2014
DOI: 10.5530/pc.2014.3.7
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An examination of the antibacterial, antifungal, anti-Giardial and anticancer properties of Kigelia africana fruit extracts

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Cited by 57 publications
(32 citation statements)
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“…A high antioxidant capacity has been postulated as being responsible for the medicinal properties of many plants. [26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43][44] In particular, antioxidants have been linked to antibacterial, antifungal and antiviral activities, as well as anticancer properties. 26-44 . However, other studies have indicated that antioxidants may protect cells from oxidative stress and thus protect against cell death.…”
Section: Discussionmentioning
confidence: 99%
“…A high antioxidant capacity has been postulated as being responsible for the medicinal properties of many plants. [26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43][44] In particular, antioxidants have been linked to antibacterial, antifungal and antiviral activities, as well as anticancer properties. 26-44 . However, other studies have indicated that antioxidants may protect cells from oxidative stress and thus protect against cell death.…”
Section: Discussionmentioning
confidence: 99%
“…[25][26][27] Briefly, 100 µL of each bacterial culture was grown in 10 mL of fresh nutrient broth until they reached a count of ~10 8 cells/mL. A volume of 100 µL of the bacterial suspension was spread onto nutrient agar plates and extracts were tested for antibacterial activity using 5 mm sterilised filter paper discs.…”
Section: Evaluation Of Antimicrobial Activitymentioning
confidence: 99%
“…The antioxidant capacity of each sample was assessed using the DPPH free radical scavenging method 30,33 with modifications. Briefly, DPPH solution was prepared fresh each day as a 400 µM solution by dissolving DPPH (Sigma) in AR grade methanol (Ajax, Australia).…”
Section: Antioxidant Capacity Determinationmentioning
confidence: 99%
“…30,33 Briefly, 1 mL of trypsin (Sigma) was added to the culture flasks and incubated at 37 o C, 5% CO 2 for 15 min to dislodge the cancer cells. The cell suspensions were then transferred to a 10 mL centrifuge tube and sedimented by centrifugation.…”
Section: Evaluation Of Cancer Cell Anti-proliferative Activitymentioning
confidence: 99%