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Drug release mechanisms of hot-melt extruded starch-based pellets

机译:热熔挤出淀粉基药丸的释药机理

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摘要

Hot-melt extrusion with die-face pelletisation is an excellent technique to continuously F produce almost monodisperse spherical starch pellets. For a better understanding of drug release mechanisms from hot-melt extruded starch-based pellets the swelling behaviour in Ac the release medium was examined by reflected-light microscopy. From the microscopic images it can be concluded that the drug release mechanism of wx corn starch pellets is almost solely based on erosion. The release mechanism of cornstarch, pea starch and potato starch pellets is primarily a swelling-based process. Although the release mechanism of a swelling dosage form is theoretically complex, it was found that the fractional drug release from the hot-melt extruded starch pellets can be described with the Noyes-Whitney equation. This facilitates the evaluation of the influence of the physicochemical properties of the matrix and the chemical properties of the active ingredient on the drug release rate. It was found that pellet size, porosity and velocity with which the penetrant diffuses into the pellet-core the water solubility of the drug as well as the molecular structure and composition of the starches are the main factors influencing drug release from the swelling starch pellets.
机译:具有模面造粒的热熔挤出是连续F生产几乎单分散的球形淀粉粒料的一项出色技术。为了更好地了解热熔挤出淀粉基团粒的药物释放机理,通过反射光显微镜检查了AC中的溶胀行为。从显微图像可以得出结论,wx玉米淀粉颗粒的药物释放机理几乎完全基于侵蚀。玉米淀粉,豌豆淀粉和马铃薯淀粉颗粒的释放机理主要是基于溶胀的过程。尽管溶胀剂型的释放机理在理论上是复杂的,但发现可以用Noyes-Whitney方程描述从热熔挤出淀粉颗粒中释放的部分药物。这有助于评估基质的物理化学性质和活性成分的化学性质对药物释放速率的影响。已经发现,丸剂的尺寸,孔隙率和渗透剂扩散到丸剂芯中的速度,药物的水溶性以及淀粉的分子结构和组成是影响药物从膨胀淀粉丸剂中释放的主要因素。

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