Targeting Inhaled Therapy beyond the Lungs

被引:30
作者
Mortensen, Ninell P. [1 ]
Hickey, Anthony J. [2 ]
机构
[1] RTI Int, Syst & Translat Sci, Res Triangle Pk, NC 27709 USA
[2] RTI Int, Technol Ind & Environm Discovery Sci Technol Grp, Res Triangle Pk, NC 27709 USA
关键词
Aerosolization; Drug delivery; Drug release; Dissolution rate; Inhaled therapy; Systemic delivery; PROTEIN CORONA; ALVEOLAR MACROPHAGES; PULMONARY EPITHELIUM; DRUG-DELIVERY; PHASE-I; SIZE; METABOLISM; ABSORPTION; INSULIN; AIRWAYS;
D O I
10.1159/000367852
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Pulmonary disease has been the primary target of inhaled therapeutics for over 50 years. During that period, increasing interest has arisen in the use of this route of administration to gain access to the systemic circulation for the treatment of a number of diseases beyond the airways. In order to effectively employ this route, the barriers to transport from the lungs following deposition of aerosols must be considered, including the nature of the disease (whether proximal, as in pulmonary hypertension, or distal, as in diabetes). Delivery to the systemic circulation begins with the efficiency of aerosol generation and subsequent deposition in the airways and proceeds to the influence of mechanisms of clearance, including absorption, metabolism, and mucociliary and cell-mediated transport, on the residence time of the drugs in the lungs. The nature of the drug (small or large molecules/low or high molecular weight), susceptibility to degradation and general physicochemical properties play a role in the chemistry of its formulation, physics of aerosol delivery and biology of disposition. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:353 / 364
页数:12
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