49 research outputs found

    High efficacy of ozonated oils on the removal of biofilms produced by methicillin-resistant staphylococcus aureus (MRSA) from infected diabetic foot ulcers

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    © 2020 by the authors. Ozone has a high wound healing capacity and antibacterial properties and can be used as a complementary treatment in infections. Methicillin-resistant S. aureus (MRSA) is the most common pathogen found in infected diabetic foot ulcers. Most of MRSA are resistant to several classes of antibiotics and, therefore, there is a need for new, effective, and well-tolerated agents. Thus, we aimed evaluate the antimicrobial and antibiofilm potentials of ozonated vegetable oils against MRSA strains isolated from diabetic foot ulcers. Six ozonated oils were produced with concentrations of ozone ranging from 0.53 to 17 mg of ozone/g of oil. The peroxide values were determined for each oil. Ozonated oils content on fatty acid was determined by gas chromatography equipped with a flame ionization detector. The antimicrobial susceptibility testing was performed by the Kirby-Bauer disk diffusion method and the effect of ozonated oils on biofilm formation ability and on established biofilms was investigated. In general, the content in identified unsaturated fatty acid in oils decreased with the increase of ozonation time and, consequently, the peroxide value increased. Most bacterial strains were inhibited by ozonated oil at a concentration of 4.24 mg/g. Ozonated oils had moderate to high ability to remove adhered cells and showed a high capacity to eradicate 24 h old biofilms. Our results show promising use of ozonated oils on the treatment of infections, in particular those caused by multidrug-resistant MRSA strains.This work was funded by the R&D Project CAREBIO2—Comparative assessment of antimicrobial resistance in environmental biofilms through proteomics—towards innovative theranostic biomarkers, with reference NORTE-01-0145-FEDER-030101 and PTDC/SAU-INF/30101/2017, financed by the European Regional Development Fund (ERDF) through the Northern Regional Operational Program (NORTE 2020) and the Foundation for Science and Technology (FCT). This work was supported by the Associate Laboratory for Green Chemistry—LAQV, which is financed by national funds from FCT/MCTES (UIDB/50006/2020). Joana S. Amaral is grateful to the Foundation for Science and Technology (FCT, Portugal) for financial support by national funds FCT/MCTES to CIMO (UIDB/00690/2020). Vanessa Silva is grateful to FCT (Fundação para a CiĂȘncia e a Tecnologia) for financial support through PhD grant SFRH/BD/137947/2018.info:eu-repo/semantics/publishedVersio

    Dose response assessment of conventional Fricke: a relationship between UV-Visible and nuclear magnetic resonance techniques

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    Conventional Fricke is an aqueous ferrous sulfate solution that has been widely studied in the field of chemical dosimetry. The feasibility of its use has become attractive for high dose measurements that are of clinical interest in the field of radiotherapy and for industrial purposes, in the irradiation of blood bags and the sterilization of surgical material. The derivation of the absorbed dose of Fricke depends on the radiation-induced oxidation of iron (II) ions (Fe2+) present in the aqueous solution to iron (III) ions (Fe3+), which occurs after exposure to ionising radiation. In this paper, it is proposed to evaluate the dose response of the Fricke dosimeter using two different analytical techniques, ultraviolet-visible spectrophotometry (UV-Vis) and nuclear magnetic resonance spectroscopy (NMR). Twelve groups of samples were analysed in triplicate, irradiated with doses between 0 and 800 Gy, using a cobalt-60 source (60Co). The dose rate of Fricke dosimeters was evaluated against the practical values obtained. The different methods allowed an analytical correlation of the species of oxidised iron (Fe3+) using a linearity curve as a function of the applied radiation dose

    Occurrence of postural deviations in children of a school of JaguariĂșna, SĂŁo Paulo, Brazil

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    OBJECTIVE: Evaluate the posture of students from a public school in Brazil and to identify the differences between normal deviation during growth and compensatory alterations. METHODS: Students from first to fourth grade of a public school in the city of JaguariĂșna, SĂŁo Paulo, Brazil, were evaluated. The students were positioned at sagital anterior and posterior coronal planes for postural assessment. Kendall points were used as the normal reference. RESULTS: 247 students were evaluated, 131 boys and 116 girls, and the main postural deviations found were: shoulder unbalance (50.2%), protracted shoulder (39.7%), abducted scapula (40.5%), knock-knee (29.6%), pelvic unbalance (21.5%), pelvic anteversion (19%), knee hyperextension (19%), medial rotation of hip (12.9%), protracted cervical (11.7%), head tilt (15.4%), thoracic hyperkyphosis (9.7%) and lumbar hyperlordosis (26.3%). CONCLUSIONS: A high incidence of postural alterations was detected in school children. Some of the postural alterations, such as abducted scapula, unbalance and protraction of the shoulders, knock-knee and lumbar hiperlordosis, normally occur and they are naturally corrected during growth. However, some postural problems, such as protraction and inclination of the cervical spine, were also prevalent and they require early intervention.OBJETIVO: Avaliar a postura de escolares do ensino pĂșblico fundamental e diferenciar as alteraçÔes que fazem parte do crescimento normal das compensatĂłrias. MÉTODOS: Trata-se de um estudo analĂ­tico, descritivo, de corte transversal, no qual se realizou avaliação postural em escolares de primeira a quarta sĂ©rie de uma escola pĂșblica da cidade de JaguariĂșna, situada no interior do Estado de SĂŁo Paulo. Cada aluno foi avaliado nos planos coronal-anterior, coronal-posterior e sagital, utilizando-se o mĂ©todo de Kendall como referĂȘncia de alinhamento postural normal. RESULTADOS: A avaliação postural de 247 escolares (131 masculinos e 116 femininos) identificou a seguinte incidĂȘncia de alteraçÔes: desnĂ­vel (50,2%) e protrusĂŁo de ombro (39,7%), escĂĄpula alada (40,5%), aumento do Ăąngulo valgo de joelho (29,6%), inclinação (21,5%) e anteroversĂŁo pĂ©lvica (19%), hiperextensĂŁo de joelho (19%), rotação de fĂȘmur (12,9%), protrusĂŁo (11,7%) e inclinação cervical (15,4%), cifose torĂĄcica (9,7%) e hiperlordose lombar (26,3%). CONCLUSÕES: Houve elevada incidĂȘncia de escĂĄpula alada, desnĂ­vel e protrusĂŁo de ombro, aumento do Ăąngulo valgo de joelho e hiperlordose lombar, consideradas normais durante o desenvolvimento da criança. As inclinaçÔes e a protrusĂŁo cervical, alteraçÔes que necessitam de intervenção precoce, tambĂ©m foram identificadas.748

    Canagliflozin and renal outcomes in type 2 diabetes and nephropathy

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    BACKGROUND Type 2 diabetes mellitus is the leading cause of kidney failure worldwide, but few effective long-term treatments are available. In cardiovascular trials of inhibitors of sodium–glucose cotransporter 2 (SGLT2), exploratory results have suggested that such drugs may improve renal outcomes in patients with type 2 diabetes. METHODS In this double-blind, randomized trial, we assigned patients with type 2 diabetes and albuminuric chronic kidney disease to receive canagliflozin, an oral SGLT2 inhibitor, at a dose of 100 mg daily or placebo. All the patients had an estimated glomerular filtration rate (GFR) of 30 to <90 ml per minute per 1.73 m2 of body-surface area and albuminuria (ratio of albumin [mg] to creatinine [g], >300 to 5000) and were treated with renin–angiotensin system blockade. The primary outcome was a composite of end-stage kidney disease (dialysis, transplantation, or a sustained estimated GFR of <15 ml per minute per 1.73 m2), a doubling of the serum creatinine level, or death from renal or cardiovascular causes. Prespecified secondary outcomes were tested hierarchically. RESULTS The trial was stopped early after a planned interim analysis on the recommendation of the data and safety monitoring committee. At that time, 4401 patients had undergone randomization, with a median follow-up of 2.62 years. The relative risk of the primary outcome was 30% lower in the canagliflozin group than in the placebo group, with event rates of 43.2 and 61.2 per 1000 patient-years, respectively (hazard ratio, 0.70; 95% confidence interval [CI], 0.59 to 0.82; P=0.00001). The relative risk of the renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causes was lower by 34% (hazard ratio, 0.66; 95% CI, 0.53 to 0.81; P<0.001), and the relative risk of end-stage kidney disease was lower by 32% (hazard ratio, 0.68; 95% CI, 0.54 to 0.86; P=0.002). The canagliflozin group also had a lower risk of cardiovascular death, myocardial infarction, or stroke (hazard ratio, 0.80; 95% CI, 0.67 to 0.95; P=0.01) and hospitalization for heart failure (hazard ratio, 0.61; 95% CI, 0.47 to 0.80; P<0.001). There were no significant differences in rates of amputation or fracture. CONCLUSIONS In patients with type 2 diabetes and kidney disease, the risk of kidney failure and cardiovascular events was lower in the canagliflozin group than in the placebo group at a median follow-up of 2.62 years
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