Design and Evaluation of Soluble Ocular Insert For Controlled Release of Chloramphenicol

Authors

Shahla MirzaeeiShahla Mirzaeei ORCID1, 2,*, Moslem Alizadeh3
1Pharmaceutical Sciences Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran
2Nano Drug Delivery Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran
3Student Research Committee, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran
*Corresponding Author: Corresponding author: Nano Drug Delivery Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran. Email:[email protected]

Journal of Reports in Pharmaceutical Sciences:Vol. 6, issue 2; 123-133
Published online:Jul 03, 2017
Article type:Research Article
Received:May 07, 2017
Accepted:Jun 25, 2017
How to Cite:Mirzaeei S, Alizadeh M. Design and Evaluation of Soluble Ocular Insert For Controlled Release of Chloramphenicol. J Rep Pharm Sci. 2017;6(2):e147610. doi:

Abstract

Soluble ocular inserts of chloramphenicol were prepared with the aim of achieving once a day administration. Drug reservoir was prepared using hydrophilic polymer and rate-controlling hydrophobic polymer; Eudragit L100, Eudragit S100, Eudragit RL100. All the formulations indicated no interaction between drug and polymer in FTIR studies. The Inserts were evaluated for the several parameters, viscosity, drug–polymer interaction, in vitro drug release, sterility testing. They were also evaluated for % moisture loss, % moisture uptake,thickness, and tensile strength. Ophthalmic inserts provide that prolonged and sustained drug release. Ocular inserts prepared were smooth and passed all the evaluation tests performed. Mechanical properties and in vitro drug release were dependent on film composition. The release profile of all the formulations showed a steady, controlled drug release. Ocular inserts formulated also passed the test for sterility. In vitro studies demonstrated that P5 insert can ensure a sustained drug release on the ocular surface for a prolonged over 20 hours’ time period. Also, reduction in frequency of administration, may improve the patient compliance.

Copyright

© 2017, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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