Isolation and quantitative analysis of phenolic antioxidants, free sugars, and polyols from mango (Mangifera indica L.) stem bark aqueous decoction used in Cuba as a nutritional supplement

被引:216
作者
Sellés, AJN
Castro, HTV
Agüero-Agüero, J
González-González, J
Naddeo, F
De Simone, F
Rastrelli, L
机构
[1] Univ Salerno, Dipartimento Sci Farmaceut, I-84084 Fisciano, SA, Italy
[2] Ctr Quim Farmaceut, Havana, Cuba
关键词
Mangifera indica L; nutritional supplement; phytomedicine; phenolic constituents; free sugars; polyols; antioxidant activity; 1D and 2D NMR; HPLC; GC-MS;
D O I
10.1021/jf011064b
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
An aqueous decoction of mango (Mangifera indica L.) stem bark has been developed in Cuba on an industrial scale to be used as a nutritional supplement, cosmetic, and phytomedicine. Previously we reported its antioxidant activity, and we concluded that the product could be useful to prevent the production of reactive oxygen species and oxidative tissue damage in vivo. A phytochemical investigation of mango stem bark extract has led to the isolation of seven phenolic constituents: gallic acid, 3,4-dihydroxy benzoic acid, gallic acid methyl ester, gallic acid propyl ester, mangiferin, (+)-catechin, (-)-epicatechin, and benzoic acid and benzoic acid propyl ester. All structures were elucidated by ES-MS and NMR spectroscopic methods. Quantitative analysis of the compounds has been performed by HPLC, and mangiferin was found to be the predominant component. Total polyphenols were assayed also by the Folin-Ciocalteu method. The free sugars and polyols content was also determined by GC-MS.
引用
收藏
页码:762 / 766
页数:5
相关论文
共 21 条
[1]   Catechin contents of foods commonly consumed in The Netherlands. 1. Fruits, vegetables, staple foods, and processed foods [J].
Arts, ICW ;
van de Putte, B ;
Hollman, PCH .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (05) :1746-1751
[2]   CONSTITUTION OF MANGIFERIN [J].
BHATIA, VK ;
RAMANATHAN, JD ;
SESHADRI, TR .
TETRAHEDRON, 1967, 23 (03) :1363-+
[3]   Plant-derived phenolic antioxidants [J].
Duthie, G ;
Crozier, A .
CURRENT OPINION IN LIPIDOLOGY, 2000, 11 (01) :43-47
[4]   C-13-NMR SPECTROSCOPY OF SUBSTITUTED XANTHONES .2. C-13 NMR SPECTRAL STUDY OF POLYHYDROXY XANTHONES [J].
FRAHM, AW ;
CHAUDHURI, RK .
TETRAHEDRON, 1979, 35 (17) :2035-2038
[5]   Antitumor, immunomodulatory and anti-HIV effect of mangiferin, a naturally occurring glucosylxanthone [J].
Guha, S ;
Ghosal, S ;
Chattopadhyay, U .
CHEMOTHERAPY, 1996, 42 (06) :443-451
[6]   OLIGOSACCHARIDE CONFORMATIONS - APPLICATION OF NMR AND ENERGY CALCULATIONS [J].
HOMANS, SW .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 1990, 22 :55-81
[7]   Examination of the inhibitory effect of norathyriol in formylmethionyl-leucyl-phenylalanine-induced respiratory burst in rat neutrophils [J].
Hsu, MF ;
Raung, SL ;
Tsao, LT ;
Lin, CN ;
Wang, JP .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 23 (07) :1035-1045
[8]  
Khan M.A., 1993, J SCI IND RES INDIA, V35, P276
[9]   Inhibition of xanthine oxidase and suppression of intracellular reactive oxygen species in HL-60 cells by theaflavin-3,3′-digallate, (-)-epigallocatechin-3-gallate, and propyl gallate [J].
Lin, JK ;
Chen, PC ;
Ho, CT ;
Lin-Shiau, SY .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (07) :2736-2743
[10]   INVERSE-DETECTED 2-DIMENSIONAL NMR METHODS - APPLICATIONS IN NATURAL-PRODUCTS CHEMISTRY [J].
MARTIN, GE ;
CROUCH, RC .
JOURNAL OF NATURAL PRODUCTS, 1991, 54 (01) :1-70