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Comparative anticancer and antimicrobial activity of aerial parts of , , and grown in Saudi Arabia. | LitMetric

Comparative anticancer and antimicrobial activity of aerial parts of , , and grown in Saudi Arabia.

Saudi Pharm J

Pharmaceutical Biotechnology Laboratory, Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11541, KSA.

Published: December 2017

AI Article Synopsis

Article Abstract

The standardized ethanol extract (EE) of aerial parts of four species [ (ASEE), (ALEE), (AHEE), and (ATEE)] were examined in order to compare their cytotoxic and antimicrobial activities. All the extracts were standardized by UPLC- PDA method using rutin as standard compound. The extracts ALEE, AHEE and ATEE were found to contain rutin along with several other phytoconstituents while rutin was absent in ASEE. All the extracts showed varying level of antimicrobial activity with zone of inhibition ranged from 11 to 21 mm against , , and . The ALEE and ATEE showed relatively high antimicrobial potency (MIC = 0.2 to 1.6 mg mL) in comparison to other extracts. All the extracts were found to reduce the biofilm of PAO1 strain significantly in comparison to the untreated control. The cytotoxic property of ASEE, ALEE, AHEE, ATEE were evaluated against HepG2 (Liver), HEK-293 (Kidney), MCF-7 (Breast) and MDA-MB 231 (Breast) cancer cells. Of these, ALEE, AHEE and ATEE exhibited moderate cytotoxic property against human liver carcinoma cells (HepG2; IC50 = 46.2, 39.2 and 42.3 μg mL, respectively) and breast cancer cell lines (MCF-7; IC50 = 57.2, 55.3 and 65.7 μg mL, respectively). The ATEE and ALEE showed moderate cytotoxicity against HEK-293 (kidney) cells with IC50 = 49.1 and 53.5 μg mL, respectively. Since, species ( and ) contains numerous polyphenols which might prove to be highly cytotoxic and antimicrobial agents, we suggest that these species can be further subjected to the isolation of more cytotoxic and antimicrobial compounds.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688228PMC
http://dx.doi.org/10.1016/j.jsps.2017.09.010DOI Listing

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