BRINE SHRIMP LETHALITY BIOASSAY OF ABRUS PRECATORIUS (LINN) LEAVES AND ROOT EXTRACT

Authors

  • Wakawa H. Y. Department of Biochemistry, FSTS/FRST Universiti Malaysia Sarawak, Kuching, 94300 Kota Samarahan
  • Prof D. R. Department of Biochemistry, FSTS/FRST Universiti Malaysia Sarawak, Kuching, 94300 Kota Samarahan
  • Fasihuddin B. A. Department of Biochemistry, FSTS/FRST Universiti Malaysia Sarawak, Kuching, 94300 Kota Samarahan

DOI:

https://doi.org/10.22159/ijpps.2017v9i1.15057

Keywords:

Insert Brine shrimp, cytotoxicity, extracts, LC50, Abrus precatorius

Abstract

Objective: The present study was conducted to test for in vivo Brine Shrimp Lethality Assay (BSLA) of Abrus precarious leaves and root extracts after successive maceration in four solvents (n-hexane, dichloromethane (DCM) ethyl acetate and methanol) and correlate cytotoxicity results with known pharmacological activities of the plant.

Methods: Cytotoxicity was evaluated in terms of LC50 (lethality concentration), 10 nauplii were added into three replicates of each concentration of the plant extracts, and after 24 h the surviving brine shrimp larvae were counted, and LC50 was assessed.

Results: Potent cytotoxicity was found for both the leaves and root extracts of Abrus precatorius, results showed a concentration dependent increment in mortality rate of the brine shrimp nauplii and the n-hexane and dichloromethane fractions of the root and leaves extracts were more potent against the brine shrimp with LC50 values of 7.870 ppm and 19.135 ppm (µg/ml) respectively, whereas methanol fractions of both the extracts exhibited low potent activity with LC50 values 61.575 ppm and 226.053 ppm (µg/ml) in root and leaves respectively.

Conclusion: The result indicated bioactive components are present in this plant that could be accounted for its pharmacological effects.

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Published

01-01-2017

How to Cite

Y., W. H., P. D. R., and F. B. A. “BRINE SHRIMP LETHALITY BIOASSAY OF ABRUS PRECATORIUS (LINN) LEAVES AND ROOT EXTRACT”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 9, no. 1, Jan. 2017, pp. 179-81, doi:10.22159/ijpps.2017v9i1.15057.

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