dc.contributor.author | Valianou, L | en |
dc.contributor.author | Karapanagiotis, I | en |
dc.contributor.author | Chryssoulakis, Y | en |
dc.date.accessioned | 2014-03-01T02:46:04Z | |
dc.date.available | 2014-03-01T02:46:04Z | |
dc.date.issued | 2009 | en |
dc.identifier.issn | 1618-2642 | en |
dc.identifier.uri | https://dspace.lib.ntua.gr/xmlui/handle/123456789/32517 | |
dc.subject | Archaeometry | en |
dc.subject | Fine arts | en |
dc.subject | HPLC | en |
dc.subject | Natural products | en |
dc.subject | Sampling | en |
dc.subject.classification | Biochemical Research Methods | en |
dc.subject.classification | Chemistry, Analytical | en |
dc.subject.other | Acid treatments | en |
dc.subject.other | Archaeometry | en |
dc.subject.other | Bisdemethoxycurcumin | en |
dc.subject.other | Carminic acid | en |
dc.subject.other | Cotinus coggygria | en |
dc.subject.other | Curcuma longa | en |
dc.subject.other | Curcumin | en |
dc.subject.other | Curcuminoids | en |
dc.subject.other | Demethoxycurcumin | en |
dc.subject.other | Diode array detectors | en |
dc.subject.other | Extraction method | en |
dc.subject.other | Extraction yield | en |
dc.subject.other | Fine arts | en |
dc.subject.other | Flavonoid glycosides | en |
dc.subject.other | HPLC | en |
dc.subject.other | HPLC-DAD | en |
dc.subject.other | Indirubin | en |
dc.subject.other | Natural dye | en |
dc.subject.other | Natural products | en |
dc.subject.other | Oxalic Acid | en |
dc.subject.other | Peak area | en |
dc.subject.other | Tinctoria | en |
dc.subject.other | Chromatographic analysis | en |
dc.subject.other | Chromatography | en |
dc.subject.other | Derivatives | en |
dc.subject.other | Dimethyl sulfoxide | en |
dc.subject.other | Dyes | en |
dc.subject.other | Fabrics | en |
dc.subject.other | High performance liquid chromatography | en |
dc.subject.other | High pressure liquid chromatography | en |
dc.subject.other | Liquids | en |
dc.subject.other | Mass spectrometry | en |
dc.subject.other | Signal to noise ratio | en |
dc.subject.other | Silk | en |
dc.subject.other | Substrates | en |
dc.subject.other | Sugars | en |
dc.subject.other | Wool | en |
dc.subject.other | Wool fibers | en |
dc.subject.other | Yarn | en |
dc.subject.other | Extraction | en |
dc.subject.other | Cotinus coggygria | en |
dc.subject.other | Curcuma longa | en |
dc.subject.other | Dactylopius coccus | en |
dc.subject.other | Isatis | en |
dc.subject.other | Isatis tinctoria | en |
dc.subject.other | Reseda luteola | en |
dc.subject.other | Rubia | en |
dc.subject.other | Rubia tinctorum | en |
dc.title | Comparison of extraction methods for the analysis of natural dyes in historical textiles by high-performance liquid chromatography | en |
heal.type | conferenceItem | en |
heal.identifier.primary | 10.1007/s00216-009-3137-6 | en |
heal.identifier.secondary | http://dx.doi.org/10.1007/s00216-009-3137-6 | en |
heal.language | English | en |
heal.publicationDate | 2009 | en |
heal.abstract | Different methods for the extraction of Dactylopius coccus Costa, Rubia tinctorum L., Isatis tinctoria L., Reseda luteola L., Curcuma longa L. and Cotinus coggygria Scop. from wool fibres are investigated using high-performance liquid chromatography with diode array detector (HPLC-DAD). The efficiencies of five extraction methods which include the use of HCl (widely used extraction method), citric acid, oxalic acid, TFA and a combination of HCOOH and EDTA are compared on the basis of the (a) number, (b) relative quantities, measured as HPLC peak areas and (c) signal-to-noise ratios (S/N) of the compounds extracted from the wool substrates. Flavonoid glycosides and curcuminoids contained in R. luteola L. and C. longa L., respectively, according to liquid chromatography with mass spectrometry (LC-MS) identifications, are not detected after treating the fibres with HCl. All the other milder methods are successful in extracting these compounds. Experiments are performed using HPLC-DAD to compare the HPLC peak areas and the S/N of the following extracted compounds: indigotin, indirubin, curcumin, demethoxycurcumin, bisdemethoxycurcumin, fisetin, sulfuretin, luteolin, luteolin-7-O-glucoside, apigenin, carminic acid, alizarin, puruprin and rubiadin. It is shown that the TFA method provides overall the best results as it gives elevated extraction yields except for fisetin, luteolin, apigenin and luteolin-7-O-glucoside and highest S/N except for fisetin and luteolin-7-O-glucoside. It is noteworthy that treatment of the fibres with the typical HCl extraction method results overall in very low S/N. The TFA method is selected for further studies, as follows. First, it is applied on silk dyed samples and compared with the HCl method. The same relative differences of the TFA and HCl methods observed for the wool dyed samples are reported for the silk dyed samples too, except for rubiadin, luteolin and apigenin. Thus, in most cases, the nature of the substrate (wool or silk) appears to have negligible effects on the relative difference of the two extraction methods. Second, the selected TFA method is applied to treat wool and silk historical samples extracted from textiles of the Mamluk period, resulting in the identification of several colouring compounds. In all extraction methods mentioned above, DMSO is used to dissolve the dyes, after acid treatment. © 2009 Springer-Verlag. | en |
heal.publisher | SPRINGER HEIDELBERG | en |
heal.journalName | Analytical and Bioanalytical Chemistry | en |
dc.identifier.doi | 10.1007/s00216-009-3137-6 | en |
dc.identifier.isi | ISI:000272017000025 | en |
dc.identifier.volume | 395 | en |
dc.identifier.issue | 7 | en |
dc.identifier.spage | 2175 | en |
dc.identifier.epage | 2189 | en |
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