Issue 6, 2024

Nanomedicines for targeted pulmonary delivery: receptor-mediated strategy and alternatives

Abstract

Pulmonary drug delivery of nanomedicines is promising for the treatment of lung diseases; however, their lack of specificity required for targeted delivery limit their applications. Recently, a variety of pulmonary delivery targeting nanomedicines (PDTNs) has been developed for enhancing drug accumulation in lung lesions and reducing systemic side effects. Furthermore, with the increasing profound understanding of the specific microenvironment of different local lung diseases, multiple targeting strategies have been employed to promote drug delivery efficiency, which can be divided into the receptor-mediated strategy and alternatives. In this review, the current publication trend on PDTNs is analyzed and discussed, revealing that the research in this area has been attracting much attention. According to the different unique microenvironments of lung lesions, the reported PDTNs based on the receptor-mediated strategy for lung cancer, lung infection, lung inflammation and pulmonary fibrosis are listed and summarized. In addition, several other well-established strategies for the design of these PDTNs, such as charge regulation, mucus delivery enhancement, stimulus-responsive drug delivery and magnetic force-driven targeting, are introduced and discussed. Besides, bottlenecks in the development of PDTNs are discussed. Finally, we highlight the challenges and opportunities in the development of PDTNs. We hope that this review will provide an overview of the available PDTNs for guiding the treatment of lung diseases.

Graphical abstract: Nanomedicines for targeted pulmonary delivery: receptor-mediated strategy and alternatives

Article information

Article type
Minireview
Submitted
30 Okt. 2023
Accepted
18 Janv. 2024
First published
18 Janv. 2024

Nanoscale, 2024,16, 2820-2833

Nanomedicines for targeted pulmonary delivery: receptor-mediated strategy and alternatives

W. Wang, Z. Zhong, Z. Huang, T. N. Hiew, Y. Huang, C. Wu and X. Pan, Nanoscale, 2024, 16, 2820 DOI: 10.1039/D3NR05487J

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