2018
DOI: 10.1186/s12951-018-0369-7
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Improving cytocompatibility of CdTe quantum dots by Schiff-base-coordinated lanthanides surface doping

Abstract: BackgroundSuitable fluorophores are the core of fluorescence imaging. Among the most exciting, yet controversial, labels are quantum dots (QDs) with their unique optical and chemical properties, but also considerable toxicity. This hinders QDs applicability in living systems. Surface chemistry has a profound impact on biological behavior of QDs. This study describes a two-step synthesis of QDs formed by CdTe core doped with Schiff base ligand for lanthanides [Ln (Yb3+, Tb3+ and Gd3+)] as novel cytocompatible f… Show more

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Cited by 11 publications
(7 citation statements)
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References 49 publications
(55 reference statements)
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“…Among cell surface proteins, hNET is one of the best candidates for high-resolution homology modeling due to the recent elucidation of homolog proteins dDAT and hSERT [18]. Nanomedicine-based approaches are under development for targeting hNET via antibodies [22] or non-radioactive MIBG-linked ligands [23], and provide rational less-invasive alternative strategy to radiotherapy. The present work explores a better method of targeting hNET via non-toxic homing peptides.…”
Section: Discussionmentioning
confidence: 99%
“…Among cell surface proteins, hNET is one of the best candidates for high-resolution homology modeling due to the recent elucidation of homolog proteins dDAT and hSERT [18]. Nanomedicine-based approaches are under development for targeting hNET via antibodies [22] or non-radioactive MIBG-linked ligands [23], and provide rational less-invasive alternative strategy to radiotherapy. The present work explores a better method of targeting hNET via non-toxic homing peptides.…”
Section: Discussionmentioning
confidence: 99%
“…Haemocompatibility of TNTs was evaluated on commercially available human red blood cells (RBCs) (Zen-Bio, Durham, NC, USA) by adopting the protocol published in our previous study [47]. In addition, formation of protein coronas and activation of third complement component (C3) due to TNTs exposure in vitro were studied according to [48].…”
Section: Evaluation Of Interactions Between Tnts and Blood Componentsmentioning
confidence: 99%
“…The relative quantity of the metallothioneins (MT1A, MT2A, MT3) were normalized against the reference gene, glyceraldehyde 3-phosphate dehydrogenase (GAPDH). Fold change differences were determined using the 2-ΔΔCT method compared with untreated cells (Livak and Schmittgen, 2001;Buchtelova et al, 2018). Sequences of all primers used in qPCR analyses are listed in Tab.…”
Section: Isolation Rna and Quantitative Real-time Polymerase Chain Rementioning
confidence: 99%
“…After washing, membranes were incubated with antimouse horseradish peroxidase (HRP)-labelled secondary antibody (1:5,000, Dako, Santa Clara, CA, USA) for GAPDH and MT1, anti-rabbit HRPlabelled secondary antibody (1:5,000) for MT3 or streptavidin-conjugated HRP (1:35,000 in PBS-T) for 1 h at 20 ℃. Signals were developed using Clarity Western ECL Blotting Substrate (Bio-Rad, Hercules, CA, USA) and blots were visualized using Azure c600 imager (Azure Biosystems, Dublin, CA, USA) (Buchtelova et al, 2018).…”
Section: Western Blottingmentioning
confidence: 99%