Please use this identifier to cite or link to this item: https://doi.org/10.1155/2015/704817
DC FieldValue
dc.titleTargeted in vivo imaging of mouse hindlimb ischemia using fluorescent gelatin nanoparticles
dc.contributor.authorZhang, J
dc.contributor.authorWang, G
dc.contributor.authorMao, D
dc.contributor.authorHan, A
dc.contributor.authorXiao, N
dc.contributor.authorQi, X
dc.contributor.authorDing, D
dc.contributor.authorKong, D
dc.date.accessioned2020-10-27T05:50:30Z
dc.date.available2020-10-27T05:50:30Z
dc.date.issued2015
dc.identifier.citationZhang, J, Wang, G, Mao, D, Han, A, Xiao, N, Qi, X, Ding, D, Kong, D (2015). Targeted in vivo imaging of mouse hindlimb ischemia using fluorescent gelatin nanoparticles. Journal of Nanomaterials 2015 : 704817. ScholarBank@NUS Repository. https://doi.org/10.1155/2015/704817
dc.identifier.issn16874110
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/180951
dc.description.abstractCritical limb ischemia is one of the most advanced forms of peripheral artery disease, which seriously threat the human health and even cause amputation. In this study, we developed a fluorescent gelatin nanoparticle (FGNP) by covalent conjugation of the nanoparticles with two fluorogens, Cy7 and rhodamine B. The FGNPs have a volume average hydrodynamic diameter of about 168 nm, which also show low cytotoxicity against NIH/3T3 normal cells. The in vivo ischemia bioimaging studies in live mice and in ischemic limb slices demonstrate that the FGNPs can be preferentially accumulated to the ischemic site, which can thus serve as a safe and effective probe for targeted visualization of ischemia in the limb. © 2015 Ju Zhang et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectFluorescence
dc.subjectHealth risks
dc.subjectMammals
dc.subjectBio-imaging
dc.subjectGelatin nanoparticles
dc.subjectHuman health
dc.subjectHydrodynamic diameter
dc.subjectIn-Vivo imaging
dc.subjectIschemic limbs
dc.subjectLow cytotoxicities
dc.subjectPeripheral artery disease
dc.subjectNanoparticles
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1155/2015/704817
dc.description.sourcetitleJournal of Nanomaterials
dc.description.volume2015
dc.description.page704817
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