RESUMEN
Background and Objectives: Plasma radiation is a widely used technique for sterilization or decontamination in various industries, as well as in some healthcare settings such as dentistry. The primary aim of this study was to assess the potential of plasma radiation to create a new population of Staphylococcus aureus cells with distinct characteristics that could lead to novel healthcare challenges. Materials and Methods: A homemade non-thermal plasma apparatus was applied and the effects of plasma treatment on S. aureus ATCC25923 was assessed. Plasma radiation was applied under controlled conditions to ensure that some bacterial cells remained viable. The treatment was repeated 10 times, with each round followed by a recovery phase to collect any surviving bacterial cells. To assess the potential changes in the bacterial population, we examined the antibiotic susceptibility pattern, micro-structural characteristics using scanning electron microscopy (SEM), and total protein profile using the matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) technique. Results: The experimental results revealed slight variations in the antibiotic susceptibility patterns of certain cell wall agents (imipenem, cephalothin, and cefepime), as well as in the MALDI-TOF spectra. However, no changes were observed in the SEM images. Conclusion: The insufficient application of non-thermal plasma in bacterial decontamination may lead to physiological changes that could enrich or select certain subpopulations of S. aureus.
RESUMEN
Wool fiber is a natural protein fiber, which is used for the manufacturing of apparels, and floorcoverings because of its excellent fire retardancy, stain-resistance, antistatic and odor control properties along with exceptional warmth and resilience. However, wool fiber has several serious demerits, such as garments made of wool fibers extensively shrink during their laundering. To overcome this problem, wool fibers, especially those are used in apparel, are frequently shrink-resist treated to make them machine-washable. A wide range of treatments including oxidative, enzymatic, radiation, polymeric coatings, sol-gel coatings, and plasma treatments have been investigated to make wool fiber shrink-resistant. In this review, the mechanisms of wool fiber shrinkage, the research carried out until recently to make wool fiber shrink-resistant, and the current status of the sustainable alternatives developed, have been compiled and presented. The various methods investigated have been critically discussed with their merits and demerits, shrink-resist performance, and their shrink-resistance mechanisms. The chemistry and synthesis of various polymers used for the shrink-resistance and their reactions with wool fiber have been outlined. This review also includes the current challenges to make shrink-resist treatments green and sustainable, and also the future directions to meet these challenges. Some of the treatments investigated may affect the biodegradability of wool fibers, especially those are based on coating with synthetic polymers. A sustainable alternative polymeric coating based on sustainably produced polymeric resins, especially bio-based resins, needs to be developed so that the future treatments become sustainable.
RESUMEN
This work evaluated the effects of UV irradiation, plasma radiation, steam and 70% ethanol treatments on the sterilization and integrity of auto-crosslinked hyaluronic acid (HA-ACP) scaffolds structured in microparticles and sponges aiming in vivo applications for regenerative medicine of bone tissue. The integrity of the microparticles was characterized by rheological behavior, while for the sponges, it was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy and differential scanning calorimetry. The effectiveness of the sterilization treatment was verified by the number of microorganism colonies in the samples after the treatments. In conclusion, plasma radiation was the best treatment for the sponges, while steam sterilization in the autoclave at 126°C (1.5 kgf/cm2) for 5 min was the best treatment for the microparticles.