Department of Biopharmaceutics and Pharmaceutical Technology, Saarland University, Saarbrücken, Germany; Institut Galien Paris-Sud, CNRS UMR 8612, LabEx, LERMIT, University Paris-Sud, Paris, France.
Department of Biopharmaceutics and Pharmaceutical Technology, Saarland University, Saarbrücken, Germany.
Lancet Respir Med. 2013 Jul;1(5):402-13. doi: 10.1016/S2213-2600(13)70072-9. Epub 2013 Jun 4.
Research in pulmonary drug delivery has focused mainly on new particle or device technologies to improve the aerosol generation and pulmonary deposition of inhaled drugs. Although substantial progress has been made in this respect, no significant advances have been made that would lead pulmonary drug delivery beyond the treatment of some respiratory diseases. One main reason for this stagnation is the still very scarce knowledge about the fate of inhaled drug or carrier particles after deposition in the lungs. Improvement of the aerosol component alone is no longer sufficient for therapeutic success of inhalation drugs; a paradigm shift is needed, with an increased focus on the pulmonary barriers to drug delivery. In this Review, we discuss some pathophysiological disorders that could benefit from better control of the processes after aerosol deposition, and pharmaceutical approaches to achieve improved absorption across the alveolar epithelium, prolonged pulmonary clearance, and targeted delivery to specific cells or tissues.
肺部药物输送的研究主要集中在新的颗粒或设备技术上,以改善吸入药物的气溶胶生成和肺部沉积。尽管在这方面已经取得了实质性的进展,但并没有取得任何重大进展,可以使肺部药物输送超越治疗一些呼吸道疾病的范围。造成这种停滞不前的一个主要原因是,人们对吸入药物或载体颗粒在肺部沉积后的命运仍然知之甚少。仅改善气溶胶成分对于吸入药物的治疗成功已不再足够;需要进行范式转变,更加关注药物输送的肺部屏障。在这篇综述中,我们讨论了一些病理生理紊乱,可以从更好地控制气溶胶沉积后的过程中受益,以及药物学方法可以改善肺泡上皮的吸收、延长肺部清除和靶向特定细胞或组织的输送。