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Tiêu đề Chromatographic Fingerprint Analysis of Herbal Medicines: Thin-layer and High Performance Liquid Chromatography of Chinese Drugs
Tác giả Hildebert Wagner, Rudolf Bauer, Dieter Melchart, Pei-Gen Xiao, Anton Staudinger
Trường học Ludwig-Maximilians-University
Chuyên ngành Pharmacy
Thể loại Book
Năm xuất bản 2009
Thành phố Munich
Định dạng
Số trang 466
Dung lượng 9,26 MB

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Nội dung

Chromatographic fingerprint analysis of herbal medicines: Thin-layer and high performance liquid chromatography of Chinese drugs is a reference work for the analysis/identification of herbal drugs since it gives the extraction conditions and the specific chromatographic procedures to be used. This volume 1 is divided into 2 parts, please refer to part 1!

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Chromatographic Fingerprint Analysis of Herbal Medicines

Thin-layer and High Performance Liquid Chromatography of Chinese Drugs

Second, Revised and Enlarged Edition

Vol 1

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Center of Pharma Research

Univ.-Prof Dr med Dieter Melchart

Compentence Centre for Complementary Medicine and Naturopathy

Technical University Munich

Germany, Munich

Prof Pei-Gen Xiao

The Editorial Offi ce of Chinese Herbal Medicine, Beijing

Institute of Medicinal Plant Development

Chinese Academy of Medical Sciences

Beijing, China

Dipl.Kfm Anton Staudinger

Visiting Professor at Beijing University of Chinese Medicine

Executive Council Member of WFCMS

TCM hospital Bad Kötzting, First German hospital of Traditional Chinese Medicine

Hospital for Psychosomatically and Psychotherapeutically

General Manager Bad Kötzting, Germany

Printed with fi nancial support of TCM-Klinik Bad Kötzting, Germany

“Chinese Drug Monographs and Analysis” originally published by Verlag für Ganzheitliche Medizin, Dr Erich Wühr GmbH, © 2004

This work is subject to copyright.

All rights are reserved, whether the whole or part of the material is concerned, specifi cally those of translation, reprinting, re-use of tions, broadcasting, reproduction by photocopying machines or similar means, and storage in data banks.

illustra-Product Liability: The publisher can give no guarantee for all the information contained in this book This does also refer to information about drug dosage and application thereof In every individual case the respective user must check its accuracy by consulting other phar- maceutical literature.

The use of registered names, trademarks, etc in this publication does not imply, even in the absence of a specifi c statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use.

© 2011 Springer-Verlag/Wien

SpringerWienNewYork is part of Springer Science+Business Media

springer.at

Photocredits:

© Cover illustration and all fi gures with courtesy of the editors and authors

Coverdesign: WMXDesign GmbH, Heidelberg, Germany

Typesetting: Thomson Press (India) Ltd., Chennai, India

Printed on acid-free and chlorine-free bleached paper

SPIN: 80025669

With 376 (partly coloured) fi gures

Library of Congress Control Number 2011926593

ISBN 978-3-7091-0762-1 SpringerWienNewYork

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On the occasion of the twentieth anniversary of the establishment of the ¿ rst hospital of

Traditional Chinese Medicine (TCM) in Germany, the editors are pleased to present a new analytical manual for the quality proof of Chinese herbal drugs that meets the high standards of the European Drug Regulatory Authority

The chromatographic TLC-, HPLC- and GC-¿ ngerprint analytical technique described in the monographs has never been used in any Pharmacopoeia, although it is the most comprehensive, non-sophisticated chromatographic method for a science-based identity and stability proof of Chinese Herbal Drugs and includes the detection of possible falsi¿ cations or adulterations This

¿ ngerprint analysis enables, for the ¿ rst time, the detection of the complex entities of all main low-molecular constituents of a plant drug with the advantage that the single constituents can be made visible in coloured TLC photographs and HPLC-peak pro¿ les Using online recordable UV-spectra with the Diode Array technique, it is also possible to gain information about the chemical structure of single constituents

Each new monograph also contains a description of the macroscopic descriptions, an updated list

of all the main bioactive constituents of a drug identi¿ ed to date, and the pharmacological and biological activities of the single herbal drugs and their therapeutic application A comprehensive reference list informs the reader about new analytical topics and trends

The eighty individual herbal drug monographs were ¿ rst published by Dr Wühr Publishers,Bad Kötzting and are now offered in an updated and corrected form in this new, two-volume manual published by Springer Publishing Company A third volume containing further 40 herbal drug monographs will be completed by the end of 2012

Scienti¿ c experts from theUniversities of Munich (Germany) and Graz (Austria), along with around 25 scienti¿ c co-workers and technicians, contributed to this comprehensive work All participants in the project are most grateful to the owner of the TCM-hospital Bad Kötzting who has supported the projectfrom its very beginning In the later phases of the project, wealso received ¿ nancial support from the AiF-program of the German Ministry of Economics in Berlin (Germany)

The editors: H Wagner, R Bauer, D Melchart, Xiao Pei-Gen, A Staudinger

April 2011

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Vol I: Monographs No 1 – 40

Vol II: Monographs No 41 – 80

Table of Contents Vol I

Contents alphabetically (lat names) xi

Contents alphabetically (chin names) xv

Acknowledgements xix

Introduction xxi

Practical work guidelines xxv

TCM-Analytical Monographs Vol I 1 Bupleuri, Radix 1

2 Frittilariae, Bulbus 13

3 Rehmanniae, Radix 23

4 Schisandrae, Fructus 37

5 Asari, Radix et Rhizoma 45

6 Houttuyniae cordatae, Herba 59

7 Pinelliae, Rhizoma 71

8 Astragali, Radix 83

9 Angelicae pubescentis, Radix 99

10 Atractylodis macrocephalae, Rhizoma 113

11 Belamcandae sinensis, Rhizoma 127

12 Lycopi lucidi, Herba 141

13 Notopterygii, Rhizoma seu Radix 151

14 Angelicae sinensis, Radix 161

15 Angelicae dahuricae, Radix 171

16 Ligustici chuanxiong, Radix 181

17 Zanthoxyli, Pericarpium 191

18 Magnoliae offi cinalis, Cortex 203

19 Drynariae, Rhizoma 211

20 Puerariae, Radix 221

21 Codonopsis pilosulae, Radix 233

22 Gardeniae, Fructus 245

23 Gastrodiae, Rhizoma 255

24 Ecliptae, Herba 263

25 Andrographis, Herba 273

26 Paeoniae albae/rubrae, Radix 281

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27 Sophorae, Flos 291

28 Coptidis, Rhizoma 301

29 Stephaniae tetrandrae, Radix 311

30 Ziziphi spinosae, Semen 325

31 Amomi rotundus, Fructus 335

32 Uncariae cum Uncis, Ramulus 343

33 Clematidis, Radix 355

34 Sinomenii, Caulis 369

35 Forsythiae, Fructus 381

36 Evodiae, Fructus 391

37 Anemarrhenae, Rhizoma 403

38 Acanthopanacis senticosi, Radix 415

39 Scrophulariae, Radix 427

40 Polygoni multifl ori, Radix 439

Appendix: Basic Solvent Systems, reagents and columns for the TLC-, GC- and HPLC-fi ngerprint Analysis of main structure types of natural products 451

Index 457

Drug monograph, Marker compounds, Chemical classifi cation, Processing 461

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Vol I: Monographs No 1 – 40

Vol II: Monographs No 41 – 80

TCM-Analytical Monographs Vol II

41 Alismatis, Rhizoma 467

42 Carthami, Flos 475

43 Epimedii, Herba 485

44 Cnidii, Fructus 499

45 Lycii radicis, Cortex 509

46 Lycii, Fructus 521

47 Mori radicis, Cortex 535

48 Mori, Folium 549

49 Cimicifugae, Rhizoma 559

50 Phellodendri amurensis, Cortex Phellodendri chinensis, Cortex 573

51 Lonicerae, Flos Lonicerae japonicae, Flos Lonicerae japonicae, Caulis 587

52 Curcumae, Radix Curcumae longae, Rhizoma Curcumae, Rhizoma 601

53 Dioscoreae oppositae, Rhizoma Dioscoreae hypoglaucae, Rhizoma Dioscoreae nipponicae, Rhizoma Dioscoreae septemlobae, Rhizoma 615

54 Ganoderma 633

55 Citri reticulatea, Pericarpium Citri reticulatea viride, Pericarpium 647

56 Corydalis, Rhizoma 665

57 Dipsaci, Radix 677

58 Atractylodis lanceae, Radix 691

59 Leonuri, Herba 707

60 Magnoliae, Flos 719

61 Piperis longi, Fructus 729

62 Sophorae fl avescentis, Radix 743

63 Scutellariae, Radix 755

64 Chaenomelis, Fructus 767

65 Acori calami, Rhizoma Acori tatarinowii, Rhizoma 777

66 Isatidis, Radix 791

67 Tribuli, Fructus 805

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68 Ophiopogonis, Radix 819

69 Eucommiae, Cortex 831

70 Notoginseng, Radix et Rhizoma 843

71 Rhei, Radix et Rhizoma 857

72 Ginseng, Radix et Rhizoma Panacis Quinquefolii, Radix 875

73 Siegesbeckiae, Herba 893

74 Salviae miltiorrhizae, Radix et Rhizoma 903

75 Poria 923

76 Cassiae, Semen 935

77 Camelliae, Folium 951

78 Artemisiae Scopariae, Herba 967

79 Aconiti lateralis praeparata, Radix 977

Aconiti kusnezoffi i praeparata, Radix 80 Cinnamomi, Cortex 991

Appendix: Basic Solvent Systems, reagents and columns for the TLC-, GC- and HPLC-fi ngerprint Analysis of main structure types of natural products 1009

Index 1015

Drug monograph, Marker compounds, Chemical classifi cation, Processing 1019

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Ɣ The editors wish to express their deep gratitude to the TCM-Hospital Bad Kötzting

A Staudinger and the Federal Ministry for Economics and Technology (AiF) Berlin, Germany for ¿ nancial support as well as to CEO Biol Chem H Rausch, Phytochem Reference substances, Ichenhausen/Neu Ulm, Prof A Vollmar, LMU Munich, Department

of Pharmacy, and Prof F Bracher, LMU Munich for their cooperation in the development

of the Chinese Herbal Monographs We also thank Prof Dai Jingzhang TCM-Hospital Bad Kötzting/Beijing, University of Chinese Medicine and Dr C-H Hempen, Center of Chinese Medicine Munich for their valuable explanation of the standard therapy using Chinese drugs

Ɣ We are deeply indebted our many scienti¿ c coworkers and colleagues at the University

of Munich (Germany) and the University of Graz (Austria), as well as to the Technical Assistants of the Department of Pharmacy, Munich named following:

Department of Pharmacy Munich, Scienti¿ c Assistants: Bauer Michael, Fischer

Mathilde, Liu Yong, Michler Hans, Müller-Jakic Barbara, Nenninger Anneli, Nörr

Heidrun, Offermann Franziska, Plößl Florian, Pröbstle Andrea, Wild Bernice, Zschocke

Sibylle Technical Assistants: Bächer Silvia, Grieblinger Elisabeth, Koch Stefanie,

Marotel Dana, Mayr Christine

Pharmacognosy University Graz: Adams Michael, Lehmann Reg, Liu Jianghua,

Reininger Eveline, Resch Marion Sylvia, Schühly Wolfgang Martin, Schwarte Anne, Seibt Anette, Stöhr Jochen

Ɣ The editors gratefully acknowledge the excellent cooperation with the Springer Publ

Comp and Mrs Dr Claudia Panuschka and Mrs Angelika Heller in particular

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Facts and Perspectives on Chinese Herbal Drugs

When we began our work on the new analytical monographs 15 years ago, we faced the challenge of how the quality proof should be performed in order to meet both the requirements of a science-based authenticity proof of the Chinese drugs and the high standards of the European Drug Regulatory Authority Based on the experience we had gained from our fi rst TLC-fi ngerprinting of herbal drugs (Wagner and Bladt 2001), we decided to use the chromatographic TLC and HPLC fi ngerprint analytical technique This method enables the researcher, for the fi rst time, to detect the complex entities of all main low molecular constituents of a plant drug, with the advantage that the single constituents can be made visible in coloured TLC photographs and in a quantifi able HPLC-peak

profi ling At the same time, for safety reasons, these new techniques can be used to exclude possible falsifi cations and adulterations of herbal drugs These criteria and advantages have also persuaded the Chinese scientifi c experts who advocated this analytical method as the best, presently available, non-sophisticated and feasible method for quality proof of herbal drugs (Liang et al 2010) The fi ngerprint technology for identifi cation of herbal drugs

is also the favored method in the framework of the international ISO-Standardisation*

of the “Quality and Safety of TCM” If the barcode DNA-analysis of all frequently used Chinese drugs becomes available in the near future, we can supplement and correlate the chromatographic analyses with those of the DNA-fi ngerprint analyses and thereby optimize the quality proof of the drugs in general (Heubl 2010)

Ɣ Authenticity of TCM-drugs not defi nitely assessed

Many TCM herbal drugs are not yet produced under controlled cultivations, but originate from wild collections Even if the drugs are derived from cultivations, it must be taken into account that they can originate from quite varied climate zones and that they may

be harvested under altered conditions Therefore, in the past, the botanical authenticity and homogeneity within a defi ned plant species could not be guaranteed We have thus investigated as many herbal drug samples of one plant species as we were able to acquire from different districts and markets in China, along with reference drugs from German herbal drug fi rms (Wagner et al 2011)

Ɣ Uncertain botanical nomenclature

The non-uniform nomenclature for the same plant in various regions of China is

a signifi cant problem This uncertainty can cause impermissible substitutions or

falsifi cations, as occurred 15 years ago when the root of Stephania tetrandra (Hanfangji) was mistaken for the root of Aristolochia fangji (Guanfangji) and administered to women

*Resolution 18 of the 2nd plenary meeting of ISO/TC 249 held in The Haque, Netherlands on May 2-4th 2011 [Establishment of the working group “Quality and Safety of TCM products” under german convenorship] www.iso.org and www.din.de

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as tea medication that produced severe nephrotoxic side effects The Aristolochia herbal

drug contains the carcinogenic aristolochic acid After the detection of this falsifi cation, the drug was banned from the Chinese Pharmacopoeia in 2002 Meanwhile, special

TLC- and HPLC-fi ngerprint methods were developed which allow the detection of even micrograms of these acids in an herbal drug or drug mixtures: see Radix Stephaniae

p 311 Mo No 29, Radix Clematidis p 355 Mo No 33 and Caulis Sinomenii p 369 Mo

No 34 A similar example is the Chinese tetraploid Acorus calamus/tatarinowii drug, Mo

No 65 p 777, which differs in its very high content of carcinogenic ß-asarone from the

diploid Acorus calamus drug known offi cially in most western countries.

Ɣ Great variability of plant species

A further diffi culty in the identifi cation of TCM-drugs is the fact that, in many Chinese monographs, more than 2 species or subspecies (sometimes up to 9 species) are listed and are often labelled as synonyms, subspecies or subvarieties For example in Fritillariae bulbus Mo No 2 p 13, nine species are listed, and the monographs for Epimedii herba-

Mo No 43 p 485, Dioscoreae rhizoma Mo No 53 p 615 and Uncariae ramulus c uncis Mo No 32 p 343 list fi ve species each without any evidence that the chemical composition of the various “species” are qualitatively and/or quantitatively equivalent and can be substituted for one another As a result of our fi ngerprinting investigations,

we could show that in many cases considerable differences were detectable between the single species and the main offi cial herbal drug Correspondingly it may be suggested that a great number of these “subspecies” do not possess pharmacological and therapeutic equivalence

Ɣ Conclusion: What have we learned from the authenticity proof of Chinese herbal drugs?

In addition to a continuation of further pharmacological and molecular-biological

investigations, we must immediately initiate comprehensive bar-code DNA-fi ngerprint analyses of the most frequently used offi cial Chinese plant drugs The fi rst priority should

be given to those Chinese plants within taxa that are frequently substituted or adulterated with other species and could be nearly indistinguishable morphologically or chemically (see herbal drugs of the Apiaceae familiy Mo No 9, 14, 15, 16, 44)

Ɣ Processing of TCM-drugs

Apart from the simple cutting and cleaning of the raw drugs, the Chinese Pharmacopoeia describes many other types of pre-treatment or processing unknown to western

Pharmacopoeias In the Chinese Pharmacopoeia 2005 (People’s Republic of China,

English Edition Vol I Appendix II A – 24) the processing is to be defi ned “to fulfi l the requirements of drugs”, whatever that may mean for each single drug In one recent publication, the purpose of processing is explained as “to alter the appearance, the physical characteristics and chemical constituents of a herbal drug” (see Zhao Z et al 2010) In none of the monographs, however those crude drugs containing toxic constituents, the necessity of the various processing is rationalized and clearly substantiated According to the Chinese Pharmacopoeia, processing can be achieved primarily through the following methods: roasting and broiling, scalding, calcining, carbonizing, steaming, boiling,

stewing, processing with wine, vinegar, or salt water, and different kinds of stir baking Some chemicals or herbal drugs may also be used for the processing

In the Monograph No 79 p 977, we describe a TLC- and HPLC-fi ngerprint analysis of

two unprocessed (non-pretreated) and processed Aconitum spp., Aconitum carmichaeli

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and “Baifupian” instructions of the Chinese Pharmacopoeia, with salted water and Radix Glycyrrhizae, black beans and water or after scalding by heating at high temperature with sand (clamshell or talc) The TLC- and HPLC-fi ngerprint analyses showed that in the processed roots, the alkaloids Aconitine and Mesaconitine were degraded to a great extent and detectable only in a very small amount as compared with the content of these alkaloids

in the raw unprocessed roots Another herbal drug which requires processing is Rhizoma Pinelliae (Mo No 7 p 71) which is not permitted to be prescribed in unprocessed form for oral therapy

Conclusion: Modern analytical techniques using the HPLC-quantitation should replace the classical methods of processing described in the Chinese Pharmacopoeia Recent publications demand a safe limit to be stipulated for the Aconitine content in processed

Aconitum drugs (Singhuber et al 2009).

Ɣ Endo (Phyto) Fungi in Chinese Herbs

During the development of the new monographs, we discovered a conspicuous occurrence

of very lipophilic acetylenic compounds of the Falcarin(di)ol type in the roots of three

Angelica spp (Mo No 9, 14 and 15 p 99, 161 and 171), in the root of Ligusticum

chuanxiong (Mo No 16 p 181) and in three Panax spp (Mo No 70, 72 p 843,

875) Initially, we considered them to be constituents biosynthesized from the plants Meanwhile, however, several publications appeared in which the original production of these compounds from endo(phyto)fungi in Chinese plants could be assessed (Strobel and Daisy 2003; Li et al 2007) The most famous example of the production of a long-

known terpene alkaloid by an endo(phyto) fungus is the Taxus brevifolia tree, the bark

of which contains the symbiotic living fungus Taxomyces andreanae This fungus is able to biosynthesize the same terpene alkaloid, paclitaxel, as the Taxus tree (Stierle et

al 1993) Which organism, the fungus or the plant, fi rst produced paclitaxel and was the gene supplier for the other organism is not known The acetylene compounds falcarinols possess antibiotic and antitumoral activity They are very lipophilic and can be easily detected because of their very characteristic UV-spectra Therefore they are of interest for the “identity proof” of a plant and it can also be suggested that they contribute to the pharmacological and therapeutic effect of some Chinese plants containing these

compounds It can be expected that in the future, additional metabolites produced by phytofungi will be detected There is no doubt that this surprising new knowledge will initiate a promising new area of research

References

Chinese Pharmacopoeia of the People’s Republic of China, English Edition 2005 Vol I

Appendix II A – 24.

Heubl G (2010): New Aspects of DNA-based Authentication of Chinese Medicinal Plants by

Molecular Biological Techniques, Planta Med 76: 1963-1974.

Liang Y-Z, Xie P, Chan R (2010): Perspective of Chemical Fingerprinting of Chinese Herbs,

Planta Med 76: 1997-2003.

Li WC, Zhou J, Guo SY, Guo LD (2007): Endophytic fungi associated with lichens in

Baihua mountain of Beijing, China Fungal Divers 25: 95-106.

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Singhuber I, Zhu M, Painz S, Kopp B (2009): Aconitum in Traditional Chinese Medicine:

a valuable drug or an unpredictable risk? J Ethnopharmacol 126: 18-30.

Stierle A, Strobel G, Stierle D (1993): Taxol and taxane production by Taxomyces andreanae

an endophytic fungus of Pacifi c yew, Science 5105: 214-216.

Strobel G, Daisy B (2009): Bioprospecting for microbial Endophytes and their natural products, Microbiology and Molecular Biology Reviews 5: 535-544.

Wagner H, Bladt S (2001): Plant Drug Analysis 2nd ed Springer, Berlin, Heidelberg,

New York.

Wagner H, Bauer R, Melchart D, Pei-Gen X, Staudinger A (eds) (2011): Chromatographic Fingerprint Analysis of Herbal Medicines Thin-layer and High Performance Liquid

Chromatography of Chinese Drugs Vol I + II, Springer-Verlag, Vienna.

Zhao Z, Liang Z, Chan K, Lu G, Lee GLM, Chen H, Li L (2010): A Unique Issue in the Standardization of Chinese Materia Medica: Processing, Planta Med 76: 1975-1986.

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Source of the herbal drugs

As described above, the herbal drugs must originate from clearly identi¿ ed botanical species Additionally, it must be taken into consideration that differences in cultivations, climatic

conditions, time of harvest, drying and storing conditions can cause slight chromatographic deviations which cannot be avoided and are normal Therefore it is worthwhile to investigate as many herbal drug samples of one species as possible from different geographic and ecological areas

Extraction conditions

The chosen extraction procedures should be rapid, but ef¿ cient according to present scienti¿ c knowledge and should include of the total entity of the low molecular constituents of a herbal drug This can be achieved in most cases using alcohol (MeOH or EtOH) Additional ¿ ngerprints can be obtained by extraction using petroleum ether/hexane or chloroform (for lipophilic

compounds) or water/water-acetone mixtures (for tannins, high polymeric procyanidines, and amino acids) as solvents Polysaccharides and proteins can be characterized using their sugar- or amino acid-¿ ngerprints after enrichment and acidic or enzymatic hydrolysis

Chromatographic conditions

Plates/columns:

For the chromatography

plates, in some speci¿ c cases also aluminum oxide- or cellulose coated plates (Merck) are used HPTLC-plates are precoated with Silica Gel of an average particle size and a narrow size distribution of 5 —m as opposed to TLC material of 15 —m average particle size and a broader size distribution

• GC-analysis is shown e.g for Monograph No 65 Rhizoma Acori Apparatus: Varian

GC 3800, Varian Saturn 2200 (El/Cl, msn) ion trap-mass spectrometer, Autosampler: CTC CombiPal, Separation column: Varian VF-5ms with 10 m precolumn (deactivated methyl-polysiloxan), Carrier gas: Helium

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can be purchased from special ¿ rms In Germany the ¿ rm Phytolab in Vestenbergsgreuth

(www.phytolab.com) offers many reference compounds which are listed as “marker compounds”

in the Chinese Pharmacopoeia

Reproducibility of the ¿ ngerprint analysis

If the same technical conditions described are used, it can be expected that even with the use

of instruments from other ¿ rms, very similar TLC- and HPLC-¿ ngerprints can be obtained

If, however, for any reason, the grade of separation and/or the Rf- and Rt-values deviate from

those stipulated in the Monographs, the sequence and the overall TLC-zone- and HPLC-peak pro¿ les must still be in agreement with those documented in our Monographs

Photography

The TL-chromatograms were developed by a Canon PowerShot G2 digital camera in a CAMAG Reprostar 3 cabinet using WinCats software (www.camag.com)

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Chromatographic Fingerprint Analysis of Herbal Medicines

Thin-layer and High Performance Liquid Chromatography of Chinese Drugs

Second, Revised and Enlarged Edition

Vol 2

Trang 30

© Cover illustration and all fi gures with courtesy of the editors and authors

Coverdesign: WMXDesign GmbH, Heidelberg, Germany

Typesetting: Thomson Press (India) Ltd., Chennai, India

Printed on acid-free and chlorine-free bleached paper

SPIN: 80025669

With 376 (partly coloured) fi gures

Library of Congress Control Number 2011926593

Univ.-Prof Dr med Dieter Melchart

Compentence Centre for Complementary Medicine and Naturopathy

Technical University Munich

Germany, Munich

Prof Pei-Gen Xiao

The Editorial Offi ce of Chinese Herbal Medicine, Beijing

Institute of Medicinal Plant Development

Chinese Academy of Medical Sciences

Beijing, China

Dipl.Kfm Anton Staudinger

Visiting Professor at Beijing University of Chinese Medicine

Executive Council Member of WFCMS

TCM hospital Bad Kötzting, First German hospital of Traditional Chinese Medicine

Hospital for Psychosomatically and Psychotherapeutically

General Manager Bad Kötzting, Germany

Printed with fi nancial support of TCM-Klinik Bad Kötzting, Germany

“Chinese Drug Monographs and Analysis” originally published by Verlag für Ganzheitliche Medizin, Dr Erich Wühr GmbH, © 2004

This work is subject to copyright.

All rights are reserved, whether the whole or part of the material is concerned, specifi cally those of translation, reprinting, re-use of tions, broadcasting, reproduction by photocopying machines or similar means, and storage in data banks.

illustra-Product Liability: The publisher can give no guarantee for all the information contained in this book This does also refer to information about drug dosage and application thereof In every individual case the respective user must check its accuracy by consulting other phar- maceutical literature.

The use of registered names, trademarks, etc in this publication does not imply, even in the absence of a specifi c statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use.

© 2011 Springer-Verlag/Wien

SpringerWienNewYork is part of Springer Science+Business Media

springer.at

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Table of Contents Vol II

Vol I: Monographs No 1 – 40

Vol II: Monographs No 41 – 80

TCM-Analytical Monographs Vol II

50 Phellodendri amurensis, Cortex

Phellodendri chinensis, Cortex 573

51 Lonicerae, Flos

Lonicerae japonicae, Flos

Lonicerae japonicae, Caulis 587

Curcumae, Rhizoma 601

53 Dioscoreae oppositae, Rhizoma

Dioscoreae hypoglaucae, Rhizoma

Dioscoreae nipponicae, Rhizoma

Dioscoreae septemlobae, Rhizoma 615

54 Ganoderma 633

55 Citri reticulatea, Pericarpium

Citri reticulatea viride, Pericarpium 647

61 Piperis longi, Fructus 729

62 Sophorae fl avescentis, Radix 743

63 Scutellariae, Radix 755

64 Chaenomelis, Fructus 767

65 Acori calami, Rhizoma

Acori tatarinowii, Rhizoma 777

66 Isatidis, Radix 791

67 Tribuli, Fructus 805

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69 Eucommiae, Cortex 831

70 Notoginseng, Radix et Rhizoma 843

71 Rhei, Radix et Rhizoma 857

72 Ginseng, Radix et Rhizoma

Panacis Quinquefolii, Radix 875

78 Artemisiae Scopariae, Herba 967

79 Aconiti lateralis praeparata, Radix 977 Aconiti kusnezoffi i praeparata, Radix

80 Cinnamomi, Cortex 991

Appendix:

Basic Solvent Systems, reagents and columns for the TLC-, GC- and HPLC-fi ngerprint

Analysis of main structure types of natural products 1009Index 1015Drug monograph, Marker compounds, Chemical classifi cation, Processing 1019

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lat name chapter volume page

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chin name Chapter volume page

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Pharmacopoeias: Pharmacopoeia of the People’s Republic of China

English Edition, 1992/2005(1)

Japanese Pharmacopoeia 1986 (Jap XI)

Of¿ cial drugs: In Chinese Pharmacopoeia: the roots of Bupleurum chinense DC (= B falcatum

auct Sin non L.) and Bupleurum scorzonerifolium Willd (= B falcatum var

scorzonerifolium (Willd.) Ledeb.) - Apiaceae - The drugs differ both in their

morphology and in their origin Beichaihu (B chinense) originates from northern China (north of the Yellow River), while Nanchaihu (B

scorzonerifolium) is indigenous to the southern provinces(1) The Japanese

Pharmacopoeia requires Bupleurum falcatum L (= B scorzonerifolium Willd var stenophyllum Nakai) or varieties of this species(3, 4)

Adulterations: B longiradiatum Turcz (toxic!)(1), occasionally contaminations with roots of

Aconitum spec.(3)

Description of the drugs:(1)

B chinense: frequently branched roots, 6-15 cm long, 3-8 cm in diameter, exter nally

blackish-brown or light brown, texture hard and tenacious, not easy to break

B scorzonerifolium: relatively thin roots, non or slightly branched, externally reddish-brown or

black-brown, texture slightly soft

Pretreatment of the raw drug:

Stalk-remnants are removed, the drug is washed and moistened, cut into thick slices and dried (Chaihu) The sliced drug is then soaked in vine gar and dried under mild heat (Cuchaihu)

Medicinal use: Often in combination with other drugs as antihepatotoxic, antipyretic, analgesic,

sedative, and antidepressive agents, in cases of menstrual complaints, uterine and anal prolaps, sudden loss of hearing and malaria(1, 4, 5)

H Wagner et al (eds.), Chromatographic Fingerprint Analysis of Herbal Medicines

© Springer-Verlag/Wien 2011

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