酮咯酸氨丁三醇
材料科学
生物利用度
超声
药品
药物输送
色谱法
酮咯酸
纳米技术
药理学
化学
医学
止痛药
作者
Pankaj Jadhav,Adhikrao Vyankatrao Yadav
标识
DOI:10.4155/tde-2019-0045
摘要
Aim: At present, various ophthalmic formulations show low bioavailability. The rationale of present work was to design and develop stable ketorolac tromethamine nanosuspension with sustained effect and greater permeability for ocular drug delivery and increased ocular residence. Materials & methods: Formulations were designed by using central composite design, developed by combined nanoprecipitation and probe sonication method. Results & discussion: Nanosuspensions depicted the size range of the particles in between 199 and 441 nm with slight reduction in crystallinity of drug. In vitro drug release revealed that higher % entrapment efficiency of drug in nanosuspension delays the drug release. Conclusion: Eudragit RL-100-based nanosuspension increases viscosity and avoids problems like drug loss from precorneal surface and rapid drainage through nasolacrimal areas.
科研通智能强力驱动
Strongly Powered by AbleSci AI