ABSTRACT
La tripanosomiasis americana es una enfermedad infecciosa desatendida, causada por el parásito protozoo Trypanosoma cruzi, que no cuenta con tratamiento en la fase crónica de esta enfermedad mortal, uno de los desafíos es encontrar terapias efectivas para esta compleja enfermedad, dado que no presenta síntomas asociables a la parasitosis por lo que es desconocida entre los médicos tradicionales. Nuestra Facultad está evaluando la medicina tradicional tacana como fuente de agentes antiparasitarios potenciales. El objetivo de este trabajo fue identificar productos naturales trypanocidas utilizando el método colorimétrico XTT-PMS. Para ello, se realizaron curvas de crecimiento de epimastigotes de T. cruzi y determinamos el tiempo óptimo de realización de los ensayos. Se seleccionó la población inicial de trabajo (3x106 parásitos/mL), las condiciones de incubación (medio LIT, 27ºC, 72 horas) y revelado (XTT-PMS, 4 horas). Con el protocolo optimizado, se realizaron evaluaciones de actividad de drogas control, controles naturales y 20 extractos crudos de plantas medicinales de la amazonía. La actividad se basó en cálculos de concentración inhibitoria media y se consideraron activos las sustancias con CI50<50µg/mL. De los 20 extractos evaluados, el 40% fueron activos. Las plantas más interesantes fueron Sipu sipu (CI50=8.9±1.7µg/mL), Ejije bid'u (CI50=9.1±1.5µg/mL) e Id'ene eidhue (CI50=10.8±1.1µg/mL) con valores de CI50 cercanos a los controles, confirmando la utilidad y potencial del protocolo desarrollado
American trypanosomiasis is listed among the unattended infectious disease, is caused by the protozoan parasite Trypanosoma cruzi, and has no treatment in the chronic phase of this deadly disease. One of the challenges is finding effective therapies for this complex disease, given that it does not present any associated symptoms to the parasitism and is unknown among traditional doctors. Our Faculty is evaluating tacana traditional medicine as a source of potential antiparasitic agents. The objective of this work was to identify trypanocidal natural products using the XTTPMS colorimetric method. For this, growth curves of T. cruzi epimastigotes were made to determine the optimal time to carry out the tests. The initial work population (3x106 parasites/mL), the incubation conditions (medium LIT, 27ºC, 72 hours) and revealed process (XTT-PMS, 4 hours) were selected. With the optimized protocol, activity evaluations of control drugs, natural controls and 20 crude extracts of medicinal plants of the Amazon were carried out. The activity was based on calculations of mean inhibitory concentration and substances with IC50 <50µg/mL were considered active. Of the 20 extracts evaluated, 40% were active. The most interesting plants were Sipu sipu (IC50=8.9±1.7µg/mL), Ejije bid'u (IC50=9.1±1.5µg/mL) and Id'ene eidhue (IC50=10.8±1.1µg/mL) with values of IC50 close to the controls, confirming the usefulness and potential of the developed protocol.
Subject(s)
Plants, Medicinal , Inhibitory Concentration 50 , Medicine, Traditional , Therapeutics , Trypanosoma cruzi , Pharmaceutical PreparationsABSTRACT
PURPOSE: The aim of this in vitro study was to evaluate the effect of aging on the tear strength and cytotoxicity of four soft denture lining materials. MATERIALS AND METHODS: Four commonly used soft denture lining materials, (Coe-Comfort(TM) GC America Inc., Alsip, IL, USA; Coe-Soft(TM) GC America Inc., Alsip, IL, USA; Visco-gel Dentsply Caulk Milford, DE, USA; and Sofreliner Tough M Tokuyama Dental Corporation Tokyo, Japan) were selected. Sixty trouser-leg designed specimens per lining material were fabricated using a stainless steel mold for tear strength testing. The specimens were divided into non-thermocycling and 1000-, and 3000- thermocycling groups. For the cytotoxicity test, twenty-four disk shaped specimens per material were fabricated using a stainless steel mold. The specimens were soaked in normal saline solution for 24 h, 48 h and 72 h. Cytotoxicity was measured by XTT assay in L929 mouse fibroblasts. Data were analyzed by two way analysis of variance and Dunnett's test (P<.05). RESULTS: Before thermocycling, Sofreliner Tough M (10.36 +/- 1.00 N) had the highest tear strength value while Coe-Comfort(TM) (0.46 +/- 0.10 N) had the lowest. After 3000 cycles, Sofreliner Tough M (9.65 +/- 1.66 N) presented the highest value and Coe-Comfort(TM) (0.42 +/- 0.08 N) the lowest. Sofreliner Tough M, in all incubation periods was the least toxic with significant differences compared to all other materials (P<.05). Coe-Comfort(TM), Coe-Soft(TM), and Sofreliner Tough M did not show any significant differences within their material group for all incubation periods. CONCLUSION: This in vitro study revealed that aging can affect both the tear strength and cytotoxicity of soft denture materials depending on the composition.
Subject(s)
Animals , Mice , Aging , Americas , Dentures , Fibroblasts , Fungi , Sodium Chloride , Stainless SteelABSTRACT
Aims: Candida species cause a wide spectrum of diseases, including hospital-acquired and device-associated infections. The biofilm formation is a major virulence factor in Candida pathogenesis and the cells in biofilm show enhanced resistance to disinfectants. Our aim was to evaluate the efficiency of the commonly used hospital disinfectants (glutaraldehyde (GLU), hydrogen peroxide (HP), peracetic acid (PA), ortho-phtalaldehyde (OPA) and sodium hypochlorite (SH) on biofilms of clinical Candida (C. albicans, C. glabrata, C. parapsilosis, C. krusei and C. tropicalis) isolates. Study Design: An experimental study. Place and Duration of Study: Department of Microbiology, Faculty of Medicine and Electron Microscope Laboratory, Eskisehir Osmangazi University, between January 2011 and May 2011. Methodology: These disinfectants were selected due to their common application in hospital environment. Their concentrations were adjusted to manufacturer’s recommendations for instrument disinfection: 5% HP, 0.2% PA, 5.25% SH (5000 ppm of chlorine), 2% GLU and 0.55% OPA. They were also prepared at the 1:2 and 1:4 times of recommended concentration to evaluate the activity of lower concentrations. The biofilms were grown in microplates and treated with disinfectants at contact times 1, 5 and 10 minutes (20 min for GLU), then stained with the biomass indicator (2, 3-Bis [2-methoxy-4- nitro-5-(sulfenylamino) carbonyl-2H-tetrazolium-hydroxide]). Results: The disinfectants reduced the biofilm for all concentrations studied, however none of them completely removed the biofilm. When they were used at low concentration, longer contact times were more effective. However, when the disinfectants were used in recommended concentration, results showed many variations depending on the disinfectant type, contact times and species. Conclusion: Our results also emphasize the importance of regular disinfection, before the starting of biofilm formation.
ABSTRACT
El presente estudio evaluó el desempeño de dos sales de tetrazolio, una tradicional: INT y una de nueva generación: XTT, para estimar la densidad de microorganismos degradadores de hidrocarburos (HCs) en suelos empleando la técnica del Número Más Probable (NMP). Se analizaron 96 muestras de suelo provenientes de la Ecorregión Cafetera de Colombia. Los microorganismos fueron recuperados en agar mínimo de sales en atmósfera saturada de HCs y la capacidad degradadora fue confirmada por repiques sucesivos utilizando diesel como fuente de carbono. No se observaron diferencias significativas en los recuentos de microorganismos degradadores obtenidos con las dos sales (t de Student, p < 0,05), pero el XTT permitió mejor visualización de los pozos positivos dada la solubilidad del producto reducido, mientras que el INT produjo precipitación, debido al formazán insoluble generado, dificultando su lectura. Se obtuvo un mayor porcentaje de aislamientos empleando XTT (67%), lo cual podría indicar que el tipo de sal es determinante en la viabilidad de estas bacterias. Adicionalmente, se evaluó el límite de detección celular, las condiciones óptimas de concentración de XTT y el tiempo de incubación necesario para la detección de actividad degradadora utilizando la cepa Acinetobacter sp. El aumento en la concentración de XTT de 0,5 mM a 2 mM y el tiempo de incubación tuvieron un efecto inhibitorio y favorable respectivamente, en la recuperación de células viables, adicionalmente, límite de detección de la técnica fue de 10² UFC/ml.
The objective of this study was to evaluate the performance of two tetrazolium indicators: a traditional one: INT and a new generation one: XTT, for the estimation of hydrocarbon (HC) degrading microorganism s density using the Most Probable Number Technique (MPN). Ninety six composite soil samples were taken and analyzed from Ecorregión Cafetera Colombiana. Degrading microorganisms were recovered in minimum salt medium with saturated HC atmosphere. Degrading HC capacity of the microorganisms was confirmed by successive subcultures in the same medium using diesel as only carbon source. Counts obtained with the two salts were not significantly different (Student t test, p < 0,05) but XTT allowed an easier visualization of positive wells due to product solubility of the reduce product. A greater percentage of isolates was obtained using XTT (67%), which suggests that salt type is relevant for recovering of these microorganisms. Additionally, cell detection limit, optimal conditions of XTT concentration and incubation times for detection of activity were evaluated. This evaluation was performed by means of microplate format for hydrocarbon degrading microorganisms using Acinetobacter sp. An inhibitory effect was observed in the recovering of cultivable cells when XTT concentrations increased from 0,5 mM to 2 mM. Incubation time favored this recovering. Detection limit of this technique was established at 10² UFC/ml. Production of the XTT-formazan was positively related with initial cell concentration and negatively with incubation time.
ABSTRACT
2, 3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino) carbonyl]-2H-tetrazolium hydroxide (XTT) reduction assay has been used to study Candida biofilm formation. However, considering that the XTT reduction assay is dependent on cell activity, its use for evaluating mature biofilms may lead to inaccuracies since biofilm bottom cell layers tend to be relatively quiescent at later stages of biofilm formation. The aim of this study was to improve XTT reduction assay by adding glucose supplements to the standard XTT formulation. Candida albicans ATCC 90028 was used to form 24-, 48- and 72-h biofilms. The oxidative activity at 90, 180 and 270 min of incubation was evaluated. The control consisted of standard XTT formulation without glucose supplements, and was modified by the addition of 50, 100 and 200 mM of glucose. The XTT assay with 200 mM glucose showed more accurate and consistent readings correlating with biofilm development at 24, 48 and 72 h. Biofilm growth yield after 180 min incubation, when evaluated with the 200 mM glucose supplemented XTT, produced the most consistent readings on repetitive testing. It may be concluded that glucose supplementation of XTT could minimize variation and produce more accurate data for the XTT assay.
O teste de redução do 2,3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino) carbonyl]-2H-tetrazolium hydroxide (XTT) tem sido utilizado para mensurar o desenvolvimento de biofilmes de Candida. Contudo, a reação de XTT é dependente da atividade celular e o seu uso para biofilmes maduros pode ser questionado, considerando que diferentes camadas celulares têm atividade metabólica diferenciadas. O objetivo deste estudo foi avaliar se a adição de glicose à formula de XTT diminuiria a variabilidade na mensuração da atividade metabólica. Biofilmes de Candida albicans ATCC 90028 com tempos de crescimento de 24, 48 e 72 h foram utilizados. Para avaliar o melhor tempo de incubação do XTT, este foi mantido a temperatura de 37 °C, em tempos de 90 180 e 270 min. A fórmula padrão do teste XTT (controle) foi modificada com a adição de 50, 100 e 200 mM de glicose para os grupos experimentais. Os melhores resultados para a incubação foi observado com tempo de 180 min e para a suplementação de glicose à concentração de 200 mM (p<0.001). Concluiu-se que a incubação de 180 min utilizando a suplementação de 200 mM de glicose apresenta resultados de atividade metabólica celular com a menor variação para o estudo de biofilmes de Candida albicans.
Subject(s)
Biofilms/growth & development , Candida albicans/growth & development , Colony Count, Microbial/methods , Culture Media/chemistry , Indicators and Reagents/chemistry , Glucose , Oxidation-Reduction , Reproducibility of Results , Tetrazolium Salts/chemistryABSTRACT
STATEMENT OF PROBLEM: The role of calcium sulfate in stimulating the growth of gingival soft tissue has been reported in few studies. Such a unique property of calcium sulfate could serve as a trouble-solving broker in compensating for the lack of soft tissues in various oral surgeries. PURPOSE: The purpose of this study was to compare the proliferating activities of human gingival fibroblasts seeded on various bone graft barrier materials of calcium sulfate, collagen, and polytetrafluorethylene (PTFE). MATERIAL AND METHODS: Two calcium sulfates (CAPSET(R) and CalForma(R), Lifecore Biomedical Inc., St. Paul, Minnesota, USA), a resorbable natural collagen (Bio-Gide(R), Geistlich Pharma Ag., Wolhusen, Switzerland), and a non-resorbable PTFE (TefGen-FD(R), Lifecore Biomedical Inc., St. Paul, Minnesota, USA) served as the human gingival fibroblasts'substrates and comprised the four experimental groups, whereas the untreated floors of culture plastics were used in the control group, in this study. Cells were trypsinized, seeded, and incubated for 48 h. The proliferating activities of fibroblasts were determined by XTT and SRB assay and absorbance (optical density, OD) was measured. One-way ANOVA was used to analyze the differences in the mean OD values between the groups of CAPSET, CalForma, Bio-Gide, TefGen, and the control (p<0.05). RESULTS: From the XTT assay, the mean OD value of the control group, the highest, was significantly greater than that of any of the four experimental groups followed by CalForma, CAPSET, TefGen, and Bio-Gide. Further, the mean OD value of CalForma, was significantly greater compared to that of Bio-Gide. From the SRB assay, Calforma showed the highest mean OD value, which was significantly greater than that of any other groups, followed by the control, CAPSET, Bio-Gide, and TefGen. The mean OD values of both the control and CAPSET were significantly greater compared to that of TefGen (p<0.05). CONCLUSION: Assessment of the viability and proliferation of cultured fibroblasts seeded and incubated for 48 h on various barrier-material substrates using XTT and SRB assay showed that calcium sulfate CalForma(R) promotes the proliferating activity of human gingival fibroblasts.