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Abstract Background Colorectal adenocarcinoma cells (Caco-2) are a widely used model of intestinal barrier to study cancer development, toxicological assessments, absorption and metabolism in food science or drug discovery. Caco-2 spontaneously differentiate into a monolayer expressing several specific characteristics, typically showed by mature enterocytes. For in vitro experiments, it is crucial to identify non-invasive and non-destructive techniques able to evaluate the integrity and differentiation of the cells monolayer. Thus, we aimed to assess these properties by analyzing electrical impedance measurements. Methods Caco-2 cells were differentiated for 21 days. The monolayer integrity and differentiation were primarily evaluated by means of morphological, biochemical and molecular data. Impedance measurements in a range of frequencies from 400 Hz to 50 kHz were performed using a dedicated set up, including customized Aerosol Jet Printed carbon-based sensors. Results The trends of RI observed at three different frequencies were able to describe cell growth and differentiation. In order to evaluate which frequencies better correlate with cell differentiation, Principal Component Analysis have been employed and the concordance analysis between RI magnitude and morphological, biochemical and molecular data, highlighted 40 kHz as the optimal frequency to assess Caco-2 cells differentiation process. Conclusion We demonstrated the feasibility and reliability of applying impedance-based measurements not only to provide information about the monolayer status, but also for cell differentiation monitoring. General significance This study underlined the possibility to use a dedicated sensor to assess the integrity and differentiation of Caco-2 monolayer, as a reliable non-destructive alternative to conventional approaches. Highlights • Electrochemical sensors can provide information about cell adhesion, growth and differentiation. • Monitoring of Caco-2 to enterocyte-like cells differentiation with impedance-based sensors. • Relative Impedance at specific frequencies could describe cell growth and differentiation. • 40 kHz highlighted as the optimal frequency to assess Caco-2 cells differentiation process. [ABSTRACT FROM AUTHOR]

An extremely promising methodology able to obtain feedbacks from cell cultures is represented by the direct integration within culture substrates of specific sensitive elements capable to provide information related to cell adhesion, migration, differentiation and growth. At present, the most common materials used in the implementation of sensors monitoring 2D cell culture are noble metals. However, printed electronics allow instead an innovative approach, from both sensor realization technique and utilization of sensitive materials. This project aims to develop and test 2D ink-jet printed sensors, focusing on biocompatible substrates and conductive inks. Both biocompatibility and printability of two different sensor designs were evaluated, followed by electronic measurements that estimate fibroblast adhesion. Preliminary findings show a good biocompatibility of the Kapton® substrate coupled with PEDOT:PSS ink. This solution allowed us to correlate cell adhesion with an increase of impedance module, in agreement with the optical observation. On-going works rely on the evaluation of different materials used for both substrates and inks, addressing the possibility to monitor cardiomyocyte activity. [ABSTRACT FROM AUTHOR]

Alzheimer disease (AD), despite representing the most common type of dementia in elderly, is still lacking reliable methodologies for early diagnosis. A potential biomarker associated to AD development has been recently identified in the open isoform of p53, redox sensitive protein, currently quantified using a specific blood-based enzyme-linked immunosorbent assay (ELISA). In order to overcome ELISA limitations (level of detection, standardization and reliability), this study aimed to realize a low cost highly sensitive portable point-of-care (PoC) testing system based on screen printed electrochemical sensors (SPES). The study specifically reported the design of the platform, including the sensing probe and the electronic circuit devoted to the conditioning of the electric signal. Preliminary results were obtained from circuit testing by using controlled concentrations of electrolytic solutions and from an initial calibration stage by using Anodic Stripping Voltammetry (ASV) measurements. Future works will address the quantification of unknown concentration of unfolded p53 in peripheral blood samples, thus to validate the here-presented low cost, easy to use and highly precise platform. [ABSTRACT FROM AUTHOR]

Our skin is in close contact with clothes most of the time thus risking potentially noxious chemicals contact. One of the potentially harmful manufacturing by-products that can be released by textiles when sweating is formaldehyde, used as an anti-crease treatment. As it is known to be carcinogenic to humans and a potent skin sensitizer, the aim of this study was to investigate its effects on both normal human keratinocytes (HaCaT cells) and on a highly invasive malignant melanoma cell line (SK-MEL-28) in order to contribute to the definition of safety cut-off to be applied to the production processes. Formaldehyde concentrations below the commonly accepted limits (10–50 μM) were obtained by diluting formaldehyde in simulated sweat (UNI EN ISO 105-E04). The effects on cell proliferation were evaluated by cell counting, while ERK pathway activation was evaluated by western blot. Low concentrations of formaldehyde (10 μM) in both acidic and alkaline simulated sweat were able to increase malignant melanoma cell proliferation, while not affecting normal keratinocytes. Melanoma proliferation increase was greater in acidic (pH = 5.5) than in alkaline (pH = 8) conditions. Moreover, formaldehyde stimulation was able to induce ERK pathway activation. The data obtained suggest the need for an even increasing attention to the potentially harmful effects of textile manufacturing by-products. [ABSTRACT FROM AUTHOR]