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Drug administration for nano-suspension with increased dissolution rate and saturation solubility

机译:用于纳米悬浮液的药物管理,具有更高的溶解速率和饱和溶解度

摘要

(57) Abstract The system whose saturation solubility (Cs) is high considerably can by manufacturing the nano- suspensoid of the medicine. Therefore, it is possible to raise the saturation solubility of the medicine whose organism utilization characteristic is low. You can obtain the melting speed which is higher than the melting speed which is obtained with this addition increase of saturation solubility, by the simple increase of the surface area of the medicine. Quite stability you can obtain nano- suspensoid very low with the surface active agent of density and using the stabilizer. It is possible to manufacture the nano- suspensoid which does not contain boundary activity. The nano- suspensoid whose contents of the particle which possesses the grain size of the micrometer range are very few can be produced on a large scale without impairing the advantage making use of cavitation method. Because the powdered medicine particle is thought, that the gap of almost 25 millimicrons is blocked, until recently manufacturing the nano- suspensoid which is by cavitation method was made impossible. It flows from the viewpoint of optimum stability and the surface active agent non- containing formulation and, it is possible to manufacture nano- suspensoid with shearing or the shocking action which uses the dispersed device.
机译:(57)<摘要>可以通过制造药物的纳米悬浮液来实现饱和溶解度(Cs)很高的系统。因此,可以提高生物利用度低的药物的饱和溶解度。通过简单地增加药物的表面积,可以获得高于通过增加饱和溶解度而获得的熔融速度的熔融速度。使用密度高的表面活性剂并使用稳定剂,可以获得相当低的纳米悬浮液。可以制造不具有边界活性的纳米悬浮体。具有微米范围的晶粒尺寸的颗粒的含量非常少的纳米悬浮体可以大规模地生产而不会损害利用空化方法的优点。因为认为是粉末状的药物颗粒,所以近25微米的间隙被阻塞了,直到最近才通过气穴法制造纳米悬浮体成为不可能。从最佳稳定性和不含表面活性剂的配方的观点出发,可以使用分散装置通过剪切或冲击作用制造纳米悬浮体。

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