RESUMO
Life-threatening Candida infections have increased with the COVID-19 pandemic, and the already limited arsenal of antifungal drugs has become even more restricted due to its side effects associated with complications after SARS-CoV-2 infection. Drug combination strategies have the potential to reduce the risk of side effects without loss of therapeutic efficacy. The aim of this study was to evaluate the combination of ent-hardwickiic acid with low concentrations of amphotericin B against Candida strains. The minimum inhibitory concentration (MIC) values were determined for amphotericin B and ent-hardwickiic acid as isolated compounds and for 77 combinations of amphotericin B and ent-hardwickiic acid concentrations that were assessed by using the checkerboard microdilution method. Time-kill assays were performed in order to assess the fungistatic or fungicidal nature of the different combinations. The strategy of combining both compounds markedly reduced the MIC values from 16 µg/mL to 1 µg/mL of amphotericin B and from 12.5 µg/mL to 6.25 µg/mL of ent-hardwickiic acid, from isolated to combined, against C. albicans resistant to azoles. The combination of 1 µg/mL of amphotericin B with 6.25 µg/mL of ent-hardwickiic acid killed all the cells of the same strain within four hours of incubation.
RESUMO
Desmostachya bipinnata (L.) Stapf, Poaceae, or Kusha in Sanskrit, is a sacred grass used extensively in Indian Vedic practices. It is well known for its medicinal value and is used in traditional Indian medicine to treat microbial infection in combination with other herbs. An effort has been made to isolate and characterize the bioactive compounds from the hydroalcoholic extract of D. bipinnata through bioassay guided fractionation, column chromatography. Their individual or combined antimicrobial properties were determined by the Resazurin Microtitre Assay, the checkerboard assay in combination with antibiotics, and by time kill curve analysis. β-Sitosterol-D-glucopyranoside was the bioactive compound identified to have the best antimicrobial activity (MIC 6-50 µg/ml) and it works synergistically with most antibiotics, especially with ciprofloxacin. Time kill curves showed that BS kills most of the pathogens within 5-10 h. To our knowledge at its best, this is the first time report of antibacterial synergy of β-sitosterol-D-glucopyranoside from D. bipinnata.
RESUMO
A clear understanding of the pharmacodynamic properties of antifungal agents is important for the adequate treatment of fungal infections like candidiasis. For certain antifungal agents, the determination of Minimal Fungicidal Concentration (MFC) and time kill curve could be clinically more relevant than the determination of the Minimal Inhibitory Concentration (MIC). In this study, MIC and MFC to fluconazole, amphotericin B and caspofungin against C. albicans isolates and the killing patterns obtained with caspofungin and amphotericin B against susceptible and resistant strains to fluconazole were determined. The results of MICs showed that all C. albicans isolates were highly susceptible to amphotericin B, but two isolates were fluconazole resistant. The comparative analysis between MIC and MFC showed that MFC of fluconazole was fourfold higher than MIC in 41.9% of the C. albicans isolates. Same values of MFC and MIC of amphotericin B and caspofungin were found for 71% of the isolates. Correlation between time kill curves and MFC of amphotericin B and caspofungin against all 4 isolates tested was observed. The caspofungin killing effect was more evident at MFC in 6 hours of incubation than at MIC in this time, suggesting dependence of concentration. The similarity of results of time-kill curve and MFC values indicate that determination of MFC is an alternative for the detection of the fungicidal activity of these drugs.
Um claro entendimento das propriedades farmacodinâmicas dos agentes antifúngicos é de grande importância para o adequado tratamento das infecções fúngicas como a candidíase. Em alguns casos de escolha do agente antifúngico, a determinação da concentração fungicida minima (CFM) e a curva do tempo de morte podem ser mais clinicamente relevantes do que a concentração inibitória minima (CIM). Nesse estudo, foi avaliado a CIM e a CFM de fluconazol, anfotericina B e caspofungina em Candida albicans e ainda os padrões de morte obtidos com caspofungina e anfotericina B de isolados suscetíveis e resistentes ao fluconazol. Os resultados de CIM mostraram que todos os isolados de Candida albicans foram altamente suscetíveis à anfotericina B, entretanto dois isolados foram fluconazol resistentes. A análise comparativa de CIM e da CFM mostrou que o CFM de fluconazol foi quatro vezes superior à CIM para 41,9% dos isolados de Candida albicans. Valores iguais de CFM e CIM de anfotericina B e caspofungina foram encontrados para 71% dos isolados. Correlação entre a curva do tempo de morte e a CFM de anfotericina B e caspofungina contra quatro isolados testados foi observada. O efeito de morte de caspofungina foi mais evidente na CFM até 6 horas de incubação do que na CIM nesse mesmo tempo, sugerindo a dependência da concentração. A similaridade dos resultados da curva do tempo de morte e os valores de CFM indicam que a determinação da CFM é uma escolha alternativa na detecção da atividade fungicida destes agentes antifúngicos.
Assuntos
Humanos , Antibacterianos/isolamento & purificação , Candida albicans/isolamento & purificação , Suscetibilidade a Doenças , Mucosa Bucal , Micoses , Cinética , Métodos , Pacientes , Técnicas e Procedimentos DiagnósticosRESUMO
A clear understanding of the pharmacodynamic properties of antifungal agents is important for the adequate treatment of fungal infections like candidiasis. For certain antifungal agents, the determination of Minimal Fungicidal Concentration (MFC) and time kill curve could be clinically more relevant than the determination of the Minimal Inhibitory Concentration (MIC). In this study, MIC and MFC to fluconazole, amphotericin B and caspofungin against C. albicans isolates and the killing patterns obtained with caspofungin and amphotericin B against susceptible and resistant strains to fluconazole were determined. The results of MICs showed that all C. albicans isolates were highly susceptible to amphotericin B, but two isolates were fluconazole resistant. The comparative analysis between MIC and MFC showed that MFC of fluconazole was fourfold higher than MIC in 41.9% of the C. albicans isolates. Same values of MFC and MIC of amphotericin B and caspofungin were found for 71% of the isolates. Correlation between time kill curves and MFC of amphotericin B and caspofungin against all 4 isolates tested was observed. The caspofungin killing effect was more evident at MFC in 6 hours of incubation than at MIC in this time, suggesting dependence of concentration. The similarity of results of time-kill curve and MFC values indicate that determination of MFC is an alternative for the detection of the fungicidal activity of these drugs.
RESUMO
A clear understanding of the pharmacodynamic properties of antifungal agents is important for the adequate treatment of fungal infections like candidiasis. For certain antifungal agents, the determination of Minimal Fungicidal Concentration (MFC) and time kill curve could be clinically more relevant than the determination of the Minimal Inhibitory Concentration (MIC). In this study, MIC and MFC to fluconazole, amphotericin B and caspofungin against C. albicans isolates and the killing patterns obtained with caspofungin and amphotericin B against susceptible and resistant strains to fluconazole were determined. The results of MICs showed that all C. albicans isolates were highly susceptible to amphotericin B, but two isolates were fluconazole resistant. The comparative analysis between MIC and MFC showed that MFC of fluconazole was fourfold higher than MIC in 41.9% of the C. albicans isolates. Same values of MFC and MIC of amphotericin B and caspofungin were found for 71% of the isolates. Correlation between time kill curves and MFC of amphotericin B and caspofungin against all 4 isolates tested was observed. The caspofungin killing effect was more evident at MFC in 6 hours of incubation than at MIC in this time, suggesting dependence of concentration. The similarity of results of time-kill curve and MFC values indicate that determination of MFC is an alternative for the detection of the fungicidal activity of these drugs.
Um claro entendimento das propriedades farmacodinâmicas dos agentes antifúngicos é de grande importância para o adequado tratamento das infecções fúngicas como a candidíase. Em alguns casos de escolha do agente antifúngico, a determinação da concentração fungicida minima (CFM) e a curva do tempo de morte podem ser mais clinicamente relevantes do que a concentração inibitória minima (CIM). Nesse estudo, foi avaliado a CIM e a CFM de fluconazol, anfotericina B e caspofungina em Candida albicans e ainda os padrões de morte obtidos com caspofungina e anfotericina B de isolados suscetíveis e resistentes ao fluconazol. Os resultados de CIM mostraram que todos os isolados de Candida albicans foram altamente suscetíveis à anfotericina B, entretanto dois isolados foram fluconazol resistentes. A análise comparativa de CIM e da CFM mostrou que o CFM de fluconazol foi quatro vezes superior à CIM para 41,9% dos isolados de Candida albicans. Valores iguais de CFM e CIM de anfotericina B e caspofungina foram encontrados para 71% dos isolados. Correlação entre a curva do tempo de morte e a CFM de anfotericina B e caspofungina contra quatro isolados testados foi observada. O efeito de morte de caspofungina foi mais evidente na CFM até 6 horas de incubação do que na CIM nesse mesmo tempo, sugerindo a dependência da concentração. A similaridade dos resultados da curva do tempo de morte e os valores de CFM indicam que a determinação da CFM é uma escolha alternativa na detecção da atividade fungicida destes agentes antifúngicos.