A fluorescence resonance energy transfer pair consisting of a colloidal quantum dot donor and multiple organic fluorophores as acceptors is reported and the photophysics of the system is characterized. Most nanoparticle-based biosensors reported so far use the detection of specific changes of the donor/acceptor distance under the influence of analyte binding. Our nanoparticle design on the other hand leads to sensors that detect spectral changes of the acceptor (under the influence of analyte binding) at fixed donor/acceptor distance by the introduction of the acceptor into the polymer coating. This approach allows for short acceptor-donor separation and thus for high-energy transfer efficiencies. Advantageously, the binding properties of the hydrophilic polymer coating further allows for addition of poly(ethylene glycol) shells for improved colloidal stability.
Water-soluble luminescent CdSe quantum dots surface-modified with 2-mercaptoethane sulfonate were synthesized for the selective determination of free cyanide in aqueous solution with high sensitivity (detection limit of 1.1 x 10(-6) M), via analyte-induced changes in their photoluminescence after photoactivation.
Carbon dots have demonstrated great potential as luminescent nanoparticles in bioapplications. Although such nanoparticles appear to exhibit low toxicity compared to other metal luminescent nanomaterials, today we know that the toxicity of carbon dots (C-dots) strongly depends on the protocol of fabrication. In this work, aqueous fluorescent C-dots have been synthesized from cinnamon, red chilli, turmeric and black pepper, by a one-pot green hydrothermal method. The synthesized C-dots were firstly characterized by means of UV–vis, fluorescence, Fourier transform infrared and Raman spectroscopy, dynamic light scattering and transmission electron microscopy. The optical performance showed an outstanding ability for imaging purposes, with quantum yields up to 43.6%. Thus, the cytotoxicity of the above mentioned spice-derived C-dots was evaluated in vitro in human glioblastoma cells (LN-229 cancer cell line) and in human kidney cells (HK-2 non-cancerous cell line). Bioimaging and viability studies were performed with different C-dot concentrations from 0.1 to 2 mg·mL−1, exhibiting a higher uptake of C-dots in the cancer cultures compared to the non-cancerous cells. Results showed that the spice-derived C-dots inhibited cell viability dose-dependently after a 24 h incubation period, displaying a higher toxicity in LN-229, than in HK-2 cells. As a control, C-dots synthesized from citric acid did not show any significant toxicity in either cancerous or non-cancerous cells, implying that the tumour cell growth inhibition properties observed in the spice-derived C-dots can be attributed to the starting material employed for their fabrication. These results evidence that functional groups in the surface of the C-dots might be responsible for the selective cytotoxicity, as suggested by the presence of piperine in the surface of black pepper C-dots analysed by ESI-QTOF-MS.
In this mini-review recent applications of quantum dots in bioanalytics and biolabeling are discussed. The state-of-the-art of the field is summarized, some selected applications are highlighted, and future directions are suggested.
Optical labelling reagents (dyes and fluorophores) are an essential component of probe-based biomolecule detection, an approach widely employed in a variety of areas including environmental analysis, disease diagnostics, pharmaceutical screening, and proteomic and genomic studies. Recently, functional nanomaterials, as a new generation of high-value optical labels, have been applied to molecular detection. The great potential of such recent optical labels has paved the way for the development of new biomolecule assays with unprecedented analytical performance characteristics, related to sensitivity, multiplexing capability, sample throughput, cost-effectiveness and ease of use. This review aims to provide an overview of recent advances using different nanoparticles (such as quantum dots, rare earth doped nanoparticles or gold nanoparticles) for analytical genomics and proteomics, with particular emphasis on the outlook for different strategies of using nanoparticles for bioimaging and quantitative bioanalytical applications, as well as possibilities and limitations of nanoparticles in such a growing field.
The intentional introduction of transition metal impurities into semiconductor nanocrystals is an attractive approach for tuning quantum dot photoluminescence emission. Particularly, doping of ZnS quantum dots with Mn(2+) (Mn:ZnS QDs) results in a phosphorescence-type emission, attributed to the incorporation of manganese ions into the nanocrystal structure, so that delayed radiational deactivation of the energy of nanoparticles, excited through the energy levels of the metal, is enabled. However, the development of effective doping strategies can be challenging, especially if a highly efficient photoluminescent emission within a known crystalline core structure, is required (e.g. for analytical phosphorescence applications). The spectroscopic properties and the crystal structure of Mn(2+)-doped ZnS QDs are studied here to provide a better understanding on how the luminescence emission and the crystalline composition are influenced by the presence of Mn(2+) and its concentration used during the synthesis. In order to further control and optimize the synthesis of doped QDs for future bioanalytical applications, different complementary techniques including photoluminescence and X-ray powder diffraction have been employed. The information obtained has allowed standardization of the synthesis conditions of these doped QDs and the identification and quantification of the crystal phases obtained under different synthesis conditions.
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