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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  • Προβολή τεκμηρίου
  •   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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Rapid quantification of insulin degludec by immunopurification combined with liquid chromatography high-resolution mass spectrometry

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Συγγραφέας
Reverter-Branchat G., Groessl M., Nakas C.T., Prost J.-C., Antwi K., Niederkofler E.E., Bally L.
Ημερομηνία
2020
Γλώσσα
en
DOI
10.1007/s00216-020-02971-4
Λέξη-κλειδί
Clinical research
Drug products
Industrial research
Liquid chromatography
Mass spectrometry
Patient monitoring
Patient treatment
Clinical application
High resolution mass spectrometry
High-throughput method
Human blood samples
Liquid chromatography-high resolution mass spectrometries
Lower limit of quantifications
Pharmaceutical industry
US Food and Drug Administration
Insulin
insulin degludec
long acting insulin
adult
human
isolation and purification
limit of detection
liquid chromatography
male
mass spectrometry
procedures
reproducibility
Adult
Chromatography, Liquid
Humans
Insulin, Long-Acting
Limit of Detection
Male
Mass Spectrometry
Reproducibility of Results
Springer Science and Business Media Deutschland GmbH
Εμφάνιση Μεταδεδομένων
Επιτομή
Insulin degludec is an ultra-long-acting insulin analogue that is increasingly being used in diabetes due to its favourable efficacy and safety profile. Thus, there is an increasing demand for a reliable and specific analytical method to quantify insulin degludec for research, pharmaceutical industry and clinical applications. We developed and validated an automated, high-throughput method for quantification of insulin degludec in human blood samples across the expected clinical range combining immunopurification with high-resolution mass spectrometry. Validation was performed according to the requirements of the US Food and Drug Administration. The method satisfyingly met the following parameters: lower limit of quantification (120 pM), linearity, accuracy (error < 5%), precision (CV < 7.7%), selectivity, carry-over, recovery (89.7–97.2%), stability and performance in the presence of other insulin analogues. The method was successfully applied to clinical samples of patients treated with insulin degludec showing a good correlation with the administered dose (r2 = 0.78). High usability of the method is supported by the small specimen volume, automated sample processing and short analysis time. In conclusion, this reliable, easy-to-use and specific mass spectrometric insulin degludec assay offers great promise to address the current unmet need for standardized insulin analytics in academic and industrial research. [Figure not available: see fulltext.]. © 2020, The Author(s).
URI
http://hdl.handle.net/11615/78497
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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