Design, development and characterization of ketorolac tromethamine polymeric nanosuspension

被引:10
|
作者
Jadhav, Pankaj A. [1 ]
Yadav, Adhikrao, V [2 ]
机构
[1] Annasaheb Dange Coll B Pharm, Dept Pharmaceut, Sangli 416301, MS, India
[2] Gourishankar Inst Pharmaceut Educ & Res, Satara 415015, MS, India
关键词
ketorolac tromethamine; lyophilization; nanoprecipitation; nanosuspension; probe sonication; ORAL BIOAVAILABILITY; EUDRAGIT RS100(R); DRUG NANOCRYSTALS; DELIVERY; FORMULATION; NANOPARTICLES; FLURBIPROFEN; VARIABLES; SYSTEM; PH;
D O I
10.4155/tde-2019-0045
中图分类号
R9 [药学];
学科分类号
1007 ;
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.
引用
收藏
页码:585 / 596
页数:12
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