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. 2016 Jun 27;11(3):230–235. doi: 10.1049/iet-nbt.2015.0061

Table 2.

Inhibitory rate (%) of FeNPs synthesised using Azadirachta indica leaf extract against various plants pathogenic fungi at different concentrations in vitro

Fungi Inhibition rates (%)A
Ai a Feb FeNP Ai FeNP Ai  + Ai
10 ppm 25 ppm 50 ppm 100 ppm 10 ppm 25 ppm 50 ppm 100 ppm 10 ppm 25 ppm 50 ppm 100 ppm 10 ppm 25 ppm 50 ppm 100 ppm
B. dothidea 27.1 ± 0.5 38.1 ± 2.1 52.4 ± 1.3 67 ± 0.2 15 ± 1.0 32 ± 2.1 40 ± 1.2 53 ± 2.2 30 ± 1.2 45 ± 1.3 63 ± 2.1 83 ± 1.4 29.1 ± 1.2 44.2 ± 3.1 68.1 ± 0.6 82.5 ± 1.2
D. seriata 21.1 ± 2.1 40.2 ± 0.3 63.8 ± 2.1 75 ± 0.5 11 ± 2.1 18 ± 2.1 29 ± 2.1 44 ± 1.6 28 ± 2.1 41 ± 3.5 58 ± 3.1 79 ± 1.3 35.1 ± 0.4 50.1 ± 1.5 68.2 ± 3.1 80.3 ± 1.5
A. mali 33.1 ± 1.0 48.2 ± 0.5 55.2 ± 0.3 68.7 ± 3.1 1.3 ± 2.1 10 ± 2 16 ± 2.0 30 ± 0.5 27 ± 2.0 37 ± 1.0 53 ± 2.0 78.5 ± 1.0 25.3 ± 0.9 40.1 ± 0.2 59.2 ± 2.5 79.2 ± 1.3

A Inhibition rate =  mycelialgrowthincontrolplatesmycelialgrowthintreatedplatesmycelialgrowthincontrolplates×100.

Colony diameters were measured at 7 days post‐inoculation: inhibition rates were determined based on four replicates of each experiment represented as means ± SD: inhibition rate of control for each fungus = 0%.

a Ai  = A. indica leaf extract solution.

b Fe = Fe2+ ion solution.

FeNP Ai : solution of FeNP synthesised by using A. indica leaf extract.