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1.
World J Microbiol Biotechnol ; 40(1): 6, 2023 Nov 07.
Artículo en Inglés | MEDLINE | ID: mdl-37932532

RESUMEN

Urinary tract infections (UTIs) are a significant cause of morbidity in healthcare systems and are prominently associated with applying urethral catheters, particularly in surgeries. Polyvinyl chloride (PVC) is extensively utilized in the fabrication of catheters. Biofilms, complex polymeric constructions, provide a protective milieu for cell multiplication and the enhancement of antibiotic resistance. Strategies to counteract biofilm development on medical apparatuses' surfaces incorporate antimicrobial agents such as N,N-dodecyl, and methyl polyethylenimine (DMPEI). This research endeavored to characterize the morphology of PVC and PVC-DMPEI surfaces utilizing Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM) and to gauge hydrophobicity through contact angle measurements. Employing Escherichia coli, Staphylococcus aureus, and Candida albicans in adhesion assays enabled the assessment of DMPEI's efficacy in preventing microbial adherence to PVC. Butanol successfully solubilized 2 mg.mL-1 DMPEI without altering the PVC structure. SEM results substantiated the formation of a DMPEI layer on the PVC surface, which led to decreased surface roughness, as validated by AFM, and increased hydrophilicity, as demonstrated by contact angle evaluations. E. coli, S. aureus, and C. albicans exhibited significant adhesion reduction, 89.3%, 94.3%, and 86.6% on PVC-DMPEI surfaces. SEM visualizations confirmed reduced cellular colonization on PVC-DMPEI and highlighted considerable morphological modifications in E. coli. Consequently, DMPEI films effectively minimize the adhesion of E. coli, S. aureus, and C. albicans on PVC surfaces. DMPEI, with its potential as a protective coating for innovative medical devices, promises to inhibit biofilm adherence effectively.


Asunto(s)
Escherichia coli , Polietileneimina , Polietileneimina/farmacología , Staphylococcus aureus , Catéteres , Biopelículas , Candida albicans
2.
Food Res Int ; 140: 110061, 2021 02.
Artículo en Inglés | MEDLINE | ID: mdl-33648284

RESUMEN

This study aimed to evaluate the effects of ohmic heating (OH) on probiotic inactivation, cell viability and morphology of the probiotic strains Lactobacillus acidophilus LA 05 (LA), Lacticaseibacillus casei 01 (LC), and Bifidobacterium animalis Bb 12 (BA) to develop paraprobiotics. OH at different electric field magnitudes (4, 8, and 12 V/cm at 60 Hz) and conventional heat treatment (CONV) were performed to determine the most adequate condition for the obtainment of paraprobiotics. Analysis of culturability, flow cytometry (FC), and Scanning electron microscope (SEM) was carried out. The complete inactivation by CONV was achieved only in the following conditions: LA - 95 °C/5 min, LC and BA - 95 °C/7 min. The same temperature profile was used in OH treatments to study the OH electrical effects. The OH treatment (8 V/cm) caused lower damage to the cell membrane integrity compared to the CONV treatment (p < 0.05). The OH showed to be adequate technology for the efficient production of paraprobiotics.


Asunto(s)
Bifidobacterium animalis , Probióticos , Citometría de Flujo , Calefacción , Lactobacillus acidophilus , Probióticos/análisis
3.
Food Microbiol ; 97: 103737, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-33653516

RESUMEN

The effect of ohmic heating (OH) (50, 55, and 60 °C, 6 V/cm) on the inactivation kinetics (Weibull model) and morphological changes (scanning electron microscopy and flow cytometry) of Salmonella spp. in infant formula (IF) was evaluated. In addition, thermal load indicators (hydroxymethylfurfural and whey protein nitrogen index, HMF, and WPNI) and bioactive compounds (DPPH, total phenolics, ACE, α-amylase, and α-glucosidase inhibitory activities) were also studied. OH presented a more intense inactivation rate than conventional heating, resulting in a reduction of about 5 log CFU per mL at 60 °C in only 2.91 min, being also noted a greater cell membrane deformation, higher formation of bioactive compounds, and lower values for the thermal load parameters. Overall, OH contributed to retaining the nutritional value and improve food safety in IF processing.


Asunto(s)
Conservación de Alimentos/métodos , Fórmulas Infantiles/química , Fórmulas Infantiles/microbiología , Salmonella/crecimiento & desarrollo , Microbiología de Alimentos , Conservación de Alimentos/instrumentación , Furaldehído/análogos & derivados , Furaldehído/química , Calor , Salmonella/química , Salmonella/fisiología , Proteína de Suero de Leche/química
4.
Food Chem ; 351: 129290, 2021 Jul 30.
Artículo en Inglés | MEDLINE | ID: mdl-33631613

RESUMEN

The effect of different types of sugar (sucrose, demerara, brown, fructose, coconut sugar, and honey) on sheep milk kefir was evaluated. Microbial counts (Lactobacillus, Lactococcus, Leuconostoc, yeast), antagonistic activity against foodborne pathogens, microstructure (scanning electron microscopy), and antiproliferative activity of cancer cells were evaluated. Furthermore, the antioxidant activity (DPPH), inhibitory activity of angiotensin-converting enzyme (ACE), α-amylase, and α-glucosidase, lactose content, lactic and acetic acids and ethanol, fatty acid profile and volatile organic compounds were determined. The addition of sugars increased the Lactobacillus population (up to 2.24 log CFU/mL), metabolites concentration, antagonistic activity against pathogens, antioxidant activity (11.1 to 24.1%), ACE inhibitory activity (27.5 to 37.6%), α-amylase inhibition (18 to 37.4%), and anti-proliferative activity. Furthermore, it improved the fatty acid profile and volatile compounds. The results suggest that the replacement of sucrose with different types of sugar constitute an interesting option to be used in sheep milk kefir formulations.


Asunto(s)
Kéfir/análisis , Sacarosa/química , Animales , Antioxidantes/química , Línea Celular , Proliferación Celular/efectos de los fármacos , Humanos , Concentración de Iones de Hidrógeno , Kéfir/microbiología , Kéfir/toxicidad , Lactobacillus/aislamiento & purificación , Lactobacillus/metabolismo , Lactococcus/aislamiento & purificación , Lactococcus/metabolismo , Leche/química , Peptidil-Dipeptidasa A/química , Peptidil-Dipeptidasa A/metabolismo , Análisis de Componente Principal , Ovinos , Compuestos Orgánicos Volátiles/análisis , Levaduras/aislamiento & purificación , Levaduras/metabolismo , alfa-Amilasas/antagonistas & inhibidores , alfa-Amilasas/metabolismo
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