Stimuli-bioresponsive hydrogels as new generation materials for implantable, wearable, and disposable biosensors for medical diagnostics: Principles, opportunities, and challenges.

Hydrogels are excellent water-swollen polymeric materials for use in wearable, implantable, and disposable biosensors. Hydrogels have unique properties such as low cost, ease of preparation, transparency, rapid response to external conditions, biocompatibility and self-adhesion to the skin, flexibility, and strain sensitivity, making them ideal for use in biosensor platforms. This review provides a detailed overview of advanced applications of stimuli-responsive hydrogels in biosensor platforms, from hydrogel synthesis and functionalization for bioreceptor immobilization to several important diagnostic applications. Emphasis is placed on recent advances in the fabrication of ultrasensitive fluorescent and electrically conductive hydrogels and their applications in wearable, implantable, and disposable biosensors for quantitative measurements. Design, modification, and assembly techniques of fluorescent, ionically conductive, and electrically conductive hydrogels to improve performance will be addressed. The advantages and performance improvements of immobilizing bioreceptors (e.g., antibodies, enzymes, and aptamers), and incorporating fluorescent and electrically conductive nanomaterials are described, as are their limitations. Potential applications of hydrogels in implantable, wearable, disposable portable biosensors for quantitative detection of the various bioanalytes (ions, molecules, drugs, proteins, and biomarkers) are discussed. Finally, the global market for hydrogel-based biosensors and future challenges and prospects are discussed in detail.

Interaction of CO2 with MnOx /Pd(111) Reverse Model Catalytic Interfaces.

Understanding the activation of CO2 on the surface of the heterogeneous catalysts comprised of metal/metal oxide interfaces is of critical importance since it is not only a prerequisite for converting CO2 to value-added chemicals but also often, a rate-limiting step. In this context, our current work focuses on the interaction of CO2 with heterogeneous bi-component model catalysts consisting of small MnOx clusters supported on the Pd(111) single crystal surface. These metal oxide-on-metal 'reverse' model catalyst architectures were investigated via temperature programmed desorption (TPD) and x-ray photoelectron spectroscopy (XPS) techniques under ultra-high vacuum (UHV) conditions. Enhancement of CO2 activation was observed upon decreasing the size of MnOx nanoclusters by lowering the preparation temperature of the catalyst down to 85 K. Neither pristine Pd(111) single crystal surface nor thick (multilayer) MnOx overlayers on Pd(111) were not capable of activating CO2 , while CO2 activation was detected at sub-monolayer (∼0.7 ML) MnOx coverages on Pd(111), in correlation with the interfacial character of the active sites, involving both MnOx and adjacent Pd atoms.

Comparative efficacy of biogenic zinc oxide nanoparticles synthesized by Pseudochrobactrum sp. C5 and chemically synthesized zinc oxide nanoparticles for catalytic degradation of dyes and wastewater treatment.

Discharge of untreated textile wastewaters loaded with dyes is not only contaminating the soil and water resources but also posing a threat to the health and socioeconomic life of the people. Hence, there is a need to devise the strategies for effective treatment of such wastewaters. The present study reports the catalytic potential of biogenic ZnO nanoparticles (ZnO NPs) synthesized by using a bacterial strain Pseudochrobactrum sp. C5 for degradation of dyes and wastewater treatment. The catalytic potential of the biogenic ZnO NPs for degradation of dyes and wastewater treatment was also compared with that of the chemically synthesized ones. The characterization of the biogenic ZnO NPs through FT-IR, XRD, and field emission scanning electron microscopy (FESEM) indicated that these are granular agglomerated particles having a size range of 90-110 nm and zeta potential of -27.41 mV. These catalytic NPs had resulted into almost complete (> 90%) decolorization of various dyes including the methanol blue and reactive black 5. These NPs also resulted into a significant reduction in COD, TDS, EC, pH, and color of two real wastewaters spiked with reactive black 5 and reactive red 120. The findings of this study suggest that the biosynthesized ZnO NPs might serve as a potential green solution for treatment of dye-loaded textile wastewaters.

Visual detection of in vitro nucleic acid replication by submicro- and nano-sized materials.

The rapid growth of in vitro nucleic acid replication has offered a powerful tool for clinical diagnosis, food safety detection and environmental monitorning. Successful implementation of various isothermal nucleic acid amplification methods enables rapid replication of target sequences without the participant of a thermal cycler. Point-of-need analysis possesses great superiorities in user-friendly, instant results analysis, low manufacturing, and consumable costs. To meet the great challenge of point-of-need analysis, developing simple and rapid visual methods becomes crucial. Submicro- and nanomaterials possess unique surface properties, which enables their rapid response to DNA amplicons. Their unique optical, magnetic, catalytic, and other physical/chemical properties have been frequently employed for the visual detection of in vitro nucleic acid replications. Herein, we aim to review the submicro- and nanomaterials-based visual methods for detection of nucleic acid amplification. The visual methods are classified according to the designing strategies (e.g. LSPR, bridging flocculation, luminescence, catalytic reaction, separation, etc.). The basic principles, merits and drawbacks of each strategy are described. The application in analysis of nucleic acid targets and non-nucleic acid targets are discussed. The main challenges and future research directions are also highlighted in this rapidly emerging field.

Synthesis of Positively and Negatively Charged CeO2 Nanoparticles: Investigation of the Role of Surface Charge on Growth and Development of Drosophila melanogaster.

Monodispersed cerium oxide nanoparticles (CeO2 NPs) with positive and negative surface potential were synthesized by co-precipitation method using hexamethylenetetramine (HMT) and poly(vinylpyrrolidone) (PVP), respectively, as precipitating agents. Synthesized NPs were characterized with scanning electron microscopy (SEM), UV-Visible (UV-Vis) spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, and powder X-ray diffraction (XRD). Positively charged NPs of about 30 ± 10 nm in size formed within 5 h, aggregated in number, and resulted in larger-sized NPs as a function of time. The CeO2 NPs were administered to Drosophila as a part of their diet to study the effects on the growth and development of Drosophila. While the positively charged NPs did not affect the growth of the third instar larvae, the negatively charged NPs delayed the growth of larvae by about 7 days. It required 7 more days to reach the stage of adult fly. TEM imaging of the larvae gut showed that positively charged NPs were found to be smaller, whereas the size of negatively charged NPs remained unchanged. This biodegradability could be the reason for the delayed larvae growth in the case of negatively charged particles. The distance covered by such second instar larvae fed with diet containing negatively charged CeO2 NPs was significantly lower, and their size was significantly smaller when compared to the crawling activity and size of the third instar larvae of the control group. Such positively charged NPs have high potential for use as drug delivery carriers for the treatment of disease, and negatively charged NPs may play a rather detrimental role.

Ultrasensitive electrochemical immunoassay for melanoma cells using mesoporous polyaniline.

We report the development of an antibody (anti-MC1R antibody)-functionalized polyaniline nanofibers modified screen-printed electrode capable of efficient electrochemical detection of melanoma cells at levels (1 cell per mL) not readily achieved by other methods. This immunosensor is highly selective in its detection of melanoma cells over normal human cells.

Highly selective colorimetric and electrochemical sensing of iron (III) using Nile red functionalized graphene film.

We report a highly selective method for identification and detection of iron (III) (ferric iron, Fe3+) using Nile red (NR) as a complexing agent. Fe3+ preferentially binds with NR in dimethylformamide (DMF)/water (1:1) solution over other cations such as Fe2+, Cu2+, Pb2+, Hg2+, Mn2+, Ni2+, Zn2+, Co2+ and Cd2+ at room temperature. In the presence of Fe3+, the color of NR solution changes from purple to dark brown, which is detectable with bare eyes. Using UV-vis spectroscopy, we could measure the amount of Fe3+ in the sample solution by monitoring changes in absorption from 540 to 580nm; the linear range and the limit of detection are 30-1000µM and 24.9µM, respectively. Taking advantage of the NR selectivity, we treated partially oxidized graphene sheets (po-Gr) with NR to obtain po-Gr-NR dispersion by ultrasonication. The NR-treated po-Gr flakes (po-Gr-NR) were characterized by UV-vis, FT-IR, and Raman spectroscopies and FE-SEM, which indicated attachment of NR on po-Gr sheets. The po-Gr-NR hybrid film deposited glassy carbon electrode (po-Gr-NR/GCE) served as the Fe3+ sensor. Differential pulse voltammetry was used to investigate the detection of Fe3+ in 0.05M HCl+0.05M KCl solution. The linear range and the limit of detection of Fe3+ were from 37.5nM to 21.53µM and 18.7nM, respectively. Furthermore, this sensor was successfully used to measure Fe3+ content in red wine samples.