High-performance liquid chromatographic analysis of Black Cohosh (Cimicifuga racemosa) constituents with in-line evaporative light scattering and photodiode array detection

被引:55
作者
Li, WK
Chen, SN
Fabricant, D
Angerhofer, CK
Fong, HHS
Farnsworth, NR
Fitzloff, JF
机构
[1] Univ Illinois, Coll Pharm, Program Collaborat Res Pharmaceut Sci, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Pharm, Dept Med Chem & Pharmacognosy, Chicago, IL 60612 USA
[3] Univ Illinois, Coll Pharm, Funct Food Hlth Core Analyt Lab, Chicago, IL 60612 USA
[4] Univ Illinois, Coll Pharm, NIH, Ctr Bot Dietary Supplements Res, Chicago, IL 60612 USA
[5] Toms Maine Corp, Lafayette Ctr, Kennebunk, ME 04043 USA
关键词
Black Cohosh; Cimicifuga racemosa; triterpene glycosides; phenolic acids; flavonoids; HPLC; PDA; ELSD;
D O I
10.1016/S0003-2670(02)00776-6
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A validated and reproducible high-performance liquid chromatography (HPLC) method with in-line evaporative light scattering and photodiode array detection was developed for the analysis of major constituents in Black Cohosh (Cimicifuga racemosa L.). The method is based on the baseline chromatographic separation of 18 compounds reported to be present in Black Cohosh on a C-18 column (5 mum, 4.6 mm, x 250 nun) with water (0.05% trifluoroacetic acid, TFA)-acetonitrile-water as the mobile phase, and their in-line detection using photodiode array detector (PDA) and evaporative light scattering detector (ELSD). Sixteen of these (caffeic acid, ferulic acid, isoferulic acid, cimicifugoside H-1, cimiracemoside A, cimicifugoside H-2, (26R)-actein, 26-deoxycimicifugoside, (26S)-actein, 23-epi-26-deoxyactein, 23-OAc-shengmanol-3-O-beta-D-xyloside, 26-deoxyactoin, 25-OAc-cimigenol-3-O-alpha-L-arabinoside, 25-OAc-cimigenol-3-O-beta-D-xyloside, cimigenol-3-O-alpha-L-arabinoside, cimigenol-3-O-beta-D-xyloside) were detected to be present and quantifiable. The reputed two flavonoid constituents (kaempferol and formononetin) were not detectable. The validation of the method included tests for sensitivity, linearity, reproducibility, recovery and stability. The detection limits were found to be in the range of 26-55 ng (10 mul per injection) in ELSD for the 16 constituents of Black Cohosh. The exponential linear calibration curves were observed for all the constituents tested with r(2) being >0.99. The reproducibility of the method was evaluated by analyzing three sets of controls on three consecutive days (n = 3) with R.S.D. (%) and relative error (%) <8.14 and 11.27%, respectively. The observed recovery rates were better than 91.75%. The stability of Black Cohosh methanolic sample solution was assessed by consecutively analyzing the methanolic solutions prepared from liquid extract (Sample A), powered extract (Sample B), milled plant material (Sample Q and one of the commercial product (Sample D I) for the content of 16 major constituents with the relative standard deviations (R.S.D., %) <6.39%, indicating the sample matrix of Black Cohosh is stable. Contrary to literature reports, kaempferol and formononetin were not detected in either our field collected plant materials or commercial products of Black Cohosh in the current assay. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:61 / 75
页数:15
相关论文
共 34 条
[1]  
Bedir E, 2000, CHEM PHARM BULL, V48, P425
[2]  
Bedir E, 2001, PHARMAZIE, V56, P268
[3]   RP-HPLC peptide mapping of proteins with an evaporative light scattering detector [J].
Bongers, J ;
Chen, TK .
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2000, 23 (06) :925-933
[4]   EVAPORATIVE LIGHT-SCATTERING AND THERMOSPRAY MASS-SPECTROMETRY - 2 ALTERNATIVE METHODS FOR DETECTION AND QUANTITATIVE LIQUID-CHROMATOGRAPHIC DETERMINATION OF GINKGOLIDES AND BILOBALIDE IN GINKGO-BILOBA LEAF EXTRACTS AND PHYTOPHARMACEUTICALS [J].
CAMPONOVO, FF ;
WOLFENDER, JL ;
MAILLARD, MP ;
POTTERAT, O ;
HOSTETTMANN, K .
PHYTOCHEMICAL ANALYSIS, 1995, 6 (03) :141-148
[5]   Isolation, structure elucidation, and absolute configuration of 26-deoxyactein from Cimicifuga racemosa and clarification of nomenclature associated with 27-deoxyactein [J].
Chen, SN ;
Li, WK ;
Fabricant, DS ;
Santarsiero, BD ;
Mesecar, A ;
Fitzloff, JF ;
Fong, HHS ;
Farnsworth, NR .
JOURNAL OF NATURAL PRODUCTS, 2002, 65 (04) :601-605
[6]   Phylogeny of Actaea including Cimicifuga (Ranunculaceae) inferred from nrDNA ITS sequence variation [J].
Compton, JA ;
Culham, A ;
Gibbings, JG ;
Jury, SL .
BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 1998, 26 (02) :185-197
[7]   Reclassification of Actaea to include Cimicifuga and Souliea (Ranunculaceae): phylogeny inferred from morphology, nrDNA ITS, and cpDNA trnL-F sequence variation [J].
Compton, JA ;
Culham, A ;
Jury, SL .
TAXON, 1998, 47 (03) :593-634
[8]  
DUKE JA, 1985, CRC HDB MED HERBS, P677
[9]  
Foster S., 1999, HerbalGram, P35
[10]   Separation of Cimicifuga racemosa triterpene glycosides by reversed phase high performance liquid chromatography and evaporative light scattering detection [J].
Ganzera, M ;
Bedir, E ;
Khan, IA .
CHROMATOGRAPHIA, 2000, 52 (5-6) :301-304