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. 2016 Jul 14;6(3):154–164. doi: 10.1016/j.ijpddr.2016.07.001

Table 2.

IC50 of Bz and 1g on epimastigotes (Epi), trypomastigotes (Tryp) amastigotes (Ama), Vero cells and Cardiomyocytes (Vero/CM) incubated in medium with and without hemin. Results represent the mean and standard deviation of at least three experiments in duplicate.

Medium 1g
Bz
Epia Trypb Amac Vero/CMd Epia Trypb Amac Vero/CMd
Without heme 19.5 ± 2.5 >100 12.2 ± 2.6 >100 2.9 ± 0.6 13 ± 5.7 3.25 ± 0.3 >100
With heme* <1** 11.7 ± 4** 6.3 ± 2.5** >100 9.5 ± 5.2** 12 ± 6.5 2.5 ± 1.4 >100

*30 μM of heme diluted in BHI, RPMI and DMEM medium.

**Statistically significant p < 0.05 using one-way ANOVA.

a

IC50 (Concentration that inhibits the growth of 50% of T. cruzi Y epimastigote forms within 72 h). Viability was measure counting motile parasites in Neubauer chamber.

b

IC50 (Concentration that kills 50% of T. cruzi Y trypomastigotes within 24 h). Viability was measure using resazurin.

c

IC50 (Concentration that inhibits 50% of T. cruzi Y amastigotes after 72 h of treatment). Measured by counting the number of parasites stained with GIEMSA.

d

CC50 (Concentration that inhibits 50% of host cell growth after 72 h of treatment). Viability was measure using resazurin.