Source:http://linkedlifedata.com/resource/pubmed/id/12851046
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2003-7-9
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pubmed:abstractText |
Betamethasone (BTM)-loaded microparticles prepared by a spray drying method using chitosan (CTS) as raw material, type-A gelatin and ethylene oxide-propylene oxide block copolymer (Pluronic F68) as modifiers. The BTM-loaded in varied chitosan/Pluronic F68/gelatin microparticle formulations was investigated. By properly choosing excipient type and concentration a high degree of control was achieved over the physical properties of the BTM-loaded microparticles. Microparticle characteristics (zeta potential, tap density, particle size and yield), loading efficiencies, microparticle morphology and in-vitro release properties were examined. Surface morphological characteristics and surface charges of prepared microparticles were observed by using scanning electron microscopy (SEM) and microelectrophoresis. A SEM micrograph shows that the particle sizes of the varied chitosan composed microparticles ranged from 1.1-4.7 microm and the external surfaces appear smooth. The BTM-loaded microparticles entrapped in the chitosan/Pluronic F68/gelatin microparticles with trapping efficiencies up to 93%, collected yield rate 44%, and mean particle size varied between 1-3 microm, positive surface charge (20-40 mv), and tap densities (0.04-0.40 g/cm3) were obtained. The collected BTM yield and size of particle was increased with increasing BTM-loaded amount but both zeta potential and tap density of the particles decreased with increasing BTM-loaded amount. The in vitro release of BTM showed a dose-dependent burst followed by a slower release phase that was proportional to the drug concentration in the concentration range between 5-30%w/w. The in vitro drug release from the chitosan/Pluronic F68/gelatin 1/0.1/0.4 microspheres had a prolong release pattern. These formulation factors were correlated to particulate characteristics for optimizing BTM microspheres in pulmonary delivery.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Inflammatory Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Betamethasone,
http://linkedlifedata.com/resource/pubmed/chemical/Biocompatible Materials,
http://linkedlifedata.com/resource/pubmed/chemical/Chitin,
http://linkedlifedata.com/resource/pubmed/chemical/Chitosan,
http://linkedlifedata.com/resource/pubmed/chemical/Delayed-Action Preparations,
http://linkedlifedata.com/resource/pubmed/chemical/Drug Carriers,
http://linkedlifedata.com/resource/pubmed/chemical/Excipients,
http://linkedlifedata.com/resource/pubmed/chemical/Poloxamer
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pubmed:status |
MEDLINE
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pubmed:issn |
0265-2048
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
459-72
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pubmed:dateRevised |
2009-7-21
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pubmed:meshHeading |
pubmed-meshheading:12851046-Anti-Inflammatory Agents,
pubmed-meshheading:12851046-Betamethasone,
pubmed-meshheading:12851046-Biocompatible Materials,
pubmed-meshheading:12851046-Chitin,
pubmed-meshheading:12851046-Chitosan,
pubmed-meshheading:12851046-Delayed-Action Preparations,
pubmed-meshheading:12851046-Drug Carriers,
pubmed-meshheading:12851046-Drug Compounding,
pubmed-meshheading:12851046-Excipients,
pubmed-meshheading:12851046-Humans,
pubmed-meshheading:12851046-Microspheres,
pubmed-meshheading:12851046-Particle Size,
pubmed-meshheading:12851046-Poloxamer,
pubmed-meshheading:12851046-Surface Properties
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pubmed:articleTitle |
The characteristics of betamethasone-loaded chitosan microparticles by spray-drying method.
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pubmed:affiliation |
Graduate Institute of Life Sciences, National Defense Medical Center, University of National Defense, Taipei, Taiwan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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