Ultra-high-performance liquid chromatography-mass spectrometry method for neutrophil gelatinase-associated lipocalin as a predictive biomarker in acute kidney injury.


Journal

Talanta
ISSN: 1873-3573
Titre abrégé: Talanta
Pays: Netherlands
ID NLM: 2984816R

Informations de publication

Date de publication:
01 Apr 2019
Historique:
received: 13 07 2018
revised: 14 11 2018
accepted: 16 11 2018
entrez: 11 1 2019
pubmed: 11 1 2019
medline: 21 3 2019
Statut: ppublish

Résumé

Neutrophil gelatinase associated lipocalin (NGAL) is a protein that was found to be overexpressed in acute kidney injury (AKI). The rise in NGAL concentration, both in urine or plasma, appears earlier than for other classical renal function markers such as serum creatinine, thus making it a suitable marker for early pathology detection. The aim of this study was to develop a method involving tryptic digestion, solid phase extraction and LC-MS/MS analysis to analyze NGAL in plasma medium using an isotope labeled surrogate protein, containing NGAL signature tags, as internal standard (QPrEST). The method was validated for the analysis of NGAL in an analytical range from 50 to 1250 ng/mL using two different proteotypic peptides. The method was further used to quantify the NGAL in human plasma samples for whom elevated NGAL values were expected. NGAL values were between 190.8 and 242.6 ng/mL for control group and between 228.1 and 3526.2 ng/mL for patient group. This study proved that the selection of the right internal standard is of utmost importance in targeted proteomics studies as the digestion steps might cause high variability. This study also confirmed that, although NGAL is highly resistant to proteases such as trypsin, the method could be fully validated according to FDA guidelines and subsequently used to assess NGAL levels in patient plasma with high analytical confidence.

Identifiants

pubmed: 30625599
pii: S0039-9140(18)31201-3
doi: 10.1016/j.talanta.2018.11.050
pii:
doi:

Substances chimiques

Biomarkers 0
LCN2 protein, human 0
Lipocalin-2 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

668-675

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Valentin Ion (V)

Laboratory for the Analysis of Medicines (LAM), Department of Pharmacy, CIRM, University of Liège, 4000 Liège, Belgium; Analytical Chemistry and Drug Analysis Department, Faculty of Pharmacy, University of Medicine, Pharmacy, Sciences and Technology from Tîrgu Mureș, 540139 Tîrgu Mureș, Romania.

Gwenaël Nys (G)

Laboratory for the Analysis of Medicines (LAM), Department of Pharmacy, CIRM, University of Liège, 4000 Liège, Belgium.

Gaël Cobraiville (G)

Laboratory for the Analysis of Medicines (LAM), Department of Pharmacy, CIRM, University of Liège, 4000 Liège, Belgium.

Etienne Cavalier (E)

Clinical Chemistry Department, CIRM, University of Liège, CHU Sart-Tilman, 4000 Liège, Belgium.

Jacques Crommen (J)

Laboratory for the Analysis of Medicines (LAM), Department of Pharmacy, CIRM, University of Liège, 4000 Liège, Belgium.

Anne-Catherine Servais (AC)

Laboratory for the Analysis of Medicines (LAM), Department of Pharmacy, CIRM, University of Liège, 4000 Liège, Belgium.

Daniela-Lucia Muntean (DL)

Analytical Chemistry and Drug Analysis Department, Faculty of Pharmacy, University of Medicine, Pharmacy, Sciences and Technology from Tîrgu Mureș, 540139 Tîrgu Mureș, Romania.

Marianne Fillet (M)

Laboratory for the Analysis of Medicines (LAM), Department of Pharmacy, CIRM, University of Liège, 4000 Liège, Belgium. Electronic address: marianne.fillet@ulg.ac.be.

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Classifications MeSH