Universal hydrophilic coating of thermoplastic polymers currently used in microfluidics

A number of materials used to fabricate disposable microfluidic devices are hydrophobic in nature with water contact angles on their surface ranging from 80 to over 100. This characteristic makes them unsuitable for a number of microfluidic applications. Both the wettability and analyte adsorption parameters are highly dependent on the surface hydrophobicity. In this article, we propose a general method to coat the surface of five materials: polydimethylsiloxane (PDMS), cyclic olefin copolymer (COC), polyethylene terephthalate (PET), polycarbonate (PC), and polytetrafluoroethylene (PTFE). This fast and robust process, which is easily implementable in any laboratory including microfabrication clean room facilities, was devised by combining gas-phase and wet chemical modification processes. Two different coatings that improve the surface hydrophilicity were prepared via the "dip and rinse" approach by immersing the plasma oxidized materials into an aqueous solution of two different poly(dimethylacrylamide) copolymers incorporating a silane moiety and functionalized with either N-acryloyloxysuccinimide (NAS) (poly(DMA-NAS-MAPS) or glycidyl methacrylate (GMA) (poly(DMA-GMA-MAPS). The coating formation was confirmed by contact angle (CA) analysis comparing the variation of CAs of uncoated and coated surfaces subjected to different aging treatments. The antifouling character of the polymer was demonstrated by fluorescence and interferometric detection of proteins adsorbed on the surafce. This method is of great interest in microfluidics due to its broad applicability to a number of materials with varying chemical compositions

Preparation and Carbonization of Glucose and Pyromellitic Dianhydride Crosslinked Polymers

In this work, four types of nanosponges were prepared from pyromellitic dianhydride (PMDA) and D-glucose (GLU) with different molar ratios (1.5:1, 2:1, 2.5:1 and 3:1). The obtained PMDA/GLU nanosponges were then pyrolyzed at 800 °C for 30 min under N2 gas flow. The prepared polymeric nanosponges were investigated by FTIR spectroscopy, elemental and thermogravimetric analyses to unravel the role played by the different molar ratio of the precursors in the formation of the polymer. The pyrolyzed nanosponges were investigated by means of porosity measurements, X-ray diffraction analysis, Raman spectroscopy and high-resolution transmission electron microscopy. Notably, no significant correlation of the amounts of used precursors with the porous texture and structure was evidenced. The results corroborate that PMDA and GLU can be easily combined to prepare nanosponges and that the carbon materials produced by their pyrolysis can be associated with glassy carbons with a microporous texture and relatively high surface area. Such hard carbons can be easily obtained and shrewdly used to segregate relatively small molecules and organic contaminants; in this study methylene blue adsorption was investigated

Dual-domain reporter approach for multiplex identification of major SARS-CoV-2 variants of concern in a microarray-based assay

: Since the emergence of the COVID-19 pandemic in December 2019, the SARS-CoV-2 virus continues to evolve into many variants emerging around the world. To enable regular surveillance and timely adjustments in public health interventions, it is of the utmost importance to accurately monitor and track the distribution of variants as rapidly as possible. Genome sequencing is the gold standard for monitoring the evolution of the virus, but it is not cost-effective, rapid and easily accessible. We have developed a microarray-based assay that can distinguish known viral variants present in clinical samples by simultaneously detecting mutations in the Spike protein gene. In this method, the viral nucleic acid, extracted from nasopharyngeal swabs, after RT-PCR, hybridizes in solution with specific dual-domain oligonucleotide reporters. The domains complementary to the Spike protein gene sequence encompassing the mutation form hybrids in solution that are directed by the second domain ("barcode" domain) at specific locations on coated silicon chips. The method utilizes characteristic fluorescence signatures to unequivocally differentiate, in a single assay, different known SARS-CoV-2 variants. In the nasopharyngeal swabs of patients, this multiplex system was able to genotype the variants which have caused waves of infections worldwide, reported by the WHO as being of concern (VOCs), namely Alpha, Beta, Gamma, Delta and Omicron variants

Agronomic efficiency of granulated organomineral fertilizers based on poultry litter and phosphates.

This paper has as aim to evaluate the agronomic efficiency of granulated organomineral fertilizers produced from poultry litter and mineral sources of phosphorus

Nanostructures in Dye-Sensitized and Perovskite Solar Cells

Due to increase of attention in energy and environmental concerns, there has been much interest developed in clean and renewable energy technologies. The utilization of green and eco-friendly sunlight through solar cells like photovoltaic cells, photo-electrochemical cells, and dye-sensitize and perovskite solar cells (DSSCs and PSCs) produces energy demand. Due to high electron mobility, suitable band alignment, and high optical transparency, the binary and ternary transition metal oxide materials such as TiO2, SnO2, ZnO, WO3, Bi2O3 and SrTiO3, Zn2SnO4, BaSnO3, etc. have attracted considerable attention as DSSC and PSC electrode materials. Highly efficient solar cells with sustainable performance under severe mechanical deformations are in great demand in forming wearable power supply devices, essential for space technologies. In this regard, myriads of studies have progressed in developing the said metal oxides by various means of nanostructure forms. The aim of this chapter is to highlight research background, basic concepts, operating parameters, working principles, theoretical aspects, and selection of materials with essential properties for DSSCs and PSCs applications

Unreported resistance in the charge transport limits the photoconversion efficiency of aqueous dye-sensitised solar cells: An electrochemical impedance spectroscopy study

In this work, a thorough electrochemical impedance spectroscopy study is performed of both liquid and polymeric aqueous dye-sensitized solar cells (a-DSSCs), which are also compared with conventional organic solvent-based devices. The main purpose is unveiling phenomena limiting the efficiency of water-based photovoltaics. Indeed, electrochemical impedance spectroscopy spectra of a-DSSCs show two peculiar (and unreported) features that are not observed in organic-based DSSCs. The higher frequency one (R45°) is likely associated with a slowdown of the diffusion kinetics of the redox mediator: it is due to the breakdown of the hydrogen-bond network of the aqueous environment, which was also supported by density functional theory calculations. The lower-frequency feature is associated with the additional amount of energy required for the breakdown at the semiconductor/FTO interface of the adducts between protons (coming from the solvent) and electrons localized in the TiO2 surface trap-states. This ‘disruption energy’ results in a resistive element (RIC) that inversely correlates with the device efficiency. Very interestingly, RIC depends on the applied potential and becomes negligible only at much more positive values than VOC. Tailored equivalent circuits implementing simultaneously R45° and RIC are currently under investigation

Novel blocked functionality copolymers as surface coatings in DNA microarray technology

AbstractNew copolymers made of 2-(dimethyl amino) ethyl methacrylate (DMAEM) and isocyanate ethyl methacrylate blocked with methyl ethyl ketoxime (IEMB) was synthesized in various composition ratios in order to obtain water reducible copolymers after acidification. They were characterized by infrared spectroscopy, chemical titration for the determination of amine equivalent weight, and by differential scanning calorimetry (DSC). Calorimetric analysis showed the presence of a former broad endothermal peak followed by a latter, stronger exothermal one, which can be respectively attributed to the deblocking of isocyanate groups and to their subsequent reactions. Some copolymer compositions were dip coated onto microscope glass slides and surfaces were characterized by static and dynamic contact angles, revealing a clear effect of the salifying agent and a likely surface rearrangement of polar groups while in contact with water. Finally, oligonucleotides surface immobilization and molecular recognition capability of the coated glass slides were positively assessed by hybridization tests with fluorescently labelled complementary probes