We have demonstrated a novel platform of quantum dots (QDs) core-shell conjugated graphene oxide (GO) biosensor for effective protein detection. The advantage in making core shell nanostructure allows preserving stable QDs, by improving quantum yield, and lowering the toxicity of the core. Both QDs and GO are efficient nanoparticle systems that can potentially be used for drug delivery, diagnosis, and biosensors scaffolds. However, our study indicates that the conjugation between these two nanoparticle systems makes their properties even more effective. The change in fluorescent intensity through fluorescence resonance energy transfer from quantum dots to GO produced a novel method for detection of the target and allows for the optimization of the recognition limit of Bovine serum albumin (BSA) due to efficient fluorescence resonance energy transfer as observed through time resolved relaxation spectroscopy. It is observed that the quenching of photoluminescence peak of QDs due to GO shell produced an applicable strategy and could be conveniently extended for detection of other biomolecules. We obtained significantly enhanced spectral signal through successful conjugation of GO with CdSe/CdS core shell, which can potentially be used for the detection of biomolecules with high sensitivity and selectivity. Our study underlines the efficiency of QD conjugated GO core shell in spectral detection of proteins even at very low concentration (0.25 mmol).

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A highly sensitive biosensing platform comprised of CdSe-ZnO core–shell nanostructures for targeted applications in protein detection is demonstrated. This innovative technique uses a microwave-assisted thermal decomposition method to produce a rapid, less hazardous, and user-friendly procedure to synthesize a semiconductor core surrounded by nanometer-thick metal oxide shells. The benefit of using a metal oxide shell includes mitigating the toxicity of the CdSe core, thus increasing its biocompatibility and minimizing its photochemical corrosion and oxidation. We present a simple one-pot microwave-assisted protocol for the formation of CdSe-ZnO core–shell quantum dots (QDs). These QDs optimize the recognition limit of bovine serum albumin (BSA) protein through a spectral signal at a considerably low concentration (2.5 × 10−6 M), thus demonstrating its potential to become a highly effective surface-plasmon-enhanced Raman spectroscopy (SERS)-like sensing platform. We report a QD material that can mimic a strong SERS-like behavior due to charge transfer affecting the local electric field.

The formation of self-assembled monolayers (SAM) of noble metals for optical sensing applications faces serious challenges when trying to achieve simplicity, cost efficacy, specificity, and versatility. Utilizing stable, SAM-forming alkanethiols, such as glutathione (GSH), enable for simple assembly and specific detection of proteins, trace metals, oxidants, etc., thus providing a sensing platform that not only can detect low levels of reactive oxygen species (ROS) for early determination of neurodegenerative diseases, but can also assess trace metals in freshwaters and marine waters, for example. Providing a universal device for detecting varieties of target materials would adapt, simplify, and reduce costs that come from current detection methods. Our research on improving these detection methods is demonstrated using the frequency-controlled self-assembly of a GSH-functionalized gold nanoparticle (Au NP) film as a platform for highly specific and sensitive sensing. We have previously demonstrated the use of an eco-friendly and highly sensitive surface enhanced Raman spectroscopy (SERS) substrate for biomedical diagnostic applications using an ultraviolet photochemical reaction of gold (III) chloride trihydrate (HAuCl4) to create a densely packed Au NP film that exhibits localized surface plasmon resonances [1]. By the firm anchoring of a thiol group to the Au NP surface, GSH assembles the Au NPs for SERS into a densely packed, dendritic structure. At a pH of ~1 in solution, GSH forms a y-shape [2], allowing its carboxyl and amino groups to create a hydrophilic interface and, therefore, be fully available for bonding to various functional molecules. Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), and ultraviolet-visible spectroscopy (UV-vis) were used to confirm the presence of GSH and enhancement capabilities of the SERS substrate. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) confirmed the Au NP film to be 90nm thick, with an average Au NP size of 125nm in diameter [1], and visually confirmed the dendritic assembly of the GSH-functionalized Au NPs. For application purposes, this study will evaluate the trace metal Pb2+ in water. The contamination of lead, and heavy metals in general, have a damaging impact on the health of both humans and our planet. The chelation of the GSH ligands with Pb2+ enables highly specific detection of Pb2+ in water. This method provides a simple, versatile SERS substrate with a dendritic assembly that creates intriguing optical properties and broadens the capability for potential applications. [1] G. Rutherford et al., ECS J. Solid State Sci. Tech. 4, S3071 (2015). [2] M. Bieri and T. Burgi, Langmuir 2005, 21, 1354-1362. Figure 1

The detection of the lead heavy metal (Pb) in water is crucial in many chemical processes, as it is associated with serious health hazards. Here, we report the selective and precise colorimetric detection of Pb2+ ions in water, exploiting the aggregation and self-assembly mechanisms of glutathione (GSH)-functionalized gold nanoparticles (GNPs). The carboxyl functional groups are able to create coordination complexes with Pb2+, inducing aggregation amongst the GSH-GNPs in the presence of Pb2+ due to the chelation of the GSH ligands. The resulting aggregation amongst the GSH-GNPs in the presence of Pb2+ increases the aggregate size depending on the available Pb2+ ions, affecting the plasmonic coupling. This causes a substantial shift in the plasmon wavelength to a longer wavelength side with increasing Pb2+ concentration, resulting in a red-to-blue colorimetric or visual change, enabling the instant determination of lead content in water.