RESUMO

The aim of this study was to evaluate in vitro and in vivo the effect of sodium dodecyl sulfate (SDS) on the caprine lentivirus (CLV) in colostrum and milk. This was performed to develop a practical and efficient method of blocking the lactogenic transmission of the virus. In the in vitro experiment, colostrum and milk were treated with 0.25%; 0.50% and 1% SDS. Then, somatic cells of colostrum and milk were submitted to co-culture with caprine synovial membrane cells (CSM). In the in vivo test, goats were fed with colostrum and milk provided from CLV-positive goats treated with SDS in the same concentrations used in the in vitro experiment. Animals were tested by nested polymerase chain reaction (nPCR) and Western blot (WB) assays. In the in vitro experiment, inhibitory activity against CLV without inactivation occurred in colostrum with all SDS concentrations. However, concentrations of 0.25 and 0.5% SDS presented only inhibitory activity against CLV in milk cells, and 1% concentration provided inactivation of the virus. In the in vivo tests, none of the three concentrations of SDS was effective in inactivating LVC in colostrum or goat milk, which was confirmed by seroconversion and presence of proviral DNA in animals afterwards.(AU)

O objetivo da pesquisa foi avaliar in vitro e in vivo o efeito do dodecil sulfato de sódio (SDS) sobre o lentivírus caprino (LVC) no colostro e no leite, a fim de desenvolver um método prático e eficiente no bloqueio da via de transmissão lactogênica do vírus. No experimento in vitro, o colostro e o leite de cabras positivas foram tratados com SDS a 0,25%, 0,50% e 1,0%. Em seguida, as células somáticas do colostro e do leite foram obtidas e direcionadas ao cocultivo com células de membrana sinovial caprina (MSC). No teste in vivo, os cabritos foram alimentados com colostro e leite providos de cabras positivas para LVC, tratados com SDS nas mesmas concentrações usadas no teste in vitro. Os animais foram acompanhados pelos testes de reação em cadeia da polimerase nested (nPCR) e western blot (WB). Nos resultados in vitro, no colostro, observou-se que, em todas as concentrações de SDS, ocorreu uma atividade inibitória contra o LVC, sem a inativação. Em relação às células do leite, o SDS apresentou, nas concentrações de 0,25 e 0,5%, atividade inibitória contra o LVC, e na concentração de 1%, houve inativação viral. Nos testes in vivo, as três concentrações de SDS testadas não foram efetivas na inativação do LVC no colostro e no leite caprino, o que se comprovou pela soroconversão e pela presença de DNA proviral nos animais.(AU)

Assuntos

RESUMO

The aim of this study was to evaluate in vitro and in vivo the effect of sodium dodecyl sulfate (SDS) on the caprine lentivirus (CLV) in colostrum and milk. This was performed to develop a practical and efficient method of blocking the lactogenic transmission of the virus. In the in vitro experiment, colostrum and milk were treated with 0.25%; 0.50% and 1% SDS. Then, somatic cells of colostrum and milk were submitted to co-culture with caprine synovial membrane cells (CSM). In the in vivo test, goats were fed with colostrum and milk provided from CLV-positive goats treated with SDS in the same concentrations used in the in vitro experiment. Animals were tested by nested polymerase chain reaction (nPCR) and Western blot (WB) assays. In the in vitro experiment, inhibitory activity against CLV without inactivation occurred in colostrum with all SDS concentrations. However, concentrations of 0.25 and 0.5% SDS presented only inhibitory activity against CLV in milk cells, and 1% concentration provided inactivation of the virus. In the in vivo tests, none of the three concentrations of SDS was effective in inactivating LVC in colostrum or goat milk, which was confirmed by seroconversion and presence of proviral DNA in animals afterwards.(AU)

O objetivo da pesquisa foi avaliar in vitro e in vivo o efeito do dodecil sulfato de sódio (SDS) sobre o lentivírus caprino (LVC) no colostro e no leite, a fim de desenvolver um método prático e eficiente no bloqueio da via de transmissão lactogênica do vírus. No experimento in vitro, o colostro e o leite de cabras positivas foram tratados com SDS a 0,25%, 0,50% e 1,0%. Em seguida, as células somáticas do colostro e do leite foram obtidas e direcionadas ao cocultivo com células de membrana sinovial caprina (MSC). No teste in vivo, os cabritos foram alimentados com colostro e leite providos de cabras positivas para LVC, tratados com SDS nas mesmas concentrações usadas no teste in vitro. Os animais foram acompanhados pelos testes de reação em cadeia da polimerase nested (nPCR) e western blot (WB). Nos resultados in vitro, no colostro, observou-se que, em todas as concentrações de SDS, ocorreu uma atividade inibitória contra o LVC, sem a inativação. Em relação às células do leite, o SDS apresentou, nas concentrações de 0,25 e 0,5%, atividade inibitória contra o LVC, e na concentração de 1%, houve inativação viral. Nos testes in vivo, as três concentrações de SDS testadas não foram efetivas na inativação do LVC no colostro e no leite caprino, o que se comprovou pela soroconversão e pela presença de DNA proviral nos animais.(AU)

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RESUMO

Cefuroxime axetil immediate release tablets were formulated by direct compression method with different percentages of sodium lauryl sulphate (SLS) such as 0.5, 1.0, 1.5 and also without SLS. Resulting batches of tablets were evaluated by both pharmacopeial and non-pharmacopeial methods to ascertain the physico-mechanical properties. Dissolution test were carried out in different medium like 0.07 M HCl, distilled water, 0.1M HCl of pH 1.2 and phosphate buffers at pH 4.5 and 6.8 to observe the drug release against the respective concentration of SLS used. Later, test formulations were compared by f1 (dissimilarity) and f2 (similarity) factors using a reference brand of cefuroxime axetil. Significant differences (p<0.05) in dissolution rate were recorded with the change in concentration of SLS in different media. Test formulation T3 containing 1% SLS was found to be best optimized formulation based on assay, disintegration, dissolution and similarity and dissimilarity factors.

Formularam-se comprimidos de liberação imediata à base de cefuroxima axetil, pelo método de compressão direta, com diferentes percentagens de lauril sulfato de sódio (LSS), tais como 0,5, 1,0, 1,5, e também sem SLS. Os lotes resultantes dos comprimidos foram avaliados por ambos os métodos da farmacopeia e não farmacopeicos para determinar as propriedades físico-mecânicas. O teste de dissolução foi realizado em meios diferentes, como HCl 0,07 M, água destilada, HCl 0,1 M com pH 1,2 e os tampões fosfato (pH 4,5 e 6,8) para observar a liberação do fármaco contra a correspondente concentração de LSS utilizado. Em seguida, as formulações de teste foram comparadas por fatores f1 (dissimilaridade) e f2 (similaridade), utilizando uma marca de referência de cefuroxima axetil. Diferenças significativas (p<0,05) na taxa de dissolução foram registradas com a mudança na concentração de LSS em diferentes meios de dissolução. A formulação T3 contendo LSS a 1% foi considerada a melhor formulação otimizada com base nos ensaios de desintegração, dissolução e fatores de semelhança e dissimilaridade.

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RESUMO

O objetivo deste estudo foi avaliar o efeito do dodecil sulfato de sódio (SDS) na criopreservação do sêmen canino. Dez ejaculados foram obtidos de cinco cães machos adultos. O sêmen fresco foi avaliado subjetivamente e criopreservado. Os tratamentos consistiram em um grupo-controle, formado pelo diluente Tris-gema (20%) e pelo glicerol, e os grupos-teste, sendo o mesmo diluente acrescido de 0,1 ou 0,2% de SDS. Após a descongelação, o sêmen foi avaliado subjetivamente e por meio da análise computadorizada (CASA). Observou-se uma redução significativa da qualidade espermática após a descongelação. Entretanto, não houve diferenças entre os tratamentos e o controle (P > 0,05) para nenhum dos parâmetros seminais avaliados. Conclui-se que a adição do SDS nas concentrações de 0,1 e 0,2% ao diluente Tris-gema-glicerol não influencia a qualidade do sêmen canino após a descongelação. (AU)

The aim of this study was to evaluate the effect of sodium dodecyl sulfate (SDS) on the cryopreservation of canine semen. Ten ejaculates were obtained from five mature dogs were used. The fresh semen was subjectively evaluated and cryopreserved. The treatments consisted in a control group formed by Tris-based extender plus egg yolk (20%) and glycerol (6%); the testing groups were formed by the same extender plus 0.1 or 0.2% SDS. After thawing, semen was evaluated through light microscopy and computer-assisted analysis (CASA). A significant reduction in semen quality was verified after thawing. However, there were no differences between treatments and control for any sperm characteristic (P > 0.05). In conclusion the addition of 0.1 or 0.2% SDS to Tris-based extender does not influence the quality of the canine semen after thawing.(AU)

Assuntos

RESUMO

O objetivo deste estudo foi avaliar o efeito do dodecil sulfato de sódio (SDS) na criopreservação do sêmen canino. Dez ejaculados foram obtidos de cinco cães machos adultos. O sêmen fresco foi avaliado subjetivamente e criopreservado. Os tratamentos consistiram em um grupo-controle, formado pelo diluente Tris-gema (20%) e pelo glicerol, e os grupos-teste, sendo o mesmo diluente acrescido de 0,1 ou 0,2% de SDS. Após a descongelação, o sêmen foi avaliado subjetivamente e por meio da análise computadorizada (CASA). Observou-se uma redução significativa da qualidade espermática após a descongelação. Entretanto, não houve diferenças entre os tratamentos e o controle (P > 0,05) para nenhum dos parâmetros seminais avaliados. Conclui-se que a adição do SDS nas concentrações de 0,1 e 0,2% ao diluente Tris-gema-glicerol não influencia a qualidade do sêmen canino após a descongelação.

The aim of this study was to evaluate the effect of sodium dodecyl sulfate (SDS) on the cryopreservation of canine semen. Ten ejaculates were obtained from five mature dogs were used. The fresh semen was subjectively evaluated and cryopreserved. The treatments consisted in a control group formed by Tris-based extender plus egg yolk (20%) and glycerol (6%); the testing groups were formed by the same extender plus 0.1 or 0.2% SDS. After thawing, semen was evaluated through light microscopy and computer-assisted analysis (CASA). A significant reduction in semen quality was verified after thawing. However, there were no differences between treatments and control for any sperm characteristic (P > 0.05). In conclusion the addition of 0.1 or 0.2% SDS to Tris-based extender does not influence the quality of the canine semen after thawing.

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RESUMO

Toxicities of atrazine and sodium dodecyl sulfate (SDS) to the tropical freshwater cladoceran Pseudosida ramosa were studied in the laboratory. Acute tests showed that the 48-h LC50 of atrazine was 20.9 mg l⁻¹, while that of SDS was 11.1 mg l⁻¹. P. ramosa showed to be slightly more sensitive than the other species of temperate cladocerans, in the assay conditions specified for each one. Long-term exposure of P. ramosa individuals to atrazine decreased the 21-day fecundity, the 21-day fertility and r(m), at concentrations ranging from 0.8 to 3.2 mg l⁻¹. Furthermore, fecundity and fertility at each brood decreased from the first to the fifth, at concentrations ranging from 0.8 to 3.2 mg l⁻¹ and for the first three broods at the concentration of 0.4 mg l⁻¹. Long-term exposure of female P. ramosa to SDS decreased the 21-day fecundity, the 21-day fertility and r(m), at concentrations of 2 and 4 mg l⁻¹. Fecundity and fertility of each brood were reduced from the first to the fifth, at concentrations of 2-4 mg l⁻¹, and for the first three at concentrations of 0.5 and 1 mg l⁻¹. The survival and moulting of the adult females were not affected by either chemical at the concentrations tested. Many water quality criteria in tropical regions are based on ecotoxicological tests with non-native species and this may lead to errors in setting the maximum permissible levels of chemicals in water bodies. Therefore, we reiterate here the idea of using native species in ecotoxicological assessments.

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RESUMO

Wastewater produced in the contaminated soil washing was treated by means of coagulation-flocculation (CF) process. The wastewater contained petroleum hydrocarbons, a surfactant, i.e., sodium dodecyl sulfate (SDS) as well as salts, brownish organic matter and other constituents that were lixiviated from the soil during the washing process. The main goal of this work was to develop a process for treating the wastewaters generated when washing hydrocarbon-contaminated soils in such a way that it could be recycled to the washing process, and also be disposed at the end of the process properly. A second objective was to study the relationship among the coagulant and flocculant doses and the pH at which the CF process is developed, for systems where methylene blue active substances (MBAS) as well as oil and greases were present. The results for the selection of the right coagulant and flocculant type and dose, the optimum pH value for the CF process and the interactions among the three parameters are detailed along this work. The best coagulant and flocculant were FeCl(3) and Tecnifloc 998 at doses of 4,000 and 1 mg/L, correspondingly at pH of 5. These conditions gave color, turbidity, chemical oxygen demand (COD) and conductivity removals of 99.8, 99.6, 97.1 and 35%, respectively. It was concluded that it is feasible to treat the wastewaters generated in the contaminated soil washing process through CF process, and therefore, wastewaters could be recycled to the washing process or disposed to drainage.

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RESUMO

Synthetic wastewater samples containing a model surfactant were treated using two different Fenton-like advanced oxidation processes promoted by solar radiation; the photo-Fenton reaction and Co/PMS/UV processes. Comparison between the different experimental conditions was performed by means of the overall surfactant degradation achieved and by obtaining the initial rate in the first 15 min of reaction (IR15). It was found that, for dark Fenton reaction, the maximum surfactant degradation achieved was 14% under low iron and oxidant concentration. Increasing Fenton reagents by one magnitude order, surfactant degradation achieved 63% in 60 min. The use of solar radiation improved the reaction rate by 17% under same conditions and an additional increase of 12.5% was obtained by adjusting initial pH to 2. IR15 values for dark and irradiated Fenton reactions were 0.143 and 0.154 mmol/min, respectively, for similar reaction conditions and this value increased to 0.189 mmol/min when initial pH was adjusted. The use of the Co/PMS system allow us to determine an increase in the degradation rate, for low reaction conditions (1 mM of transition metal; 4 mM oxidant) similar to those used in dark Fenton reaction. Surfactant degradation increased from 3%, for Fenton reaction, to 44.5% in the case of Co/PMS. When solar irradiation was included in the experiments, under same reaction conditions described earlier, surfactant degradation up to 64% was achieved. By increasing Co/PMS reagent concentration by almost 9 times under irradiated conditions, almost complete (>99%) surfactant degradation was reached in 5 min. Comparing IR15 values for Co/PMS and Co/PMS/UV, it allow us to observe that the use of solar radiation increased the degradation rate in one magnitude order when compared with dark experiments and further increase of reagent concentration increased reaction rate twice.

Assuntos