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HPLC-ICPMS and Stable Isotope-Labeled Approaches To Assess Quantitatively Ti(IV) Uptake by Transferrin in Human Blood Serum

dc.contributor.authorSarmiento González, Alejandro 
dc.contributor.authorRuiz Encinar, Jorge 
dc.contributor.authorCantarero Roldán, Alicia María
dc.contributor.authorMarchante Gayón, Juan Manuel 
dc.contributor.authorSanz Medel, Alfredo 
dc.date.accessioned2013-01-30T10:05:58Z
dc.date.available2013-01-30T10:05:58Z
dc.date.issued2008
dc.identifier.citationAnalytical Chemistry, 80(22), p. 8702-8711 (2008); doi:10.1021/ac801029pspa
dc.identifier.issn0003-2700
dc.identifier.urihttp://hdl.handle.net/10651/8040
dc.description.abstractLittle is known about the effects of titanium found in patients wearing prostheses or about the biochemical pathways of this metal when used as an anticancer drug (e.g., titanocene dichloride). In this work, transferrin has been confirmed as the only carrier protein binding Ti in human blood serum samples by making use of different HPLC protein separations followed by element-specific Ti detection by ICPMS. Besides, isotope dilution analysis has been applied to the quantitative speciation of Ti−Tf in standards and human blood serum samples. Species-unspecific and species-specific isotope dilution modes have been explored. In the first case, very low Ti−Tf results were obtained even using two different chromatographic mechanisms, anion exchange (20−24%) and size exclusion (33−36%). Surprisingly, no major Ti species except Ti−Tf were observed in the chromatograms, suggesting that Ti(IV) hydrolysis and precipitation as inactive titanium oxide species could take place inside the chromatographic columns. These results demonstrate that chemical degradation of metalloproteins during analytical separations could ruin the sought speciation quantitative results. The isotope dilution species-specific mode, much more accurate in such cases, has been instrumental in demonstrating the possibility of gross errors in final metalloprotein quantification. For this purpose, an isotopically enriched standard of 49Ti−Tf was synthesized and applied to the quantitative speciation of Ti−Tf again. Using this species-specific spike, Ti−Tf dissociation inside the chromatographic columns used could be corrected, and thus, quantitative Ti−Tf binding in serum (92−102%) was observed. In other words, the usefulness and potential of a species-specific isotope dilution analysis approach to investigate quantitatively metal−protein associations, which can be dissociated at certain experimental conditions, is demonstrated here for the first time.spa
dc.format.extentp. 8702-8711spa
dc.language.isoeng
dc.relation.ispartofAnalytical Chemistryspa
dc.rights(c) Analytical Chemistry
dc.sourceWOKspa
dc.titleHPLC-ICPMS and Stable Isotope-Labeled Approaches To Assess Quantitatively Ti(IV) Uptake by Transferrin in Human Blood Serumspa
dc.typejournal article
dc.identifier.local449spa
dc.identifier.doi10.1021/ac801029p
dc.relation.publisherversionhttp://dx.doi.org/10.1021/ac801029pspa


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