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1.
J Photochem Photobiol B ; 177: 85-94, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29107206

ABSTRACT

Bacterial soft rot is responsible for the loss of about 25% of worldwide production in vegetables and fruits. Efforts have been made to develop an effective nanosponge with the capacity to load and release antibacterial drugs to protect plants. Based on the potential of the ZnO nanoparticles (ZnO-NPs) to achieve this goal, this study synthesized NP via the sol-gel and hydrothermal methods by controlling native defects, such as oxygen vacancies, using thermal treatments and reduced atmospheres. To characterize the ZnO NPs, X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), optical spectroscopy, electron paramagnetic resonance (EPR), Zeta Potential measurements and surface area with the Brunauer-Emmett-Teller (BET) method were used. The photophysical and photochemical properties via spin trapping method aligned with EPR using UVA light showed a greater formation of electron-hole pairs and hydroxyl radicals for the reduced ZnO NPs when compared with the oxidized ones. Additionally, we found that reduced ZnO-NPs have high effectively against Escherichia coli, Erwinia carotovora and Pantoea sp. bacteria using the photocatalytic effect in the UV range. Moreover, ZnO-NPs loaded with DOX release profile enables the release of DOX within 46days, where 25% was released during the first 10h followed by a second delivery phase with an interesting short-term efficacy (<1day) against E. carotovora and Pantoea sp. Bacteria. For the first time, it was demonstrated that ZnO-NPs and ZnO-NPs loaded with DOX have efficient UV photocatalytic activities against bacterial soft rot infections.


Subject(s)
Anti-Bacterial Agents/chemistry , Doxycycline/chemistry , Drug Carriers/chemistry , Metal Nanoparticles/chemistry , Zinc Oxide/chemistry , Anti-Bacterial Agents/pharmacology , Catalysis , Drug Liberation , Electron Spin Resonance Spectroscopy , Escherichia coli/drug effects , Escherichia coli/radiation effects , Microbial Sensitivity Tests , Oxidation-Reduction , Pantoea/drug effects , Particle Size , Pectobacterium carotovorum/drug effects , Pectobacterium carotovorum/radiation effects , Ultraviolet Rays
2.
Molecules ; 19(9): 13948-64, 2014 Sep 05.
Article in English | MEDLINE | ID: mdl-25197932

ABSTRACT

Current procedures for the detection and identification of bacterial infections are laborious, time-consuming, and require a high workload and well-equipped laboratories. Therefore the work presented herein developed a simple, fast, and low cost method for bacterial detection based on hydroxyapatite nanoparticles with a nutritive mixture and the fluorogenic substrate. Calcium phosphate ceramic nanoparticles were characterized and integrated with a nutritive mixture for the early detection of bacteria by visual as well as fluorescence spectroscopy techniques. The composite was obtained by combining calcium phosphate nanoparticles (Ca:P ratio, 1.33:1) with a nutritive mixture of protein hydrolysates and carbon sources, which promote fast bacterial multiplication, and the fluorogenic substrate 4-methylumbellipheryl-ß-D-glucuronide (MUG). The composite had an average particle size of 173.2 nm and did not show antibacterial activity against Gram-negative or Gram-positive bacteria. After an Escherichia coli suspension was in contact with the composite for 60-90 min, fluorescence detected under UV light or by fluorescence spectrophotometer indicated the presence of bacteria. Intense fluorescence was observed after incubation for a maximum of 90 min. Thus, this calcium phosphate nanocomposite system may be useful as a model for the development of other nanoparticle composites for detection of early bacterial adhesion.


Subject(s)
Ceramics/chemistry , Hydroxyapatites/chemistry , Nanocomposites/chemistry , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Bacterial Infections/diagnosis , Enterococcus faecalis/drug effects , Escherichia coli/drug effects , Humans , Hydroxyapatites/pharmacology , Limit of Detection , Nanocomposites/ultrastructure , Particle Size , Pseudomonas aeruginosa/drug effects , Spectrometry, Fluorescence , Staphylococcus aureus/drug effects , Surface Properties
3.
Colloids Surf B Biointerfaces ; 118: 194-201, 2014 Jun 01.
Article in English | MEDLINE | ID: mdl-24816509

ABSTRACT

Doxycycline is a semi-synthetic antibiotic commonly used for the treatment of many aerobic and anaerobic bacteria. It inhibits the activity of matrix metalloproteinases (MMPs) and affects cell proliferation. In this study, the structural and thermodynamic parameters of free DOX and a DOX/ßCD complex were investigated, as well as their interactions and effects on Staphylococcus aureus cells and cellular cytotoxicity. Complexation of DOX and ßCD was confirmed to be an enthalpy- and entropy-driven process, and a low equilibrium constant was obtained. Treatment of S. aureus with higher concentrations of DOX or DOX/ßCD resulted in an exponential decrease in S. aureus cell size, as well as a gradual neutralization of zeta potential. These thermodynamic profiles suggest that ion-pairing and hydrogen bonding interactions occur between DOX and the membrane of S. aureus. In addition, the adhesion of ßCD to the cell membrane via hydrogen bonding is hypothesized to mediate a synergistic effect which accounts for the higher activity of DOX/ßCD against S. aureus compared to pure DOX. Lower cytotoxicity and induction of osteoblast proliferation was also associated with DOX/ßCD compared with free DOX. These promising findings demonstrate the potential for DOX/ßCD to mediate antimicrobial activity at lower concentrations, and provides a strategy for the development of other antimicrobial formulations.


Subject(s)
Cell Membrane/drug effects , Doxycycline/chemistry , Doxycycline/pharmacology , Staphylococcus aureus/cytology , beta-Cyclodextrins/chemistry , beta-Cyclodextrins/pharmacology , Animals , Calorimetry , Cell Death/drug effects , Cell Proliferation/drug effects , Differential Thermal Analysis , Hydrodynamics , Light , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , Osteoblasts/cytology , Osteoblasts/drug effects , Osteoblasts/metabolism , Proton Magnetic Resonance Spectroscopy , Rats, Wistar , Scattering, Radiation , Spectroscopy, Fourier Transform Infrared , Staphylococcus aureus/drug effects , Static Electricity , Thermodynamics , Thermogravimetry
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