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. 2019 Mar 11;25:e144418. doi: 10.1590/1678-9199-JVATITD-1444-18

Table 2. Detection of phosphatidylserine expression by Annexin V method on L.(L) amazonensis promatigotes exposed to different concentrations of nitro-heterocyclic derivatives and amphotericin B.

  PI+ (%) AV+ (%) PI+ AV+ (%)
Negative Control 2.13 2.94 0.86
DMSO PA Control 3.75 1.15 0.27
[100 µM]
Amphotericin B 5.43 16.8 1.68
BSF-C4H9 4.56 11.7 4.11
BSF-CH3 7.63 7.86 3.56
BSF-Cl 11.2 14.5 5.42
BSF-H 2.61 25.1 4.1
BSF-NO2 7.67 1.25 0.29
[25 µM]
Amphotericin B 6.72 35.1 3.03
BSF-C4H9 4.06 5.87 3.52
BSF-CH3 3.64 3.87 0.93
BSF-Cl 4.68 19 6.2
BSF-H 2.49 14.3 4.06
BSF-NO2 1.22 9.28 2.21
[6.25 µM]
Amphotericin B 2.42 48.3 3.88
BSF-C4H9 1.04 7.19 2.11
BSF-CH3 0.94 6.21 1.58
BSF-Cl 1.33 7.53 1.97
BSF-H 2.23 7.53 1.96
BSF-NO2 1.72 2.7 0.67

Data expressed by the percentage of the average fluorescence intensity of Annexin V-FITC and Propidium Iodide-PE on L.(L) amazonensis promatigotes. Incubation for 48 hours, at 32 °C and 5% of CO2. AV+ (Q3): Annexin V positive; PI+ (Q1): Propidium iodide positive PI+ AV + (Q2): Annexin V and Propidium iodide positive; Negative control: promastigotes untreated.