The biological activities of 20 nature identical essential oil constituents

被引:139
作者
van Zyl, Robyn L.
Seatlholo, Sammy T.
van Vuuren, Sandy F.
Viljoen, Alvaro M.
机构
[1] Univ Witwatersrand, Fac Hlth Sci, Dept Pharm & Pharmacol, ZA-2193 Parktown, South Africa
[2] Tshwane Univ Technol, Sch Pharm, ZA-0001 Pretoria, South Africa
关键词
nature identical essential oil constituent; (-)-alpha-bisabolol; geraniol; (+/-)-linalool; (E- & Z-)-(+/-)-nerolidol; (-)-citronellal; trans-geranyl acetate; linalyl acetate; (+/-)-alpha plus beta-thujone; (+)-carvone; (-)-fenchone; (-)-menthone; (-)-pulegone; carvacrol; eugenol; (+)-alpha-pinene; (+)-beta-pinene; gamma-terpinene; p-cymene; 1,8-cineole; (+)-linionerie; antimicrobial activity; antinialarial activity; antioxidant activity; toxicity;
D O I
10.1080/10412905.2006.12067134
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Twenty nature identical essential oil constituents from seven structural groups were tested for antimalarial, antimicrobial, antioxidant and toxicity properties. The compounds displayed antimalarial activity (IC50 values ranging from 0.9 to 1528.8 mu M) with varying toxicity (IC50 values ranging from 5.5 to 1358.4 mu M). The data indicates that (-)-pulegone, (E- & Z-)-(+/-)-nerolidol, linalyl acetate and (+)-alpha-pinene have the most potent antimalaial activity. Carvacrol (MIC values ranging from <1.66 to 13.3 mM) followed by geraniol (MIC values: 19.5-51.9 mM) displayed the broadest spectrum of antimicrobial activity. The least toxic of the tested compounds, eugenol, was the only compound with antioxidant activity comparable to ascorbic acid. The results demonstrate that the 20 compounds individually display variable biological activity, although further research is required to determine how they may interact when combined.
引用
收藏
页码:129 / 133
页数:5
相关论文
共 34 条
[1]   Essential oils: their antibacterial properties and potential applications in foods - a review [J].
Burt, S .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2004, 94 (03) :223-253
[2]   Composition and antimalarial activity in vitro of the essential oil of Tetradenia riparia [J].
Campbell, WE ;
Gammon, DW ;
Smith, P ;
Abrahams, M ;
Purves, TD .
PLANTA MEDICA, 1997, 63 (03) :270-272
[3]   ANTIMICROBIAL ACTIVITY OF THE MAJOR COMPONENTS OF THE ESSENTIAL OIL OF MELALEUCA-ALTERNIFOLIA [J].
CARSON, CF ;
RILEY, TV .
JOURNAL OF APPLIED BACTERIOLOGY, 1995, 78 (03) :264-269
[4]   Radical-scavenging activities of citrus essential oils and their components: Detection using 1,1-diphenyl-2-picrylhydrazyl [J].
Choi, HS ;
Song, HS ;
Ukeda, H ;
Sawamura, M .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (09) :4156-4161
[5]   Essential oils from Piper cernuum and Piper regnellii:: Antimicrobial activities and analysis by GC/MS and 13C-NMR [J].
Costantin, MB ;
Sartorelli, P ;
Limberger, R ;
Henriques, AT ;
Steppe, M ;
Ferreira, MJP ;
Ohara, MT ;
Emerenciano, VP ;
Kato, MJ .
PLANTA MEDICA, 2001, 67 (08) :771-773
[6]  
de Macedo CS, 2002, FEMS MICROBIOL LETT, V207, P13, DOI 10.1111/j.1574-6968.2002.tb11021.x
[7]   QUANTITATIVE ASSESSMENT OF ANTI-MALARIAL ACTIVITY INVITRO BY A SEMIAUTOMATED MICRODILUTION TECHNIQUE [J].
DESJARDINS, RE ;
CANFIELD, CJ ;
HAYNES, JD ;
CHULAY, JD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1979, 16 (06) :710-718
[8]   A sensitive and quick microplate method to determine the minimal inhibitory concentration of plant extracts for bacteria [J].
Eloff, JN .
PLANTA MEDICA, 1998, 64 (08) :711-713
[9]   Terpenes arrest parasite development and inhibit biosynthesis of isoprenoids in Plasmodium falciparum [J].
Goulart, HR ;
Kimura, EA ;
Peres, VJ ;
Couto, AS ;
Duarte, FAA ;
Katzin, AM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (07) :2502-2509
[10]  
Griffin SG, 1999, FLAVOUR FRAG J, V14, P322, DOI [10.1002/(SICI)1099-1026(199909/10)14:5<322::AID-FFJ837>3.3.CO