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Phenolic profile and antioxidant evaluation of Mentha x piperita L. (peppermint) extracts.
Nat Prod Commun. 2009 Apr; 4(4):535-42.NP

Abstract

Seven extracts were prepared from Mentha x piperita (peppermint) leaves in sequence using a Soxhlet apparatus, viz. (40-60 degrees) light petroleum (PE), dichloromethane (CH2Cl2), acetonitrile (ACN), ethyl acetate (EtOAc), methanol (MeOH), n-butanol and water (H2O) extracts. The phenolic and flavonoid content of each extract were estimated using spectrophotometric methods whilst a qualitative-quantitative analysis was made by reverse-phase high performance liquid chromatography coupled with photodiode array detection (HPLC-PDA). Each extract was assessed in a battery of six antioxidant-related assays so as to determine their iron(III) reductive, iron(II) chelating and free radical scavenging abilities. The MeOH-soluble extract contained the greatest content of total phenols and flavonoids based upon the Folin-Ciocalteu and 2-aminoethyl diphenylborate reagent data and HPLC-PDA analysis. Based upon the chromatographic and UV-spectral data, the leaves principally contained the cinnamic acid caffeic acid, the depside rosmarinic acid and flavonoids (flavones and flavanones). Eriocitrin (383.3 +/- 2.2 mg/g extract) and rosmarinic acid (381.2 +/- 1.9 mg/g extract) were the most abundant components identified within the leaves, whilst naringenin-7-O-glucoside (0.8 +/- 0.01 mg/g extract) was the least abundant component identified being found only in the EtOAc-soluble extract. The EtOAc, ACN and H2O-soluble extracts demonstrated the most potent iron(III) reductive and 1,1'-diphenyl-2-picrylhydrayl, 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonate) and hydroxyl free radical scavenging properties; however, the H2O and CH2Cl2-soluble extracts were the most potent extracts in the beta-carotene-linoleic acid bleaching inhibition assay. In terms of iron(II) chelation--an important antioxidant property--the PE, MeOH and H2O extracts demonstrated moderate iron(II) chelating activity.

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 availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

19476001

Citation

Dorman, H J Damien, et al. "Phenolic Profile and Antioxidant Evaluation of Mentha X Piperita L. (peppermint) Extracts." Natural Product Communications, vol. 4, no. 4, 2009, pp. 535-42.
Dorman HJ, Koşar M, Başer KH, et al. Phenolic profile and antioxidant evaluation of Mentha x piperita L. (peppermint) extracts. Nat Prod Commun. 2009;4(4):535-42.
Dorman, H. J., Koşar, M., Başer, K. H., & Hiltunen, R. (2009). Phenolic profile and antioxidant evaluation of Mentha x piperita L. (peppermint) extracts. Natural Product Communications, 4(4), 535-42.
Dorman HJ, et al. Phenolic Profile and Antioxidant Evaluation of Mentha X Piperita L. (peppermint) Extracts. Nat Prod Commun. 2009;4(4):535-42. PubMed PMID: 19476001.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Phenolic profile and antioxidant evaluation of Mentha x piperita L. (peppermint) extracts. AU - Dorman,H J Damien, AU - Koşar,Müberra, AU - Başer,K Hüsnü C, AU - Hiltunen,Raimo, PY - 2009/5/30/entrez PY - 2009/5/30/pubmed PY - 2009/7/21/medline SP - 535 EP - 42 JF - Natural product communications JO - Nat Prod Commun VL - 4 IS - 4 N2 - Seven extracts were prepared from Mentha x piperita (peppermint) leaves in sequence using a Soxhlet apparatus, viz. (40-60 degrees) light petroleum (PE), dichloromethane (CH2Cl2), acetonitrile (ACN), ethyl acetate (EtOAc), methanol (MeOH), n-butanol and water (H2O) extracts. The phenolic and flavonoid content of each extract were estimated using spectrophotometric methods whilst a qualitative-quantitative analysis was made by reverse-phase high performance liquid chromatography coupled with photodiode array detection (HPLC-PDA). Each extract was assessed in a battery of six antioxidant-related assays so as to determine their iron(III) reductive, iron(II) chelating and free radical scavenging abilities. The MeOH-soluble extract contained the greatest content of total phenols and flavonoids based upon the Folin-Ciocalteu and 2-aminoethyl diphenylborate reagent data and HPLC-PDA analysis. Based upon the chromatographic and UV-spectral data, the leaves principally contained the cinnamic acid caffeic acid, the depside rosmarinic acid and flavonoids (flavones and flavanones). Eriocitrin (383.3 +/- 2.2 mg/g extract) and rosmarinic acid (381.2 +/- 1.9 mg/g extract) were the most abundant components identified within the leaves, whilst naringenin-7-O-glucoside (0.8 +/- 0.01 mg/g extract) was the least abundant component identified being found only in the EtOAc-soluble extract. The EtOAc, ACN and H2O-soluble extracts demonstrated the most potent iron(III) reductive and 1,1'-diphenyl-2-picrylhydrayl, 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonate) and hydroxyl free radical scavenging properties; however, the H2O and CH2Cl2-soluble extracts were the most potent extracts in the beta-carotene-linoleic acid bleaching inhibition assay. In terms of iron(II) chelation--an important antioxidant property--the PE, MeOH and H2O extracts demonstrated moderate iron(II) chelating activity. SN - 1934-578X UR - https://www.unboundmedicine.com/medline/citation/19476001/Phenolic_profile_and_antioxidant_evaluation_of_Mentha_x_piperita_L___peppermint__extracts_ L2 - https://medlineplus.gov/antioxidants.html DB - PRIME DP - Unbound Medicine ER -