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Process, Physicochemical Characterization and In-Vitro Assessment of Albendazole Microcrystals

Purpose: Albendazole is a poorly soluble drug which limits its oral bioavailability. The study was focussed to enhance the solubility by in-situ micronization. Methods: Albendazole microcrystals were prepared by solvent change method using gum karaya and hupu gum as stabilizing agents and the effect...

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Autores principales: KR, Vandana, Yalavarthi, Prasanna Raju, Vadlamudi, Harini Chowdary, Kalluri, Jagadesh Kumar Yadav, Rasheed, Arun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651063/
https://www.ncbi.nlm.nih.gov/pubmed/29071224
http://dx.doi.org/10.15171/apb.2017.050
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author KR, Vandana
Yalavarthi, Prasanna Raju
Vadlamudi, Harini Chowdary
Kalluri, Jagadesh Kumar Yadav
Rasheed, Arun
author_facet KR, Vandana
Yalavarthi, Prasanna Raju
Vadlamudi, Harini Chowdary
Kalluri, Jagadesh Kumar Yadav
Rasheed, Arun
author_sort KR, Vandana
collection PubMed
description Purpose: Albendazole is a poorly soluble drug which limits its oral bioavailability. The study was focussed to enhance the solubility by in-situ micronization. Methods: Albendazole microcrystals were prepared by solvent change method using gum karaya and hupu gum as stabilizing agents and the effect of each stabilizer on the prepared microcrystals were studied. FT-IR, DSC, XRD and SEM analysis were performed as a part of characterization studies. The formulations were evaluated for micromeritics, solubility and drug release. The microcrystals that had shown optimized properties were filled into suitable capsules. Results: The formulations showed reduction in particle size with uniform size distribution and three folds increase in drug release. The microcrystals had shown more than 100-folds increase in solubility compared to pure drug. Surface energy, enthalpy and crystalline nature of microcrystals were found to be reduced. Microcrystals containing gum karaya had shown more drug release. The filled-in capsules also showed increase in drug release rate. The solubility enhancement of albendazole microcrystals was mainly due to the surface adsorption of the stabilizing agents that led to reduction in surface energy and crystalline nature as substantiated by the DSC and XRD studies. The type of stabilizing agent had significant effect on dissolution rate. High affinity of albendazole with gum karaya led to faster drug release profiles. Conclusion: The study proved that in-situ micronization is an effective technique to enhance the solubility and dissolution rate of poorly soluble drugs like albendazole.
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spelling pubmed-56510632017-10-25 Process, Physicochemical Characterization and In-Vitro Assessment of Albendazole Microcrystals KR, Vandana Yalavarthi, Prasanna Raju Vadlamudi, Harini Chowdary Kalluri, Jagadesh Kumar Yadav Rasheed, Arun Adv Pharm Bull Research Article Purpose: Albendazole is a poorly soluble drug which limits its oral bioavailability. The study was focussed to enhance the solubility by in-situ micronization. Methods: Albendazole microcrystals were prepared by solvent change method using gum karaya and hupu gum as stabilizing agents and the effect of each stabilizer on the prepared microcrystals were studied. FT-IR, DSC, XRD and SEM analysis were performed as a part of characterization studies. The formulations were evaluated for micromeritics, solubility and drug release. The microcrystals that had shown optimized properties were filled into suitable capsules. Results: The formulations showed reduction in particle size with uniform size distribution and three folds increase in drug release. The microcrystals had shown more than 100-folds increase in solubility compared to pure drug. Surface energy, enthalpy and crystalline nature of microcrystals were found to be reduced. Microcrystals containing gum karaya had shown more drug release. The filled-in capsules also showed increase in drug release rate. The solubility enhancement of albendazole microcrystals was mainly due to the surface adsorption of the stabilizing agents that led to reduction in surface energy and crystalline nature as substantiated by the DSC and XRD studies. The type of stabilizing agent had significant effect on dissolution rate. High affinity of albendazole with gum karaya led to faster drug release profiles. Conclusion: The study proved that in-situ micronization is an effective technique to enhance the solubility and dissolution rate of poorly soluble drugs like albendazole. Tabriz University of Medical Sciences 2017-09 2017-09-25 /pmc/articles/PMC5651063/ /pubmed/29071224 http://dx.doi.org/10.15171/apb.2017.050 Text en ©2017 The Authors. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, as long as the original authors and source are cited. No permission is required from the authors or the publishers.
spellingShingle Research Article
KR, Vandana
Yalavarthi, Prasanna Raju
Vadlamudi, Harini Chowdary
Kalluri, Jagadesh Kumar Yadav
Rasheed, Arun
Process, Physicochemical Characterization and In-Vitro Assessment of Albendazole Microcrystals
title Process, Physicochemical Characterization and In-Vitro Assessment of Albendazole Microcrystals
title_full Process, Physicochemical Characterization and In-Vitro Assessment of Albendazole Microcrystals
title_fullStr Process, Physicochemical Characterization and In-Vitro Assessment of Albendazole Microcrystals
title_full_unstemmed Process, Physicochemical Characterization and In-Vitro Assessment of Albendazole Microcrystals
title_short Process, Physicochemical Characterization and In-Vitro Assessment of Albendazole Microcrystals
title_sort process, physicochemical characterization and in-vitro assessment of albendazole microcrystals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651063/
https://www.ncbi.nlm.nih.gov/pubmed/29071224
http://dx.doi.org/10.15171/apb.2017.050
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