A novel scheme of pre-surface modification of media using mixed argon-nitrogen plasma is proposed to improve the protection performance of 1.5 nm carbon overcoats (COC) on media produced by a facile pulsed DC sputtering technique. We observe stable and lower friction, higher wear resistance, higher oxidation resistance, and lower surface polarity for the media sample modified in 70%Ar + 30%N2 plasma and possessing 1.5 nm COC as compared to samples prepared using gaseous compositions of 100%Ar and 50%Ar + 50%N2 with 1.5 nm COC. Raman and X-ray photoelectron spectroscopy results suggest that the surface modification process does not affect the microstructure of the grown COC. Instead, the improved tribological, corrosion-resistant and oxidation-resistant characteristics after 70%Ar + 30%N2 plasma-assisted modification can be attributed to, firstly, the enrichment in surface and interfacial bonding, leading to interfacial strength, and secondly, more effective removal of ambient oxygen from the media surface, leading to stronger adhesion of the COC with media, reduction of media corrosion and oxidation, and surface polarity. Moreover, the tribological, corrosion and surface properties of mixed Ar + N2 plasma treated media with 1.5 nm COCs are found to be comparable or better than ~2.7 nm thick conventional COC in commercial media.
Understanding and engineering interfaces, and controlling the friction and wear of materials, are extremely important for many technological applications, particularly for magnetic storage technologies and micro-and nanoelectromechanical systems (MEMS and NEMS), where one sliding/moving surface comes into contact with another. Ultrathin carbon fi lms are generally employed in most of these technologies. However, their wear and friction mechanisms are not well understood, especially the role of the fi lm-substrate (FS) interface has not been deeply explored and discussed to date. This limits further developments in this fi eld. Through experimental and theoretical experiments, we are able to report on the engineering of a FS interface consisting of high sp 3and high sp 2 -bonded ultrathin carbon fi lms on Al 2 O 3 -TiC substrates by introducing a silicon nitride (SiN x ) interlayer and tuning the carbon ion energy. All carbon-based overcoats show a low coeffi cient of friction (COF) in the range of 0.08-0.16; however, the high sp 3 -bonded C/SiN x bilayer overcoat reveals the lowest and most stable friction. The friction mechanism is explained using an integrated framework of surface passivation, rehybridization, material transfer, tribolayer formation, and interfaces. We discover that FS interface engineering substantially reduces the wear of ultrathin carbon fi lms while maintaining/ reducing the friction. In general, this approach can be applied to control the friction and wear of ultrathin fi lms of diverse materials.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a new virus in coronavirus family that causes coronavirus disease (COVID-19), emerges as a big threat to the human race. To date, there is no medicine and vaccine available for COVID-19 treatment. While the development of medicines and vaccines are essentially and urgently required, what is also extremely important is the repurposing of smart materials to design effective systems for combating COVID-19. Graphene and graphene-related materials (GRMs) exhibit extraordinary physicochemical, electrical, optical, antiviral, antimicrobial, and other fascinating properties that warrant them as potential candidates for designing and development of high-performance components and devices required for COVID-19 pandemic and other futuristic calamities. In this article, we discuss the potential of graphene and GRMs for healthcare applications and how they may contribute to fighting against COVID-19.
The design of a drug delivery system and the fabrication of efficient, successful, and targeted drug carriers are two separate issues that require slightly different design parameters. The geometry of the drug carrier such as its size and shape, chemical structure, surface chemistry, and surface charge are among the key parameters that need to be optimized to achieve the desired therapeutic behaviour.We review here the effects of the size of the drug delivery carrier on its biodistribution, target specificity, body clearance rate and, most importantly, the therapeutic action of the drug. Pulmonary and intravenous drug administration are the main focus, with special emphasis on cancer therapeutics and lung-targeted drug delivery. The significance of the effect of the dimensional variations and size of the drug delivery carriers on appropriate controlled and targeted drug delivery is explored with the aim of both prohibiting excessive therapeutic loss via different clearance routes and overcoming sideeffects and toxicity.
In an era of relentless evolution of antimicrobial resistance, there is an increasing demand for the development of efficient antimicrobial coatings or surfaces for food, biomedical, and industrial applications. This study reports the laccase-catalyzed room-temperature synthesis of mechanically robust, thermally stable, broad spectrum antimicrobial films employing interfacial interactions between poly(vinyl alcohol), PVA, and 14 naturally occurring catecholamines and polyphenols. The oxidative products of catecholamines and polyphenols reinforce the PVA films and also alter their surface and bulk properties. Among the catecholamines-reinforced films, optimum surface and bulk properties can be achieved by the oxidative products of epinephrine. For polyphenols, structure-property correlation reveals an increase in surface roughness and elasticity of PVA films with increasing number of phenolic groups in the precursors. Interestingly, PVA films reinforced with oxidized/polymerized products of pyrogallol (PG) and epinephrine (EP) display potent antimicrobial activity against pathogenic Gram-positive and Gram-negative strains, whereas hydroquinone (HQ)-reinforced PVA films display excellent antimicrobial properties against Gram-positive bacteria only. We further demonstrate that HQ and PG films retain their antimicrobial efficacy after steam sterilization. With an increasing trend of giving value to natural and renewable resources, our results have the potential as durable self-defensive antimicrobial surfaces/films for advanced healthcare and industrial applications.
Bacterial colonization
of acute and chronic wounds is often associated
with delayed wound healing and prolonged hospitalization. The rise
of multi-drug resistant bacteria and the poor biocompatibility of
topical antimicrobials warrant safe and effective antimicrobials.
Antimicrobial agents that target microbial membranes without interfering
with the mammalian cell proliferation and migration hold great promise
in the treatment of traumatic wounds. This article reports the utility
of superhydrophilic electrospun gelatin nanofiber dressings (NFDs)
containing a broad-spectrum antimicrobial polymer, ε-polylysine
(εPL), crosslinked by polydopamine (pDA) for treating second-degree
burns. In a porcine model of partial thickness burns, NFDs promoted
wound closure and reduced hypertrophic scarring compared to untreated
burns. Analysis of NFDs in contact with the burns indicated that the
dressings trap early colonizers and elicit bactericidal activity,
thus creating a sterile wound bed for fibroblasts migration and re-epithelialization.
In support of these observations, in porcine models of Pseudomonas aeruginosa and Staphylococcus
aureus colonized partial thickness burns, NFDs decreased
bacterial bioburden and promoted wound closure and re-epithelialization.
NFDs displayed superior clinical outcome than standard-of-care silver
dressings. The excellent biocompatibility and antimicrobial efficacy
of the newly developed dressings in pre-clinical models demonstrate
its potential for clinical use to manage infected wounds without compromising
tissue regeneration.
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