干粉气溶胶输送系统:当前和未来的研究方向。

Hak-Kim Chan
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引用次数: 101

摘要

干粉气溶胶输送系统的开发涉及粉末生产、配方、分散、输送和粉末气溶胶在气道中的沉积。传统的结晶和磨粉生产方法的不足导致了替代技术的发展。在过去的十年中,通过使用工程药物颗粒和赋形剂系统,粉末配方的性能得到了显着改善,这些系统(i)具有低空气动力学直径(多孔或低颗粒密度),和/或(ii)凝聚力和粘合剂较差(通过波纹表面,低体积密度,降低表面能和颗粒相互作用,疏水添加剂和细载体颗粒)。原子力显微镜(AFM)和反相气相色谱(IGC)等分析技术提供了对粒子力和表面能的早期见解,有助于解释这种改进。相对湿度通过毛细管力和静电相互作用对干粉吸入器(DPI)产品的性能至关重要。现在可以使用改进的低压冲击器(ELPI)来测量气溶胶中不同粒径组分的静电荷。与粉末相比,在基本水平上对吸入器装置所做的工作要少得多。最近,计算流体动力学已被应用于了解吸入器的设计(如吹口、网格结构、进气口)如何影响粉末的分散。众所周知,USP咽喉不足以代表DPI气溶胶的口咽部沉积。使用磁共振成像(MRI)模型模型进行了研究,以解释口咽沉积的受试者之间和受试者内部的变化。大多数对商业产品进行的肺沉积研究都不能彻底了解影响体内肺沉积的决定因素。需要一个更系统的方法来建立一个有用的数据库,了解肺沉积对呼吸参数、吸入器设计和粉末配方特性的依赖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dry powder aerosol delivery systems: current and future research directions.

Development of dry powder aerosol delivery system involves powder production, formulation, dispersion, delivery, and deposition of the powder aerosol in the airways. Insufficiency of conventional powder production by crystallization and milling has led to development of alternative techniques. Over the last decade, performance of powder formulations has been improved significantly through the use of engineered drug particles and excipient systems which are (i) of low aerodynamic diameters (being porous or of low particle density), and/or (ii) less cohesive and adhesive (via corrugated surfaces, low bulk density, reduced surface energy and particle interaction, hydrophobic additives, and fine carrier particles). Early insights into particle forces and surface energy that help explain the improvement have been provided by analytical techniques such as the atomic force microscopy (AFM) and inverse gas chromatography (IGC). Relative humidity is critical to the performance of dry powder inhaler (DPI) products via capillary force and electrostatic interaction. Electrostatic charge of different particle size fractions of an aerosol can now be measured using a modified electrical low-pressure impactor (ELPI). Compared with powders, much less work has been done on the inhaler devices at the fundamental level. Most recently, computational fluid dynamics has been applied to understand how the inhaler design (such as mouthpiece, grid structure, air inlet) affects powder dispersion. The USP throat is known to under-represent the oropharyngeal deposition of DPI aerosols. Studies using magnetic resonance imaging (MRI) model casts have been undertaken to explain the inter- and intra- subject variation in oropharyngeal deposition. Most of the lung deposition studies performed on commercial products did not allow a thorough understanding of the determinants affecting in vivo lung deposition. A more systematic approach would be necessary to build a useful database on the dependence of lung deposition on the breathing parameters, inhaler design, and powder formulation properties.

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