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1.
Chinese Journal of Cardiology ; (12): 330-333, 2010.
Article Dans Chinois | WPRIM | ID: wpr-341223

Résumé

<p><b>OBJECTIVE</b>To evaluate the clinical value of 3D visualization method for simulating percutaneous transcatheter closure of atrial septal defect (ASD).</p><p><b>METHODS</b>3D volume render method was used for visualizing ASD and surrounding structures and 3D modeling method was applied for simulate the shape of occlusion device. The size and the distance between the lower edge of device and atria-ventricular valve of simulation occluder and actual selected atrial septal occluder (ASO) were compared in 30 patients underwent successful transcatheter closure of ASD.</p><p><b>RESULTS</b>The location, geometry, size, extent of ASDs in children were displayed in 3D visualization. No significant difference was found between simulation occluder and ASO size measured from left atrium [(26.07 +/- 5.32) cm vs. (25.91 +/- 5.32) cm] and right atrium [(22.13 +/- 5.31) cm vs. (22.08 +/- 5.26) cm, all P > 0.05]. The distances from simulation occluder to mitral valves [(5.76 +/- 2.39) cm] and to tricuspid valves [(8.25 +/- 2.40) cm] were similar as ASO to atria-ventricular valves [(5.61 +/- 2.26) cm and (8.02 +/- 2.48) cm, respectively, all P > 0.05].</p><p><b>CONCLUSIONS</b>The simulating percutaneous transcatheter closure of ASD by 3D visualization technique could be a helpful noninvasive approach for ASO selection before the procedure of transcatheter occlusion of ASD.</p>


Sujets)
Enfant , Enfant d'âge préscolaire , Femelle , Humains , Mâle , Cathétérisme cardiaque , Méthodes , Simulation numérique , Échocardiographie tridimensionnelle , Communications interauriculaires , Imagerie diagnostique , Thérapeutique , Résultat thérapeutique
2.
Acta Pharmaceutica Sinica ; (12): 138-141, 2006.
Article Dans Chinois | WPRIM | ID: wpr-253484

Résumé

<p><b>AIM</b>To investigate the intestinal absorption of silybin (SLB) in male rats.</p><p><b>METHODS</b>Single-pass intestinal perfusion (SPIP) technique was performed in each isolated region of the small intestine at a flow rate of 0.1 mL x min(-1). The samples of perfusate and portal plasma were collected at the designated periods of time after rat intestinal perfusion and analyzed for drug by HPLC.</p><p><b>RESULTS</b>The absorption rate constant (k(a)) and the effective permeability (P(eff)) of SLB at 190 microg x mL(-1) were determined for each segment. These data indicated the absorption rate were duodenum > jejunum > ileum > colon. SPIP was also performed in duodenum with three concentrations of SLB (80, 190 and 300 microg x mL(-1)). The concentration dependent changes of k(a) and P(eff) were evident in the duodenum perfusion of silybin. At silybin perfusate concentrations of 80 microg x mL(-1), k(a) and P(eff) were different from the values at either of the two higher concentrations (190 and 300 microg x mL(-1), P < 0.05). However there was no difference between 190 microg x mL(-1) and 300 microg x mL(-1) groups. The drug mass appearing in the plasma further indicated the absorption were duodenum > jejunum > ileum > colon.</p><p><b>CONCLUSION</b>SLB can be absorbed in whole intestinal sections. When the concentration raises to a certain level, the uptake of SLB will not increase.</p>


Sujets)
Animaux , Mâle , Rats , Côlon , Métabolisme , Duodénum , Métabolisme , Iléum , Métabolisme , Absorption intestinale , Intestin grêle , Métabolisme , Jéjunum , Métabolisme , Silybium marianum , Chimie , Perfusion , Plantes médicinales , Chimie , Rat Sprague-Dawley , Silymarine , Sang , Pharmacocinétique
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