造粒
色谱法
羟丙基纤维素
材料科学
聚合物
生物利用度
流化床
剂型
甲基纤维素
化学
纤维素
化学工程
复合材料
药理学
有机化学
医学
工程类
作者
Pham-Thi-Phuong Dung,Thanh-Dat Trinh,Quoc-Hoai Nguyen,Huu-Manh Nguyen,Ngoc-Chien Nguyen,Nguyen‐Phuong‐Dung Tran,Cao-Son Tran,Nguyen Thi Hong Ngọc,Nguyen-Thach Tung
标识
DOI:10.1080/02652048.2023.2209639
摘要
This research aims to develop bitter taste-masking microcapsules containing azithromycin (AZI) by a simpler and familiar method, fluid-bed coating technology, in comparison with Zithromax®. Cores of microcapsules, AZI microparticles, were prepared by fluid-bed granulation, then taste-masking polymer was covered on by fluid-bed coating technique. Eudragit L100, Eudragit RL100, and ethyl cellulose in single and combined with Eudragit L100 and Eudragit E100 were used as taste-masking polymers. The obtained microcapsules were characterised by taste-masking ability, in vitro release, SEM, coating thickness, and coating efficiency. Combination of ethyl cellulose and Eudragit E100 (3:1) in coating thickness of 45.13 ± 2.12% w/w prevents AZI release from microcapsules below bitter taste threshold (1.78 ± 1.17 µg/ml). Bioavailability of powders containing AZI microcapsules and pH modulators (50 mg Na3PO4 and 35 mg Mg(OH)2) was not significantly different from the reference product (Zithromax®, Pfizer, New York, NY) in the rabbit model (p > 0.05). These results support the possibility of developing a generic product containing AZI.
科研通智能强力驱动
Strongly Powered by AbleSci AI