Akosua B. Anane?Adjei
Effects of Polymer 3D Architecture, Size, and Chemistry on Biological Transport and Drug Delivery In Vitro and in Orthotopic Triple Negative Breast Cancer Models
Anane?Adjei, Akosua B.; Pearce, Amanda K.; Anane-Adjei, Akosua B.; Cavanagh, Robert J.; Monteiro, Patricia F.; Bennett, Thomas M.; Taresco, Vincenzo; Clarke, Phil A.; Ritchie, Alison A.; Alexander, Morgan R.; Grabowska, Anna M.; Alexander, Cameron
Authors
Amanda K. Pearce
Akosua B. Anane-Adjei
Dr ROBERT CAVANAGH ROBERT.CAVANAGH1@NOTTINGHAM.AC.UK
RESEARCH FELLOW
Patricia F. Monteiro
Thomas M. Bennett
Dr VINCENZO TARESCO VINCENZO.TARESCO@NOTTINGHAM.AC.UK
NOTTINGHAM RESEARCH FELLOW
Phil A. Clarke
Alison A. Ritchie
Professor MORGAN ALEXANDER MORGAN.ALEXANDER@NOTTINGHAM.AC.UK
PROFESSOR OF BIOMEDICAL SURFACES
Anna M. Grabowska
Professor CAMERON ALEXANDER CAMERON.ALEXANDER@NOTTINGHAM.AC.UK
PROFESSOR OF POLYMER THERAPEUTICS
Abstract
© 2020 Wiley-VCH GmbH The size, shape, and underlying chemistries of drug delivery particles are key parameters which govern their ultimate performance in vivo. Responsive particles are desirable for triggered drug delivery, achievable through architecture change and biodegradation to control in vivo fate. Here, polymeric materials are synthesized with linear, hyperbranched, star, and micellar-like architectures based on 2-hydroxypropyl methacrylamide (HPMA), and the effects of 3D architecture and redox-responsive biodegradation on biological transport are investigated. Variations in “stealth” behavior between the materials are quantified in vitro and in vivo, whereby reduction-responsive hyperbranched polymers most successfully avoid accumulation within the liver, and none of the materials target the spleen or lungs. Functionalization of selected architectures with doxorubicin (DOX) demonstrates enhanced efficacy over the free drug in 2D and 3D in vitro models, and enhanced efficacy in vivo in a highly aggressive orthotopic breast cancer model when dosed over schedules accounting for the biodistribution of the carriers. These data show it is possible to direct materials of the same chemistries into different cellular and physiological regions via modulation of their 3D architectures, and thus the work overall provides valuable new insight into how nanoparticle architecture and programmed degradation can be tailored to elicit specific biological responses for drug delivery.
Citation
Anane‐Adjei, A. B., Pearce, A. K., Anane-Adjei, A. B., Cavanagh, R. J., Monteiro, P. F., Bennett, T. M., Taresco, V., Clarke, P. A., Ritchie, A. A., Alexander, M. R., Grabowska, A. M., & Alexander, C. (2020). Effects of Polymer 3D Architecture, Size, and Chemistry on Biological Transport and Drug Delivery In Vitro and in Orthotopic Triple Negative Breast Cancer Models. Advanced Healthcare Materials, 9(22), Article 2000892. https://doi.org/10.1002/adhm.202000892
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 6, 2020 |
Online Publication Date | Oct 19, 2020 |
Publication Date | Nov 18, 2020 |
Deposit Date | Oct 7, 2020 |
Publicly Available Date | Oct 20, 2021 |
Journal | Advanced Healthcare Materials |
Print ISSN | 2192-2640 |
Electronic ISSN | 2192-2659 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 9 |
Issue | 22 |
Article Number | 2000892 |
DOI | https://doi.org/10.1002/adhm.202000892 |
Keywords | biomedical applications, bionanotechnology, drug delivery, polymeric materials, stimuli‐responsive materials |
Public URL | https://nottingham-repository.worktribe.com/output/4944205 |
Publisher URL | https://onlinelibrary.wiley.com/doi/full/10.1002/adhm.202000892 |
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adhm.202000892
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
Supporting information - Variable Architecture Polymers ESI
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