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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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On-line SPE sample treatment as a tool for method automatization and detection limits reduction: Quantification of 25-hydroxyvitamin D3/D2

Thumbnail
Συγγραφέας
Palaiogiannis D., Bekou E., Pazaitou-Panayiotou K., Samanidou V., Tsakalof A.
Ημερομηνία
2017
Γλώσσα
en
DOI
10.1016/j.jchromb.2016.10.006
Λέξη-κλειδί
Biochemistry
Biomolecules
Metabolites
Phase separation
Instrumental analysis
Large volume injection
Large-volume sample injection
Method detection limits
On-line preconcentration
On-line sample preconcentration
On-line solid phase extraction
Vitamin-D
Vitamins
25 hydroxyergocalciferol
calcifediol
drug metabolite
25 hydroxyergocalciferol
calcifediol
Article
assay
automation
controlled study
human
injection
limit of detection
plasma
priority journal
protein binding
serum
solid phase extraction
switching valve
ultra performance liquid chromatography
blood
chemistry
high performance liquid chromatography
isolation and purification
limit of detection
procedures
reproducibility
solid phase extraction
statistical model
25-Hydroxyvitamin D 2
Calcifediol
Chromatography, High Pressure Liquid
Humans
Limit of Detection
Linear Models
Reproducibility of Results
Solid Phase Extraction
Elsevier B.V.
Εμφάνιση Μεταδεδομένων
Επιτομή
The development and approbation of new, automated UHPLC-DAD method for the quantification of 25-hydroxyvitamin D3/D2 (25OH-D3/D2) metabolites in plasma/serum for the evaluation of patient's vitamin D status are presented. The method was developed on the Ultimate 3000 UHPLC dual gradient system supplied with the on-line SPE-concentration column coupled through six port switching valve to analytical column. This configuration and materials selected enable large volume sample injection (500 μL) and on-line sample preconcentration, clean up and subsequent selective metabolites transfer onto the analytical column. The new method abrogates main conventional time consuming and error source off-line steps of analysis and thus simplifies analysis. The large volume injection increases the sensitivity of instrumental analysis by about ten-fold on-line pre-concentration of metabolites. The instrument response is linear (R > 0.99) in the investigated concentration range 10–100 ng mL−1 which covers all the possible vitamin D status from serious deficiency (<12 ng mL−1) to excess. The method detection limits (S/N = 3) are LOD (25OH-D3) = 0.94 ng mL−1 and LOD (25OH-D2) = 2.4 ng mL−1. The method performance was assessed with the use of certified reference samples and perfect agreement between certified and measured values is demonstrated. The method was applied to human samples previously analyzed for total vitamin D by Competitive Protein-binding assay and findings of the two methods are compared. © 2016 Elsevier B.V.
URI
http://hdl.handle.net/11615/77432
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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