betadex and cadmium-telluride

Fluorescent CdTe nanocrystals (NCs) capped with beta-cyclodextrin (β-CD) are successfully synthesized by host-guest supramolecular assembly of the hydrophobic alkyl chains of N-acetyl-l-cysteine (NAC) on the surface of CdTe NCs and eco-friendly β-CD via the promising simple hydrothermal method in our experiments. The as-prepared NCs display better stability and lower toxicity compared with traditional those only capped with NAC. Specially, cytotoxicity experiments to human umbilical vein endothelial cells in vitro and zebrafish embryo toxicological tests in vivo are performed to determine the toxicity of CdTe NCs. For their practical applications, the promising red-luminescent NCs are employed as stable and low poison red phosphors to fabricate white light-emitting diodes (WLEDs) with remarkable color-rendering index (CRI) being 91.6. This research offers significance for solving the difficulty in toxicity and instability of heavy metal based NCs, which has potential applications in future optoelectronic devices and biomarkers.

Topics: Animals; beta-Cyclodextrins; Cadmium Compounds; Cell Survival; Embryo, Nonmammalian; Human Umbilical Vein Endothelial Cells; Humans; Lethal Dose 50; Luminescent Agents; Nanoparticles; Photochemistry; Surface Properties; Tellurium; Zebrafish

Cadmium telluride quantum dots (CdTe QDs) have been proposed to induce oxidative stress, which plays a crucial role in CdTe QDs-mediated mitochondrial-dependent apoptosis in human umbilical vein endothelial cells (HUVECs). However, the direct interactions of CdTe QDs with HUVECs and their potential impairment of other organelles like endoplasmic reticulum (ER) in HUVECs are poorly understood. In this study, we reported that the negatively charged CdTe QDs (-21.63±0.91 mV), with good dispersity and fluorescence stability, were rapidly internalized via endocytosis by HUVECs, as the notable internalization could be inhibited up to 95.52% by energy depletion (NaN3/deoxyglucose or low temperature). The endocytosis inhibitors (methyl-β-cyclodextrin, genistein, sucrose, chlorpromazine, and colchicine) dramatically decreased the uptake of CdTe QDs by HUVECs, suggesting that both caveolae/raft- and clathrin-mediated endocytosis were involved in the endothelial uptake of CdTe QDs. Using immunocytochemistry, a striking overlap of the internalized CdTe QDs and ER marker was observed, which indicates that QDs may be transported to ER. The CdTe QDs also caused remarkable ER stress responses in HUVECs, confirmed by significant dilatation of ER cisternae, upregulation of ER stress markers GRP78/GRP94, and activation of protein kinase RNA-like ER kinase-eIF2α-activating transcription factor 4 pathway (including phosphorylation of both protein kinase RNA-like ER kinase and eIF2α and elevated level of activating transcription factor 4). CdTe QDs further promoted an increased C/EBP homologous protein expression, phosphorylation of c-JUN NH2-terminal kinase, and cleavage of ER-resident caspase-4, while the specific inhibitor (SP600125, Z-LEVD-fmk, or salubrinal) significantly attenuated QDs-triggered apoptosis, indicating that all three ER stress-mediated apoptosis pathways were activated and the direct participation of ER in the CdTe QDs-caused apoptotic cell death in HUVECs. Our findings provide important new insights into QDs toxicity and reveal potential cardiovascular risks for the future applications of QDs.

Topics: Apoptosis; beta-Cyclodextrins; Cadmium Compounds; Colchicine; eIF-2 Kinase; Endocytosis; Endoplasmic Reticulum Chaperone BiP; Endoplasmic Reticulum Stress; Fluorescence; Genistein; Heat-Shock Proteins; Human Umbilical Vein Endothelial Cells; Humans; Quantum Dots; Tellurium; Thiomalates

Novel, water-soluble CdTe quantum dots (QDs) capped with β-cyclodextrin (β-CD) and ~ 4.0 nm in diameter were synthesized in aqueous solution, and characterized using transmission electron microscopy (TEM). A fluorescence-sensing system based on the photoinduced electron transfer (PET) of (mono-6-thio-β-CD)-CdTe QDs was then designed to measure the interaction of phenothiazine dyes [methylene blue (MB) and methylene green (MG)] with herring sperm DNA (hsDNA). This fluorescence-sensing system was based on a fluorescence "OFF-ON" mode. First, MB/MG adsorbed on the surface of (mono-6-thio-β-CD)-CdTe QDs effectively quenches the fluorescence of (mono-6-thio-β-CD)-CdTe QDs through PET. Then, addition of hsDNA restores the fluorescence intensity of (mono-6-thio-β-CD)-CdTe QDs, because hsDNA can bind with MB/MG and remove it from the as-prepared (mono-6-thio-β-CD)-CdTe QDs. In addition, detailed reaction mechanisms of the (mono-6-thio-β-CD)-CdTe QDs-MB/MG-hsDNA solution system were studied using optical methods, by comparison with the TGA-CdTe QDs-MB/MG-hsDNA solution system.

Topics: Animals; beta-Cyclodextrins; Cadmium Compounds; DNA; Fishes; Male; Methylene Blue; Molecular Structure; Quantum Dots; Spectrometry, Fluorescence; Spermatozoa; Tellurium

An alkaline phosphatase activity detection system was constructed based on the different quenching effect of the enzyme substrate and product on the β-CD-functionalized CdTe QDs.

Topics: Alkaline Phosphatase; Animals; beta-Cyclodextrins; Biosensing Techniques; Cadmium Compounds; Humans; Quantum Dots; Sensitivity and Specificity; Spectrometry, Fluorescence; Tellurium