Please use this identifier to cite or link to this item: https://doi.org/10.1007/s12668-013-0087-4
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dc.titleWater-Soluble Upconversion Nanoparticles by Micellar Route
dc.contributor.authorNagarajan, S.
dc.contributor.authorRoullier, V.
dc.contributor.authorCortes, M.A.
dc.contributor.authorGnanasamandham, M.K.
dc.contributor.authorDif, A.
dc.contributor.authorGrasset, F.
dc.contributor.authorZhang, Y.
dc.contributor.authorMarchi, V.
dc.date.accessioned2014-06-17T09:47:27Z
dc.date.available2014-06-17T09:47:27Z
dc.date.issued2013-06
dc.identifier.citationNagarajan, S., Roullier, V., Cortes, M.A., Gnanasamandham, M.K., Dif, A., Grasset, F., Zhang, Y., Marchi, V. (2013-06). Water-Soluble Upconversion Nanoparticles by Micellar Route. BioNanoScience 3 (2) : 208-215. ScholarBank@NUS Repository. https://doi.org/10.1007/s12668-013-0087-4
dc.identifier.issn21911630
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/67348
dc.description.abstractUpconversion nanoparticles (UCNs) have been of interest in applications such as biological imaging and sensing because of properties like low autofluorescence and negligible photobleaching. In this paper, a micellar encapsulation route was worked upon to make hydrophilic UCNs that are compatible with biological systems and enable conjugation of biomolecules. Phospholipid micelles cannot be easily synthesized with chemical recognition groups of biological interest so synthetic amphiphiles with suitable functional head groups were used to encapsulate and solubilize the hydrophobic UCNs. The encapsulated nanoparticles were characterized using transmission electron microscopy, fluorescence spectroscopy, and dynamic light scattering. The micelle-encapsulated UCNs had an average diameter of 125 nm and the fluorescence emission at 540/660 nm of the bare UCNs did not show any shift after encapsulation. The cytotoxicity of the micelle-encapsulated UCNs was tested using lactose dehydrogenase/MTS (tetrazole salt) assays. The cell viability was estimated to be 80 % at the working concentration of the micelle-encapsulated UCNs. Finally, the micelle-encapsulated UCNs bearing Arg-Gly-Asp tripeptidic RGD surface functionalization were tested on cancer cells expressing integrins for specificity. The micelle-encapsulated UCNs were found to be suitable for cellular targeting and imaging. © 2013 Springer Science+Business Media New York.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s12668-013-0087-4
dc.sourceScopus
dc.subjectCancer
dc.subjectImaging
dc.subjectMicelle modification
dc.subjectNanoparticles
dc.subjectUpconversion
dc.typeArticle
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1007/s12668-013-0087-4
dc.description.sourcetitleBioNanoScience
dc.description.volume3
dc.description.issue2
dc.description.page208-215
dc.identifier.isiut000218931600012
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