2010
DOI: 10.1016/j.biomaterials.2010.01.114
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Synthesis, biocompatibility and cell labeling of l-arginine-functional β-cyclodextrin-modified quantum dot probes

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Cited by 61 publications
(27 citation statements)
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“…4 A significant amount of effort has been expended on the improvement of the intracellular delivery and bioimaging of QDs with reduced toxicity through conjugation of QDs with various molecules including biomacromolecules, [5][6][7][8] biocompatible polymer molecules, 9 and peptides. 10 Recently, QDs have been incorporated into various drug delivery systems that can be used not only as molecular imaging agents but also for therapy application.…”
mentioning
confidence: 99%
“…4 A significant amount of effort has been expended on the improvement of the intracellular delivery and bioimaging of QDs with reduced toxicity through conjugation of QDs with various molecules including biomacromolecules, [5][6][7][8] biocompatible polymer molecules, 9 and peptides. 10 Recently, QDs have been incorporated into various drug delivery systems that can be used not only as molecular imaging agents but also for therapy application.…”
mentioning
confidence: 99%
“…The surface modification of QDs with CDs has been shown to reduce cytotoxicity and enhance biocompatibility . This manipulation not only preserves the imaging capabilities of the nanocarrier but also potentially affords the nanocarrier additional therapeutic functionalities such as drug loading.…”
Section: Resultsmentioning
confidence: 99%
“…Meanwhile, a polymer film (P-β-CD-L-Arg) was formed on the surface of the CNTs@GNRs/GCE through the combination of L-Arg with each other by intermolecular condensation between -NH 2 and -COOH (Liu et al, 1999;Zhao et al, 2010).…”
Section: Characterization Of P-β-cd-l-arg/cnts@gnrsmentioning
confidence: 99%