140 research outputs found

    Enzyme-based impedimetric detection of PCR products using oligonucleotide-modified screen-printed gold electrodes.

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    Electrochemical Fingerprint of Arsenic (III) by Using Hybrid Nanocomposite-Based Platforms

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    Arsenic, one of the most abundant mineral and also one to the most toxic compounds. Due to its high toxicity sensitive analytical methods are highly important, taking into account that the admitted level is in the range of mu g L-1. A novel and easy to use platform for As(III) detection from water samples is proposed, based on gold and platinum bi metallic nanoparticles and a conductive polymer (polyaniline). The electrochemical detection was achieved after optimization of cathodic pre-concentration and stripping parameters by square wave anodic stripping voltammetry at modified screen-printed carbon-based electrochemical cells, proving its applicability for disposable and cost-effective in situ analysis of arsenic

    Mercury Detection in Novel Foods by a Smart Pocket Sensor

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    Mercury is one of the most well-known toxic contaminants of natural and anthropogenic origin in aquatic ecosystems that can bioaccumulate in vegetal and animal organisms. In this work, we propose a smart detection system for Hg(II) ions by square wave anodic stripping voltammetry at nanocomposite graphite screen-printed electrodes, as an analytical tool to be applied in food quality control. The nanocomposite surfaces were obtained by the modification of screen-printed graphite electrodes with poly(l-aspartic acid) and gold nanoparticles and were characterized by means of electrochemical techniques. An exhaustive study of the experimental conditions involved both in the electropolymerization and in the voltammetric stripping measurements was addressed to develop a reliable method capable of measuring Hg(II) concentration in the low mu g/L range, both in conventional and drop configurations. The sensor was integrated in a smart setup, comprising a Sensit Smart pocket instrument connected to a smartphone, thus proving its applicability for in situ analysis due to its cost-effectiveness. The analytical significance of the developed sensor was assessed by detecting Hg(II) in novel food samples.imag

    Nano-biosensing platforms for detection of cow’s milk allergens: An overview

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    Among prevalent food allergies, cow milk allergy (CMA) is most common and may persist throughout the life. The allergic individuals are exposed to a constant threat due to milk proteins' presence in uncounted food products like yogurt, cheese, and bakery items. The problem can be more severe due to cross-reactivity of the milk allergens in the food products due to homologous milk proteins of diverse species. This problem can be overcome by proper and reliable food labeling in order to ensure the life quality of allergic persons. Therefore, highly sensitive and accurate analytical techniques should be developed to detect the food allergens. Here, significant research advances in biosensors (specifically immunosensors and aptasensors) are reviewed for detection of the milk allergens. Different allergic proteins of cow milk are described here along with the analytical standard methods for their detection. Additionally, the commercial status of biosensors is also discussed in comparison to conventional techniques like enzyme-linked immunosorbent assay (ELISA). The development of novel biosensing mechanisms/kits for milk allergens detection is imperative from the perspective of enforcement of labeling regulations and directives keeping in view the sensitive individuals

    Carbon and gold electrodes as electrochemical transducers for DNA hybridisation sensors.

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    Platinum Nanozyme-Enabled Colorimetric Determination of Total Antioxidant Level in Saliva

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    Redox imbalance and oxidative stress-related biomarkers are raising increasing consensus in the scientific community for their significant role in a wide range of human disorders. In this framework, the total antioxidant capacity (TAC), namely, the overall pattern of both enzymatic and nonenzymatic antioxidant compounds within the body, represents an important bioanalytical parameter. To date, however, antioxidant assays require costly instrumentations, laboratory setups, and reagents, and they are invasive. Yet, their accuracy typically suffers from strong sensitivity to interfering matrices and inability to detect the complete pattern of physiological antioxidant molecules, due to the use of reaction schemes and probes/substrates that are not sensitive to the diverse range of relevant target species. Here, we exploit the enzyme-mimetic properties of platinum nanoparticles combined with hydroxyl radical probes produced at the particle surface to develop an effective detection scheme that is sensitive to both single electron transfer (SET) and hydrogen atom transfer (HAT) reactions, thus covering all the physiologically relevant antioxidant species. Importantly, the nanozyme-enabled method allows fast (5 min), accurate, and noninvasive evaluation of the body TAC through saliva via simple naked-eye or smartphone-based inspection

    New micro-and nano-technologies for biosensor development

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    Recent advances in micro- and nanotechnology have produced a number of new materials which exhibit exceptional potential for the design of novel sensing strategies and to enhance the analytical performance of biosensing systems. In this thesis three different types of miniaturisation pathways were investigated for electrochemical biosensing applications. Vertically aligned carbon nanotube thin films were designed and tested as platforms for DNA immobilisation and for the development of a model electrochemical genosensor. The sensor format involved the immobilisation of oligoucleotide probes onto the sensor surface, hybridisation with the target sequence and electrochemical detection of the duplex formation. By combining such an electrode platform with an enzyme labeling, a detection limit of oligonucleotide targets in the nanomolar range was achieved. A novel magnetic particle-based microfluidic sensor was also realised by integrating a microfluidic platform with a new analytical procedure based on the use of paramagnetic beads for the detection of real PCR samples. The hybridisation reaction was carried out on probe-modified beads in a flow-through format, thus enhancing the surface area-to-volume ratio and consequently the sensitivity. Moreover, the magnetic properties of the beads greatly facilitated the delivery and removal of reagents through the microfluidic channels. This format allowed the detection of nanomolar levels of double-stranded DNA sequences, with high reproducibility and fast time of analysis. Finally, polyaniline nanotubes arranged in an ordered structure directly on gold electrode surfaces were realised and employed to create a model molecularly imprinted (MIP) polymer -sensor for catechol detection. The advantages of using nanostructures in this particular biosensing application have been evaluated by comparing the analytical performance of the sensor with an analogous non-nanostructured MIP-sensor that we had previously developed. A significantly lower limit of detection (one order of magnitude) was achieved, thus demonstrating that the nanostructures enhanced the analytical performance of the sensor.EThOS - Electronic Theses Online ServiceGBUnited Kingdo
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