Electrospinning of gelatin fibers using solutions with low acetic acid concentration: Effect of solvent composition on both diameter of electrospun fibers and cytotoxicity

Gelatin fibers were prepared by electrospinning of gelatin/acetic acid/water ternary mixtures with the aim of studying the feasibility of fabricating gelatin nanofiber mats at room temperature using an alternative benign solvent by significantly reducing the acetic acid concentration. The results showed that gelatin nanofibers can be optimally electrospun with low acetic acid concentration (25%, v/v) combined with gelatin concentrations higher than 300 mg/mL. Both gelatin solutions and electrospun gelatin mats (prepared with different acetic acid aqueous solutions) were analyzed by Fourier transform infrared spectroscopy and differential scanning calorimetry techniques to determine the chemical and structural changes of the polymer. The electrospun gelatin mats fabricated from solutions with low acetic acid content showed some advantages as the maintenance of the decomposition temperature of the pure gelatin (～ 230°C) and the reduction of the acid content on electrospun mats, which allowed to reach a cell viability upper than 90% (analyzed by cell viability test using human dermal fibroblast and embryonic kidney cells). This study has also analyzed the influence of gelatin and acetic acid concentration both on the solution viscosity and the electrospun fiber diameter, obtaining a clear relationship between these parameters. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42115.     

Proteases to Improve the Mechanical Characteristics of Durable Press Finished Cotton Fabrics

N‐Methylol reagents are conventional crosslinking agents that are still widely used in textile industry to produce crease‐resistant cotton fabrics. In this work serine proteases were used to recover the strength of fabrics, cross‐linked with N‐hydroxymethylacrylamide. Nearly one half of the strength loss of crosslinked cotton fabrics could be restored after protease treatment, while the wrinkle recovery angle (WRA) decreased only slightly. The enzymatic hydrolysis of the amide cross‐links in the durable pressed cellulose was confirmed by FT‐IR analysis and dyeability with an acid dye.

Effect of protease concentration on the tensile strength recovery, WRA and acid dye dyeability at 30 min reaction time.     

Dyeing in catalase-treated bleaching baths

The conventional rinsing after bleaching to remove the residual hydrogen peroxide, harmful to the reactive colorants, was replaced by enzymatic cleaning using catalases. The catalase-treated bleaching liquor was reused for dyeing. Though no hydrogen peroxide was detected after the enzymatic process, the bleaching bath composition caused unacceptable colour changes on dyed fabrics. By varying the parameters of the dyeing process – dye, salt, alkali and enzyme concentrations – the colour difference could be reduced significantly and a good dyeing result could be achieved.     

Laccases to Improve the Whiteness in a Conventional Bleaching of Cotton

This study reports for the first time on the enhancement of the bleaching effect achieved on cotton using laccase enzyme. Laccases applied in short‐time batchwise or pad‐dry processes prior to conventional peroxide bleaching, improved the end fabric whiteness. The whiteness level reached in the combined enzymatic/peroxide process was comparable to the whiteness in two consecutive peroxide bleaches.

Effect of 10 min laccase pre‐treatment at 60 °C, pH 5 on fabrics whiteness before and after a conventional hydrogen peroxide bleaching.     

Effect of temperature and bath composition on the dyeing of cotton with catalase-treated bleaching effluent

Conventional rinsing to remove residual hydrogen peroxide after the bleaching of cotton fabric can be replaced by enzymatic cleaning using catalases. Our previous study showed that dyeing in such catalase-treated bleaching baths results in a shade change on the dyed fabrics. The aim of this present study was to investigate the reasons for the unacceptable colour differences of the dyed fabrics. Experiments were performed to study the possible temperature-dependent dye interactions in the standard dyebath, and in the dyebath prepared with bleaching effluent. Fluorescence emission spectra were used to detect changes in the structure of the catalase related to the thermal unfolding and denaturing of the protein. It was found that the colour difference on the dyed textiles could be attributed to the temperature-dependent dye-enzyme interaction and precipitation, as well as to the complexity of the bleaching bath composition.     

Variable Induction of Pro-Inflammatory Cytokines by Commercial SARS CoV-2 Spike Protein Reagents: Potential Impacts of LPS on In Vitro Modeling and Pathogenic Mechanisms In Vivo

Proinflammatory cytokine production following infection with severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) is associated with poor clinical outcomes. Like SARS CoV-1, SARS CoV-2 enters host cells via its spike protein, which attaches to angiotensin-converting enzyme 2 (ACE2). As SARS CoV-1 spike protein is reported to induce cytokine production, we hypothesized that this pathway could be a shared mechanism underlying pathogenic immune responses. We herein compared the capabilities of Middle East Respiratory Syndrome (MERS), SARS CoV-1 and SARS CoV-2 spike proteins to induce cytokine expression in human peripheral blood mononuclear cells (PBMC). We observed that only specific commercial lots of SARS CoV-2 induce cytokine production. Surprisingly, recombinant SARS CoV-2 spike proteins from different vendors and batches exhibited different patterns of cytokine induction, and these activities were not inhibited by blockade of spike protein-ACE2 binding using either soluble ACE2 or neutralizing anti-S1 antibody. Moreover, commercial spike protein reagents contained varying levels of lipopolysaccharide (LPS), which correlated directly with their abilities to induce cytokine production. The LPS inhibitor, polymyxin B, blocked this cytokine induction activity. In addition, SARS CoV-2 spike protein avidly bound soluble LPS in vitro, rendering it a cytokine inducer. These results not only suggest caution in monitoring the purity of SARS CoV-2 spike protein reagents, but they indicate the possibility that interactions of SARS CoV-2 spike protein with LPS from commensal bacteria in virally infected mucosal tissues could promote pathogenic inflammatory cytokine production.     

Layer‐By‐Layer Coating of Aminocellulose and Quorum Quenching Acylase on Silver Nanoparticles Synergistically Eradicate Bacteria and Their Biofilms

The emergence of antibiotic‐resistant bacteria and the failure of the existing antibacterial therapeutics call for development of novel treatment strategies. Furthermore, the formation of bacterial biofilms restricts drug penetration and efficiency, causing life‐threatening infections. Bacterial attachment and biofilm formation are regulated by the cell‐to‐cell communication phenomenon called quorum sensing (QS). In this work, antimicrobial silver nanoparticles (AgNPs) are decorated in a layer‐by‐layer fashion with the oppositely charged aminocellulose (AM) and acylase to generate hybrid nanoentities with enhanced antibacterial and antibiofilm activities as well as reduced cytotoxicity. Acylase, a quorum‐quenching enzyme that degrades the QS signals in the extracellular environment of bacteria, disrupts the bacterial QS process and together with the bactericidal AM synergistically lowers fourfold the minimum inhibitory concentration of the AgNPs templates toward Gram‐negative Pseudomonas aeruginosa (P. aeruginosa). The hybrid nanoparticles in eightfold‐lower concentration than the AgNPs inhibit 45% of the QS‐regulated virulence factors produced by the reporter Chromobacterium violaceum bacterial strain and reduce by 100% the P. aeruginosa biofilm formation. Moreover, the sequential deposition of antibacterial/antibiofilm active and biocompatible biopolymers onto the AgNPs allows the engineering of safe nanomaterials that do not affect the viability of human cells.     

Properties of the reachable set of control systems

We investigate some properties of the reachable set of a control system. Representing the system as a differential inclusion and using proximal Hamilton–Jacobi equation we describe its graph. We work in infinitely dimensional Hilbert space and use one sided Lipschitz approach. The funnel equation is considered in the last section. That equation describes the reachable set in arbitrary Banach space. We consider also the autonomous case and prove the existence of a limit of the reachable set.     

Lipases to Improve the Performance of Formaldehyde‐Free Durable Press Finished Cotton Fabrics

Lipases were used to restore partially the strength losses of cotton fabrics crosslinked with 1,2,3,4‐butanetetracarboxylic acid. The enzymatic hydrolysis of the ester linkages at low temperature and neutral pH resulted in 10% strength recovery, coupled with a slight deterioration of the crease‐resistance effect. The conventional alkaline hydrolysis provided higher strength recovery, however provoked considerable change in the durable press performance of the fabrics.     

Sonochemical synthesis and stabilization of concentrated antimicrobial silver‐chitosan nanoparticle dispersions

This work reports on a green synthetic route to produce concentrated aqueous dispersions of silver nanoparticles (AgNP) employing high‐intensity ultrasound (US) and chitosan (CS) as a nontoxic reducing agent for Ag⁺ salts and AgNP stabilizer. The sonication simultaneously boosted the synthesis and improved the stability of the AgNP, capping them with CS. Hybrid AgNP‐CS antimicrobial dispersions, stable for at least 6 months, were synthesized in a simple single step process. The use of US allowed for applying relatively mild processing temperatures (60 °C) and reaction time between 30 min and 3 h to obtain concentrated dispersions of AgNP that otherwise could not be obtained even after 72 h under mechanical stirring at the same reaction conditions. Upon sonication spherical AgNP‐CS with a size between 60 and 100 nm were generated, in contrast to the average diameter of ～200 nm of the particles obtained by stirring. The antibacterial efficiency of the AgNP‐CS hybrids was evaluated against the medically relevant pathogens Staphylococcus aureus and Escherichia coli. The US‐synthesized AgNP‐CS showed more than three fold higher antibacterial activity compared to the particles obtained under stirring, due to their higher concentration and smaller size. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45136.