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The concern regarding the harm caused by biocides to human health has been increasing over the years, making the natural products an alternative to less toxic and more efficient biocides. Therefore, this paper reports the investigation of the disinfectant potential of extracts and isolated compounds from Baccharis dracunculifolia. For this purpose, extracts of aerial parts (BD-C), tricomial wash (BD-L) and roots (BD-R) of B. dracunculifolia were obtained by maceration. The extracts were submitted to different chromatographic techniques, including high-speedy countercurrent chromatography (HSCCC) furnishing nine isolated compounds. The extracts and isolated compounds were evaluated regarding their antimicrobial activity by the broth microdilution method, according to the Clinical and Laboratory Standards Institute, and regarding their sanitizing activity according to Standard Operating Procedure No. 65·3210·007 (INCQS, 2011), developed by the National Institute for Quality Control in Health (INCQS) - Oswaldo Cruz Foundation (FIOCRUZ). In the antimicrobial evaluation the BD-C extract showed minimum inhibitory concentration (MIC) values of 200 and 100 µg/ml against Staphylococcus aureus and Tricophyton mentagrophytes, respectively. BD-L extract showed MIC value of 200 µg/ml against S. aureus. The isolated compounds caffeic acid (MBC 2·22 µmol l-1 ), ferulic acid (MBC 2·06 µmol l-1 ) and baccharin (MBC 0·27 µmol l-1 ) showed significant inhibitory activity against S. aureus. All B. dracunculifolia isolated compounds were active with exception of aromadrendin-4´-O-methyl-ether for T. mentagrophytes. Additionally, isosakuranetin was active against Salmonella choleraesuis (MIC 1·4 µmol l-1 ). Regarding the sanitizing activity, the hydroalcoholic solution containing 0·2% of B. dracunculifolia extract in 40°GL ethanol was effective in eliminating the microbial contamination on all carrier cylinders and against all microorganisms evaluated in the recommended exposure time of 10 min. Therefore, B. dracunculifolia has potential for the development of sanitizing agents to be used in hospitals, food manufactures and homes.

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BACKGROUND: Notwithstanding that concomitant exposure to different isothiazolinone derivatives may result in concomitant sensitization, clinical and animal studies have suggested cross-reactivity between these derivatives, notably between methylisothiazolinone (MI) and octylisothiazolinone (OIT). OBJECTIVE: To investigate if patients sensitized to MI show cross-reactions to OIT and/or to benzisothiazolinone (BIT) by applying the concept of the re-test method. PATIENTS AND METHODS: From March to October 2019 consecutive patients were patch tested with MI 0.2% aqueous in duplicate at the two lower corners of both shoulder blades. Patients sensitized to MI, but not to OIT 0.1% petrolatum (pet.) nor to BIT 0.1% pet., were re-tested, 2 months later, with the latter two derivatives at the skin sites where the MI reactions had fully disappeared. RESULTS: Of 116 patients, 15 (13%) were sensitized to MI, eight of these not sensitized to BIT nor to OIT. Of these, seven patients, all (very) strongly sensitized to MI, were re-tested: five patients showed positive patch test reactions to OIT 0.1% pet.; one patient to OIT 0.1% pet. and BIT 0.1% pet.; and one other patient showed no reactions. CONCLUSION: This study suggests that patients primarily and strongly sensitized to MI may show immunologic cross-reactions to OIT, and to a far lesser extent to BIT.

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Abstract Background: Stress test is used to detect coronary artery disease (CAD). The QTc interval dispersion (dQTc) is an electrocardiographic index of ventricular repolarization heterogeneity. Some researchers have linked transient myocardial ischemia induced by physical exertion with increased heterogeneity of ventricular repolarization measured by dQTc. Objectives: To study the patterns of dQT in patients with and without chronic obstructive CAD and to define a reliable cutoff point for dQT that could become a diagnostic criterion for myocardial ischemia. Methods: We retrospectively analyzed the electrocardiogram in resting and in exercise of 63 patients submitted to exercise test and cardiac catheterization. We divided the patients into three groups: true negative (VN), true positive (VP) and false positive (FP). VN: patients with coronary lesion lower than 70% and exercise test without myocardial ischemia; VP: individuals with stenosis greater than 70% in coronary arteries and a test suggestive of myocardial ischemia; FP: people with stenosis lower than 70% in the coronary arteries and stress test with ischemia criteria. Values of p < 0.05 were considered statistically significant. Results: Resting dQTc was not different among the three groups. However, for the dispersion of the QTc interval in exercise was, respectively, 47 ± 17 ms, 72 ± 42 ms, and 61 ± 31 ms for VN, VP and FP (p = 0.003). Conclusions: Obstructive chronic coronary disease patients have an increase in dQTc during exercise. Measurement of dQTc may be helpful in the diagnosis of myocardial ischemia in the stress test.

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RESUMO A concentração de óleos e graxas em amostras de águas contaminadas com resíduos oleosos pode ser determinada pelos procedimentos estabelecidos no Standard Methods for the Examination of Water and Wastewater. No entanto, sua aplicação nem sempre resulta em valores adequados ou níveis de precisão satisfatórios para atendimento de padrões normativos. Nesse sentido, este artigo apresenta uma proposta de ensaio para determinação da concentração de óleos minerais em águas provenientes de áreas pavimentadas, sujeitas ao derramamento de óleos e graxas. Tal método tem por base o método de partição gravimétrica (5520 B), estabelecido pelo Standard Methods. No novo procedimento, a etapa de separação entre o solvente de extração contendo os resíduos e o restante da fase aquosa foi substituída pela evaporação de toda a água da amostra, em estufa a 85ºC. Para avaliar a eficiência do método, foram preparadas amostras com concentrações conhecidas de óleo de 200, 100, 50, 25 e 15 mg.L-1 em água destilada e realizados ensaios de laboratório para determinação do teor de óleo, conforme tal procedimento. Os valores obtidos para as concentrações de óleo são bastante satisfatórios, apresentando comportamento linear em relação às concentrações de referência. Esse fato evidencia a confiabilidade do método proposto e sua aplicabilidade na determinação da concentração de óleos em amostras de águas contaminadas provenientes do escoamento superficial em pavimentos.

ABSTRACT Oil and grease concentration in water samples contaminated by oily residues can be determined by the procedures established in the Standard Methods for the Examination of Water and Wastewater. However, its application does not always result in adequate values or satisfactory accuracy levels in order to meet regulatory standards. In this sense, this paper presents a test-method proposal for determining mineral oil concentration in water samples from runoff of paved areas subject to oil and grease spillages. This method is based on the partition-gravimetric method (5520 B) established by the Standard Methods. In the new procedure, the separation between the extraction solvent containing residues and the aqueous phase remainder was replaced by the whole water sample evaporation in an oven at 85ºC. In order to assess the proposed method's efficiency, samples were prepared with known oil concentrations of 200, 100, 50, 25 and 15 mg.L-1, in distilled water and laboratory tests were performed to determine the oil content, according to the new procedure. The values obtained for the oil concentrations through the proposed procedure are quite satisfactory, presenting linear behavior in relation to the reference concentrations. This fact evidences the reliability of the new method and its applicability in determining the oil concentration in contaminated water samples from runoff in pavement surfaces.