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Novel HPLC-ICP-MS strategy for the determination of β2-Transferrin, the biomarker of cerebrospinal fluid (CSF) leakage

Autor(es) y otros:
Castillo Busto, María Estela delAutoridad Uniovi; Montes Bayón, MaríaAutoridad Uniovi; García Alonso, José IgnacioAutoridad Uniovi; Caruso, Joseph A.; Sanz Medel, AlfredoAutoridad Uniovi
Palabra(s) clave:

Inductively Coupled Plasma/Ms

Lc/Ms

Quantitative Organic Analyses

Biomarkers

Transferrin

Biological Fluids

Fecha de publicación:
2010
Editorial:

Royal Society of Chemistry

Versión del editor:
http://dx.doi.org/10.1039/c0an00207k
Citación:
Analyst, 135(7), p. 1538-1540 (2010); doi:10.1039/c0an00207k
Descripción física:
p. 1538-1540
Resumen:

Asialo-Transferrin (S0) or β2-Transferrin is an accepted marker of cerebrospinal fluid (CSF) leakage from the subarachnoid space into the nasal or aural cavity as the result of a head trauma. At this time, the S0 detection method of choice is isoelectric focusing on polyacrylamide gel with direct immunofixation of transferrin (Tf) and silverstaining which are time-consuming techniques (> 5 h). The aim of this study is to present an alternative methodology for determination of Tf sialoforms present in CSF samples, specifically S0, based on the detection of the Fe associated with those forms. A double spiking methodology is developed by saturating the protein with isotopically enriched iron (57Fe) and conducting post-column Isotope Dilution Analysis (IDA) with 54Fe after separation of the different sialoforms by anion exchange chromatography. The results obtained have been validated using a certified serum (ERM®-DA470) and applied with satisfactory results to a pooled CSF sample.

Asialo-Transferrin (S0) or β2-Transferrin is an accepted marker of cerebrospinal fluid (CSF) leakage from the subarachnoid space into the nasal or aural cavity as the result of a head trauma. At this time, the S0 detection method of choice is isoelectric focusing on polyacrylamide gel with direct immunofixation of transferrin (Tf) and silverstaining which are time-consuming techniques (> 5 h). The aim of this study is to present an alternative methodology for determination of Tf sialoforms present in CSF samples, specifically S0, based on the detection of the Fe associated with those forms. A double spiking methodology is developed by saturating the protein with isotopically enriched iron (57Fe) and conducting post-column Isotope Dilution Analysis (IDA) with 54Fe after separation of the different sialoforms by anion exchange chromatography. The results obtained have been validated using a certified serum (ERM®-DA470) and applied with satisfactory results to a pooled CSF sample.

URI:
http://hdl.handle.net/10651/7651
ISSN:
0003-2654
Identificador local:

20100506

DOI:
10.1039/c0an00207k
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