Multivalency in CXCR4 chemokine receptor targeted iron oxide nanoparticles

Neazar E Baghdadi; Benjamin P Burke; Tahani Alresheedi; Shubhanchi Nigam; Abdu Saeed; Farooq Almutairi; Juozas Domarkas; Abid Khan; Stephen J Archibald

doi:10.1039/d0dt02626c

Multivalency in CXCR4 chemokine receptor targeted iron oxide nanoparticles

Neazar E Baghdadi, Benjamin P Burke, Tahani Alresheedi, Shubhanchi Nigam, Abdu Saeed, Farooq Almutairi, Juozas Domarkas, Abid Khan, Stephen J Archibald

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Research output: Contribution to journal › Article › peer-review

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.

Original language	English
Journal	Dalton Transactions
DOIs	https://doi.org/10.1039/d0dt02626c
Publication status	Published - 27 Jan 2021

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10.1039/d0dt02626c

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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.",

author = "Baghdadi, {Neazar E} and Burke, {Benjamin P} and Tahani Alresheedi and Shubhanchi Nigam and Abdu Saeed and Farooq Almutairi and Juozas Domarkas and Abid Khan and Archibald, {Stephen J}",

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language = "English",

journal = "Dalton Transactions",

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T1 - Multivalency in CXCR4 chemokine receptor targeted iron oxide nanoparticles

AU - Baghdadi, Neazar E

AU - Burke, Benjamin P

AU - Alresheedi, Tahani

AU - Nigam, Shubhanchi

AU - Saeed, Abdu

AU - Almutairi, Farooq

AU - Domarkas, Juozas

AU - Khan, Abid

AU - Archibald, Stephen J

PY - 2021/1/27

Y1 - 2021/1/27

N2 - 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.

AB - 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.

U2 - 10.1039/d0dt02626c

DO - 10.1039/d0dt02626c

M3 - Article

C2 - 33502425

JO - Dalton Transactions

JF - Dalton Transactions

SN - 1477-9226

ER -

Multivalency in CXCR4 chemokine receptor targeted iron oxide nanoparticles

Abstract

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