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The low electrical conductivity of silk textile structures is a crucial factor limiting their practical applications. Silk‐based materials need modifications with different electroconductive compounds and structures. This report presents functionalization with silver nanowires (AgNWs) using polydopamine (PDA) as a linker. AgNWs create 3 and 10 g/m2 conductive networks on silk fabric. The surface resistance is estimated to be 1.5 × 105 Ω and 1.0 × 103 Ω, while volume resistance is 2.3 × 103 Ω and 6.8 × 102 Ω respectively to less and more developed AgNWs networks. AgNWs‐coated silk fabric is more thermally stable and provides thermal shielding. AgNWs functionalization makes silk fabric more hydrophilic due to PDA and polyvinylpyrrolidone (PVP) influence. PVP acts as a capping agent during AgNWs synthesis and remains on their surface. Silk fabric functionalized with AgNWs reveals above 99.94% reduction of bacterial growth against Gram‐positive and ‐negative bacteria Staphylococcus aureus and Klebsiella pneumoniae, respectively. The bacteriostatic and biocidal coefficients are respectively above 7.2 and 3.3 for both bacteria types. AgNWs do not harmfully influence excellent silk mechanical properties. The specific strength does not change significantly and the elongation at break is even improved. The presented AgNWs functionalized silk fabric has useful physical, antimicrobial, and electronic properties for designing multimodal textile products. [ABSTRACT FROM AUTHOR]

Understanding of biology of osteosarcoma malignant progression is indispensable for enhancement of conventional chemotherapy by the use of silver nanoparticles (AgNPs). We presented an in vitro model of cancer progression closely resembling processes occurring in vivo in terms of protein profile. A comparison of cytotoxic and genotoxic potential of AgNPs in Saos‐2 cells in early stages of cancerous progression (early passages) with the cells in advanced stages (late passages) demonstrated significantly reduced responsiveness of the late passage cells to nanoparticles toxicity. It was also confirmed by proteome analysis as we identified considerably higher number of differentially expressed proteins in Saos‐2 cells in early passages compared to the late passage cells. Our studies showed that the ability of AgNPs as potential drug carriers to deliver a medication and/or to evoke toxic effects might be significantly diminished in advanced stages of cancer progression. [ABSTRACT FROM AUTHOR]

Endothelial cell aging is related to changes not only in cell phenotype, such as luminal changes, intimal and medial thickening, and increased vascular stiffness, but encompasses different cell responses to various substances including drugs or nanomaterials. In the present work, time‐ and dose‐dependent elasticity changes evoked by silver nanoparticles in endothelial cells in early (below 15) passages were analyzed. Silver nanoparticle concentrations of 3, 3.6, and 16 μg/mL were selected for elasticity measurements for long incubation (24 hours) and of 1 and 3 μg/mL for monitoring dynamic elasticity changes of 1‐, 3‐, and 6‐hour incubations. Surprisingly, a significant reduction in the cells elasticity modulus at lower number of passages exposed to silver nanoparticles used at 3 μg/mL for 24 hours was demonstrated. These results are in contrast to those obtained for endothelial cells in late (33‐43) passages that may result from cellular aging in response to nanosilver. Furthermore, for short incubation times (1 and 3 hours), SNP‐induced significant increase in the cell elasticity modulus was detected. In current work, we also attempted to answer the question whether the changes in cell elasticity were induced by the silver nanoparticles stabilized with polyvinyl pyrrolidone or by stabilizer itself. Elasticity measurements were supplemented by observations made with transmission electron microscopy and scanning electron microscopy, which confirmed the presence of silver nanoparticles inside the cells and on the cell membrane. Additionally, activation of reactive oxygen species was detected for cells exposed to SNPs for 1 and 3 hours, which was accompanied by increased cell elasticity modulus suggesting a possible mechanism of observed phenomenon. [ABSTRACT FROM AUTHOR]

The hybrid technology combines an efficient material‐removal process and implant surface treatment by the laser reducing time of manufacture process compared to currently used machining technologies. It also permits precise structuring of the implant material surface. Six structures of the Ti6Al4V ELI surface were designed and studied how the structure topography prepared with the hybrid technology affected the Escherichia coli adhesion to the surface and viability, as well as the growth, adhesion, and viability of human osteogenic Saos‐2 cells cultured on the investigated surfaces. Results have confirmed that the microtopography of medical titanium alloy plays a beneficial role in bacterial adhesion and viability (number of bacteria found on reference surface: [5.9 ± 0.44] × 106 CFU/ml, sample no. 3: [8.8 ± 0.93] × 104 CFU/ml, and sample no. 5: [1.2 ± 0.23] × 107 CFU/ml; CFU ‐ Colony Forming Unit). All tested structured surfaces enabled good cell attachment and proliferation of Saos‐2 cells (viability of Saos‐2 cells [% of control] for reference surface: 81.93%; sample no. 3: 75% and sample no. 5: 100%). Transcriptome analysis of genes commonly expressed in the process of osseointegration demonstrated that the use of hybrid technology allows designing structures that enhance osseointegration but it should be coupled with other methods of preventing bacterial growth, or with a different strategy to limit microbial colonization with the satisfactory osseointegration potential. [ABSTRACT FROM AUTHOR]