Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros

Base de dados
Tipo de documento
Intervalo de ano de publicação
1.
Front Microbiol ; 13: 1062544, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36545208

RESUMO

Introduction: African Swine Fever (ASF) is a highly infectious disease of pigs, caused by African swine fever virus (ASFV). The lack of vaccines and drugs makes strict disinfection practices to be one of the main measurements to curb the transmission of ASF. Therefore, it is important to assess if all viruses are inactivated after disinfection or after long time exposure in their natural conditions. Currently, the infectivity of ASFV is determined by virus isolation and culture in a biosafety level 3 (BSL-3) laboratory. However, BSL-3 laboratories are not readily available, need skilled expertise and may be time consuming. Methods: In this study, a Triton X-100 assisted PMAxx-qPCR method was developed for rapid assessment of infectious ASFV in samples. PMAxx, an improved version of propidium monoazide (PMA), can covalently cross-link with naked ASFV-DNA or DNA inside inactivated ASFV virions under assistance of 0.1% (v/v) TritonX-100, but not with ASFV-DNA inside live virions. Formation of PMAxx-DNA conjugates prevents PCR amplification, leaving only infectious virions to be detected. Under optimum conditions, the limit of detection of the PMAxx-qPCR assay was 2.32log10HAD50/mL of infectious ASFV. Testing different samples showed that the PMAxx-qPCR assay was effective to evaluate intact ASFV virions after treatment by heat or chemical disinfectants and in simulated samples such as swine tissue homogenate, swine saliva swabs, and environmental swabs. However, whole-blood and saliva need to be diluted before testing because they may inhibit the PCR reaction or the cross-linking of PMAxx with DNA. Conclusion: The Triton X-100 assisted PMAxx-qPCR assay took less than 3 h from sample to result, offering an easier and faster way for assessing infectious ASFV in samples from places like pig farms and pork markets.

2.
J Hazard Mater ; 393: 122388, 2020 07 05.
Artigo em Inglês | MEDLINE | ID: mdl-32120218

RESUMO

Remediation of organochlorine pesticides (OCPs)-contaminated soils is urgently required especially in China. Surfactants have emerged as reliable and efficient co-solvent for the treatment of hardly soluble organic pollutants in contaminated soil. Here, we report the use of TritonX-100 (TX-100) in advanced oxidation under electrokinetic technology (EK) for OCPs removal from a historically contaminated soil from a former pharmaceutical industrial wasteland. Result shows that TX-100 (10%) played a key role in soil remediation. In effect, after a treatment period of 15 days, pollutants washed ranged from 50.68% (4,4'-DDT) to 76.07% (HCB), when TX-100 was used as the electrolyte (EK-TX-100). A simple advanced oxidation of the soil using sodium persulfate (PS) under EK approach (EK-PS) was limited to achieve good removal efficiency of the pollutants; as the result of OCPs' hardly dissolvable nature. The achieved removal efficiency were comprised between 22.62% (2,4-DDT) and 55.78% (1,2,4,5-TCB). With the application of TX-100 as co-solvent (EK-TX-100/PS), the pollutants removal efficiency significantly improved (p < 0.05). The treatment efficiency was shifted and up to 88.05% (1,2,4-TCB) was achieved, while the lowest removal efficiency was 56.36% (4,4'-DDE). We come to the conclusion that the use of TX-100-enhanced advanced oxidation (EK-TX-100/PS) as a reliable treatment for remediating organochlorine contaminated soil.

3.
Materials (Basel) ; 13(6)2020 Mar 13.
Artigo em Inglês | MEDLINE | ID: mdl-32183113

RESUMO

This study aimed to investigate the effects of single-walled carbon nanotubes (SWCNTs) on strength the properties of cement composites when surfactant (SAA) was applied as the dispersion method. TritonX-100 (TX10) was used as the SAA to pretreat SWCNTs, which has been proved to perform well in dispersing the agglomerates of SWCNTs. In this study, four different concentration of SWCNTs, namely 0.00 wt%, 0.02 wt%, 0.04 wt%, and 0.06 wt% by the mass of cement, were used to prepare cement composite specimens. The compressive strength and flexural strength of specimens were tested and recorded. The results show that the compressive and flexural strengths of cement composites decreased with the increase in the concentration of SWCNTs without the addition of TX10. However, when SWCNT suspensions were pretreated with TX10, the strength variation pattern changed; the compressive and flexural strengths of cement composites increased as a function of the concentration of SWCNTs, although there were reductions compared to non-TX10-treated specimens at all concentrations of SWCNTs. Furthermore, the relationship between the strength of cement composites and bulk density of specimens was considered.

4.
Neuroscience ; 252: 24-34, 2013 Nov 12.
Artigo em Inglês | MEDLINE | ID: mdl-23896570

RESUMO

We previously reported that the novel antidepressant-like effect of tipepidine may be produced at least partly through the activation of mesolimbic dopamine (DA) neurons via inhibiting G protein-coupled inwardly rectifying potassium (GIRK) channels. In this study, we investigated the action of tipepidine on DA D2 receptor-mediated GIRK currents (IDA(GIRK)) and membrane excitability in DA neurons using the voltage clamp and current clamp modes of the patch-clamp techniques, respectively. DA neurons were acutely dissociated from the ventral tegmental area (VTA) in rats and identified by the presence of the hyperpolarization-activated currents. Tipepidine reversibly inhibited IDA(GIRK) with IC50 7.0 µM and also abolished IDA(GIRK) irreversibly activated in the presence of intracellular GTPγS. Then tipepidine depolarized membrane potential and generated action potentials in the neurons current-clamped. Furthermore, the drug at 40 mg/kg, i.p. increased the number of cells immunopositive both for c-Fos and tyrosine hydroxylase (TH) in the VTA. These results suggest that tipepidine may activate DA neurons in VTA through the inhibition of GIRK channel-activated currents.


Assuntos
Antidepressivos/farmacologia , Neurônios Dopaminérgicos/efeitos dos fármacos , Canais de Potássio Corretores do Fluxo de Internalização Acoplados a Proteínas G/efeitos dos fármacos , Piperidinas/farmacologia , Receptores de Dopamina D2/efeitos dos fármacos , Área Tegmentar Ventral/efeitos dos fármacos , Animais , Neurônios Dopaminérgicos/metabolismo , Canais de Potássio Corretores do Fluxo de Internalização Acoplados a Proteínas G/metabolismo , Imuno-Histoquímica , Técnicas de Patch-Clamp , Ratos , Ratos Wistar , Receptores de Dopamina D2/metabolismo , Área Tegmentar Ventral/metabolismo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA