Exact(4)
Standard screening tests of the extract were carried out for various plant constituents.
Phytochemical tests of the extract were performed as previously described [ 21, 22].
EEAIT was also injected intraperitoneally by the following manner after performing the routine toxicity tests of the extract [ 9].
Standard screening tests of the extract were carried out for various plant chemical constituents; for the presence or absence of secondary metabolites such as terpenes, alkaloids, steroidal compounds, phenolic compounds, tannins, saponins and flavonoids using standard procedures [ 28, 29].
Similar(56)
When mixed with AFB1, all five tested concentrations of the extract showed inhibition exceeding 40%, reaching 80% at one concentration.
As demonstrated in Table 6, all test doses of the extract significantly reduced the intestinal weight ratio in dose dependent manner.
The OECD guidelines for testing chemicals (2000) for toxicity were adapted in testing the safety of the extract of Loxostylis alata[ 28].
To test validity of the extracted signals, a back-propagation neural network is designed and appropriately trained with "Early Stopping" technique to detect these defects automatically.
Chloroquine sensitive Plasmodium berghei (ANKA strain) was used to test the antimalarial activity of the extract.
The mice in the test groups received fractions of the extract once daily for 4 days.
The anti-inflammatory activity of the extract tested using the chick carrageenan-induced foot oedema model.
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