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The Preparating And Evaluation On Nanoemulsion Of Artesanate

Posted on:2014-01-03Degree:MasterType:Thesis
Country:ChinaCandidate:J L LiFull Text:PDF
GTID:2253330401478634Subject:Basic veterinary science
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The nanoemulsions also known as micro-emulsion. it is a particle size of10to100nm of athermodynamically stable isotropic, transparent or translucenthomogeneous dispersion system,whichformated by water, oil, surfactant and co-surfactant agent spontaneous. Nanoemulsions can increase thesolubility of insoluble drug, promote drug absorption, and slow release of the drug to improvebioavailability. Artesunate has a very substantial effect in the treatment of blood protozoan diseases.However, due to its low solubility in water, it is difficult to prepare a stable liquid formulation, theclinical application is limited. Nanoparticle delivery technology can effectively solve some of theshortcomings of the existing formulation of artesunate.To further optimize the prescription of artesunate nanoemulsion, By central composite design with5levels of3factors,we measured drug loading and average particle size of nanoemulsion obtained ineach group experiments, And the experimental data was nonlinear regression analysised and drawresponse surface with Design Expert-7to estimate the optimal formulations of artesunate nanoemulsionPreparation of artesunate nanoemulsion with the best formula, And packaged with brown ampouleand brown vials. Each packaged nanoemulsion was treated with high-temperature test, glareexperiments and accelerated test. The results show that the the two packaged artesunate nanoemulsioncould stably stored at60°C high temperature and4500lx±500lx glare. At a temperature of40°C±2°C, humidity75%RH±5%,Both brown vials packaged artesunate nanoemulsion and brown ampoulepackage artesunate nanoemulsion stably stored in the end of the first, second, third,and sixth month.In the research,we establish the method that detect the content of artesunate with highperformance liquid chromatography (HPLC) analysis. The standard curve was linear in the range of5to50μg/mL (R2=0.9992) good, Intra-day precision RSD=0.943%, Day precision RSD=0.945%, therecovery rate was98±5.3%(N=3). This method have high recovery rate, Good precision,can Accuratelyand effectively detect the content of the artesunate in nanoemulsion formulation.Throμg Insect suppression in vitro experiments, compared the in vitro insecticidal activity ofArtesunate nanoemulsion Bernier, imidocarb, hydrochloric acid acridine and other drμgs to bovineBabesia. The results showed that artesunate nanoemulsion in vitro has strong insecticidal cattle Babesia.This study prepared a artesunate nanoemulsion wich is high drug loading, good stability, andeasy to use. The nanoemulsion effective to make up for the shortcomings of the existing formulation ofartesunate poor stability, clinical inconvenient to use, and a preliminary study.about anti-Babesia abilityin vitro have be done. These work provide a foundation to nanoemulsion drug delivery system appliingin the veterinary field.
Keywords/Search Tags:Nanoemulsion, Artesunate, Babesia, Optimal design
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