Formulation and Evaluation of Microencapsulated Levofloxacin Gel
Abstract
Abstract
To treat various buccal infectious diseases, a sustained release microencapsulated levofloxacin gel was formulated. Levofloxacin microspheres were being prepared following o/w emulsion solvent evaporation technique by varying concentrations of ethyl acetate, ethyl cellulose and tween 80. Depending on their flow properties almost all the microspheres were found to be excellent. The drug-excipient compatibility study carried out using Fourier transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC) resulted that the excipients used in the formulation are compatible to the drug used and with each other. However, the microspheres containing 2 g of drug in composition with 1.5% and 1.75% ethyl cellulose, 0.9% and 1% ethyl acetate, respectively, with 4% acetone were found to have more than 50% of drug-loading efficiency, hence optimized for further study. Finally, the optimized microspheres were incorporated within a conventional gel containing varying concentration of carbopol-934P. Conclusively, the optimized microcapsule-loaded gel formulations were evaluated for their physicochemical characters such as pH, viscosity and in vitro release study. All the optimized levofloxacin containing microcapsule-loaded gel formulations were found to possess desired pH and viscosity. Further, the in vitro drug release study showed that the levofloxacin containing microcapsule-loaded gel with 0.45% carbopol-934p was found to be the best formulation.Keywords: Microcapsulated gel, levofloxacin, FTIR, DSC, in vitro drug release
Cite this Article
Pattnaik S, Priyadarshini S, Niyogi P, et al. Formulation and Evaluation of Microencapsulated Levofloxacin Gel. Research & Reviews: A Journal of Drug Formulation, Development and Production. 2016; 3(1): 39–47p.
Downloads
Published
Issue
Section
License
Copyright Transfer and Declaration Form (Please compile this form, sign and send by e-mail and post)
Journal Title:
Title of the Paper:
Corresponding Author’s Information: Name: Address:
E-mail:
Contact Number: I
t is herein agreed that: The copyright to the above-listed unpublished and original article is transferred to STM Journals. This copyright transfer covers the exclusive right to reproduce and distribute the contribution, including reprints, translations, photographic reproductions, microform, electronic form (offline, online), or any other reproductions of similar nature. I/We declare that above manuscript is not published already in part or whole (except in the form of abstract) in any journal or magazine for private or public circulation, and, is not under consideration of publication elsewhere. I/ We warrant(s) that his/her/their contribution is original, except for such excerpts from copyrighted works as may be included with the permission of the copyright holder and author thereof, that it contains no libelous statements, and does not infringe on any copyright, trademark, patent, statutory right, or propriety right of others. I/We will not publish his/her/their above said contribution anywhere else without the prior written permission of the publisher unless it has been changed substantially.I/We also agree to the authorship of the article in the following order:Author(s) Name Signature(s)
1. ________________
2. _______________
_3. ________________
4. ________________
The author(s) agree to the terms of this Copyright Notice, which will apply to this submission if and when it is published by this journal (comments if any to the editor can be added below).