Speeding up pyrogenicity testing: Identification of suitable cell components and readout parameters for an accelerated monocyte activation test (MAT). Issue 2 (28th April 2016)

• Record Type: Journal Article
• Authors: Stoppelkamp, Sandra; Würschum, Noriana; Stang, Katharina; Löder, Jasmin; Avci‐Adali, Meltem; Toliashvili, Leila; Schlensak, Christian; Wendel, Hans Peter; Fennrich, Stefan
• Is Part Of: Drug testing and analysis. Volume 9:Issue 2(2017:Feb.)
• Page Start: 260
• Page End: 273
• Publication Date: 2016-04-28
• Subjects: pyrogens -- endotoxins -- monocyte activation test -- medical devices -- parenterals; Drugs -- Analysis -- Periodicals; Drug testing -- Periodicals; Chemistry, Forensic -- Periodicals; 615.1901
• DOI: 10.1002/dta.1973
• Languages: English
• ISSNs: 1942-7603

Abstract

Abstract : Pyrogen testing represents a crucial safety measure for parental drugs and medical devices, especially in direct contact with blood or liquor. The European Pharmacopoeia regulates these quality control measures for parenterals. Since 2010, the monocyte activation test (MAT) has been an accepted pyrogen test that can be performed with different human monocytic cell sources: whole blood, isolated monocytic cells or monocytic cell lines with IL1β, IL6, or TNFα as readout cytokines. In the present study, we examined the three different cell sources and cytokine readout parameters with the scope of accelerating the assay time. We could show that despite all cell types being able to detect pyrogens, primary cells were more sensitive than the monocytic cell line. Quantitative real‐time PCR revealed IL6 mRNA transcripts having the largest change in Ct‐values upon LPS‐stimulation compared to IL1β and TNFα, but quantification was unreliable. IL6 protein secretion from whole blood or peripheral blood mononuclear cells (PBMC) was also best suited for an accelerated assay with a larger linear range and higher signal‐to‐noise ratios upon LPS‐stimulation. The unique combination with propan‐2‐ol or a temperature increase could additionally increase the cytokine production for earlier detection in PBMC. The increased incubation temperature could finally increase not only responses to lipopolysaccharides (LPS) but also other pyrogens by up to 13‐fold. Therefore, pyrogen detection can be accelerated considerably by using isolated primary blood cells with an increased incubation temperature and IL6 as readout. These results could expedite assay time and thus help to promote further acceptance of the MAT. Copyright © 2016 John Wiley & Sons, Ltd. Abstract : Pyrogen testing represents a crucial safety measure for parental drugs and medical devices, especially in direct contact with blood or liquor. Using primary human blood cells with IL6 as readout cytokine most sensitive pyrogen detection was achieved. Accelerated detection with an increased temperature or propan‐2‐ol was possible already after about 3 h incubation. These findings can speed up assay time and expedite acceptance of the in vitro pyrogen testing with the monocyte activation test.