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1.
Zhongguo Zhong Yao Za Zhi ; (24): 376-379, 2006.
Article de Chinois | WPRIM | ID: wpr-350937

RÉSUMÉ

<p><b>OBJECTIVE</b>To study the preparation of solid lipid nanoparticles loaded with Xionggui powder-supercritical carbon dioxide fluid extraction and their evaluation in vitro release.</p><p><b>METHOD</b>To prepare solid lipid nanoparticles (SLN) loaded with Xionggui powder-supercritical carbon dioxide fluid extraction (XG-CO2-SFE) using a hot dispersion- ultrasonic technique, establishing the best prescription of XG-CO2-SFE-SLN through orthogonal design methods using entrapment efficiency of nanoparticles as index, and investigating their physicochemical characterizations. The invro release action of SLN was studied in different dissolution mediums using dynamic dialyse method.</p><p><b>RESULT</b>The best prescription was: phospholipid: F-68: stearie acid glyceride = 5: 2 : 1, the entrapment efficiency of nanoparticles was 96.3%, and the results revealed the nanoparticles were sphere like with the mean size of 245.8 nm, the mean Zeta potential was -33.5 mV. The in vitro release meet to Weibull distribution in physiological brine and to single-index model in pH 7.4 phosphate liquid (40% EtOH).</p><p><b>CONCLUSION</b>The preparation method of the XG-CO2-SFE-SLN was appropriate, and the XG-CO2-SFE-SLN was released completely.</p>


Sujet(s)
Angelica sinensis , Chimie , Chromatographie en phase supercritique , Préparations à action retardée , Vecteurs de médicaments , Association médicamenteuse , Préparation de médicament , Méthodes , Systèmes de délivrance de médicaments , Médicaments issus de plantes chinoises , Ligusticum , Chimie , Nanostructures , Taille de particule , Phospholipides , Poloxamère , Solubilité
2.
Zhongguo Zhong Yao Za Zhi ; (24): 101-105, 2006.
Article de Chinois | WPRIM | ID: wpr-351000

RÉSUMÉ

From the characteristic, prepare the craft, quality control, bioavailability and clinical curative effect,etc. To do the summary to the modern research of dropping pill, analyse and is thought to dropping pill that has wide development prospects.


Sujet(s)
Animaux , Humains , Biodisponibilité , Capsules , Médicaments issus de plantes chinoises , Pharmacocinétique , Plantes médicinales , Chimie , Polyéthylène glycols , Contrôle de qualité , Solubilité , Technologie pharmaceutique , Méthodes
3.
Zhongguo Zhong Yao Za Zhi ; (24): 507-508, 2003.
Article de Chinois | WPRIM | ID: wpr-266761

RÉSUMÉ

<p><b>OBJECTIVE</b>To find the best condition of the preparation technology of Flos Magnoliae essential oil-beta-cyclodextrin inclusion complex.</p><p><b>METHOD</b>L9(3(4)) table was used to examine the effects of 4 factors, and the inclusion rate of each test was determined of orthogonal test.</p><p><b>RESULT</b>The best condition was:oil:beta-cyclodextrin:water = 1:8:60 (mL:g:mL), stirring for 1 hour at 80 degrees C.</p><p><b>CONCLUSION</b>The complex prepared on the condition aforementioned is stable and stirring has a highest inclusion rate.</p>


Sujet(s)
Cyclodextrines , Vecteurs de médicaments , Stabilité de médicament , Médicaments issus de plantes chinoises , Fleurs , Chimie , Magnolia , Chimie , Huile essentielle , Plantes médicinales , Chimie , Technologie pharmaceutique , Méthodes , Cyclodextrines bêta
4.
Zhongguo Zhong Yao Za Zhi ; (24): 721-723, 2003.
Article de Chinois | WPRIM | ID: wpr-282258

RÉSUMÉ

<p><b>OBJECTIVE</b>To study in vitro dissolution rate of geniposide in Huangqin Qingfei dispersible tablet.</p><p><b>METHOD</b>A reversed-phase HPLC method was developed for determination of geniposide. In vitro dissolution rates were compared between Huangqin Qingfei dispersible tablet and conventional tablet in the dissolution medium of pH 1.0, 2.85, 4.5, 6.8, and 8.0 accordingly. Zero-class model, single-index model, logarithm normal school model, and Weibull distributing model were used to simulate the dissolution curve.</p><p><b>RESULT</b>The dissolution rate of two tablets is not affected by pH so much, and they can dissolve within 5 to 10 minutes. Weibull distributing model is the best simulation for in vitro dissolution. Comparing with conventional tablet, dispersible tablet dissolve quickly and completely.</p><p><b>CONCLUSION</b>The in vitro dissolution rate of geniposide in Huangqin Qingfei dispersible tablet conforms to Weibull distributing model. The dispersible tablet is able to release rapidly.</p>


Sujet(s)
Chromatographie en phase liquide à haute performance , Association médicamenteuse , Médicaments issus de plantes chinoises , Chimie , Gardenia , Chimie , Iridoïdes , Cinétique , Plantes médicinales , Chimie , Pyrannes , Scutellaria , Chimie , Solubilité , Comprimés , Chimie , Facteurs temps
5.
Zhongguo Zhong Yao Za Zhi ; (24): 28-30, 2002.
Article de Chinois | WPRIM | ID: wpr-263649

RÉSUMÉ

<p><b>OBJECTIVE</b>To evaluate different methods by treating water-decocted liquid of 6 Chinese medical herbs and 4 co-prescription respectively with alcohol, ultrafilter, macroporousresin and clarifier.</p><p><b>METHOD</b>The contents of target component in those extracts were determined with HPLC or titration, and quantitative and qualitative determination of the impurity components, such as polysaccharide and protein, was made.</p><p><b>RESULT</b>Each method showed its advantages and disavantages.</p><p><b>CONCLUSION</b>Different method can be chosen according to the clinical and preparation demands or the characteristic of components.</p>


Sujet(s)
Association médicamenteuse , Médicaments issus de plantes chinoises , Méthodes , Plantes médicinales , Chimie , Polyosides
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