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Development and Evaluation of Thymol Microparticles Using Cellulose Derivatives as Controlled Release Dosage form

Thymol, an important and advantageous component of many essential oils, has been applied as an antimicrobial agent in animals. To increase the duration of action of this compound in ruminants, it was decided here to prepare a controlled release carrier for thymol. Hydroxy propyl methyl cellulose (HP...

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Autores principales: Zamani, Zahra, Alipour, Daryoush, Moghimi, Hamid Reza, Mortazavi, Seyed Ali Reza, Saffary, Mostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673930/
https://www.ncbi.nlm.nih.gov/pubmed/26664369
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author Zamani, Zahra
Alipour, Daryoush
Moghimi, Hamid Reza
Mortazavi, Seyed Ali Reza
Saffary, Mostafa
author_facet Zamani, Zahra
Alipour, Daryoush
Moghimi, Hamid Reza
Mortazavi, Seyed Ali Reza
Saffary, Mostafa
author_sort Zamani, Zahra
collection PubMed
description Thymol, an important and advantageous component of many essential oils, has been applied as an antimicrobial agent in animals. To increase the duration of action of this compound in ruminants, it was decided here to prepare a controlled release carrier for thymol. Hydroxy propyl methyl cellulose (HPMC) and ethyl cellulose (EC) were used as the matrix polymer here. Mixtures of thymol with eight different ratios of these polymers were then prepared using emulsion solvent evaporation method (F(1) to F(8)). The prepared microparticles were evaluated for production yield, entrapment efficiency, drug content, particle size, drug release behavior, release kinetics (zero order, first order and Fickian matrix diffusion for spheres) and characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). Mean particle size of microparticles was 1.03 ± 0.02 mm. SEM study revealed that the microparticles were slightly irregular, rough and porous. The formulation with HPMC: EC ratio of 5:1 (F6) showed the highest drug loading (38.8%) and entrapment efficiency (61.2%). This formulation also showed optimum in-vitro drug release. The best fit of release kinetics was achieved with Fickian matrix diffusion for spheres (linear amount released vs t(0.43)). The FTIR spectroscopic and DSC studies show possible interaction between drug and polymers. In this study, thymol was successfully loaded in microparticles prepared from HPMC and EC. These microparticles can be used in further trials to evaluate the effect of slow release thymol on rumen fermentation parameters in ruminants.
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spelling pubmed-46739302015-12-10 Development and Evaluation of Thymol Microparticles Using Cellulose Derivatives as Controlled Release Dosage form Zamani, Zahra Alipour, Daryoush Moghimi, Hamid Reza Mortazavi, Seyed Ali Reza Saffary, Mostafa Iran J Pharm Res Original Article Thymol, an important and advantageous component of many essential oils, has been applied as an antimicrobial agent in animals. To increase the duration of action of this compound in ruminants, it was decided here to prepare a controlled release carrier for thymol. Hydroxy propyl methyl cellulose (HPMC) and ethyl cellulose (EC) were used as the matrix polymer here. Mixtures of thymol with eight different ratios of these polymers were then prepared using emulsion solvent evaporation method (F(1) to F(8)). The prepared microparticles were evaluated for production yield, entrapment efficiency, drug content, particle size, drug release behavior, release kinetics (zero order, first order and Fickian matrix diffusion for spheres) and characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). Mean particle size of microparticles was 1.03 ± 0.02 mm. SEM study revealed that the microparticles were slightly irregular, rough and porous. The formulation with HPMC: EC ratio of 5:1 (F6) showed the highest drug loading (38.8%) and entrapment efficiency (61.2%). This formulation also showed optimum in-vitro drug release. The best fit of release kinetics was achieved with Fickian matrix diffusion for spheres (linear amount released vs t(0.43)). The FTIR spectroscopic and DSC studies show possible interaction between drug and polymers. In this study, thymol was successfully loaded in microparticles prepared from HPMC and EC. These microparticles can be used in further trials to evaluate the effect of slow release thymol on rumen fermentation parameters in ruminants. Shaheed Beheshti University of Medical Sciences 2015 /pmc/articles/PMC4673930/ /pubmed/26664369 Text en © 2015 by School of Pharmacy, Shaheed Beheshti University of Medical Sciences and Health Services This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zamani, Zahra
Alipour, Daryoush
Moghimi, Hamid Reza
Mortazavi, Seyed Ali Reza
Saffary, Mostafa
Development and Evaluation of Thymol Microparticles Using Cellulose Derivatives as Controlled Release Dosage form
title Development and Evaluation of Thymol Microparticles Using Cellulose Derivatives as Controlled Release Dosage form
title_full Development and Evaluation of Thymol Microparticles Using Cellulose Derivatives as Controlled Release Dosage form
title_fullStr Development and Evaluation of Thymol Microparticles Using Cellulose Derivatives as Controlled Release Dosage form
title_full_unstemmed Development and Evaluation of Thymol Microparticles Using Cellulose Derivatives as Controlled Release Dosage form
title_short Development and Evaluation of Thymol Microparticles Using Cellulose Derivatives as Controlled Release Dosage form
title_sort development and evaluation of thymol microparticles using cellulose derivatives as controlled release dosage form
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673930/
https://www.ncbi.nlm.nih.gov/pubmed/26664369
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