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Condensational growth of combination drug-excipient submicrometer particles for targeted high efficiency pulmonary delivery: comparison of CFD predictions with experimental results.

机译:结合药物-赋形剂亚微米颗粒的凝结生长,用于靶向高效肺部递送:CFD预测值与实验结果的比较。

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The objective of this study was to investigate the hygroscopic growth of combination drug and excipient submicrometer aerosols for respiratory drug delivery using in vitro experiments and a newly developed computational fluid dynamics (CFD) model.Submicrometer combination drug and excipient particles were generated experimentally using both the capillary aerosol generator and the Respimat inhaler. Aerosol hygroscopic growth was evaluated in vitro and with CFD in a coiled tube geometry designed to provide residence times and thermodynamic conditions consistent with the airways.The in vitro results and CFD predictions both indicated that the initially submicrometer particles increased in mean size to a range of 1.6-2.5?μm for the 50:50 combination of a non-hygroscopic drug (budesonide) and different hygroscopic excipients. CFD results matched the in vitro predictions to within 10% and highlighted gradual and steady size increase of the droplets, which will be effective for minimizing extrathoracic deposition and producing deposition deep within the respiratory tract.Enhanced excipient growth (EEG) appears to provide an effective technique to increase pharmaceutical aerosol size, and the developed CFD model will provide a powerful design tool for optimizing this technique to produce high efficiency pulmonary delivery.
机译:本研究的目的是使用体外实验和新开发的计算流体力学(CFD)模型,研究用于呼吸道给药的复合药物和赋形剂亚微米气雾剂的吸湿性增长。毛细管气雾发生器和Respimat吸入器。体外评估气溶胶的吸湿性生长,并采用CFD在盘管几何形状中进行设计,以提供与气道一致的停留时间和热力学条件。体外结果和CFD预测均表明,最初的亚微米颗粒的平均粒径增加到了非吸湿性药物(布地奈德)与不同吸湿性赋形剂的50:50组合使用1.6-2.5μm。 CFD结果与体外预测相符,在10%以内,并突出了液滴逐渐稳定的大小增长,这将有效地减少胸腔外沉积并在呼吸道深处产生沉积。增强的赋形剂生长(EEG)似乎提供了有效的方法技术来增加药物气雾剂的尺寸,并且开发的CFD模型将提供强大的设计工具来优化该技术以产生高效的肺部递送。

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