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Preparation and evaluation of sustained release loxoprofen loaded microspheres

The aim of present study was to formulate and evaluate the loxoprofen loaded Sustained release microspheres by emulsion solvent evaporation technique. Ethylcellulose, a biocompatible polymer is used as the retardant material. The effects of process conditions such as drug loading, polymer type and s...

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Detalles Bibliográficos
Autores principales: Venkatesan, P., Manavalan, R., Valliappan, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979224/
https://www.ncbi.nlm.nih.gov/pubmed/24826017
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author Venkatesan, P.
Manavalan, R.
Valliappan, K.
author_facet Venkatesan, P.
Manavalan, R.
Valliappan, K.
author_sort Venkatesan, P.
collection PubMed
description The aim of present study was to formulate and evaluate the loxoprofen loaded Sustained release microspheres by emulsion solvent evaporation technique. Ethylcellulose, a biocompatible polymer is used as the retardant material. The effects of process conditions such as drug loading, polymer type and solvent type on the characteristics of microspheres were investigated. The prepared microspheres were characterized for their particle size and drug loading and drug release. The in-vitro release studies were carried out in phosphate buffer at pH 7.4. The prepared microspheres were white, free flowing and spherical in shape. The drug-loaded microspheres showed 71.2% of entrapment and the in-vitro release studies showed that Loxoprofen microspheres of 1:3 ratios showed better sustained effect over a period of 8 hours
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spelling pubmed-39792242014-05-13 Preparation and evaluation of sustained release loxoprofen loaded microspheres Venkatesan, P. Manavalan, R. Valliappan, K. J Basic Clin Pharm Original Article The aim of present study was to formulate and evaluate the loxoprofen loaded Sustained release microspheres by emulsion solvent evaporation technique. Ethylcellulose, a biocompatible polymer is used as the retardant material. The effects of process conditions such as drug loading, polymer type and solvent type on the characteristics of microspheres were investigated. The prepared microspheres were characterized for their particle size and drug loading and drug release. The in-vitro release studies were carried out in phosphate buffer at pH 7.4. The prepared microspheres were white, free flowing and spherical in shape. The drug-loaded microspheres showed 71.2% of entrapment and the in-vitro release studies showed that Loxoprofen microspheres of 1:3 ratios showed better sustained effect over a period of 8 hours Medknow Publications & Media Pvt Ltd 2011-06 2011-08-15 /pmc/articles/PMC3979224/ /pubmed/24826017 Text en Copyright: © Journal of Basic and Clinical Pharmacy http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Venkatesan, P.
Manavalan, R.
Valliappan, K.
Preparation and evaluation of sustained release loxoprofen loaded microspheres
title Preparation and evaluation of sustained release loxoprofen loaded microspheres
title_full Preparation and evaluation of sustained release loxoprofen loaded microspheres
title_fullStr Preparation and evaluation of sustained release loxoprofen loaded microspheres
title_full_unstemmed Preparation and evaluation of sustained release loxoprofen loaded microspheres
title_short Preparation and evaluation of sustained release loxoprofen loaded microspheres
title_sort preparation and evaluation of sustained release loxoprofen loaded microspheres
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979224/
https://www.ncbi.nlm.nih.gov/pubmed/24826017
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