IN-VIVO ASSESSMENT OF EMBRYO TOXICITY POTENTIAL OF IMMUNE BOOSTING SIDDHA FORMULATION NELLIKAI LEGIUM DURING GESTATION PERIOD
Elakkiyaa V.*, Nisha J., Visweswaran S. and Muthukumar N. J.
Abstract
Zebrafish model provides valuable insight into teratogenic risk
assessment of drugs, chemicals, traditional medicines and other
pharmaceuticals. This model has also been recommended as an
alternative to fish acute toxicity. Embryo toxicity assay is most reliable
model for predicting the teratogenic potential of the formulation and
other new drug entities. Zebrafish (Danio rerio) attains greater
importance in the field reproductive biology due to it’s close genetical
resemblance with respect to that of the humans. The main aim of the
present investigation is to evaluate the embryo toxicity profiling of the
siddha formulation Nellikai Legium using Zebrafish embryos. The
concentration of the test drug ranging from 10μg to 320 μg/ml upon 24
to 96 hours post fertilization (HPF) exposure at 30 embryos per concentration. The results
obtained from the present investigation has clearly shown that there is no significant
difference in movement analysis of the drugs treated groups (7.1 ± 1.155 to 7.733 ± 0.90 per
min) with that of the control embryos with movement of 7.667 ± 1.184 per min. The data
obtained from the present investigation reveals that there is no significant difference in heart
rate of the drugs treated groups (124.1 ± 2.255 to 126.5 ± 2.286 beats/min) with that of the
control embryos with heart rate of 125.1 ± 2.27 beats/ min. Further there was no
abnormalities were detected in observed parameter’s such hatching rate, blood circulation, pigmentation, swimming pattern, balancing and morphogenesis. It was concluded from the results of the present investigation that siddha formulation Nellikai Legium was safe and didn’t alter any of the physiology of the developing fetus upon 24 to 96 HPF exposure.
Keywords: Siddha formulation, Nellikai Legium, Zebrafish embryos, Toxicity profiling, Hours post fertilization.
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