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A new concept for preparing drug-delivery-system (DDS) of inhaled drug

机译:准备吸入药物的药物递送系统(DDS)的新概念

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摘要

Uptake of medicine by inhalation is the unique, convenient and effective way for the application of apoprotein and DNA biomedicines, by which protecting biomedicines from the decomposition of digestion and the primary hepatic metabolism. Meanwhile, due to the individualities cannot be kept in the absence of dispersing solvent, the nano particles lose the merit, i.e. nano size, when used as inhaled drug. Therefore, in this presentation, we postulated a new concept for preparing the nano inhaled drug and its DDS device, namely, preparing the nano drug particles and simultaneously dispersing them from aggregation by using the nanofiber. As a model of this concept, poly(vinyl pyrrolidone) (PVP) was selected to prepare the crosslinked nanofiber mat while the biomimic antioxidant drug, Ebselen and an amino-acid, Creatine were used as the model drug. The nanofiber having sea-grape-like structure of PVP/Creatine was prepared, and its property of releasing drug by in the passing-through air flow was tested.
机译:吸入摄取药物是应用脱辅基蛋白和DNA生物医学的独特,便捷和有效的方法,通过这种方法可以保护生物医学免于消化和初级肝代谢的分解。同时,由于在缺乏分散溶剂的情况下不能保持个性,当用作吸入药物时,纳米颗粒失去了优点,即纳米尺寸。因此,在本演讲中,我们提出了一种制备纳米吸入药物及其DDS装置的新概念,即制备纳米药物颗粒,并同时使用纳米纤维将其分散而不会聚集。作为该概念的模型,选择了聚乙烯吡咯烷酮(PVP)制备交联的纳米纤维垫,同时使用仿生抗氧化剂Ebselen和氨基酸肌酸作为模型药物。制备具有PVP /肌酸的海草状结构的纳米纤维,并测试其在通过气流中释放药物的性质。

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