Enrichment of Biologically Active Compounds from Selected Plants

Enrichment of Biologically Active Compounds from Selected Plants

<p>TECHNISCHE UNIVERSITÄT MÜNCHEN </p><p>Lehrstuhl für Chemisch-Technische Analyse und Chemische Lebensmitteltechnologie </p><p><strong>Enrichment of Biologically Active Compounds from Selected </strong><br><strong>Plants Using Adsorptive Bubble Separation </strong></p><p>Leonor Thompson <br>Vollständiger Abdruck der von der Fakultät Wissenschaftszentrum Weihenstephan für <br>Ernährung, Landnutzung und Umwelt der Technische Universität München zur Erlangung des akademischen Grades&nbsp;eines </p><p>Doktors der Naturwissenschaften (Dr. rer. nat.) </p><p>genehmigten Dissertation. </p><p></p><ul style="display: flex;"><li style="flex:1">Vorsitzender: </li><li style="flex:1">Univ.-Prof. Dr. K. Sommer </li></ul><p>1. Univ.-Prof. Dr. H. Parlar 2. Univ.-Prof. Dr. K.-H. Engel <br>Prüfer der Dissertation: Die Dissertation wurde am 16.06.2004 bei der Technischen Universität München eingereicht und durch die Fakultät Wissenschaftszentrum Weihenstephan für Ernährung, Landnutzung und Umwelt am 22.09.2004 angenommen. </p><p><em>Dedicated to the memory of my late father, for instilling in me the desire to learn and the praise for the good values of Life </em></p><p><strong>Acknowledgements </strong></p><p>The research work presented in this PhD thesis was realised at the Chair for Chemical and Technical Analysis and Chemical Food Technology of the Technical University of Munich, in Freising, Weihenstephan. I would like to express my gratitude to: </p><p>Prof. Dr. Harun Parlar, the Head of the Chair and my supervisor, for providing me with an interesting topic for the thesis, for the freedom to implement my ideas and the availability of funds for the financing of three years of work. </p><p>Dr. Mehmet Coelhan, the head of my working group, for providing that the required means for the pursuance of my work were met, for the practical hints, particularly in relation with the HPLC and GC-MS analysis, as well as the interesting discussions regarding chemistry. </p><p>Ms. Florence Beaume, for the good atmosphere in the laboratory, the interesting discussions on chemistry and themes other than science, for a great companionship during the time of hard work and sporadic pleasant breaks. </p><p>Dr. Carsten Wattenbach, for the help given with the NMR analysis and the readiness for the innumerable and challenging discussions concerning chemistry. </p><p>Mr. Albrecht Friess, for the kind, untiring and timely help in the improvement of the linguistics and presentation aspects of this thesis, as well as for sorting out administrative details of the thesis. </p><p>Mr. Kurt Sholz, for the prompt production of special glass apparatus for the Foam Fractionation. </p><p>Ms. Johanna Strohmeier, for the good atmosphere in the laboratory and companionship. Ms. Bettina Zimmerman, for the help with the GC-ECNI/MS analysis. Ms. Mareike Wenning from the Microbial Ecology Group, Technical University of Munich, for the help with the FTIR analysis. </p><p>Prof. Dr. Matthias Hamburger, Friedrich-Schiller University, Jena, for the kind supply of the tryptanthrin standard. The Raps Institute in Freising, Weihenstephan, the Thuringian State Institute for Agriculture, Thuringia and the firma BAFA, Malsch, for the kind supply of plant raw materials. </p><p>I finally express my deepest gratitude to my wonderful family to whom I owe so much: My mother Mrs. Lucia Thompson, for the support, encouragement, caring and for being a source of strength during the difficult moments. My siblings, in particular Prof. Dr. Rachael Thompson, Prof. Dr. Gertrude Thompson and Dr. Ricardo Thompson, for the support, encouragement, and wise advice. </p><p>My husband Dr. Michael Lutze, for helping with the linguistic improvement of this thesis, for always standing by me both for the happy and difficult moments, for the understanding, encouragement and loving. My small daughter Michelle Thompson Lutze, for being such a lovely child, a source of inspiration and for her contagious joy. Contents </p><p>______________________________________________________________________________ </p><p><strong>Contents </strong></p><p><strong>1. INTRODUCTION------------------------------------------------------------------------------ 1 2. THEORETICAL BACKGROUND&nbsp;---------------------------------------------------- 5 2.1 Non-Foaming&nbsp;Adsorptive Bubble Separation and Foam Separation ------------------- 6 2.2 Foam&nbsp;Fractionation ------------------------------------------------------------------------------- 7 </strong><br><strong>2.2.1 Adsorption&nbsp;------------------------------------------------------------------------------------- 8 2.2.2 Foams&nbsp;------------------------------------------------------------------------------------------13 </strong><br><strong>2.2.2.2 Drainage&nbsp;and Thinning ---------------------------------------------------------------15 2.2.2.3 Gas&nbsp;Diffusion Coalescence and Bubble size---------------------------------------16 2.2.3.1 Foam&nbsp;Fractionation Devices ---------------------------------------------------------17 </strong><br><strong>2.2.4 Efficiency&nbsp;of Foam Fractionation --------------------------------------------------------20 2.2.5 Parameters&nbsp;Influencing the Efficiency of Foam Fractionation---------------------22 </strong><br><strong>2.2.5.1 Concentration&nbsp;of Solute and Surfactant-------------------------------------------22 2.2.5.2 Addition&nbsp;of Organic Solvents --------------------------------------------------------22 2.2.5.3 Addition&nbsp;of Electrolytes and Polyelectrolytes ------------------------------------23 2.2.5.4 Addition&nbsp;of Viscosity Enhancers ----------------------------------------------------23 2.2.5.5 pH&nbsp;of Solution---------------------------------------------------------------------------24 2.2.5.6 Ionic&nbsp;Strength---------------------------------------------------------------------------24 2.2.5.7 Gas&nbsp;Flow Rate --------------------------------------------------------------------------24 2.2.5.8 Height&nbsp;of Liquid Pool------------------------------------------------------------------25 2.2.5.9 Height&nbsp;of Foam Tower ----------------------------------------------------------------25 2.2.5.10 Internal&nbsp;Reflux Ratio ----------------------------------------------------------------25 </strong></p><p><strong>2.3 Plant&nbsp;Materials Under Investigation----------------------------------------------------------26 </strong><br><strong>2.3.1 Calendula Officinalis L. --------------------------------------------------------------------27 </strong><br><strong>2.3.1.1 General-----------------------------------------------------------------------------------27 2.3.1.2 Chemical&nbsp;Composition ----------------------------------------------------------------28 2.3.1.3 Active&nbsp;Principles------------------------------------------------------------------------29 2.3.1.4 Other&nbsp;Components---------------------------------------------------------------------33 2.3.1.5 Biological&nbsp;and Pharmacological Activity ------------------------------------------34 2.3.1.6 Toxicology&nbsp;-------------------------------------------------------------------------------34 </strong></p><p>Contents </p><p>______________________________________________________________________________ </p><p><strong>2.3.2 Camellia Sinensis L.-------------------------------------------------------------------------35 </strong><br><strong>2.3.2.1 General-----------------------------------------------------------------------------------35 2.3.2.2 Chemical&nbsp;Composition ----------------------------------------------------------------36 2.3.2.3 Active&nbsp;Principle-------------------------------------------------------------------------36 2.3.2.4 Other&nbsp;compounds ----------------------------------------------------------------------39 </strong><br><strong>2.3.3 Isatis Tinctoria L. ----------------------------------------------------------------------------44 </strong><br><strong>2.3.3.1 General-----------------------------------------------------------------------------------44 2.3.3.2 Chemical&nbsp;Composition ----------------------------------------------------------------45 2.3.3.3 Active&nbsp;Principle-------------------------------------------------------------------------45 2.3.3.5 Important&nbsp;Conversions of the Main Components -------------------------------46 2.3.3.6 Biological&nbsp;and Pharmacological Activity ------------------------------------------47 2.3.3.7 Toxicity-----------------------------------------------------------------------------------47 </strong><br><strong>2.3.4 Cannabis Sativa&nbsp;L. --------------------------------------------------------------------------48 </strong><br><strong>2.3.4.1 General-----------------------------------------------------------------------------------48 2.3.4.2 Chemical&nbsp;Composition ----------------------------------------------------------------49 2.3.4.3 Active&nbsp;Principle-------------------------------------------------------------------------50 2.3.4.4 Other&nbsp;components----------------------------------------------------------------------52 2.3.4.5 Important&nbsp;Reactions of Active Cannabinoids ------------------------------------52 2.3.4.6 Biological&nbsp;and Pharmacological Activity ------------------------------------------53 2.3.4.7 Toxicology&nbsp;-------------------------------------------------------------------------------54 </strong></p><p><strong>3. MATERIALS&nbsp;EQUIPMENTS AND METHODS -------------------------------------------55 3.1 Materials&nbsp;-------------------------------------------------------------------------------------------55 </strong><br><strong>3.1.1 Samples&nbsp;of Plant Materials ----------------------------------------------------------------55 3.1.2 Standards&nbsp;-------------------------------------------------------------------------------------56 3.1.3 Chemicals&nbsp;and Solvents--------------------------------------------------------------------58 3.1.4 Miscellaneous&nbsp;Materials--------------------------------------------------------------------59 </strong></p><p><strong>3.2 Foam&nbsp;Fractionation Unit and Equipments --------------------------------------------------59 </strong><br><strong>3.2.1 Foam&nbsp;Fractionation Unit-------------------------------------------------------------------59 3.2.2 High&nbsp;Performance Liquid Chromatography ------------------------------------------60 3.2.3 Gas&nbsp;Chromatography ----------------------------------------------------------------------61 3.2.3 UV-Vis&nbsp;Spectroscopy -----------------------------------------------------------------------61 3.2.4 Nuclear&nbsp;Magnetic Resonance Spectroscopy--------------------------------------------61 </strong></p><p>Contents </p><p>______________________________________________________________________________ </p><p><strong>3.2.5 Fourier&nbsp;Transform Infrared Microspectroscopy -------------------------------------61 3.2.6 Other&nbsp;Equipments---------------------------------------------------------------------------62 </strong></p><p><strong>3.3 Methods---------------------------------------------------------------------------------------------62 </strong><br><strong>3.3.1 Analytical&nbsp;Characterisation and Quantification --------------------------------------62 </strong><br><strong>3.3.1.1 Faradiol&nbsp;Esters--------------------------------------------------------------------------62 3.3.1.2 Catechins---------------------------------------------------------------------------------64 3.3.1.3 Tryptanthrin&nbsp;----------------------------------------------------------------------------65 3.3.1.4 Cannabinoids&nbsp;---------------------------------------------------------------------------66 </strong><br><strong>3.3.2 Extraction-------------------------------------------------------------------------------------67 </strong><br><strong>3.3.2.1 Extraction of&nbsp;Faradiol Esters -------------------------------------------------------67 3.3.2.2 Extraction&nbsp;of Catechins ---------------------------------------------------------------68 3.3.2.3 Extraction&nbsp;of Tryptanthrin-----------------------------------------------------------68 3.3.2.4 Extraction&nbsp;of Cannabinoids----------------------------------------------------------68 </strong><br><strong>3.3.3 Foam&nbsp;Fractionation -------------------------------------------------------------------------69 </strong><br><strong>3.3.3.1 Foam Fractionation of Faradiol Esters---------------------------------------------70 3.3.3.2 Foam&nbsp;Fractionation of Catechins ---------------------------------------------------74 3.3.3.3 Foam&nbsp;Fractionation of Tryptanthrin-----------------------------------------------76 </strong></p><p><strong>4. RESULTS-----------------------------------------------------------------------------------------82 4.1 Accuracy&nbsp;of Measurements and Quantification of Active Principles by HPLC -----82 4.2 Calendula Officinalis------------------------------------------------------------------------------85 </strong><br><strong>4.2.1 Analytical&nbsp;Characterisation of&nbsp;Lupeol Acetate ---------------------------------------85 </strong><br><strong>4.2.1.1 UV-Vis&nbsp;Characterisation -------------------------------------------------------------85 </strong><br><strong>4.2.1.2 HRGC-EI/MS&nbsp;Characterisation -------------------------------------------------------85 4.2.2 Extraction&nbsp;of Faradiol Esters -------------------------------------------------------------86 4.2.3 Enrichment&nbsp;of Faradiol&nbsp;Esters-----------------------------------------------------------87 </strong><br><strong>4.2.3.1 Influence&nbsp;of Surfactant and Additives ---------------------------------------------88 4.2.3.2 Influence&nbsp;of Solute Concentration and pH----------------------------------------89 4.2.3.3 Influence&nbsp;of Height of Foam Tower and Height of Liquid Pool --------------91 4.2.3.4 Influence&nbsp;of Time of Foaming and Gas Flow Rates -----------------------------92 4.2.3.5 Optimised&nbsp;Overall Enrichment Process -------------------------------------------93 </strong></p><p><strong>4.3 Camellia Sinensis----------------------------------------------------------------------------------95 </strong></p><p>Contents </p><p>______________________________________________________________________________ </p><p><strong>4.3.1 Analytical&nbsp;Characterisation of Catechins ----------------------------------------------95 </strong><br><strong>4.3.1.1 UV-Vis&nbsp;Characterisation -------------------------------------------------------------95 4.3.1.2 Nuclear&nbsp;Magnetic Resonance&nbsp;Characterisation ---------------------------------96 </strong><br><strong>4.3.2 Extraction&nbsp;of Catechins --------------------------------------------------------------------96 4.3.3 Enrichment&nbsp;of Catechins-------------------------------------------------------------------97 </strong><br><strong>4.3.3.1 Influence of Solute Concentration, Additives and pH ---------------------------98 4.3.3.2 Influence&nbsp;of Consecutive Foaming and Gas Flow Rate----------------------- 100 4.3.3.3 Optimised&nbsp;Overall Enrichment Process ----------------------------------------- 101 </strong></p>

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