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1.
J Chem Health Saf ; 28(3): 171-182, 2021 May 24.
Artigo em Inglês | MEDLINE | ID: mdl-37556257

RESUMO

Amid the coronavirus disease 2019 pandemic, demand for cloth face masks containing nanosilver has increased. Common product claims such as "antiviral" and "antimicrobial" can be attractive to buyers seeking to protect themselves from this respiratory disease, but it is important to note that filtration capabilities are the main factor to prevent virus transmission and that antimicrobial ability is a secondary protection factor. Silver has long been known to be antibacterial, and growing research supports additional antiviral properties. In this study, 40 masks claiming to contain silver were evaluated for substantiated antiviral and antimicrobial claims using methods available to the public. Criteria for determining the validity of substantiated claims included the use of patented technology, international certification for antimicrobial and/or antiviral textile by ISO or ASTM, EPA pesticide registration, and peer-reviewed literature. Our analysis showed that, of the 40 masks, 21 had substantiated claims. Using scanning electron microscopy (SEM), two of the substantiated face masks (A and B) were examined for silver identification for further confirmation. Mask A uses silver and copper ions attached to zeolite particles; the zeolite particles discovered through SEM were approximately 90-200 nm in diameter. In mask B, particles of silver and titanium at the 250 nm size were found. In conclusion, these certifications or patents are not enough to determine credibility, and stricter regulations by federal agencies on product testing for manufacturers that make claims are necessary to ensure the efficacy of the product advertised, as well as a cloth face mask inhalation standard.

2.
J Nanobiotechnology ; 17(1): 32, 2019 Feb 23.
Artigo em Inglês | MEDLINE | ID: mdl-30797235

RESUMO

BACKGROUND: The conventional approaches to assess the potential cytotoxic effects of nanomaterials (NMs) mainly rely on in vitro biochemical assays. These assays are strongly dependent on the properties of the nanomaterials, for example; specific surface area (SSA), size, surface defects, and surface charge, and the host response. The NMs properties can also interfere with the reagents of the biochemical and optical assays leading to skewed interpretations and ambiguous results related to the NMs toxicity. Here, we proposed a structured approach for cytotoxicity assessment complemented with cells' mechanical responses represented as the variations of elastic Young's modulus in conjunction with conventional biochemical tests. Monitoring the mechanical properties responses at various times allowed understanding the effects of NMs to the filamentous actin cytoskeleton. The elastic Young's modulus was estimated from the force volume maps using an atomic force microscope (AFM). RESULTS: Our results show a significant decrease on Young's modulus, ~ 20%, in cells exposed to low concentrations of graphene flakes (GF), ~ 10% decrease for cells exposed to low concentrations of multiwalled carbon nanotubes (MWCNTs) than the control cells. These considerable changes were directly correlated to the disruption of the cytoskeleton actin fibers. The length of the actin fibers in cells exposed to GF was 50% shorter than the fibers of the cells exposed to MWCNT. Applying both conventional biochemical approach and cells mechanics, we were able to detect differences in the actin networks induced by MWCNT inside the cells and GF outside the cell's membrane. These results contrast with the conventional live/dead assay where we obtained viabilities greater than 80% after 24 h; while the elasticity dramatically decreased suggesting a fast-metabolic stress generation. CONCLUSIONS: We confirmed the production of radical oxygen species (ROS) on cells exposed to CBNs, which is related to the disruption of the cytoskeleton. Altogether, the changes in mechanical properties and the length of F-actin fibers confirmed that disruption of the F-actin cytoskeleton is a major consequence of cellular toxicity. We evidenced the importance of not just nanomaterials properties but also the effect of the location to assess the cytotoxic effects of nanomaterials.


Assuntos
Módulo de Elasticidade/efeitos dos fármacos , Grafite/toxicidade , Nanotubos de Carbono/toxicidade , Células 3T3 , Citoesqueleto de Actina/metabolismo , Actinas/metabolismo , Adsorção , Animais , Membrana Celular/efeitos dos fármacos , Membrana Celular/metabolismo , Sobrevivência Celular/efeitos dos fármacos , Fibroblastos/citologia , Camundongos , Tamanho da Partícula , Propriedades de Superfície
3.
Molecules ; 23(2)2018 Feb 08.
Artigo em Inglês | MEDLINE | ID: mdl-29419803

RESUMO

Growing antimicrobial resistance is considered a potential threat for human health security by health organizations, such as the WHO, CDC and FDA, pointing to MRSA as an example. New antibacterial drugs and complex derivatives are needed to combat the development of bacterial resistance. Six new copper and cobalt complexes of azole derivatives were synthesized and isolated as air-stable solids and characterized by melting point analyses, elemental analyses, thermogravimetric analyses (TGA), and infrared and ultraviolet/visible spectroscopy. The analyses and spectral data showed that the complexes had 1:1 (M:L) stoichiometries and tetrahedral geometries, the latter being supported by DFT calculations. The antibacterial activities of the metal complexes by themselves and combined with silver nanoparticles (AgNPs; 2 µg mL-1) were assessed in vitro by broth microdilution assays against eight bacterial strains of clinical relevance. The results showed that the complexes alone exhibited moderate antibacterial activities. However, when the metal complexes were combined with AgNPs, their antibacterial activities increased (up to 10-fold in the case of complex 5), while human cell viabilities were maintained. The minimum inhibitory concentration (MIC50) values were in the range of 25-500 µg mL-1. This study thus presents novel approaches for the design of materials for fighting bacterial resistance. The use of azole complexes combined with AgNPs provides a new alternative against bacterial infections, especially when current treatments are associated with the rapid development of antibiotic resistance.


Assuntos
Antibacterianos/química , Antibacterianos/farmacologia , Azóis/química , Azóis/farmacologia , Nanopartículas Metálicas/química , Prata/química , Bactérias/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Cobalto/química , Coloides , Cobre/química , Humanos , Ligantes , Testes de Sensibilidade Microbiana , Microscopia de Força Atômica , Modelos Moleculares , Estrutura Molecular , Análise Espectral , Termogravimetria
4.
J Biomed Mater Res A ; 104(11): 2801-9, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27376695

RESUMO

Bacterial cellulose (BC) has been used as a scaffold for tissue regeneration (TR). Improving functional TR requires highly selective strategies for specific cell attraction. Embedding iron oxide nanoparticles into a BC matrix can drive magnetically labeled cells to specific tissues where they may begin to heal injured tissue. This article focuses on characterization and in vitro toxicity assessment of magnetic BC (MBC). We proposed to detect the production of radical oxygen species (ROS), esterase activity, and apoptosis to study cytotoxic interactions of MBC within its bioenvironment. Morphological characterization was performed using scanning electron microscopy where evidence shows that the diameter of MBC fibers compared to BC fibers was 33% smaller, and the pore areas were 25% bigger. Cytotoxicity assays in porcine aortic smooth muscle cells exposed for 24 hours to BC, MBC, and poly(ethylene glycol)-coated MBC (MBC-PEG) reveals 96% viability and 9% ROS production for MBC-PEG. In contrast, 25% of cells exposed to MBC were apoptotic, suggesting that even when the cells were metabolically active, MBC can induce damage. These outcomes support the need for more integral assessment in the hopes of assessing the potential biosafety and uses of nanocomposites for TR. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 2801-2809, 2016.


Assuntos
Materiais Biocompatíveis/química , Celulose/química , Gluconacetobacter xylinus/química , Nanopartículas de Magnetita/química , Miócitos de Músculo Liso/citologia , Animais , Apoptose/efeitos dos fármacos , Materiais Biocompatíveis/toxicidade , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Celulose/síntese química , Celulose/toxicidade , Compostos Férricos/química , Compostos Férricos/toxicidade , Nanopartículas de Magnetita/toxicidade , Polietilenoglicóis/síntese química , Polietilenoglicóis/química , Polietilenoglicóis/toxicidade , Suínos
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