What the devil is in your phytomedicine? Exploring species substitution in Harpagophytum through chemometric modeling of 1H-NMR and UHPLC-MS datasets

被引:30
作者
Mncwangi, Nontobeko P. [1 ]
Viljoen, Alvaro M. [1 ,2 ]
Zhao, Jianping [3 ]
Vermaak, Ilze [1 ]
Chen, Wei [1 ]
Khan, Ikhlas [3 ,4 ]
机构
[1] Tshwane Univ Technol, Dept Pharmaceut Sci, ZA-0001 Pretoria, South Africa
[2] King Abdulaziz Univ, Dept Nat Prod & Alternat Med, Fac Pharm, Jeddah 21589, Saudi Arabia
[3] Univ Mississippi, Sch Pharm, Pharmaceut Sci Res Inst, Natl Ctr Nat Prod Res, University, MS 38677 USA
[4] Univ Mississippi, Sch Pharm, Dept Pharmacognosy, University, MS 38677 USA
基金
新加坡国家研究基金会;
关键词
Harpagophytum procumbens; Harpagophytum zeyheri; Pedaliaceae; Devil's Claw; Chemometrics; Nuclear magnetic resonance; Ultra-high performance liquid chromatography-mass spectrometry; Iridoid glycosides; Harpagoside; PLANT METABOLOMICS; PROCUMBENS; HARPAGOSIDE; CLAW; HPLC; IDENTIFICATION;
D O I
10.1016/j.phytochem.2014.06.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Harpagophytum procumbens (Pedaliaceae) and its close taxonomical ally Harpagophytum zeyheri, indigenous to southern Africa, are being harvested for exportation to Europe where phytomedicines are developed to treat inflammation-related disorders. The phytochemical variation within and between natural populations of H. procumbens (n = 241) and H. zeyheri (n = 107) was explored using proton nuclear magnetic resonance (H-1-NMR) and ultra-high performance liquid chromatography coupled to mass spectrometry (UHPLC-MS) in combination with multivariate data analysis methods. The UHPLC-MS results revealed significant variation in the harpagoside content: H. procumbens (0.17-4.37%); H. zeyheri (0.00-3.07%). Only 41% of the H. procumbens samples and 17% of the H. zeyheri samples met the pharmacopoeial specification of >= 1.2%. Both principal component analysis (PCA) and orthogonal projections to latent structures discriminant analysis (OPLS-DA) indicated separation based on species (UHPLC-MS data OPLS-DA model statistics: (RX)-X-2 = 0.258, (RY)-Y-2 (cum) = 0.957 and Q(2)(cum) = 0.934; H-1-NMR data OPLS-DA model statistics: (RX)-X-2 = 0.830, (RY)-Y-2 = 0.865 (cum) and Q(2)(cum) = 0.829). It was concluded that two species are not chemically equivalent and should not be used interchangeably. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 115
页数:12
相关论文
共 30 条
[1]  
[Anonymous], 2000, People's Plants: A Guide to Useful Plants of Southern Africa
[2]   Metabolomics and its potential in drug development [J].
Beyoglu, Diren ;
Idle, Jeffrey R. .
BIOCHEMICAL PHARMACOLOGY, 2013, 85 (01) :12-20
[3]  
BP, 2012, BRIT PHARM HERB DRUG
[4]  
Cole D., 2003, IMPACT CERTIFICATION
[5]  
CZYGAN FC, 1977, PLANTA MED, V31, P305, DOI 10.1055/s-0028-1097536
[6]   Inhibition of TNF-α synthesis in LPS-stimulated primary human monocytes by Harpagophytum extract SteiHap 69 [J].
Fiebich, BL ;
Heinrich, M ;
Hiller, KO ;
Kammerer, N .
PHYTOMEDICINE, 2001, 8 (01) :28-30
[7]   Harpagoside: from Kalahari Desert to pharmacy shelf [J].
Georgiev, Milen I. ;
Ivanovska, Nina ;
Alipieva, Kalina ;
Dimitrova, Petya ;
Verpoorte, Robert .
PHYTOCHEMISTRY, 2013, 92 :8-15
[8]   Metabolic differentiations and classification of Verbascum species by NMR-based metabolomics [J].
Georgiev, Milen I. ;
Ali, Kashif ;
Alipieva, Kalina ;
Verpoorte, Robert ;
Choi, Young Hae .
PHYTOCHEMISTRY, 2011, 72 (16) :2045-2051
[9]  
Gruenwald J., 2002, NAM NAT DEV CLAW C
[10]   Comparison between HPLC and HPTLC-densitometry for the determination of harpagoside from Harpagophytum procumbens CO2-extracts [J].
Günther, M ;
Schmidt, PC .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2005, 37 (04) :817-821