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首页> 外文期刊>International Journal of Pharmaceutics >Effect of temperature-increase rate on drug release characteristics of dextran microspheres prepared by emulsion solvent evaporation process.
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Effect of temperature-increase rate on drug release characteristics of dextran microspheres prepared by emulsion solvent evaporation process.

机译:升温速率对乳液溶剂蒸发法制得的葡聚糖微球释药特性的影响。

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摘要

Microspheres containing theophylline (TH) were prepared from a hydrophobic dextran derivative by an emulsion solvent evaporation process using an acetone/liquid paraffin system. The effects of solvent evaporation rate on particle properties and drug release characteristic of the microspheres were evaluated. The solvent evaporation rate was controlled by the rate of increase in temperature of the water bath, ranging 7.5-30 degrees C/h. Drug release from the microspheres was examined using JPXIV 2nd fluid (pH 6.8) containing 0.1% Tween 80, and was found to be greatly affected by the solvent evaporation rate. The percentage of drug released until 8h varied; from 28% to 84% for 30 and 7.5 degrees C, respectively. Differential scanning calorimetry and powder X-ray diffraction studies revealed that TH partially interacted with the polymer and drug crystallinity was maintained intact in the microspheres. According to scanning electron microscopy observations, all microspheres showed a well-formed spherical particle with a solid interior. The appearances of the microspheres were, however, extremely different. Microspheres prepared at 30 degrees C/h had a very smooth surface, while those prepared at 7.5-15 degrees C/h had a rough surface with large craters. These findings demonstrated that the surface morphology and drug release characteristic were controlled by the rate of increase of temperature.
机译:含有茶碱(TH)的微球是由疏水性葡聚糖衍生物通过使用丙酮/液体石蜡系统的乳液溶剂蒸发工艺制得的。评估了溶剂蒸发速率对微球颗粒性质和药物释放特性的影响。溶剂的蒸发速率由水浴温度的升高速率控制,范围为7.5-30摄氏度/小时。使用含有0.1%Tween 80的JPXIV 2nd液体(pH 6.8)检查了微球中的药物释放,发现其受溶剂蒸发速度的影响很大。直到8h释放的药物百分比有所变化;分别在30和7.5摄氏度下从28%增至84%。差示扫描量热法和粉末X射线衍射研究表明,TH与聚合物部分相互作用,并且药物结晶度在微球中保持完整。根据扫描电子显微镜观察,所有微球均显示出具有固体内部的良好形成的球形颗粒。但是,微球的外观截然不同。以30℃/ h的速度制备的微球表面非常光滑,而以7.5-15℃/ h的速度制备的微球表面粗糙且有大坑。这些发现表明,表面形态和药物释放特性受温度升高速率的控制。

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