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Extraction and Planar Chromatographic Separation Techniques in the

Extraction and Planar Chromatographic Separation Techniques in the

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34<br />

In microchemical detection methods <strong>the</strong> TLC plate is sprayed with or dipped <strong>in</strong>to a suitable<br />

reagent to form absorb<strong>in</strong>g or fluorescent derivatives with <strong>the</strong> analytes which can <strong>the</strong>n be<br />

detected. Derivatization can take place ei<strong>the</strong>r before or after <strong>the</strong> TLC separation, <strong>and</strong> <strong>the</strong><br />

terms pre- <strong>and</strong> postchromatographic derivatization are used to separate <strong>the</strong>se two options. A<br />

great number of different universal <strong>and</strong> specific, i.e. group-characteriz<strong>in</strong>g reagents which<br />

react with a specific functional group, have been developed <strong>and</strong> new variants cont<strong>in</strong>ue to be<br />

published (e.g. STAHL 1967, JORK et al. 1990, 1994, TOUCHSTONE 1992).<br />

Biological detection of separated substances on <strong>the</strong> TLC plate <strong>in</strong> situ has been applied to <strong>the</strong><br />

screen<strong>in</strong>g of various extracts for e.g. antimicrobial <strong>and</strong> antioxidant activity or general toxicity<br />

(EBERZ et al. 1996, WEINS <strong>and</strong> JORK 1996, HOSTETTMANN et al. 1997). These methods<br />

are especially suitable for screen<strong>in</strong>g purposes as <strong>the</strong> fractions or compounds with most<br />

pronounced activity can be detected directly on <strong>the</strong> TLC plate <strong>and</strong> subjected to fur<strong>the</strong>r<br />

purification <strong>and</strong>/or identification steps.

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