7 research outputs found

    Printed Electrochemical Strip for the Detection of miRNA-29a: A Possible Biomarker Related to Alzheimer's Disease

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    The development of electrochemical strips, as extremely powerful diagnostic tools, has received much attention in the field of sensor analysis and, in particular, the detection of nucleic acids in complex matrixes is a hot topic in the electroanalytical area, especially when directed toward the development of emerging technologies, for the purpose of facilitating personal healthcare. One of the major diseases for which early diagnosis is crucial is represented by Alzheimer's disease (AD). AD is a progressive neurodegenerative disease, and it is the most common cause of dementia worldwide. In this context microRNAs (miRNAs), which are small noncoding RNAs, have recently been highlighted for their promising role as biomarkers for early diagnosis. In particular, miRNA-29 represents a class of miRNAs known to regulate pathogenesis of AD. In this work we developed an electrochemical printed strip for the detection of miRNA-29a at low levels. The architecture was characterized by the presence of gold nanoparticles (AuNPs) and an anti-miRNA-29a probe labeled with a redox mediator. The novel analytical tool has been characterized with microscale thermophoresis and electrochemical methods, and it has been optimized by selection of the most appropriate probe density to detect low target concentration. The present tool was capable to detect miRNA-29a both in standard solution and in serum, respectively, down to 0.15 and 0.2 nM. The platform highlighted good repeatability (calculated as the relative standard deviation) of ca. 10% and satisfactory selectivity in the presence of interfering species. This work has the objective to open a way for the study and possible early diagnosis of a physically and socially devastating disease such as Alzheimer's. The results demonstrate the suitability of this approach in terms of ease of use, time of production, sensitivity, and applicability

    Roadmap on printable electronic materials for next-generation sensors

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    The dissemination of sensors is key to realizing a sustainable, ‘intelligent’ world, where everyday objects and environments are equipped with sensing capabilities to advance the sustainability and quality of our lives—e.g., via smart homes, smart cities, smart healthcare, smart logistics, Industry 4.0, and precision agriculture. The realization of the full potential of these applications critically depends on the availability of easy-to-make, low-cost sensor technologies. Sensors based on printable electronic materials offer the ideal platform: they can be fabricated through simple methods (e.g., printing and coating) and are compatible with high-throughput roll-to-roll processing. Moreover, printable electronic materials often allow the fabrication of sensors on flexible/stretchable/biodegradable substrates, thereby enabling the deployment of sensors in unconventional settings. Fulfilling the promise of printable electronic materials for sensing will require materials and device innovations to enhance their ability to transduce external stimuli—light, ionizing radiation, pressure, strain, force, temperature, gas, vapours, humidity, and other chemical and biological analytes. This Roadmap brings together the viewpoints of experts in various printable sensing materials—and devices thereof—to provide insights into the status and outlook of the field. Alongside recent materials and device innovations, the roadmap discusses the key outstanding challenges pertaining to each printable sensing technology. Finally, the Roadmap points to promising directions to overcome these challenges and thus enable ubiquitous sensing for a sustainable, ‘intelligent’ world

    Combined Paper-Based Substrates for Electrochemical Detection of Copper Ions in Serum

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    The electroanalytical field has exploited great advantages in using paper-based substrates, even if the word “paper” might be general. In fact, the mainly adopted paper-based substrates are often chromatographic and office ones. They are characterized by main features (and drawbacks): chromatographic paper is well-established for storing reagents/treating samples but the sensitivity compared to traditional screen-printed is lower (due to porosity), while office paper represents a sustainable alternative to plastic (with similar sensitivity) but its porosity is not enough to load reagents. To overcome the limitations that might arise due to the adoption of a type of individual paper-based substrate, herein we describe for the first time, the development of a 2D merged paper-based devices for electrochemical copper ions detection in serum. In this work we report a novel configuration to produce an integrated all-in-one electrochemical device, in which no additional working media has to be added by the end user and the sensitivity can be tuned by rapid pre-concentration on porous paper, with the advantage of making the platform adaptable to real matrix scenario. The novel architecture has been obtained by combining office paper to screen-print a sustainable and robust electrochemical strip, the printed electrochemical strips and chromatographic one to 1) store the reagents, 2) collect real sample and 3) pre-concentrate the analyte of interest. The novel sensing platform has allowed to obtain a detection limit for copper ions down to 5 ppb in all the solutions that have been interrogated, namely standard solution and serum, and a repeatability of ca. 10% has been obtained.</p

    Technical Evaluation of a Paper-Based Electrochemical Strip to Measure Nitrite Ions in the Forensic Field

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    Nitrite is a compound used as a food additive for its preservative action and coloring capability, as well as an industrial agent for its antifreezing action and for preventing corrosion, and it is also used as a pharmaceutical in cyanide detoxification therapy. However, even recently, because of its high toxicity, it has been used as a murder and suicidal agent due to its affordability and ready availability. In this technical report, we describe an electrochemical paper-based device for selectively determining nitrite in complex biofluids, such as blood, cadaveric blood, vitreous humor, serum, plasma, and urine. The approach was validated in terms of the linearity of response, selectivity, and sensitivity, and the accuracy of the determination was verified by comparing the results with a chromatographic instrumental method. A linear response was observed in the micromolar range; the sensitivity of the method expressed as the limit of detection was 0.4 ÎŒM in buffer measurements. The simplicity of use, the portability of the device, and the performance shown make the approach suitable for detecting nitrite in complex biofluids, including contexts of forensic interest, such as murders or suicides in which nitrite is used as a toxic agent. Limits of detection of ca. 1, 2, 4, 5, 3, and 4 ÎŒM were obtained in vitreous humor, urine, serum and plasma, blood, and cadaveric blood, also highlighting a satisfactory accuracy comprised between 91 and 112%

    CyanoMetDB, a comprehensive public database of secondary metabolites from cyanobacteria

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    We created a comprehensive, publically accessible database of cyanobacterial secondary metabolites following the last ICTC in Krakow (2019). CyanoMetDB is a highly curated, flat-file, openly accessible database of cyanobacterial secondary metabolites collated from more than 850 peer-reviewed articles published since 1967. The database contains structural codes of more than 2000 cyanobacterial metabolites and facilitates the detection and dereplication of known cyanobacterial toxins and secondary metabolites as well as the identification of novel natural products from cyanobacteria. Research on biosynthesis of cyanobacterial secondary metabolite as well as investigations of their abundance, persistence, and toxicity in natural environments also benefit greatly from this comprehensive suspect list. We continue curating CyanoMetDB and integrating it into existing open access platforms. We are also generating mass spectrometry reference spectra for many entries to further facilitate the level confidence with which one can identify these metabolites when no reference materials are available
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