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10.1097/FTD.0b013e3181d46386

http://scihub22266oqcxt.onion/10.1097/FTD.0b013e3181d46386
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C5374220!5374220!20216110
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suck abstract from ncbi


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pmid20216110      Ther+Drug+Monit 2010 ; 32 (2): 145-51
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  • Multisite Analytical Evaluation of the Abbott ARCHITECT Cyclosporine Assay #MMPMID20216110
  • Wallemacq P; Maine G; Berg K; Rosiere T; Marquet P; Aimo G; Mengozzi G; Young J; Wonigert K; Krestchmer R; Wermuth B; Schmid R
  • Ther Drug Monit 2010[]; 32 (2): 145-51 PMID20216110show ga
  • The objective of this study was to evaluate the analytical performance of the Abbott ARCHITECT Cyclosporine (CsA) immunoassay in 7 clinical laboratories in comparison to liquid chromatography/tandem mass spectrometry (LC/MS/MS), Abbott TDx, Cobas Integra 800, and the Dade Dimension Xpand immunoassay. The ARCHITECT assay uses a whole blood specimen, a pretreatment step with organic reagents to precipitate proteins and extract the drug, followed by a 2-step automated immunoassay with magnetic microparticles coated with anti-CsA antibody and an acridinium-CsA tracer. Imprecision testing at the 7 evaluation sites gave a range of total % coefficient of variations of 7.5%?12.2% at 87.5 ng/mL, 6.6%?14.3% at 411 ng/mL, and 5.2%?10.7% at 916 ng/mL. The lower limit of quantification ranged from 12 to 20 ng/mL. Purified CsA metabolites AM1, AM1c, AM4N, AM9, and AM19 were tested in whole blood by the ARCHITECT assay and showed minimal cross-reactivity at all 7 sites. In particular, AM1 and AM9 cross-reactivity in the ARCHITECT assay, ranged from ?2.5% to 0.2% and ?0.8% to 2.2%, respectively, and was significantly lower than for the TDx assay, in which the values were 3.2% and 16.1%, respectively. Comparable testing of metabolites in the Dade Dimension Xpand assay at 2 evaluation sites showed cross-reactivity to AM4N (6.4% and 6.8%) and AM9 (2.6% and 3.6%) and testing on the Roche Integra 800 showed cross-reactivity to AM1c (2.4%), AM9 (10.7%), and AM19 (2.8%). Cyclosporine International Proficiency Testing Scheme samples, consisting of both pooled specimens from patients receiving CsA therapy as well as whole-blood specimens supplemented with CsA, were tested by the ARCHITECT assay at 6 sites and showed an average bias of ?24 to ?58 ng/mL versus LC/MSMS CsA and ?2 to ?37 ng/mL versus AxSYM CsA. Studies were performed with the ARCHITECT CsA assay on patient specimens with the following results: ARCHITECT CsA assay versus LC/MSMS, average bias of 31 ng/mL; ARCHITECT versus the Dade Dimension assay (4 sites), average biases of ?7 to ?228 ng/mL; ARCHITECT versus AxSYM and TDx, average biases of ?4 and ?53 ng/mL, respectively. Spearman correlation coefficients were ?0.89. The ARCHITECT CsA assay has significantly reduced CsA metabolite interference relative to other immunoassays and is a convenient and sensitive semiautomated method to measure CsA in whole blood.
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