Acute toxicity
The acute toxicity study was conducted as per
the OECD guidelines 425, w
here the limit test
dose of 5000 mg/kg was used. No treatment
-
related mortality was observed at 5000 mg/kg.
Throughout 14 days of observation, there were
no significant (
p
>0.05) changes recorded in
behavior in any of the animals such as apathy,
hyperactivi
ty, morbidity, etc. No abnormal
changes attributable to treatment were noticed in
body weights and treatment
-
related changes like
respiration rate and heart
rate. Therefore, the extract seems to be safe at a
dose level of 5000 mg/kg, and the LD
50
is
consi
dered be > 5000 mg/kg.
There were no
clinical signs of toxicity or treatment
-
related
mortality during the observation period among
the rats. The animals appeared very healthy and
their physical activity appeared normal.
Acute toxicity The acute toxicity study was conducted as per the OECD guidelines 425, where the limit test dose of 5000 mg/kg was used. No treatment-related mortality was observed at 5000 mg/kg. Throughout 14 days of observation, there were no significant (p>0.05) changes recorded in behavior in any of the animals such as apathy, hyperactivity, morbidity, etc. No abnormal changes attributable to treatment were noticed in body weights and treatment-related changes like respiration rate and heart rate. Therefore, the extract seems to be safe at a dose level of 5000 mg/kg, and the LD50is considered be > 5000 mg/kg. There were no clinical signs of toxicity or treatment-related mortality during the observation period among the rats. The animals appeared very healthy and their physical activity appeared normal.
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