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Multimodality PET/MRI agents targeted to activated macrophages

Tu, Chuqiao and Ng, Thomas S. C. and Jacobs, Russell E. and Louie, Angelique Y. (2014) Multimodality PET/MRI agents targeted to activated macrophages. Journal of Biological Inorganic Chemistry, 19 (2). pp. 247-258. ISSN 0949-8257. PMCID PMC3946888. https://resolver.caltech.edu/CaltechAUTHORS:20140304-071658174

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Abstract

The recent emergence of multimodality imaging, particularly the combination of PET and MRI, has led to excitement over the prospect of improving detection of disease. Iron oxide nanoparticles have become a popular platform for the fabrication of PET/MRI probes owing to their advantages of high MRI detection sensitivity, biocompatibility, and biodegradability. In this article, we report the synthesis of dextran-coated iron oxide nanoparticles (DIO) labeled with the positron emitter ^(64)Cu to generate a PET/MRI probe, and modified with maleic anhydride to increase the negative surface charge. The modified nanoparticulate PET/MRI probe (MDIO-^(64)Cu-DOTA) bears repetitive anionic charges on the surface that facilitate recognition by scavenger receptor type A (SR-A), a ligand receptor found on activated macrophages but not on normal vessel walls. MDIO-^(64)Cu-DOTA has an average iron oxide core size of 7–8 nm, an average hydrodynamic diameter of 62.7 nm, an r_1 relaxivity of 16.8 mM^(−1) s^(−1), and an r_2 relaxivity of 83.9 mM^(−1) s^(−1) (37 °C, 1.4 T). Cell studies confirmed that the probe was nontoxic and was specifically taken up by macrophages via SR-A. In comparison with the nonmodified analog, the accumulation of MDIO in macrophages was substantially improved. These characteristics demonstrate the promise of MDIO-^(64)Cu-DOTA for identification of vulnerable atherosclerotic plaques via the targeting of macrophages.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1007/s00775-013-1054-9DOIArticle
http://link.springer.com/article/10.1007/s00775-013-1054-9PublisherArticle
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946888/PubMed CentralArticle
http://rdcu.be/twkbPublisherFree ReadCube access
ORCID:
AuthorORCID
Jacobs, Russell E.0000-0002-1382-8486
Additional Information:© 2013 SBIC. Received: 1 July 2013. Accepted: 8 October 2013. Published online: 29 October 2013. Responsible Editor: Valerie C. Pierre. The authors wish to acknowledge the National Institutes of Health (EB008576-01 and EB000993), the Center for Molecular and Genomic Imaging at the University of California, Davis (U24 CA 110804), and the NMR award of the University of California, Davis for support of this work. We thank Jeongchan Park, Jai Woong Seo, and Ray Wong for help with TEM imaging, zeta potential measurements, and IR spectroscopy, respectively.
Funders:
Funding AgencyGrant Number
NIHEB008576-01
NIHEB000993
NIHU24 CA 110804
University of California, DavisUNSPECIFIED
Subject Keywords:Iron, Nanoparticles, MRI contrast, agents, Macrophages, Inflammation
Issue or Number:2
PubMed Central ID:PMC3946888
Record Number:CaltechAUTHORS:20140304-071658174
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20140304-071658174
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:44116
Collection:CaltechAUTHORS
Deposited By: Ruth Sustaita
Deposited On:04 Mar 2014 16:09
Last Modified:03 Oct 2019 06:14

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