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1.
Molecules ; 23(2)2018 Feb 08.
Article in English | MEDLINE | ID: mdl-29419803

ABSTRACT

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.


Subject(s)
Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Azoles/chemistry , Azoles/pharmacology , Metal Nanoparticles/chemistry , Silver/chemistry , Bacteria/drug effects , Cell Survival/drug effects , Cobalt/chemistry , Colloids , Copper/chemistry , Humans , Ligands , Microbial Sensitivity Tests , Microscopy, Atomic Force , Models, Molecular , Molecular Structure , Spectrum Analysis , Thermogravimetry
2.
J Biomed Mater Res A ; 104(11): 2801-9, 2016 11.
Article in English | MEDLINE | ID: mdl-27376695

ABSTRACT

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.


Subject(s)
Biocompatible Materials/chemistry , Cellulose/chemistry , Gluconacetobacter xylinus/chemistry , Magnetite Nanoparticles/chemistry , Myocytes, Smooth Muscle/cytology , Animals , Apoptosis/drug effects , Biocompatible Materials/toxicity , Cell Line , Cell Survival/drug effects , Cellulose/chemical synthesis , Cellulose/toxicity , Ferric Compounds/chemistry , Ferric Compounds/toxicity , Magnetite Nanoparticles/toxicity , Polyethylene Glycols/chemical synthesis , Polyethylene Glycols/chemistry , Polyethylene Glycols/toxicity , Swine
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