Multiwavelength Raman microspectroscopy for rapid prediction of soot oxidation reactivity

Multiwavelength Raman microspectroscopy (MWRM) analysis for characterization of soot structure and reactivity was developed. This new method is based on the dispersive character of carbon D mode in Raman spectra (i.e., red shift and increase in intensity at higher excitation wavelength, λ(0)). The approach was proven by investigating various diesel soot samples and related carbonaceous materials at different λ(0) (785, 633, 532, and 514 nm). In order to compare the behavior of the D mode for various samples and to derive a single parameter characterizing the soot structure, the difference of integrals for pairs of spectra collected at different λ(0) was calculated. MWRM analysis revealed substantial differences in the structural ordering which decreases from graphite, over Printex XE2 and various diesel soot samples, to spark discharge soot. To obtain the relation between structure and reactivity of soot, MWRM analysis was combined with temperature-programmed oxidation (TPO). TPO allowed us to characterize the oxidation behavior of soot in terms of the maximum emission (CO + CO(2)) temperature and reactivity index. The latter was calculated by introducing the reactivity limits: spark discharge soot containing a large amount of disorder represents the upper limit, whereas the lower limit is given by graphite powder with high structural order. The comparison of MWRM (viz., the observed Raman difference integrals) and TPO data revealed a linear correlation between soot structure and oxidation reactivity. Thus, we demonstrated for the first time the potential of MWRM for a robust and rapid prediction of diesel soot reactivity based on the structure-reactivity correlation.     

Surface plasmon resonance biosensor screening method for paralytic shellfish poisoning toxins: a pilot interlaboratory study

A surface plasmon resonance (SPR) optical biosensor method was developed for the detection of paralytic shellfish poisoning (PSP) toxins in shellfish. This application was transferred in the form of a prototype kit to seven laboratories using Biacore Q SPR optical biosensor instrumentation for interlaboratory evaluation. Each laboratory received 20 shellfish samples across a range of species including blind duplicates for analysis. The samples consisted of 4 noncontaminated samples spiked in duplicate with a low level of PSP toxins (240 μg STXdiHCl equivalents/kg), a high level of saxitoxin (825 μg STXdiHCl/kg), 2 noncontaminated, and 14 naturally contaminated samples. All 7 participating laboratories completed the study, and HorRat values obtained were <1 demonstrating that the method performance was acceptable. Mean recoveries expressed as STXdiHCl equivalents/kg were 94.6 ± 16.8% for the low level PSP toxin mix and 98.6 ± 5.6% for the high level of saxitoxin. Relative standard deviations for within-laboratory variations (RSD(r): repeatability) and between-laboratory variations (RSD(R) = reproducibility) ranged from 1.8 to 9.6% and 2.9 to 18.3% respectively. This first ever reported SPR biosensor interlaboratory study demonstrated this PSP application to be an empowering tool in the drive toward the reduction and replacement of the mouse bioassay within Europe.     

Piezo-optic, photoelastic, and acousto-optic properties of SrB4O7 crystals

On the basis of studies of the piezo-optic effect, it has been shown that SrB(4)O(7) crystals can be used as efficient acousto-optic materials in the vacuum ultraviolet spectral range. The full matrices of piezo-optic and photoelastic coefficients have been experimentally obtained for these crystals. The acousto-optic figure of merit and the diffraction efficiency have been estimated for both the visible and deep ultraviolet spectral ranges.     

Research progress on the regulation of oxidative stress by phenolics: the role of gut microbiota and Nrf2 signaling pathway

In recent years, the increase in high-calorie diets and sedentary lifestyles has made obesity a global public health problem. An unbalanced diet promotes the production of proinflammatory cytokines and causes redox imbalance in the body. Phenolics have potent antioxidant activity and cytoprotective ability. They can scavenge free radicals and reactive oxygen species, and enhance the activity of antioxidant enzymes, thus combating the body's oxidative stress. They can also improve the body's inflammatory response, enhance the enzyme activity of lipid metabolism, and reduce the contents of cholesterol and triglyceride. Most phenolics are biotransformed and absorbed into the blood after the action by gut microbiota; these metabolites then undergo phase I and II metabolism and regulate oxidative stress by scavenging free radicals and increasing expression of antioxidant enzymes. Phenolics induce the expression of genes encoding antioxidant enzymes and phase II detoxification enzymes by stimulating Nrf2 to enter the nucleus and bind to the antioxidant response element after uncoupling from Keap1, thereby promoting the production of antioxidant enzymes and phase II detoxification enzymes. The absorption rate of phenolics in the small intestine is extremely low. Most phenolics reach the colon, where they interact with the microbiota and undergo a series of metabolism. Their metabolites will reach the liver via the portal vein and undergo conjugation reactions. Subsequently, the metabolites reach the whole body to exert biological activity by traveling with the systemic circulation. Phenolics can promote the growth of probiotics, reduce the ratio of Firmicutes/Bacteroidetes (F/B), and improve intestinal microecological imbalance. This paper reviews the nutritional value, bioactivity, and antioxidant mechanism of phenolics in the body, aiming to provide a scientific basis for the development and utilization of natural antioxidants and provide a reference for elucidating the mechanism of action of phenolics for regulating oxidative stress in the body. © 2023 Society of Chemical Industry.     

Fast Fluorescence Spectroscopy Methodology to Monitor the Evolution of Extra Virgin Olive Oils Under Illumination

Detailed regions of excitation and emission wavelengths for extra virgin olive oil samples have been extracted from three dimensional front-face fluorescence spectra. Information was applied to establish a right-angle fluorescence procedure. A right-angle device was assembled and tested with simultaneous excitation from 200 to 400 nm and registration of the fluorescence signal emitted from 400 to 850 nm. A principal component analysis was performed on the signal ranging from 400 to 550 nm from spectra of olive oils officially categorized as extra virgin in order to model the expected variability of compounds related to oxidative processes. Such model was useful to monitor the spectral evolution of extra virgin olive oil samples acquired at retail markets, which were exposed to indirect light during 2 months, through the analysis of the effect on their scores. Three relevant peaks characterized such evolution, with local maxima at around 434 to 437, 464 to 469 and 510 to 518 nm. Polynomial relationship was found between the evolution of those peaks and that of the chlorophyll, at around 670 to 673 nm, with R ² values of 0.98 and 0.99.     

N-Heterocyclic Carbenes and Their Metal Complexes Based on Histidine and Histamine Derivatives of Bacteriopurpurinimide for the Combined Chemo- and Photodynamic Therapy of Cancer

Photodynamic therapy (PDT) is currently regarded as a promising method for the treatment of oncological diseases. However, it involves a number of limitations related to the specific features of the method and the specific characteristics of photosensitizer molecules, including tumor hypoxia, small depth of light penetration into the tumor tissue, and low accumulation sensitivity. These drawbacks can be overcome by combining PDT with other treatment methods, for example, chemotherapy. In this work, we were the first to obtain agents that contain bacteriopurpurinimide as a photodynamic subunit and complexes of gold(I) that implement the chemotherapy effect. To bind the latter agents, N-heterocyclic carbenes (NHC) based on histidine and histamine were obtained. We considered alternative techniques for synthesizing the target conjugates and selected an optimal one that enabled the production of preparative amounts for biological assays. In vitro studies showed that all the compounds obtained exhibited high photoinduced activity. The C-donor Au(I) complexes exhibited the maximum specific activity at longer incubation times compared to the other derivatives, both under exposure to light and without irradiation. In in vivo studies, the presence of histamine in the NHC-derivative of dipropoxy-BPI (7b) had no significant effect on its antitumor action, whereas the Au(I) metal complex of histamine NHC-derivative with BPI (8b) resulted in enhanced antitumor activity and in an increased number of remissions after photodynamic treatment.     

Genetic Biomarkers of Antipsychotic-Induced Prolongation of the QT Interval in Patients with Schizophrenia

Antipsychotics (AP) induced prolongation of the QT interval in patients with schizophrenia (Sch) is an actual interdisciplinary problem as it increases the risk of sudden death syndrome. Long QT syndrome (LQTS) as a cardiac adverse drug reaction is a multifactorial symptomatic disorder, the development of which is influenced by modifying factors (APs’ dose, duration of APs therapy, APs polytherapy, and monotherapy, etc.) and non-modifying factors (genetic predisposition, gender, age, etc.). The genetic predisposition to AP-induced LQTS may be due to several causes, including causal mutations in the genes responsible for monoheme forms of LQTS, single nucleotide variants (SNVs) of the candidate genes encoding voltage-dependent ion channels expressed both in the brain and in the heart, and SNVs of candidate genes encoding key enzymes of APs metabolism. This narrative review summarizes the results of genetic studies on AP-induced LQTS and proposes a new personalized approach to assessing the risk of its development (low, moderate, high). We recommend implementation in protocols of primary diagnosis of AP-induced LQTS and medication dispensary additional observations of the risk category of patients receiving APs, deoxyribonucleic acid profiling, regular electrocardiogram monitoring, and regular therapeutic drug monitoring of the blood APs levels.     

Polymerizable Skin Hydrogel for Full Thickness Wound Healing

The skin is the largest organ in the human body, comprising the main barrier against the environment. When the skin loses its integrity, it is critical to replace it to prevent water loss and the proliferation of opportunistic infections. For more than 40 years, tissue-engineered skin grafts have been based on the in vitro culture of keratinocytes over different scaffolds, requiring between 3 to 4 weeks of tissue culture before being used clinically. In this study, we describe the development of a polymerizable skin hydrogel consisting of keratinocytes and fibroblast entrapped within a fibrin scaffold. We histologically characterized the construct and evaluated its use on an in vivo wound healing model of skin damage. Our results indicate that the proposed methodology can be used to effectively regenerate skin wounds, avoiding the secondary in vitro culture steps and thus, shortening the time needed until transplantation in comparison with other bilayer skin models. This is achievable due to the instant polymerization of the keratinocytes and fibroblast combination that allows a direct application on the wound. We suggest that the polymerizable skin hydrogel is an inexpensive, easy and rapid treatment that could be transferred into clinical practice in order to improve the treatment of skin wounds.     

The Cytoskeletal Protein Zyxin Inhibits Retinoic Acid Signaling by Destabilizing the Maternal mRNA of the RXRγ Nuclear Receptor

Zyxin is an LIM-domain-containing protein that regulates the assembly of F-actin filaments in cell contacts. Additionally, as a result of mechanical stress, Zyxin can enter nuclei and regulate gene expression. Previously, we found that Zyxin could affect mRNA stability of the maternally derived stemness factors of Pou5f3 family in Xenopus laevis embryos through binding to Y-box factor1. In the present work, we demonstrate that Zyxin can also affect mRNA stability of the maternally derived retinoid receptor Rxrγ through the same mechanism. Moreover, we confirmed the functional link between Zyxin and Rxrγ-dependent gene expression. As a result, Zyxin appears to play an essential role in the regulation of the retinoic acid signal pathway during early embryonic development. Besides, our research indicates that the mechanism based on the mRNA destabilization by Zyxin may take part in the control of the expression of a fairly wide range of maternal genes.     

Measuring End-to-End Delay in Low Energy SDN IoT Platform

In this paper, we developed a new customizable low energy Software Defined Networking (SDN) based Internet of Things (IoT) platform that can be reconfigured according to the requirements of the target IoT applications. Technically, the platform consists of a set of low cost and energy efficient single-board computers, which are interconnected within a network with the software defined configuration. The proposed SDN switch is deployed on Raspberry Pi 3 board using Open vSwitch (OvS) software, while the Floodlight controller is deployed on the Orange Pi Prime board. We firstly presented and implemented the method for measuring a delay introduced by each component of the IoT infrastructure, ranging from the sensor, the core of SDN, the IoT broker, to an IoT subscriber. Thus, we presented the approach for estimating energy efficiency for SDN based IoT platform proportional to the traffic. The experiments carried out on a real SDN topology based on single-board computers show that our approach not only saves up to 53.56% of energy at low traffic intensity, but also provides QoS guarantee for IoT applications.