2016
DOI: 10.1039/c5tb02348c
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Highly luminescent and photostable near-infrared fluorescent polymer dots for long-term tumor cell tracking in vivo

Abstract: Near-infrared-emitting polymer dots were prepared and used as fluorescent nanoprobes for in vitro HeLa cell labeling and in vivo long-term HeLa tumor tracking. The prepared NIR polymer dots showed no obvious effect on the tumor growth, and exhibited durable brightness, long-term photostability and high sensitivity.

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Cited by 32 publications
(28 citation statements)
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“…28,30,31,34 Xiong et al developed similar MEH-PPV/NIR775-based CPNs as Rao’s group that could be used for tumor cell imaging in vitro and in vivo. 33,35 …”
Section: Nir-emissive Pdots and Cpnsmentioning
confidence: 99%
“…28,30,31,34 Xiong et al developed similar MEH-PPV/NIR775-based CPNs as Rao’s group that could be used for tumor cell imaging in vitro and in vivo. 33,35 …”
Section: Nir-emissive Pdots and Cpnsmentioning
confidence: 99%
“…Polyfluorene‐based π‐conjugated polymer nanoparticles with ultrabright fluorescence have been successfully applied for cell labeling and tracking, bioorthogonal tagging, and in vivo tumor targeting . Accordingly, we choose polyfluorene polymers to modify their side chains with oxetane groups.…”
Section: Figurementioning
confidence: 99%
“…Polyfluorene-based p-conjugated polymer nanoparticles with ultrabright fluorescenceh ave been successfully applied for cell labeling and tracking, [18,19] bioorthogonal tagging, [20] and in vivo tumort argeting. [21,22] Accordingly,w echoose polyfluorene polymers to modify their side chains with oxetane groups.M oreover,P EG has been approved by the U.S. Food and Drug Administration for clinicala pplicationsi nv arious biomedicala reas owing to its non-toxicity and non-immunogenicity.P EGylated nanoparticles exhibited important characteristics for in vivo applications such as the increased blood circulation lifetimea sw ell as the decreased clearance by the body's reticuloendothelial system.…”
mentioning
confidence: 99%
“…[10,[41][42][43][44] By taking advantage of the facile surface functionalization of Pdots, NIR Pdots conjugated with biomolecules (i.e., antibody and folic acid) can bind to specific cell surfaces or tissues. [10,[41][42][43][44] By taking advantage of the facile surface functionalization of Pdots, NIR Pdots conjugated with biomolecules (i.e., antibody and folic acid) can bind to specific cell surfaces or tissues.…”
Section: In Vitro and In Vivo Bioimaging With Nir Pdotsmentioning
confidence: 99%