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Ocimum basilicum L.: phenolic profile and antioxidant-related activity.
Nat Prod Commun. 2010 Jan; 5(1):65-72.NP

Abstract

Ocimum basilicum L. leaf material was extracted by maceration with (80:20:1 v/v/v) methanol: water: acetic acid to produce a crude extract (CE), which was further fractionated by liquid-liquid extraction to isolate light petroleum (PE), ethyl acetate (EtOAc), n-butanol (n-BuOH) and H2O-soluble sub-fractions. The total phenol and flavonoid contents of the resulting samples were estimated using colorimetric-based methods, and their iron(III) reductive and free radical scavenging activities were determined in a battery of in vitro assays. The CE and sub-fractions contained phenolic compounds and flavonoids. The samples, except for PE, gave a positive result for the presence of flavones and flavonols; however, flavanones only appeared to be present in the CE. In iron(III) reduction, CE and n-BuOH were the most potent followed by EtOAc and H2O (statistically indistinguishable, p > 0.05). However, in the ferric reducing antioxidant power assay, H2O was the most potent followed by CE and EtOAc (statistically indistinguishable, p > 0.05) and n-BuOH and PE. In 1,1-diphenyl-2-picrylhydrazyl scavenging, all the samples, except PE, were effective against this reactive nitrogen species, with CE, EtOAc and n-BuOH being the most potent (statistically indistinguishable, p > 0.05). In alkylperoxyl scavenging, all the samples, except for PE, were effective against this reactive oxygen species (ROS). In superoxide anion scavenging, all the samples were capable of scavenging this ROS with CE being the most effective, followed by n-BuOH and H2O (statistically indistinguishable, p > 0.05) and EtOAc and PE. Similarly, in hydroxyl scavenging, all the samples were capable of scavenging this ROS with CE and n-BuOH being the most effective (statistically indistinguishable, p > 0.05) followed by EtOAc and H2O (statistically indistinguishable, p > 0.05) and PE.

Authors+Show Affiliations

Faculty of Pharmacy, Division of Pharmaceutical Biology, University of Helsinki, P.O. Box 56 (Viikinkaari 5E), FIN-00014, Finland. damien.dorman@helsinki.fiNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

20184024

Citation

Dorman, H J Damien, and Raimo Hiltunen. "Ocimum Basilicum L.: Phenolic Profile and Antioxidant-related Activity." Natural Product Communications, vol. 5, no. 1, 2010, pp. 65-72.
Dorman HJ, Hiltunen R. Ocimum basilicum L.: phenolic profile and antioxidant-related activity. Nat Prod Commun. 2010;5(1):65-72.
Dorman, H. J., & Hiltunen, R. (2010). Ocimum basilicum L.: phenolic profile and antioxidant-related activity. Natural Product Communications, 5(1), 65-72.
Dorman HJ, Hiltunen R. Ocimum Basilicum L.: Phenolic Profile and Antioxidant-related Activity. Nat Prod Commun. 2010;5(1):65-72. PubMed PMID: 20184024.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Ocimum basilicum L.: phenolic profile and antioxidant-related activity. AU - Dorman,H J Damien, AU - Hiltunen,Raimo, PY - 2010/2/27/entrez PY - 2010/2/27/pubmed PY - 2010/4/9/medline SP - 65 EP - 72 JF - Natural product communications JO - Nat Prod Commun VL - 5 IS - 1 N2 - Ocimum basilicum L. leaf material was extracted by maceration with (80:20:1 v/v/v) methanol: water: acetic acid to produce a crude extract (CE), which was further fractionated by liquid-liquid extraction to isolate light petroleum (PE), ethyl acetate (EtOAc), n-butanol (n-BuOH) and H2O-soluble sub-fractions. The total phenol and flavonoid contents of the resulting samples were estimated using colorimetric-based methods, and their iron(III) reductive and free radical scavenging activities were determined in a battery of in vitro assays. The CE and sub-fractions contained phenolic compounds and flavonoids. The samples, except for PE, gave a positive result for the presence of flavones and flavonols; however, flavanones only appeared to be present in the CE. In iron(III) reduction, CE and n-BuOH were the most potent followed by EtOAc and H2O (statistically indistinguishable, p > 0.05). However, in the ferric reducing antioxidant power assay, H2O was the most potent followed by CE and EtOAc (statistically indistinguishable, p > 0.05) and n-BuOH and PE. In 1,1-diphenyl-2-picrylhydrazyl scavenging, all the samples, except PE, were effective against this reactive nitrogen species, with CE, EtOAc and n-BuOH being the most potent (statistically indistinguishable, p > 0.05). In alkylperoxyl scavenging, all the samples, except for PE, were effective against this reactive oxygen species (ROS). In superoxide anion scavenging, all the samples were capable of scavenging this ROS with CE being the most effective, followed by n-BuOH and H2O (statistically indistinguishable, p > 0.05) and EtOAc and PE. Similarly, in hydroxyl scavenging, all the samples were capable of scavenging this ROS with CE and n-BuOH being the most effective (statistically indistinguishable, p > 0.05) followed by EtOAc and H2O (statistically indistinguishable, p > 0.05) and PE. SN - 1934-578X UR - https://www.unboundmedicine.com/medline/citation/20184024/Ocimum_basilicum_L_:_phenolic_profile_and_antioxidant_related_activity_ DB - PRIME DP - Unbound Medicine ER -