纳米医学
纳米技术
背景(考古学)
食品药品监督管理局
工程伦理学
代理(哲学)
医学
风险分析(工程)
政治学
材料科学
工程类
纳米颗粒
社会学
古生物学
社会科学
生物
作者
Thomas J. Anchordoquy,Natalie Artzi,Irina V. Balyasnikova,Yechezkel Barenholz,Ninh M. La‐Beck,Jacob S. Brenner,Warren C. W. Chan,Paolo Decuzzi,Agata A. Exner,Alberto Gabizón,Biana Godin,Samuel K. Lai,Twan Lammers,Michael J. Mitchell,S. Moein Moghimi,Vladimir R. Muzykantov,Dan Peer,Juliane Nguyen,Rachela Popovtzer,Madison H Ricco
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-05-20
卷期号:18 (22): 13983-13999
被引量:64
标识
DOI:10.1021/acsnano.4c00182
摘要
In recent years, steady progress has been made in synthesizing and characterizing engineered nanoparticles, resulting in several approved drugs and multiple promising candidates in clinical trials. Regulatory agencies such as the Food and Drug Administration and the European Medicines Agency released important guidance documents facilitating nanoparticle-based drug product development, particularly in the context of liposomes and lipid-based carriers. Even with the progress achieved, it is clear that many barriers must still be overcome to accelerate translation into the clinic. At the recent conference workshop "Mechanisms and Barriers in Nanomedicine" in May 2023 in Colorado, U.S.A., leading experts discussed the formulation, physiological, immunological, regulatory, clinical, and educational barriers. This position paper invites open, unrestricted, nonproprietary discussion among senior faculty, young investigators, and students to trigger ideas and concepts to move the field forward.
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