Preparation of Low Molecular Weight Heparin-Chitosan-Sodium Carboxymethyl Cellulose Microcapsules and Its Drug-Release Performances
Qiu Guo Xiao
Abstract
Qiu Guo Xiao
Abstract
Low molecular weight heparin-chitosan-sodium carboxymethyl cellulose microcapsules were prepared bymeans of emulsion-dispersion cross-linking method. The influence factors of the different preparations on the drug-releaseperformances of the microcapsules were investigated. The results showed that the microcapsules prepared by optimizedconditions were smooth spherical with 2~7μm diameter. Encapsulation efficiency and drug loading were 92.3% and 6.47%,respectively. The release rate of the microcapsules was dependent on pH value of the media. The result tested in rabbitsindicated that the microcapsules had a significant sustained release effect compared with the injection.
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Low molecular weight heparin-chitosan-sodium carboxymethyl cellulose microcapsules were prepared bymeans of emulsion-dispersion cross-linking method. The influence factors of the different preparations on the drug-releaseperformances of the microcapsules were investigated. The results showed that the microcapsules prepared by optimizedconditions were smooth spherical with 2~7μm diameter. Encapsulation efficiency and drug loading were 92.3% and 6.47%,respectively. The release rate of the microcapsules was dependent on pH value of the media. The result tested in rabbitsindicated that the microcapsules had a significant sustained release effect compared with the injection.
Key concepts: Chemistry, Carboxymethyl cellulose, Chitosan, Sodium alginate, Drug, Emulsion, Chromatography, Sodium