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新型共喷雾干燥妥布霉素纳米粒-克拉霉素吸入粉系统治疗囊性纤维化患者肺部感染。

New co-spray-dried tobramycin nanoparticles-clarithromycin inhaled powder systems for lung infection therapy in cystic fibrosis patients.

机构信息

Laboratory of Pharmaceutics and Biopharmaceutics, Université Libre de Bruxelles (ULB), Brussels, Belgium.

Aptis, Liege, Belgium.

出版信息

J Pharm Sci. 2013 Jun;102(6):1836-1846. doi: 10.1002/jps.23525. Epub 2013 Apr 9.

Abstract

The aim of the study was to produce easily dispersible and porous agglomerates of tobramycin nanoparticles surrounded by a matrix composed of amorphous clarithromycin. Nanoparticles of tobramycin with a median particle size of about 400 nm were produced by high-pressure homogenisation. The results from the spray-dried powders showed that the presence of these nanoparticles enhanced powder dispersion during inhalation. Moreover, local drug deposition profiles were similar for the two antibiotics, allowing them to reach the target simultaneously. The dissolution-release profiles showed that tobramycin and clarithromycin might dissolve without any difficulties in the lung. The fine particle fraction increased from 35% and 31% for the physical blend for tobramycin and clarithromycin, respectively, to 63% and 62% for the spray-dried formulation containing nanoparticles. These new formulations, showing high lung deposition properties, even at sub-optimal inspiratory flow rates, represent a great possibility for advancing pulmonary drug administration and local therapy of lung infections.

摘要

本研究旨在制备妥布霉素纳米粒易于分散的多孔团聚体,其周围为无定形克拉霉素组成的基质。采用高压均质法制备妥布霉素纳米粒,平均粒径约为 400nm。喷雾干燥粉末的结果表明,这些纳米粒的存在增强了吸入过程中粉末的分散性。此外,两种抗生素的局部药物沉积分布相似,可使它们同时到达靶位。释放溶解曲线表明,妥布霉素和克拉霉素在肺部可能没有任何困难溶解。对于妥布霉素和克拉霉素的物理混合物,细颗粒分数分别从 35%和 31%增加到含有纳米粒的喷雾干燥制剂的 63%和 62%。这些新制剂显示出高的肺部沉积特性,即使在亚最佳吸气流速下,也为推进肺部药物输送和肺部感染的局部治疗提供了巨大的可能性。

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