A quality control system for ligand-binding assay of plasma renin activity: Proof-of-concept within a pharmacodynamic study

•Customized quality control system comprised regulator standards and scientific recommendations.•Comprehensive intra- and interrun monitoring based on a lean six-step approach.•The easy-to-handle inter-run assessment ensured comparability from the first to the last study sample.•Applicability of the...

Full description

Saved in:

Bibliographic Details
Published in:	Journal of pharmaceutical and biomedical analysis Vol. 181; p. 113090
Main Authors:	Suessenbach, Fabian Konstantin, Makowski, Nina, Feickert, Martin, Gangnus, Tanja, Tins, Jutta, Burckhardt, Bjoern Bengt, Läer, Stephanie, Breitkreutz, Jörg, Klingmann, Ingrid, Lagler, Florian, de Hoon, Jan, Dalinghaus, Michiel, Bajcetic, Milica, de Wildt, Saskia, Clarke, Anne Keatley, Breur, Johannes, Male, Christoph, Ablonczy, Laslo, Mir, Thomas, Vukomanovic, Vladislav, Dukic, Milan, Jovanovic, Ida, Burckhardt, Bjoern B., Cawello, Willi, Kleine, Karl, Moder, Angelika, Obarcanin, Emina, Wagner, Peter, Walsh, Jennifer, van Hecken, Anne, Spatenkova, Lucie, Ali, Mohsin, Božić, Bojana, Burdman, Maja Bijelić Ilja, Ciplea, Agnes, Faisal, Muhammad, Farahani, Samieh, Lazic, Milica, Suessenbach, Fabian, van der Meulen, Marijke, Popović, Saša, Parezanović, Miro, Smeets, Nori, Swoboda, Vanessa, Bojanin, Dragana, Đorđević, Stefan, Dragić, Jasminka, Holle, Ann-Kathrin, Jovičić, Bosiljka, Košutić, Jovan, Kozomara, Gordana, Majid, Haidara, Mitrović, Jadranka, Ninić, Sanja, Parezanovic, Miro, Parezanovic, Vojislav, Pavlović, Andrija, Prijić, Sergej, Rebić, Branislava, Stefanović, Igor, Tordas, Daniel, Vulićević, Irena, Bartels, Anke, Čeko, Andjelka, Herborts, Marissa, Hennink, Annelies, Kosanović, Bosiljka, Kostic, Sanja, Isailović, Ljiljana, Maksimovic, Jasmina, Manai, Badies, Martinović, Nada, Máté, Gyöngyi, Perišić, Miloš, Reljić, Jelena, Salamomovic, Regina Pirker Marta, Schlesner, Claudia, Wissmann, Eva
Format:	Journal Article
Language:	English
Published:	England Elsevier B.V 20-03-2020
Subjects:	Incurred sample reanalysis Ligand-binding assay Pediatric clinical trial Plasma renin activity Quality control system LoD QCS GCLP LLOQ FDA RAAS Ligand-binding assay LENA AngI SD QC Quality control system OD Incurred sample reanalysis EMA Pediatric clinical trial Plasma renin activity ULOQ CLSI ISR RIA RfB CS CV RE PD SST PK HF LoB PRA ELISA
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Summary:	•Customized quality control system comprised regulator standards and scientific recommendations.•Comprehensive intra- and interrun monitoring based on a lean six-step approach.•The easy-to-handle inter-run assessment ensured comparability from the first to the last study sample.•Applicability of the system in academic environment was proven.•System contributed to a reliable acquisition of 940 pediatric PRA samples. While the role of plasma renin activity (PRA) in heart failure has been widely studied in adults, comprehensive data on pediatric heart failure remain lacking. This drawback is increasingly being addressed by academic research. Nevertheless, such pediatric investigations are commonly conducted only once due to ethical constraints. Therefore, the quality of bioanalytical data must be ensured to acquire meaningful insights into maturing humoral parameters. However, appropriate post-validation assessment of bioanalytical runs is currently underrepresented by regulatory guidance. Thus, for applications in an academic environment, an easy-to-handle six-step bioanalytical quality control system was designed based on regulatory guidelines (e.g. U.S. Food and Drug Administration) combined with international recommendations (e.g. Clinical and Laboratory Standards Institute) and current scientific discussion. Its applicability to an enzyme-linked immunosorbent assay for determination of PRA was investigated within three pediatric trials of the EU-funded “Labeling of Enalapril in Neonates up to Adolescents” project. This quality control system identified 15 % bioanalytical runs as non-compliant to the predefined specifications and ensured the reliable quantification of 940 pharmacodynamic samples. The inter-run assessment of quality controls was able to demonstrate the comparability of the study results. Furthermore, 86 % of incurred sample reanalysis pairs complied with regulatory requirements (>67 %), thus underlining the long-term reproducibility of the utilized ligand-binding assay. Successful participation in interlaboratory testing confirmed the accuracy of the applied method throughout the entire study period. Further investigations showed no notable differences between the five applied lots of the PRA assay. The applicability of this quality control system was proven in an academic environment and ensured reliable results for PRA over the entire 24-month study period.
Bibliography:	ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3
ISSN:	0731-7085 1873-264X
DOI:	10.1016/j.jpba.2019.113090