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COMPARISON OF ARCHITECT I 2000 FOR DETERMINATION OF CYCLOSPORINE WITH AXSYM
BACKGROUND: Cyclosporine has been shown effective drug in suppressing acute rejection in recipients of allograft organ transplants. METHODS: The cyclosporine concentration of 96 blood samples was determined using CMIA (chemiluminesecent microparticle immnoassay) Architect i 2000 and FPIA (fluorescen...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AVICENA
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558302/ https://www.ncbi.nlm.nih.gov/pubmed/23378685 http://dx.doi.org/10.5455/aim.2012.20.214-217 |
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author | Serdarevic, Nafija Zunic, Lejla |
author_facet | Serdarevic, Nafija Zunic, Lejla |
author_sort | Serdarevic, Nafija |
collection | PubMed |
description | BACKGROUND: Cyclosporine has been shown effective drug in suppressing acute rejection in recipients of allograft organ transplants. METHODS: The cyclosporine concentration of 96 blood samples was determined using CMIA (chemiluminesecent microparticle immnoassay) Architect i 2000 and FPIA (fluorescence polarization immunoassay) AxSYM Abbott diagnostic. All patients have transplantation of kidneys and were hospitalized at Department of Nephrology at the Clinical center of University of Sarajevo. The reference serum range of cyclosporine for kidney organ transplantation for maintenance lies between 50 and 150 ng/mL. The quality control, precision and accurancy of Architect i 2000 were assessed. RESULTS: The quality control was done using quality control serums for low (= 91 ng/mL), medium (= 328 ng/mL) and high (= 829 ng/mL). We have used commercial BIORAD controls and got reproducibility CV 5.83 % to 13 % for Architect i 2000. It was established that the main difference between Architect i 2000 and AxSYM and it was statistically significant for P < 0.05 according to Student t-test. Correlation coefficient was r = 0.903. CONCLUSION: The CMIA Architect assay has significant reduced cyclosporine metabolite interference relative to other immunoassay and is a convenient and sensitive automated method to measure cyclosporine in whole blood. |
format | Online Article Text |
id | pubmed-3558302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | AVICENA |
record_format | MEDLINE/PubMed |
spelling | pubmed-35583022013-02-01 COMPARISON OF ARCHITECT I 2000 FOR DETERMINATION OF CYCLOSPORINE WITH AXSYM Serdarevic, Nafija Zunic, Lejla Acta Inform Med Original Research BACKGROUND: Cyclosporine has been shown effective drug in suppressing acute rejection in recipients of allograft organ transplants. METHODS: The cyclosporine concentration of 96 blood samples was determined using CMIA (chemiluminesecent microparticle immnoassay) Architect i 2000 and FPIA (fluorescence polarization immunoassay) AxSYM Abbott diagnostic. All patients have transplantation of kidneys and were hospitalized at Department of Nephrology at the Clinical center of University of Sarajevo. The reference serum range of cyclosporine for kidney organ transplantation for maintenance lies between 50 and 150 ng/mL. The quality control, precision and accurancy of Architect i 2000 were assessed. RESULTS: The quality control was done using quality control serums for low (= 91 ng/mL), medium (= 328 ng/mL) and high (= 829 ng/mL). We have used commercial BIORAD controls and got reproducibility CV 5.83 % to 13 % for Architect i 2000. It was established that the main difference between Architect i 2000 and AxSYM and it was statistically significant for P < 0.05 according to Student t-test. Correlation coefficient was r = 0.903. CONCLUSION: The CMIA Architect assay has significant reduced cyclosporine metabolite interference relative to other immunoassay and is a convenient and sensitive automated method to measure cyclosporine in whole blood. AVICENA 2012-12 /pmc/articles/PMC3558302/ /pubmed/23378685 http://dx.doi.org/10.5455/aim.2012.20.214-217 Text en © 2012 AVICENA http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Serdarevic, Nafija Zunic, Lejla COMPARISON OF ARCHITECT I 2000 FOR DETERMINATION OF CYCLOSPORINE WITH AXSYM |
title | COMPARISON OF ARCHITECT I 2000 FOR DETERMINATION OF CYCLOSPORINE WITH AXSYM |
title_full | COMPARISON OF ARCHITECT I 2000 FOR DETERMINATION OF CYCLOSPORINE WITH AXSYM |
title_fullStr | COMPARISON OF ARCHITECT I 2000 FOR DETERMINATION OF CYCLOSPORINE WITH AXSYM |
title_full_unstemmed | COMPARISON OF ARCHITECT I 2000 FOR DETERMINATION OF CYCLOSPORINE WITH AXSYM |
title_short | COMPARISON OF ARCHITECT I 2000 FOR DETERMINATION OF CYCLOSPORINE WITH AXSYM |
title_sort | comparison of architect i 2000 for determination of cyclosporine with axsym |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558302/ https://www.ncbi.nlm.nih.gov/pubmed/23378685 http://dx.doi.org/10.5455/aim.2012.20.214-217 |
work_keys_str_mv | AT serdarevicnafija comparisonofarchitecti2000fordeterminationofcyclosporinewithaxsym AT zuniclejla comparisonofarchitecti2000fordeterminationofcyclosporinewithaxsym |