Effect of Galardin and its Solvents on the Microtensile Bond Strength of Different Adhesive Systems to Dentin

Objective: To evaluate the effect of a synthetic inhibitor of MMPs (Galardin) and its solvents [ethanol and dimethyl sulfoxide (DMSO)] on the microtensile bond strength (µTBS) of adhesive systems to dentin. Material and Methods: Sound human third molars (n=180) were randomly assigned into 5 based on solution type: DMSO; ethanol; Galardin + DMSO; Galardin + ethanol; and distilled water as control. Then were further subdivided into 6 based on the adhesive system, i.e. 3-step and 2-step etch-and-rinse (ER), one-step and 2-step self-etch (SE) and universal in ER and SE strategies. The samples underwent a 500-round thermocycling procedure at 5±5/55±5°C and were sectioned into 1-mm2 pieces perpendicularly in a cutting machine. The µTBS was measured at a strain rate of 1 mm/min. Data were analyzed with two-way ANOVA and post hoc Games-Howell tests (p<0.05). Results: The adhesive system and the solution had significant effects on the µTBS (p<0.001). The universal adhesive in the SE mode resulted in a significant decrease in µTBS compared to the other adhesives (p<0.05). Ethanol, too, resulted in a significant decrease in µTBS compared to other solutions (p<0.05). Conclusion: Galardin and its solvents, except for ethanol, had no detrimental effects on the immediate µTBS.

Cigarrillos eléctrónicos: ¿Podemos recomendar su uso? / Electronic cigarettes: can we recommend its use?

Los cigarrillos electrónicos (Cig-e) son dispositivos que contienen un líquido compuesto por un solvente, saborizantes y, en la mayoría de los casos, nicotina. Este liquido, al ser calentado en el dispositivo, se vaporiza, siendo aspirado por el usuario. En los últimos años, el uso de los Cig-e ha aumentado rápidamente, especialmente entre escolares y gente joven, sin existir hasta el día de hoy evidencias ciertas sobre su seguridad y efectos a largo plazo. En este artículo revisamos la evidencia existente en cuanto a los efectos y seguridad de cada uno de los componentes de los Cig-e y analizamos sus potenciales indicaciones en distintos escenarios clínicos.

Electronic cigarettes (Cig-e) are devices that contain a liquid composed of a solvent, flavors and, in most cases, nicotine. This liquid, when heated in the device, vaporizes, being aspirated by the user. In recent years, the use of Cig-e has increased rapidly, especially among schoolchildren and young people, with no clear evidence of safety and long-term effects to date. In this article we review the existing evidence regarding the effects and safety of each of the components of Cig-e and analyze their potential indications in different clinical scenarios.

Applying Nightingale charts to evaluate the heterogeneity of biomedical waste in a Hospital / Aplicação de gráficos nightingaleanos para avaliação da heterogeneidade de Resíduos de Serviço de Saúde de um hospital / Aplicación de gráficos Nightingale para la evaluación de la heterogeneidad de los residuos sanitarios en un Hospital

OBJECTIVES: to evaluate the heterogeneity of biomedical waste (BW) using Nightingale charts. METHOD: cross-sectional study consisting of data collection on wastes (direct observation of receptacles, physical characterisation, and gravimetric composition), development of a Management Information System, and creation of statistical charts. RESULTS: the wastes with the greatest degree of heterogeneity are, in order, recyclable, infectious, and organic wastes; chemical waste had the most efficient segregation; Nightingale charts are useful for quick visualisation and systematisation of information on heterogeneity. CONCLUSION: the development of a management information system and the use of Nightingale charts allows for the identification and correction of errors in waste segregation, which increase health risks and contamination by infectious and chemical wastes and reduce the sale and profit from recyclables. .

OBJETIVO: avaliar a heterogeneidade dos Resíduos de Serviço de Saúde por meio da aplicação de gráficos nightingaleanos. MÉTODO: estudo transversal, que consiste na coleta de dados sobre resíduos (observação direta dos locais de armazenamento, caracterização física e composição gravimétrica), desenvolvimento de um Sistema de Informação Gerencial e construção de gráficos estatísticos. RESULTADOS: os resíduos que apresentam maior grau de heterogeneidade são os recicláveis, infectantes e orgânicos, respectivamente; o resíduo químico atingiu maior eficiência na segregação; os gráficos nightingaleanos são úteis na visualização rápida e na sistematização das informações sobre a heterogeneidade. CONCLUSÃO: o desenvolvimento de um sistema de informação gerencial e a utilização dos gráficos nigthingaleanos permite identificar e corrigir erros na segregação dos resíduos que impactam tanto no aumento de riscos à saúde e de contaminação por resíduos infectantes e químicos como na redução da comercialização e receita com os recicláveis. .

OBJETIVO: evaluar la heterogeneidad de los residuos sanitarios (RS) usando gráficos Nightingale. MÉTODO: estudio transversal que consiste en la recopilación de datos sobre los residuos (observación directa de los recipientes, caracterización física y composición gravimétrica), desarrollo de un Sistema de Información para la Gestión y creación de gráficos estadísticos. RESULTADOS: los residuos con el mayor grado de heterogeneidad son los reciclables, infecciosos, y los residuos orgánicos, respectivamente; la segregación de los residuos químicos fue la más eficiente; los gráficos Nightingale son útiles para la visualización rápida y sistematización de la información sobre la heterogeneidad. CONCLUSIÓN: el desarrollo de un sistema de información para la gestión y el uso de gráficos Nightingale permiten la identificación y corrección de errores en la separación de los residuos; dichos errores aumentan los riesgos de salud y la contaminación por residuos infecciosos y químicos, y reducen la venta y beneficio obtenible de los materiales reciclables. .

Screening and isolation of halophilic bacteria producing industrially important enzymes

Halophiles are excellent sources of enzymes that are not only salt stable but also can withstand and carry out reactions efficiently under extreme conditions. The aim of the study was to isolate and study the diversity among halophilic bacteria producing enzymes of industrial value. Screening of halophiles from various saline habitats of India led to isolation of 108 halophilic bacteria producing industrially important hydrolases (amylases, lipases and proteases). Characterization of 21 potential isolates by morphological, biochemical and 16S rRNA gene analysis found them related to Marinobacter, Virgibacillus, Halobacillus, Geomicrobium, Chromohalobacter, Oceanobacillus, Bacillus, Halomonas and Staphylococcus genera. They belonged to moderately halophilic group of bacteria exhibiting salt requirement in the range of 3-20%. There is significant diversity among halophiles from saline habitats of India. Preliminary characterization of crude hydrolases established them to be active and stable under more than one extreme condition of high salt, pH, temperature and presence of organic solvents. It is concluded that these halophilic isolates are not only diverse in phylogeny but also in their enzyme characteristics. Their enzymes may be potentially useful for catalysis under harsh operational conditions encountered in industrial processes. The solvent stability among halophilic enzymes seems a generic novel feature making them potentially useful in non-aqueous enzymology.

Kinetic analysis of batch ethanol acetylation in isothermal non-stationary multiphase systems by lyophilized mycelium of Aspergillus oryzae

A relatively complex network of reactions has been investigated, using as a network model the isothermal batch esterification of acetic acid with ethanol in n-heptane catalyzed by lyophilized mycelium of Aspergillus oryzae. The kinetic analysis was firstly carried out on the whole system, without any simplification, by means of the well-known integral method. Owing to the poor results obtained by this way, we developed an alternative approach, combining initial rates and integral analysis and reducing the number of empirical parameters to be determined by the use of equilibrium data. All the values of the parameters calculated according to this "composite" approach to kinetic analysis well correlate with experimental data.

Purification and characterization of an extreme halothermophilic protease from a halophilic bacterium Chromohalobacter sp. TVSP101

An extreme halophilic bacterium was isolated from solar saltern samples and identified based on biochemical tests and 16S r RNA sequencing as Chromohalobacter sp. strain TVSP101. The halophilic protease was purified using ultrafiltration, ethanol precipitation, hydrophobic interaction column chromatography and gel permeation chromatography to 180 fold with 22% yield. The molecular mass of the protease determined by SDS PAGE was 66 kDa. The purified enzyme was salt dependent for its activity and stability with an optimum of 4.5 M NaCl. The optimum temperature for maximum protease activity was 75ºC. The protease was optimally active at pH 8 and retained more than 80% of its activity in the range of pH 7-10. Sucrose and glycine at 10% (w/v) were the most effective osmolytes, retained 100% activity in the absence of NaCl. The activity was completely inhibited by ZnCl2 (2 mM), 0.1% SDS and PMSF (1mM). The enzyme was not inhibited by 1mM of pepstatin, EDTA and PCMB. The protease was active and retained 100% it activity in 10% (v/v) DMSO, DMF, ethanol and acetone.

Residual solvent analysis in hydrochloride salts of active pharmaceutical ingredients

GMP conditions commands to control adequately the quality of APIs by checking the levels of residual solvents. Organic solvents such as acetone, ethyl acetate, isopropyl alcohol, methanol, tetrahydrofuran and toluene frequently used in pharmaceutical industry for the manufacturing of Active Pharmaceutical ingredients [APIs]. A selective Gas Chromatographic [GC] method has been developed and validated as per ICH guidelines for residual solvent analysis in 10 different hydro chloride salts of APIs. Residual solvents in APIs were monitored using gas chromatography [GC] with Flame Ionisation detector [FID]. The separation was carried out on BP 624 column [30m X 0.53mm i.d. X 0.25micro m coating thickness], using GC 17 A shimadzu, with nitrogen as carrier gas in the split mode by direct injection method. The method described is simple, sensitive, rugged, reliable and reproducible for the quantitation of acetone, ethyl acetate, isopropyl alcohol, methanol, tetrahydrofuran and toluene at residual level from hydrochloride chloride salts of APIs

TLC-spectrophometric separation and trace determination of monocrotophos and dichlorvos in enviromental and biological samples.

Organophosphorus insecticides, monocrotophos and dichlrovos are increasingly being used in agriculture to control insects on a wide range of crops. Their ready access has resulted in misuse in many instances of homicidal and suicidal poisoning cases. This paper describes about a chromogenic spray reagent for the detection/determination of monocrophos and dichlrovos in environmental and biological samples by TLC and spectrophotometric method. Monocrotophos and dichlorvos on alkaline hydrolysis yield N-methyl acetoacetamide and dichlroacetaldehyde respectively, which in turn react with diazotized p-amino acetophenone to give red-violet and red coloured compounds. Other organophosphorus insecticides do not give this reaction. Moreover, organochlorine and synthetic pyrethroid insecticides and constituents of viscera (amino acids, peptides, proteins etc), which are generally coextracted with the insecticides, do not interfere. However, phenolic compounds and hydrolysed product of carbamate insecticides may interfere and differentiate from monocrotophos and dichlrovos by Rf values. The lower limit of detection is 0.2 mg for monocrotophos and 0.1 mg for dichlorovos. The absorption maxima of the reddish-violet and red colour formed by monocrotophos and dichlrovos, are measured at 560 nm and 540 nm respectively. Beer's Law is obeyed over the concentration range of 1.2 to 6.8 mg and 6.2 to 35 mg in the final solution volume of 25 mL. The molar absorptivity and Sandell's sensitivity of monocrotophos and dichlrovos were found to be 7.1 x 10(5) (+100) 1 mole(-1) cm(-1) and 0.008 mg cm(-2), 1.2 x 10(5) 1 mole(-1) cm(-1) and 0.003 mg cm(-2) respectively. The standard deviation and relative standard deviation were found be +/- 0.005 and 2.05% +/- 0.007 and 2.02% respectively. The developed method has been successfully applied to the detection and determination of monocrotophos and dichlrovos in environmental and biological samples.

Avaliaçäo do poder solvente de guta-percha, de quatro substâncias químicas / Evaluation of the gutta-percha solvent ability of four chemicals substances

Utilizando-se de peso e lupa estereoscópica avaliou-se as seguintes substâncias: clorofórmio, eucalipto, xilol e terebintina quanto à capacidade de dissolver guta-percha, tendo como controle negativo o tergentol. Os resultados demostraram que o clorofórmio e o xilol foram mais eficientes. Verificou-se também, que as substâncias promoveram mais a plastificaçäo do que a total dissoluçäo da guta-percha, com vantagem para o clorofórmio e o xilol

Determinacao espectrofotometrica e cromatografica em fase gasosa de tricloretanol em urina / Spectrophotometric and gas chromatographic determination of trichlorethanol in urine

O tricloretanol (TCE), produto de biotransformacao dos solventes 1,1,1-tricloretano (1,1,1-TRI) e tricloretileno, e usado como indicador biologico de dose interna na vigilancia de individuos expostos ocupacionalmente a estes compostos. Neste trabalho foi realizada a otimizacao de metodo espectrofotometrico e cromatografico em fase gasosa para a determinacao do TCE, bem como se estudou a aplicacao destes metodos a analise de urina de trabalhadores expostos ao 1,1,1-TRI. A analise cromatografica com detector de captura eletronica foi efetuada em coluna SE-30 - 15//, usando-se o diclorobenzeno como padrao externo. Ambos os metodos mostraram precisao e recuperacao adequados, respectivamente de 2,2//de CV e 95,6//para o espectrofotometrico e de 2,3//de CV e 95,1//para o cromatografico. O teor medio de tricloretanol em urina, expresso em mg/g de creatinina, foi de 4,4 quando usada a espectrofotometria e de 2,4 pela cromatografia, para o grupo de individuos expostos ao 1,1,1-tricloretano. Os resultados obtidos mostraram a maior sensibilidade e especificidade da cromatografia em fase gasosa na determinacao do tricloretanol em urina

Emprego do tubo U na validaçäo da determinaçäo de vapores de solventes orgânicos coletados sobre carväo ativo em ambientes de trabalho / Use of U tube in validation of steam determination of organic solvents collected over activated carbon at working environment

No presente trabalho foi desenvolvido um sistema simples e prático para produzir quantidades conhecidas de vapores de benzeno, tolueno, xilenos (mistura dos isômeros orto, para e meta), n-hexano e ciclo-hexano em experimentos de campo, visando a validaçäo da determinaçäo da eficiência de recuperaçäo desses compostos adsorvidos sobre carväo ativo. Um tubo U (tubo de cloreto de cálcio para secagem) foi utilizado como câmara de geraçäo de amostras. O sistema do tubo U foi utilizado pelo laboratório de Higiene Industrial da Fundacentro, nos testes de campo, durante a coleta de vapores de solventes orgânicos, em três tipos de indústrias: petroquímica, gráfica e de calçados.

Influencia del solvente de extracción de proteínas de trigo para su detección por electroforesis en alimentos para celiacos / Influence of solvent extraction on wheat electrophoregram in order to control gluten free products

Se estudió la influencia de distintos solventes de extracción, sobre el perfil electroforético de proteínas de trigo, como etapa previa a su posible detección en alimentos para celiacos. Se utilizó electroforesis en placas de gel de poliacrimida en sistema discontinuo y disociante. Los solventes de extracción estudiados para gliadinas fueron: 1) etanol 70§, 2) dioxano 40§, 3) isopropanol 55§, 4) isopropanol 55§ + 2 mercaptoetanol, y para proteínas totales: 5) Buffer conteniendo dodecilsulfato de sodio y 2 Mercaptoetanol. Del análisis de los densitogramas, surge que los solventes 4) y 5), son los más adecuados, debido a la buena extracción y resolución proteica. Si bien con el resto de los solventes se obtienen pocas bandas proteicas, en principio es conveniente extraer también con el solvente 3 en caso de mezclas con otras proteinas que pudieran presentar perfiles proteicos complejos con los solventes 4 y 5. Los resultados se aplican al análisis de trigo sarraceno