Neazar E. Baghdadi
Multivalency in CXCR4 chemokine receptor targeted iron oxide nanoparticles
Baghdadi, Neazar E.; Burke, Benjamin P.; Alresheedi, Tahani; Nigam, Shubhanchi; Saeed, Abdu; Almutairi, Farooq; Domarkas, Juozas; Khan, Abid; Archibald, Stephen J.
Authors
Benjamin P. Burke
Tahani Alresheedi
Shubhanchi Nigam
Abdu Saeed
Farooq Almutairi
Juozas Domarkas
Abid Khan
Professor Steve Archibald S.J.Archibald@hull.ac.uk
Professor in Molecular Imaging
Abstract
The CXCR4 chemokine receptor is an important biomolecular target in cancer diagnostics and therapeutics. In a new multivalent approach, iron oxide nanoparticles were conjugated with multiple binding units of a low affinity azamacrocylic CXCR4 antagonist. The silica coated nanostructure has good suspension stability, a mode size of 72 nm and high affinity for CXCR4, showing >98% inhibition of anti-CXCR4 mAb binding in a receptor binding competition assay on Jurkat cells.
Citation
Baghdadi, N. E., Burke, B. P., Alresheedi, T., Nigam, S., Saeed, A., Almutairi, F., Domarkas, J., Khan, A., & Archibald, S. J. (2021). Multivalency in CXCR4 chemokine receptor targeted iron oxide nanoparticles. Dalton Transactions : an international journal of inorganic chemistry, 50(5), 1599-1603. https://doi.org/10.1039/d0dt02626c
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 6, 2021 |
Online Publication Date | Jan 19, 2021 |
Publication Date | Feb 7, 2021 |
Deposit Date | Jan 19, 2021 |
Publicly Available Date | Jan 20, 2021 |
Journal | Dalton Transactions |
Print ISSN | 1477-9226 |
Electronic ISSN | 1477-9234 |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Volume | 50 |
Issue | 5 |
Pages | 1599-1603 |
DOI | https://doi.org/10.1039/d0dt02626c |
Keywords | Inorganic Chemistry |
Public URL | https://hull-repository.worktribe.com/output/3697058 |
Publisher URL | https://pubs.rsc.org/en/content/articlelanding/2021/dt/d0dt02626c#!divAbstract |
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Publisher Licence URL
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Copyright Statement
This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
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