Preparation and characterization of cephalexin loaded PLGA microspheres

The aim of this study was to evaluate the effects of emulsion type and process parameters on the properties of CPX-loaded PLGA microspheres in order to obtain delivery systems suitable for the treatment of dairy mastitis. The microsphere size was analyzed by photon correlation spectrophotometry. Det...

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Main Authors: Chaisri W., Hennink W.E., Okonogia S.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-61849100574&partnerID=40&md5=5c1057d66b195974689a97551091461a
http://www.ncbi.nlm.nih.gov/pubmed/19418958
http://cmuir.cmu.ac.th/handle/6653943832/4549
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-45492014-08-30T02:42:35Z Preparation and characterization of cephalexin loaded PLGA microspheres Chaisri W. Hennink W.E. Okonogia S. The aim of this study was to evaluate the effects of emulsion type and process parameters on the properties of CPX-loaded PLGA microspheres in order to obtain delivery systems suitable for the treatment of dairy mastitis. The microsphere size was analyzed by photon correlation spectrophotometry. Determination of the drug loading was achieved by HPLC. It was found that CPX-loaded PLGA microspheres prepared using a w/o/w double emulsion technology were slightly larger (∼ 3-5 μm) but much higher in drug content (∼ 18 % w/w) than those obtained using o/w single emulsion preparation technology (average size was 2 μm, encapsulation efficiency was less than 2%). It was also demonstrated that stirring during emulsification and a change in both the internal and external phase of the emulsion, affected the size and the drug entrapment efficiency of the microspheres obtained. A 60/40 v/v mixture of chloroform and acetone was found to be the best organic solvent system for creating the primary emulsion. To obtain a high yield (>90%) of microspheres with a desirable size and high drug entrapment efficacy, a stirring rate of 8,000-10,000 rpm gave the best results. It is concluded CPX-loaded PLGA microspheres with suitable characteristics for the treatment of cows with dairy mastitis can be prepared by a w/o/w double emulsion preparation method. © 2009 Bentham Science Publishers Ltd. 2014-08-30T02:42:35Z 2014-08-30T02:42:35Z 2009 Article 15672018 10.2174/156720109787048186 19418958 http://www.scopus.com/inward/record.url?eid=2-s2.0-61849100574&partnerID=40&md5=5c1057d66b195974689a97551091461a http://www.ncbi.nlm.nih.gov/pubmed/19418958 http://cmuir.cmu.ac.th/handle/6653943832/4549 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description The aim of this study was to evaluate the effects of emulsion type and process parameters on the properties of CPX-loaded PLGA microspheres in order to obtain delivery systems suitable for the treatment of dairy mastitis. The microsphere size was analyzed by photon correlation spectrophotometry. Determination of the drug loading was achieved by HPLC. It was found that CPX-loaded PLGA microspheres prepared using a w/o/w double emulsion technology were slightly larger (∼ 3-5 μm) but much higher in drug content (∼ 18 % w/w) than those obtained using o/w single emulsion preparation technology (average size was 2 μm, encapsulation efficiency was less than 2%). It was also demonstrated that stirring during emulsification and a change in both the internal and external phase of the emulsion, affected the size and the drug entrapment efficiency of the microspheres obtained. A 60/40 v/v mixture of chloroform and acetone was found to be the best organic solvent system for creating the primary emulsion. To obtain a high yield (>90%) of microspheres with a desirable size and high drug entrapment efficacy, a stirring rate of 8,000-10,000 rpm gave the best results. It is concluded CPX-loaded PLGA microspheres with suitable characteristics for the treatment of cows with dairy mastitis can be prepared by a w/o/w double emulsion preparation method. © 2009 Bentham Science Publishers Ltd.
format Article
author Chaisri W.
Hennink W.E.
Okonogia S.
spellingShingle Chaisri W.
Hennink W.E.
Okonogia S.
Preparation and characterization of cephalexin loaded PLGA microspheres
author_facet Chaisri W.
Hennink W.E.
Okonogia S.
author_sort Chaisri W.
title Preparation and characterization of cephalexin loaded PLGA microspheres
title_short Preparation and characterization of cephalexin loaded PLGA microspheres
title_full Preparation and characterization of cephalexin loaded PLGA microspheres
title_fullStr Preparation and characterization of cephalexin loaded PLGA microspheres
title_full_unstemmed Preparation and characterization of cephalexin loaded PLGA microspheres
title_sort preparation and characterization of cephalexin loaded plga microspheres
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-61849100574&partnerID=40&md5=5c1057d66b195974689a97551091461a
http://www.ncbi.nlm.nih.gov/pubmed/19418958
http://cmuir.cmu.ac.th/handle/6653943832/4549
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