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合理的粒子设计克服肺部障碍治疗阻塞性肺疾病。

Rational particle design to overcome pulmonary barriers for obstructive lung diseases therapy.

机构信息

State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macau.

Department of Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region.

出版信息

J Control Release. 2019 Nov 28;314:48-61. doi: 10.1016/j.jconrel.2019.10.035. Epub 2019 Oct 20.

Abstract

Pulmonary delivery of active drugs has been applied for the treatment of obstructive lung diseases, including asthma, chronic obstructive pulmonary disease and cystic fibrosis, for several decades and has achieved progress in symptom management by bronchodilator inhalation. However, substantial progress in anti-inflammation, prevention of airway remodeling and disease progression is limited, since the majority of the formulation strategies focus only on particle deposition, which is insufficient for pulmonary delivery of the drugs. The lack of knowledge on lung absorption barriers in obstructive lung diseases and on pathogenesis impedes the development of functional formulations by rational design. In this review, we describe the physiological structure and biological functions of the barriers in various regions of the lung, review the pathogenesis and functional changes of barriers in obstructive lung diseases, and examine the interaction of these barriers with particles to influence drug delivery efficiency. Subsequently, we review rational particle design for overcoming lung barriers based on excipients selection, particle size and surface properties, release properties and targeting ability. Additionally, useful particle fabrication strategies and commonly used drug carriers for pulmonary delivery in obstructive lung diseases are proposed in this article.

摘要

几十年来,主动药物的肺部给药一直被用于治疗阻塞性肺部疾病,包括哮喘、慢性阻塞性肺疾病和囊性纤维化,通过支气管扩张剂吸入在症状管理方面取得了进展。然而,在抗炎、预防气道重塑和疾病进展方面的进展有限,因为大多数制剂策略仅关注颗粒沉积,而这对于药物的肺部给药是不够的。由于缺乏对阻塞性肺部疾病中肺吸收屏障和发病机制的了解,阻碍了通过合理设计来开发功能性制剂。在这篇综述中,我们描述了肺部各区域吸收屏障的生理结构和生物学功能,回顾了阻塞性肺部疾病中屏障的发病机制和功能变化,并研究了这些屏障与颗粒的相互作用对药物输送效率的影响。随后,我们根据辅料选择、粒径和表面特性、释放特性和靶向能力,综述了克服肺部屏障的合理颗粒设计。此外,本文还提出了阻塞性肺部疾病中肺部给药有用的颗粒制造策略和常用药物载体。

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