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Microbial infections are a global health challenge often treated with antibiotics, but their overuse can lead to antibiotic resistance. To address this, there is a need for more efficient personal protective equipment (PPE) with novel antimicrobial techniques. One such technique involves using carbon dots (CDs) to create self-disinfecting fabrics. This study focused on synthesizing phenylboronic-acid-functionalized piperine-based carbon dots (PBA-PPCDs) and boronic acid carbon dots (BACDs) as potential antimicrobial agents. The materials were successfully synthesized using a hydrothermal method and characterized using various techniques to confirm the size, charge, fluorescence properties, and inner morphology of the CDs. The CDs showed bactericidal activity against gram-positive and gram-negative bacteria, with potent inhibition in growth especially in the presence of simulated sunlight. The antibacterial properties of the CDs were tested on cellulose discs, demonstrating strong adherence and significant inhibition of bacterial cells. The cytotoxicity studies showed that these CDs, at concentrations up to 0.1 mg/mL, and the CD-modified fibers are benign to mammalian cells, emphasizing their safety for human use. Overall, the study concluded that PBA-PPCDs and BACDs are promising candidates for modifying fibers and inducing antimicrobial activity in fabrics made of cellulose fibers.Article highlights: New self-disinfecting fabrics kill bacteria with light-activated carbon dots, no harsh chemicals needed. Self-disinfecting fabrics fight bacteria, reduce antibiotic use, and slow superbug growth. Safe and effective: Carbon dot fabrics harmless to humans, promising for PPE. [ABSTRACT FROM AUTHOR]

In situ preparation of bifunctional thiazolo[5,4‐d]thiazole (TTz)‐based fluorophore cross‐linked nanofibers is successfully performed. These multifunctional nanofibers are used as both crystal growth template and antibacterial substrate that makes bacterial detection possible simultaneously. These highly fluorescent nanofibers act as optical sensors toward many analytes. The acid, base, and metal cation‐sensitive nature of the 2,5‐bis(4‐hydroxyphenyl)thiazolo[5,4‐d]thiazole (HPhTT) dye makes the prepared PVA nanofibers sensitive against these chemicals. Metal nanoparticles (MNPs) or metal oxide crystal formation occurs on the surface of nanofibers without any reducing agent. The strong interaction between metal cations and fluorophores results in crystal formation on the surface, which is named for the first time as "complexation‐triggered crystalization." These dye cross‐linked and metal‐interacted nanofibers exhibit antibacterial effect against E. coli (ATCC 25922), S. aureus (ATCC 25923), P. aeruginosa (ATCC 27853), and E. faecalis (ATCC 25922) strains. Also, the emission wavelength change of nanofibers in bacterial contamination makes it possible to use smart nanofiber films for optical bacteria detection. These novel materials pave the way for new applications such as smart wound bands, optical sensors, and one‐step preparation of surface‐enhanced Raman spectroscopy substrate. [ABSTRACT FROM AUTHOR]

[Display omitted] The widespread resistance of clinically relevant bacteria against established antibiotics emphasizes the urgent need for novel therapeutics. In this context, wound infections constitute a specific challenge, as most systemically applied antibiotics are insufficiently available at the site of infection. Therefore, the local treatment of infected wounds poses a particular challenge regarding the appropriate release kinetics of actives and their residence time in the wound bed. Consequently, design and development of novel, drug-loaded wound dressings constitute a major research focus for the effective treatment of wound infections. In this study, we employed electrospinning to design drug-loaded wound dressings, incorporating the therapeutically promising antimicrobial peptide tyrothricin. By parallel electrospinning, we combined different ratios of water-soluble polyvinylpyrrolidone and water-insoluble methacrylate copolymer (Eudragit E), in order to take advantage of their specific mechanical stability and dissolution properties. We fabricated fiber mats constituting mechanically stable wound dressings with a controlled drug release profile, combining an initial burst release above the minimal inhibitory concentration of known wound pathogens and a subsequent prolonged antimicrobial effect of the active ingredient. Antimicrobial activity against Staphylococcus aureus and Staphylococcus epidermidis was successfully proven, thereby introducing our tyrothricin-loaded fiber mats as a promising prospective therapy against typical wound-associated pathogens. [ABSTRACT FROM AUTHOR]

The dynamic development of the world economy entails an increasing exchange of goods and population. This means that we are globally struggling with increasing levels of nosocomial infections. The increasing use of antimicrobial agents triggers the microorganisms’ immune system, which in turn contributes to the increasing amount of antibiotic-resistant microorganisms, making it necessary to control the development of unwanted microorganisms, including bacteria, especially those carried on the body and clothing.

Abstract The state-of-the-art hernia meshes, used in hospitals for hernia repair, are predominantly polymeric textile-based constructs that present high mechanical strength, but lack antimicrobial properties. Consequently, preventing bacterial colonization of implanted prosthetic meshes is of major clinical relevance for patients undergoing hernia repair. In this study, the co-axial electrospinning technique was investigated for the development of a novel mechanically stable structure incorporating dual drug release antimicrobial action. Core/shell structured nanofibers were developed, consisting of Nylon-6 in the core, to provide the appropriate mechanical stability, and Chitosan/Polyethylene oxide in the shell to provide bacteriostatic action. The core/shell structure consisted of a binary antimicrobial system incorporating 5-chloro-8-quinolinol in the chitosan shell, with the sustained release of Poly(hexanide) from the Nylon-6 core of the fibers. Homogeneous nanofibers with a "beads-in-fiber" architecture were observed by TEM, and validated by FTIR and XPS. The composite nanofibrous meshes significantly advance the stress–strain responses in comparison to the counterpart single-polymer electrospun meshes. The antimicrobial effectiveness was evaluated in vitro against two of the most commonly occurring pathogenic bacteria; S. aureus and P. aeruginosa, in surgical site infections. This study illustrates how the tailoring of core/shell nanofibers can be of interest for the development of active antimicrobial surfaces.

The state-of-the-art hernia meshes, used in hospitals for hernia repair, are predominantly polymeric textile-based constructs that present high mechanical strength, but lack antimicrobial properties. Consequently, preventing bacterial colonization of implanted prosthetic meshes is of major clinical relevance for patients undergoing hernia repair. In this study, the co-axial electrospinning technique was investigated for the development of a novel mechanically stable structure incorporating dual drug release antimicrobial action. Core/shell structured nanofibers were developed, consisting of Nylon-6 in the core, to provide the appropriate mechanical stability, and Chitosan/Polyethylene oxide in the shell to provide bacteriostatic action. The core/shell structure consisted of a binary antimicrobial system incorporating 5-chloro-8-quinolinol in the chitosan shell, with the sustained release of Poly(hexanide) from the Nylon-6 core of the fibers. Homogeneous nanofibers with a "beads-in-fiber" architecture were observed by TEM, and validated by FTIR and XPS. The composite nanofibrous meshes significantly advance the stress–strain responses in comparison to the counterpart single-polymer electrospun meshes. The antimicrobial effectiveness was evaluated in vitro against two of the most commonly occurring pathogenic bacteria; S. aureus and P. aeruginosa, in surgical site infections. This study illustrates how the tailoring of core/shell nanofibers can be of interest for the development of active antimicrobial surfaces. [ABSTRACT FROM AUTHOR]

Sensitivity of dyes' colors to the surrounding environment causes lower durability and stability of color, which reflects the importance of durable finishing treatment. Current technique offered antimicrobial/durable finishing of viscose fibers through direct formation of AuNPs inside fibers macromolecules without using any external agents. By using the reducing properties of cellulose in viscose, Au +3 was reduced to AuNPs and CHO/OH of cellulose subsequently were oxidized to COOH. For comparison, two different media were used; aqueous and alkaline. Increasing the reactivity and accessibility of cellulose macromolecules in alkali leaded to enlargement of the reduction process and more incorporation of AuNPs. Size of AuNPs inside fiber was recorded to be in range of 22–112 nm and 14–100 nm, in case of using aqueous and alkaline medium, respectively. Structure and properties of fibers were not changed by treatment according to XRD and ATR-FTIR data. The treated fibers were acquired durable violet color by the action of LSPR for AuNPs and darker color obtained using higher Au +3 concentration. The treated fibers exhibited good inhibition against different pathogenic microbes including bacteria and fungi. One-pot, quite simple, inexpensive, green and industrial viable are the significant advantages of the current technique for viscose finishing (pigmentation and antimicrobial action). [ABSTRACT FROM AUTHOR]

This paper gives an overview of the current state in the field of cellulosic fibers functionalization by chemical modification. The emphasis is placed on the selective (periodate and TEMPO oxidation) and non-selective (permanganate and peroxide) cellulose oxidation, non-conventional methods for obtaining man-made cellulosic fibers, methods for obtaining antimicrobial cellulosic fibers, as well as method for obtaining two-component polysaccharide fibers. To provide evidence on the achieved functionalities we mainly used capillary rise method, moisture and iodine sorption method, water retention power, NaOH uptake, different ions sorption, Cu-number, carbonyl-and carboxyl-selective labelling and antimicrobial tests.

Antimicrobial fibers based on biodegradable polymers, poly(lactic acid) (PLA), and poly(butylene adipate-co-terephthalate) (PBAT) are prepared by electrospinning. For this purpose, a biodegradable/bio-based polyitaconate containing azoles groups (PTTI) is incorporated at 10 wt.% into the electrospinning formulations. The resulting fibers functionalized with azole moieties are uniform and free of beads. Then, the accessible azole groups are subjected to N-alkylation, treatment that provides cationic azolium groups with antibacterial activity at the surface of fibers. The positive charge density, roughness, and wettability of the cationic fibers are evaluated and compared with flat films. It is confirmed that these parameters exert an important effect on the antimicrobial properties, as well as the length of the alkylating agent and the hydrophobicity of the matrix. The quaternized PLA/PTTI fibers exhibit the highest efficiency against the tested bacteria, yielding a 4-Log reduction against S. aureus and 1.7-Log against MRSA. Then, biocompatibility and bioactivity of the fibers are evaluated in terms of adhesion, morphology and viability of fibroblasts. The results show no cytotoxic effect of the samples, however, a cytostatic effect is appreciated, which is ascribed to the strong electrostatic interactions between the positive charge at the fiber surface and the negative charge of the cell membranes., (© 2022 The Authors. Macromolecular Bioscience published by Wiley-VCH GmbH.)

Two methods were used to incorporate silver ions into poly(trimethylene terephthalate) (PTT) fibers. The first technique involved the direct addition of silver (I) sulfadiazine into PTT polymer prior to extrusion. The second method involved the use of silver-exchanged zeolites. Although no optimization with silver-exchanged zeolites was conducted, this study clearly showed that PTT fibers containing sufficient amounts of silver ions are effective in reducing pathological microorganisms such as Escherichia coli. Incorporation of silver-exchanged zeolites into PTT imparted a silver color to the fibers which may be attributed to the partial reduction of silver ions during spinning at 256°C. Because of the decomposition of silver (I) sulfadiazine, the spinnability of PTT fiber sample was not satisfactory and, therefore, this compound cannot be used as a carrier of silver ions in PTT. The thermal, tensile and antimicrobial properties of the spun filaments are reported in this paper. [ABSTRACT FROM AUTHOR]

Smart textiles based on conjugated polymers have been highlighted as promising fabrics that can intelligently respond to environmental stimuli based on the electrical properties of polymer semiconductors. However, there has been limited interest in the photothermal properties of conjugated polymers that can be applied to smart textiles. We prepared nanoparticles by assembling a conjugated polymer with a fatty acid via an emulsion process and nanocomposite fibers by distributing the conjugated polymer nanoparticles in a polyacrylonitrile matrix. We then fabricated the textiles using the fibers. The resulting fabrics based on nanocomposite fibers show a temperature increase to 50 °C in 10 min under white light irradiation because of efficient photothermal conversion by the conjugated polymer light harvester, while the temperature of a pristine polyacrylonitrile fabric increases to only 35 °C. In addition, excellent antimicrobial activity was confirmed by a 99.9% decrease in the populations of Staphylococcus aureus and Escherichia coli over 24 h because of the effect of the fatty acid in the nanocomposite films and fabrics. Furthermore, the fabric showed efficient durability after a laundry test, suggesting the usefulness of these smart textiles based on conjugated polymer nanoparticles for practical applications. [ABSTRACT FROM AUTHOR]

Smart textiles based on conjugated polymers have been highlighted as promising fabrics that can intelligently respond to environmental stimuli based on the electrical properties of polymer semiconductors. However, there has been limited interest in the photothermal properties of conjugated polymers that can be applied to smart textiles. We prepared nanoparticles by assembling a conjugated polymer with a fatty acid via an emulsion process and nanocomposite fibers by distributing the conjugated polymer nanoparticles in a polyacrylonitrile matrix. We then fabricated the textiles using the fibers. The resulting fabrics based on nanocomposite fibers show a temperature increase to 50 °C in 10 min under white light irradiation because of efficient photothermal conversion by the conjugated polymer light harvester, while the temperature of a pristine polyacrylonitrile fabric increases to only 35 °C. In addition, excellent antimicrobial activity was confirmed by a 99.9% decrease in the populations of Staphylococcus aureus and Escherichia coli over 24 h because of the effect of the fatty acid in the nanocomposite films and fabrics. Furthermore, the fabric showed efficient durability after a laundry test, suggesting the usefulness of these smart textiles based on conjugated polymer nanoparticles for practical applications.