Deshpande Deepa, Blanchard James, Srinivasan Sudarshan, Fairbanks Dallas, Fujimoto Jun, Sawa Teiji, Wiener-Kronish Jeanine, Schreier Hans, Gonda Igor
Aradigm Corporation, 3929 Point Eden Way, Hayward, CA 94545, USA.
AAPS PharmSci. 2002;4(3):E13. doi: 10.1208/ps040313.
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.
肺是基因治疗的一个有吸引力的靶点,可实现基因产物的局部递送并可能实现全身递送。本研究的目的是评估AERx肺部给药系统将非病毒基因治疗制剂递送至肺部的可行性。我们发现,“裸”DNA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配制的DNA(脂质体复合物)没有完整性损失。此外,脂质体复合物在挤出后粒径、ζ电位或络合度没有显著变化。数据表明,与阳离子脂质络合对挤出后的制剂有保护作用。此外,通过在培养的A-549细胞中进行的转染研究确定,制剂的效力没有显著变化。我们还发现,用乳糖制备的DNA制剂雾化效果不佳。当向制剂中添加NaCl等电解质时,雾化效率有显著提高。总之,数据表明使用AERx肺部给药系统递送脂质体复合物可能是肺部基因治疗的一种可行方法。