Abstract
ABSTRACTLeaf and gel extracts of Aloe schweinfurthii and A. vera were subjected to in vitro antioxidant assay using 2,2-diphennyl-1-picryl hydrazyl (DPPH), brine shrimp lethality bioassay, and cytotoxicity using the MTT assay with two human cancer cell lines: Rd and Hep-2c. Extracts of A. schweinfurthii gel had IC50 values of 44.59; A. vera gel, 41.48, and A. vera leaf, 38.84 µg.mL–1, had similar DPPH radical-scavenging properties and were more active than A. schweinfurthii leaf. Ascorbic acid had an IC50 of 9.26 ± 0.14 µg.mL–1. Aloe vera leaf (LC50 = 325 ± 5.38 µg.mL–1) was more active than the other three extracts in the BSL assay. The gel extracts of A. schweinfurthii (CC50 = 4.06 µg.mL–1on Rd and 9.00 µg.mL–1 on Hep-2c) and A. vera (CC50 = 4.31 µg.mL–1 on Rd, 9.06 µg.mL–1 on Hep-2c) elicited similar and more potent cytotoxicity comparable to cyclophosphamide, with CC50 = 2.2 µg.mL–1 on Rd and 2.66 µg.mL–1 on Hep-2c. Leaf extracts were less active than gel extracts. This study showed that A. schweinfurthii gel, A. vera gel and leaf had weak DPPH activity which were similar. Aloe vera and A. schweinfurthii did not elicit potent cytotoxicity in BSL assay. The gels from both Aloe species displayed antipoliferative activity on Rd and Hep-2c, two human cell cancer lines.
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