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Trojan particles: Large porous carriers of nanoparticles for drug delivery

机译:木马颗粒:用于药物输送的大型纳米颗粒多孔载体

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摘要

We have combined the drug release and delivery potential of nanoparticle (NP) systems with the ease of flow, processing, and aerosolization potential of large porous particle (LPP) systems by spray drying solutions of polymeric and nonpolymeric NPs into extremely thin-walled macroscale structures. These hybrid LPPs exhibit much better flow and aerosolization properties than the NPs; yet, unlike the LPPs, which dissolve in physiological conditions to produce molecular constituents, the hybrid LPPs dissolve to produce NPs, with the drug release and delivery advantages associated with NP delivery systems. Formation of the large porous NP (LPNP) aggregates occurs via a spray-drying process that ensures the drying time of the sprayed droplet is sufficiently shorter than the characteristic time for redistribution of NPs by diffusion within the drying droplet, implying a local Peclet number much greater than unity. Additional control over LPNPs physical characteristics is achieved by adding other components to the spray-dried solutions, including sugars, lipids, polymers, and proteins. The ability to produce LPNPs appears to be largely independent of molecular component type as well as the size or chemical nature of the NPs.
机译:通过将聚合物和非聚合物NP喷雾干燥成极薄壁的宏观结构,我们将纳米颗粒(NP)系统的药物释放和传递潜力与大多孔颗粒(LPP)系统的易流动性,加工性和雾化潜力相结合。这些混合的LPP表现出比NP更好的流动性和雾化特性。然而,与在生理条件下溶解以产生分子成分的LPP不同,杂化LPP溶解以产生NP,具有与NP递送系统相关的药物释放和递送优势。大型多孔NP(LPNP)聚集体的形成是通过喷雾干燥过程实现的,该过程可确保喷雾液滴的干燥时间比通过在干燥液滴中扩散而重新分配NP的特征时间足够短,这意味着局部Peclet数要大得多。大于统一。通过向喷雾干燥溶液中添加其他成分(包括糖,脂质,聚合物和蛋白质),可以进一步控制LPNP的物理特性。产生LPNP的能力似乎在很大程度上与分子组分类型以及NP的大小或化学性质无关。

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