Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/81040
Title: Synthesis and in vivo magnetic resonance imaging evaluation of biocompatible branched copolymer nanocontrast agents
Authors: Jackson, Alexander W.
Chandrasekharan, Prashant
Shi, Jian
Rannard, Steven P.
Liu, Quan
Yang, Chang-Tong
He, Tao
Keywords: MRI
RAFT polymerization
branched copolymer nanoparticles
gadolinium chelate
Issue Date: 2015
Source: Jackson, A. W., Chandrasekharan, P., Shi, J., Rannard, S. P., Liu, Q., Yang, C.-T., et al. (2015). Synthesis and in vivo magnetic resonance imaging evaluation of biocompatible branched copolymer nanocontrast agents. International Journal of Nanomedicine, 10, 5895-5907.
Series/Report no.: International Journal of Nanomedicine
Abstract: Branched copolymer nanoparticles (Dh =20–35 nm) possessing 1,4,7, 10-tetraazacyclododecane-N,N',N",N'"-tetraacetic acid macrocycles within their cores have been synthesized and applied as magnetic resonance imaging (MRI) nanosized contrast agents in vivo. These nanoparticles have been generated from novel functional monomers via reversible addition–fragmentation chain transfer polymerization. The process is very robust and synthetically straightforward. Chelation with gadolinium and preliminary in vivo experiments have demonstrated promising characteristics as MRI contrast agents with prolonged blood retention time, good biocompatibility, and an intravascular distribution. The ability of these nanoparticles to perfuse and passively target tumor cells through the enhanced permeability and retention effect is also demonstrated. These novel highly functional nanoparticle platforms have succinimidyl ester-activated benzoate functionalities within their corona, which make them suitable for future peptide conjugation and subsequent active cell-targeted MRI or the conjugation of fluorophores for bimodal imaging. We have also demonstrated that these branched copolymer nanoparticles are able to noncovalently encapsulate hydrophobic guest molecules, which could allow simultaneous bioimaging and drug delivery.
URI: https://hdl.handle.net/10356/81040
http://hdl.handle.net/10220/39076
ISSN: 1176-9114
DOI: 10.2147/IJN.S88764
Rights: © 2015 Jackson et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License. The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. Permissions beyond the scope of the License are administered by Dove Medical Press Limited. Information on how to request permission may be found at: http://www.dovepress.com/permissions.php
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:LKCMedicine Journal Articles
SCBE Journal Articles

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