使用AERx肺输送系统雾化脂丛。

AAPS PharmSci Pub Date : 2002-01-01 DOI:10.1208/ps040313
Deepa Deshpande, James Blanchard, Sudarshan Srinivasan, Dallas Fairbanks, Jun Fujimoto, Teiji Sawa, Jeanine Wiener-Kronish, Hans Schreier, Igor Gonda
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引用次数: 33

摘要

肺代表了一个有吸引力的目标,以提供基因治疗,以实现局部和潜在的全身传递基因产物。本研究的目的是评估AERx肺输送系统将非病毒基因治疗制剂输送到肺部的可行性。我们发现“裸”DNA在通过AERx喷嘴系统雾化后会发生降解。然而,用摩尔过量的阳离子脂质(脂丛)配制的DNA没有完整性损失。此外,挤压后的脂质体在粒径、zeta电位或络合度方面没有明显变化。数据表明,阳离子脂质络合对挤压后的配方有保护作用。此外,通过对培养的a -549细胞的转染研究确定,该制剂的效力没有显著变化。我们还发现,用乳糖制备的DNA制剂雾化效果很差。在配方中加入电解质(如NaCl)可显著提高雾化效率。总之,数据表明,使用AERx肺输送系统输送脂肪丛可能是一种可行的肺基因治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aerosolization of lipoplexes using AERx Pulmonary Delivery System.

The lung represents an attractive target for delivering gene therapy to achieve local and potentially systemic delivery of gene products. The objective of this study was to evaluate the feasibility of the AERx Pulmonary Delivery System for delivering nonviral gene therapy formulations to the lung. We found that "naked" DNA undergoes degradation following aerosolization through the AERx nozzle system. However, DNA formulated with a molar excess of cationic lipids (lipoplexes) showed no loss of integrity. In addition, the lipoplexes showed no significant change in particle size, zeta (zeta) potential, or degree of complexation following extrusion. The data suggest that complexation with cationic lipids had a protective effect on the formulation following extrusion. In addition, there was no significant change in the potency of the formulation as determined by a transfection study in A-549 cells in culture. We also found that DNA formulations prepared in lactose were aerosolized poorly. Significant improvements in aerosolization efficiency were seen when electrolytes such as NaCl were added to the formulation. In conclusion, the data suggest that delivery of lipoplexes using the AERx Pulmonary Delivery System may be a viable approach for pulmonary gene therapy.

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