Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/107648
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorLiao, Jen_US
dc.creatorZhou, Len_US
dc.creatorWu, Yen_US
dc.creatorQian, Zen_US
dc.creatorLi, Pen_US
dc.date.accessioned2024-07-09T03:53:40Z-
dc.date.available2024-07-09T03:53:40Z-
dc.identifier.urihttp://hdl.handle.net/10397/107648-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© 2024 The Author(s). Published by the Royal Society of Chemistryen_US
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/).en_US
dc.rightsThe following publication Liao, J., Zhou, L., Wu, Y., Qian, Z., & Li, P. (2024). Enhancing MRI through high loading of superparamagnetic nanogels with high sensitivity to the tumor environment. Nanoscale Advances, 6, 3367-3376 is available at https://doi.org/10.1039/D4NA00014E.en_US
dc.titleEnhancing MRI through high loading of superparamagnetic nanogels with high sensitivity to the tumor environmenten_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage3367en_US
dc.identifier.epage3376en_US
dc.identifier.volume6en_US
dc.identifier.issue13en_US
dc.identifier.doi10.1039/d4na00014een_US
dcterms.abstractTumors pose a significant threat to human health, and their occurrence and fatality rates are on the rise each year. Accurate tumor diagnosis is crucial in preventing untimely treatment and late-stage metastasis, thereby reducing mortality. To address this, we have developed a novel type of hybrid nanogel called γ-Fe2O3@PNIPAM/PAm/CTS, which contains iron oxide nanoparticles and poly(N-isopropyl acrylamide)/polyacrylamide/chitosan. The rationale for this study relies on the concept that thermosensitive PNIPAM has the ability to contract when exposed to elevated temperature conditions found within tumors. This contraction leads to a dense clustering of the high-loading γ-Fe2O3 nanoparticles within the nanogel, thus greatly enhancing the capabilities of MRI. Additionally, the amino groups in chitosan on the particle surface can be converted into ammonium salts under mildly acidic conditions, allowing for an increase in the charge of the nanogel specifically at the slightly acidic tumor site. Consequently, it promotes the phagocytosis of tumor cells and effectively enhances the accumulation and retention of nanogels at the tumor site. The synthesis of the hybrid nanogels involves a surfactant-free emulsion copolymerization process, where vinyl-modified γ-Fe2O3 superparamagnetic nanoparticles are copolymerized with the monomers in the presence of chitosan. We have optimized various reaction parameters to achieve a high loading content of the superparamagnetic nanoparticles, reaching up to 60%. The achieved r2 value of 517.74 mM−1 S−1 significantly surpasses that of the clinical imaging contrast agent Resovist (approximately 151 mM−1 S−1). To assess the performance of these magnetic nanogels, we conducted experiments using Cal27 oral tumors and 4T1 breast tumors in animal models. The nanogels exhibited temperature- and pH-sensitivity, enabling magnetic targeting and enhancing diagnosis through MRI. The results demonstrated the potential of these hybrid nanogels as contrast agents for magnetic targeting in biomedical applications.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNanoscale advances, 7 July 2024, v. 6, no. 13, p. 3367-3376en_US
dcterms.isPartOfNanoscale advancesen_US
dcterms.issued2024-07-07-
dc.identifier.scopus2-s2.0-85193720880-
dc.identifier.eissn2516-0230en_US
dc.description.validate202407 bcwh-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Others-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextPolyU Lo Ka Chung Centre for Natural Anti-Cancer Drug Development; Chengdu International Science and Technology Cooperation Project; National Natural Science Foundation of China, NSFC; National Natural Science Foundation of China, NSFCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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