Introduction to Essential Oils as New Agents for Corrosion Inhibition

Corrosion is a widespread problem that affects a variety of sectors, causing considerable economic losses and safety risks. Traditional corrosion inhibitors frequently use synthetic compounds, which can be poisonous and environmentally hazardous. Essential oils have recently emerged as interesting alternatives due to their natural origin, biodegradability, and potential anti-corrosion properties. This review introduces the use of essential oils as novel corrosion inhibitors. It addresses the chemical composition of essential oils, their corrosion-prevention processes, and the benefits they provide over traditional inhibitors. The review also includes contemporary research findings and case studies that demonstrate the effectiveness of essential oils in a variety of acidic situations. By investigating the potential of essential oils for corrosion inhibition, this research hopes to contribute to the development of safer and more sustainable corrosion control systems

Comparative study of inhibitory efficacy of methionine and its derivatives in acidic medium by mild steel

Corrosion inhibition effect of L-Methionine (MT1), L-Methionine sulfoxide (MT2) and L-Methionine sulfone (MT3) on mild steel corrosion in 1M HCl solution was studied by using weight loss, electrochemical polarization and electrochemical impedance spectroscopy (EIS) techniques. The experimental results showed that the inhibitory efficiency of the three aminoacids improves with the increase of concentration to reach the maximum value of 95.20% for MT1, 94.14% for MT2 and 88.92% for MT3 for a concentration of 10-3M, which translates that the surface covered by the inhibitor increases with the concentration. The effect of temperature on the corrosion rate was investigated and some thermodynamic parameters were calculated. Polarization studies show that three studied inhibitors suggested that three inhibitors control the anodic as well as cathodic reactions and act as mixed type in nature. The results show that MT1, MT2 and MT3 are good inhibitors, and the adsorption of each inhibitor on mild steel surface obeys Flory-Huggins and Langmuir, with a better fit of the Langmuir isotherm through mixed adsorption (physisorption as well as chemisorption) process. In addition, the quantum approach based on density functional theory (DFT), monte Carlo (MC) and molecular dynamics (MD) simulations was confirmed the reactivity of the studied compound towards the corrosion process

A microRNA profile of human CD8(+) regulatory T cells and characterization of the effects of microRNAs on Treg cell-associated genes.

Recently, regulatory T (Treg) cells have gained interest in the fields of immunopathology, transplantation and oncoimmunology. Here, we investigated the microRNA expression profile of human natural CD8(+)CD25(+) Treg cells and the impact of microRNAs on molecules associated with immune regulation. We purified human natural CD8(+) Treg cells and assessed the expression of FOXP3 and CTLA-4 by flow cytometry. We have also tested the ex vivo suppressive capacity of these cells in mixed leukocyte reactions. Using TaqMan low-density arrays and microRNA qPCR for validation, we could identify a microRNA 'signature' for CD8(+)CD25(+)FOXP3(+)CTLA-4(+) natural Treg cells. We used the 'TargetScan' and 'miRBase' bioinformatics programs to identify potential target sites for these microRNAs in the 3'-UTR of important Treg cell-associated genes. The human CD8(+)CD25(+) natural Treg cell microRNA signature includes 10 differentially expressed microRNAs. We demonstrated an impact of this signature on Treg cell biology by showing specific regulation of FOXP3, CTLA-4 and GARP gene expression by microRNA using site-directed mutagenesis and a dual-luciferase reporter assay. Furthermore, we used microRNA transduction experiments to demonstrate that these microRNAs impacted their target genes in human primary Treg cells ex vivo. We are examining the biological relevance of this 'signature' by studying its impact on other important Treg cell-associated genes. These efforts could result in a better understanding of the regulation of Treg cell function and might reveal new targets for immunotherapy in immune disorders and cancer

Conference highlights of the 15th international conference on human retrovirology: HTLV and related retroviruses, 4-8 june 2011, Leuven, Gembloux, Belgium

The June 2011 15th International Conference on Human Retrovirology: HTLV and Related Viruses marks approximately 30 years since the discovery of HTLV-1. As anticipated, a large number of abstracts were submitted and presented by scientists, new and old to the field of retrovirology, from all five continents. The aim of this review is to distribute the scientific highlights of the presentations as analysed and represented by experts in specific fields of epidemiology, clinical research, immunology, animal models, molecular and cellular biology, and virology

Empowering the immune fate of bone marrow mesenchymal stromal cells: gene and protein changes

Objective and design: Bone marrow mesenchymal stromal cells (BM-MSCs) are referred as a promising immunotherapeutic cell product. New approaches using empowered MSCs should be developed as for the treatment or prevention of different immunological diseases. Such preconditioning by new licensing stimuli will empower the immune fate of BM-MSCs and, therefore, promote a better and more efficient biological. Here, our main goal was to establish the immunological profile of BM-MSCs following inflammatory priming and in particular their capacity to adjust their immune-related proteome and transcriptome. Material and methods: To run this study, we have used BM-MSC cell cultures, a pro-inflammatory cytokine cocktail priming, flow cytometry analysis, qPCR and ELISA techniques. Results: Different expression levels of several immunological mediators such as COX-1, COX-2, LIF, HGF, Gal-1, HO-1, IL-11, IL-8, IL-6 and TGF-β were constitutively observed in BM-MSCs. Inflammation priming substantially but differentially modulated the gene and protein expression profiles of these mediators. Thus, expressions of COX-2, LIF, HGF, IL-11, IL-8 and IL-6 were highly increased/induced and those of COX-1, Gal-1, and TGF-β were reduced. Conclusions: Collectively, we demonstrated that BM-MSCs are endowed with a specific and modular regulatory machinery which is potentially involved in immunomodulation. Moreover, BM-MSCs are highly sensitive to inflammation and respond to such signal by properly adjusting their gene and protein expression of regulatory factors. Using such preconditioning may empower the immune fate of MSCs and, therefore, enhance their value for cell-based immunotherapy.SCOPUS: ar.jinfo:eu-repo/semantics/publishe