2013
DOI: 10.1002/elps.201200653
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Determination of carbohydrate‐deficient transferrin in human serum by capillary zone electrophoresis: Evaluation of assay performance and quality assurance over a 10‐year period in the routine arena

Abstract: The performance of high-resolution CZE for determination of carbohydrate-deficient transferrin (CDT) in human serum based on internal and external quality data gathered over a 10-year period is reported. The assay comprises mixing of serum with a Fe(III) ion-containing solution prior to analysis of the iron saturated mixture in a dynamically double-coated capillary using a commercial buffer at alkaline pH. CDT values obtained with a human serum of a healthy individual and commercial quality control sera are sh… Show more

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Cited by 17 publications
(18 citation statements)
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References 37 publications
(60 reference statements)
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“…The CEofix assays are characterized with a high precision performance [29,30,83] and were routinely used in our laboratory since 2002. Assay performance and stringent quality assurance over a 10-year period were assessed and reported [104]. The robustness of the HR-CEofix assays was thereby documented with data obtained by analysis of the serum of a healthy individual, of commercial QC sera, and by participation at external QC schemes.…”
Section: Monitoring Of Cdtmentioning
confidence: 99%
“…The CEofix assays are characterized with a high precision performance [29,30,83] and were routinely used in our laboratory since 2002. Assay performance and stringent quality assurance over a 10-year period were assessed and reported [104]. The robustness of the HR-CEofix assays was thereby documented with data obtained by analysis of the serum of a healthy individual, of commercial QC sera, and by participation at external QC schemes.…”
Section: Monitoring Of Cdtmentioning
confidence: 99%
“…CE techniques demonstrated successful applications for analysis of small analytes from biological matrices usually using proper IS without tedious sample preparation . However, in order to guarantee the accuracy of a main assay and to reliably control all degradation products of pharmaceuticals or biopharmaceuticals, orthogonal assays with different separation efficiency are indispensable .…”
Section: Determination Of (Bio)pharmaceuticalsmentioning
confidence: 99%
“…Saturated Tf solution (1500 g/mL) was prepared to avoid the heterogeneity in glycoform charge caused by incomplete iron saturation by dissolving the protein in an aqueous solution containing 0.27 mM FeCl 3 and 18.7 mM NaHCO 3 [17,[23][24][25][26][27][28]. Saturated Tf solution (1500 g/mL) was prepared to avoid the heterogeneity in glycoform charge caused by incomplete iron saturation by dissolving the protein in an aqueous solution containing 0.27 mM FeCl 3 and 18.7 mM NaHCO 3 [17,[23][24][25][26][27][28].…”
Section: Electrolytes Sheath Liquid and Standardsmentioning
confidence: 99%
“…The BGE (25 mM ammonium acetate) was adjusted to pH 8.5 with ammonia, while applying a separation voltage of 5 kV. No improvements were obtained either with decreasing the sample injection volume or analyzing Tf after saturation with Fe to ensure a constant metal content in Tf [17,[23][24][25][26][27][28]. 1A can be observed that S3, S4, S5 and S6 Tf sialoforms were poorly resolved after the negative dip indicating the EOF [23].…”
Section: Ce-uvmentioning
confidence: 99%
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