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Rapid quantification of insulin degludec by immunopurification combined with liquid chromatography high-resolution mass spectrometry.
Reverter-Branchat, Gemma; Groessl, Michael; Nakas, Christos T; Prost, Jean-Christophe; Antwi, Kwasi; Niederkofler, Eric E; Bally, Lia.
Afiliação
  • Reverter-Branchat G; Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital, University of Bern, 3010, Bern, Switzerland.
  • Groessl M; Department of Nephrology and Hypertension, Inselspital, Bern University Hospital, University of Bern, Freiburgstrasse, 3012, Bern, Switzerland. michael.groessl@dbmr.unibe.ch.
  • Nakas CT; Laboratory of Biometry, School of Agriculture, University of Thessaly, 38446, Nea Ionia, Magnesia, Greece.
  • Prost JC; University Institute of Clinical Chemistry, Inselspital, Bern University Hospital, University of Bern, 3010, Bern, Switzerland.
  • Antwi K; University Institute of Clinical Chemistry, Inselspital, Bern University Hospital, University of Bern, 3010, Bern, Switzerland.
  • Niederkofler EE; Thermo Fisher Scientific, Tempe, AZ, 85280, USA.
  • Bally L; Thermo Fisher Scientific, Tempe, AZ, 85280, USA.
Anal Bioanal Chem ; 412(30): 8351-8359, 2020 Dec.
Article em En | MEDLINE | ID: mdl-33006670
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. Graphical Abstract.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espectrometria de Massas / Cromatografia Líquida / Insulina de Ação Prolongada Limite: Adult / Humans / Male Idioma: En Revista: Anal Bioanal Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suíça País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espectrometria de Massas / Cromatografia Líquida / Insulina de Ação Prolongada Limite: Adult / Humans / Male Idioma: En Revista: Anal Bioanal Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suíça País de publicação: Alemanha