John P M, Minatoya H, Rosenberg F J
J Pharm Sci. 1979 Apr;68(4):475-81. doi: 10.1002/jps.2600680422.
Spheronized cores produced by extrusion and marumerization were microencapsulated with ethylcellulose by organic phase separation to produce beads exhibiting controlled-release characteristics. In vitro dissolution studies indicated that the drug was released as a first-order model and that the release rates were proportional to the amount of film on the bead. The bronchodilator activity in the anesthetized dog and the heart rate effect in the unanesthetized trained dog were evaluated. Microencapsulated beads were prepared which produced controlled release as assayed by bronchodilation. The heart rate increases induced by the controlled-release formulations were gradual in onset, and the total increase in heart rate over a 6-hr period was less than that associated with the plain drug powder.
通过挤出和滚圆造粒法制备的球形颗粒芯材,采用有机相分离法用乙基纤维素进行微囊化,以制备具有控释特性的微丸。体外溶出度研究表明,药物以一级模型释放,且释放速率与微丸上的包衣量成正比。对麻醉犬的支气管扩张活性和未麻醉的训练犬的心率影响进行了评估。制备了经支气管扩张测定具有控释作用的微囊化微丸。控释制剂引起的心率增加起效缓慢,在6小时内的心率总增加量低于与普通药粉相关的增加量。