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Metal-Phenolic-Mediated Assembly of Functional Small Molecules into Nanoparticles: Assembly and Bioapplications.
Chen, Jingqu; Cortez-Jugo, Christina; Kim, Chan-Jin; Lin, Zhixing; Wang, Tianzheng; De Rose, Robert; Xu, Wanjun; Wang, Zhaoran; Gu, Yuang; Caruso, Frank.
Afiliação
  • Chen J; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Cortez-Jugo C; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Kim CJ; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Lin Z; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Wang T; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • De Rose R; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Xu W; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Wang Z; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Gu Y; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
  • Caruso F; Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
Angew Chem Int Ed Engl ; 63(12): e202319583, 2024 Mar 18.
Article em En | MEDLINE | ID: mdl-38282100
ABSTRACT
Small molecules, including therapeutic drugs and tracer molecules, play a vital role in biological processing, disease treatment and diagnosis, and have inspired various nanobiotechnology approaches to realize their biological function, particularly in drug delivery. Desirable features of a delivery system for functional small molecules (FSMs) include high biocompatibility, high loading capacity, and simple manufacturing processes, without the need for chemical modification of the FSM itself. Herein, we report a simple and versatile approach, based on metal-phenolic-mediated assembly, for assembling FSMs into nanoparticles (i.e., FSM-MPN NPs) under aqueous and ambient conditions. We demonstrate loading of anticancer drugs, latency reversal agents, and fluorophores at up to ~80 % that is mostly facilitated by π and hydrophobic interactions between the FSM and nanoparticle components. Secondary nanoparticle engineering involving coating with a polyphenol-antibody thin film or sequential co-loading of multiple FSMs enables cancer cell targeting and combination delivery, respectively. Incorporating fluorophores into FSM-MPN NPs enables the visualization of biodistribution at different time points, revealing that most of these NPs are retained in the kidney and heart 24 h post intravenous administration. This work provides a viable pathway for the rational design of small molecule nanoparticle delivery platforms for diverse biological applications.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nanopartículas Idioma: En Ano de publicação: 2024 Tipo de documento: Article