CEDIA Tacrolimus Application Ortho Clinical Diagnostics VITROS 5600 Integrated System and VITROS 5,1 FS and 4600 Chemistry Systems
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1 Microgenics Corporation Part of Thermo Fisher Scientific CEDIA Tacrolimus Application Ortho Clinical Diagnostics VITROS 5600 Integrated System and VITROS 5,1 FS and 4600 Chemistry Systems Catalog No Intended for the Quantitative Determination of Tacrolimus in Human Whole Blood For In Vitro Diagnostic Use Only Intended Use The information provided in this application sheet is intended as a supplement to the package insert. Refer to the package insert for information on intended use, reagent storage, reagent preparation, specimen collection, specimen storage, quality control and additional performance data. Ordering Information Materials available from Microgenics: Item Catalog Number CEDIA Tacrolimus Assay Reagents CEDIA Tacrolimus Calibrator Kit More Diagnostics Rap/Tac/CsA Control Level More Diagnostics Rap/Tac/CsA Control Level More Diagnostics Rap/Tac/CsA Control Level To place an order or for technical service contact (North America): Microgenics Corporation, part of Thermo Fisher Scientific Fremont Boulevard, Fremont, CA USA U.S. Toll free: (800) / Tel: (510) U.S. Toll free fax: (800) / Fax: (510) EC REP Microgenics GmbH, Spitalhofstrasse 94D Passau Germany Tel: +49 (0) /Fax: +49 (0) Page 1 of APPS, Rev
2 ADD UDA Template A new UDA template containing protocol *2PT R1-S-R2 is available on ADD DRV5604 forward and should be used for this assay. Please order ADD DRV5604 from Ortho Clinical Diagnostics; it is not available from Microgenics. Reagent Pack Storage Reconstituted reagents are stable for 60 days at 2-8 C when stored in their original container or in UDxx reagent packs. Reconstituted reagents stored in UDxx reagent packs onboard the analyzer are stable for 3 days. Reagent life can be extended by storing the reagent packs in a refrigerator at 2-8 C between use. Depending on the anticipated reagent utilization, it is recommended that reconstituted reagents be split into multiple UDxx reagent packs so that each UDxx pack contains only sufficient reagents for 3 days. To split the reconstituted reagent among reagent packs of the same UDxx ID, follow the chart below: Number of packs EA (ml) in ED (ml) in Tests/pack UDxx/A UDxx/B Note: Once the individual UDxx pack number is selected for use during the protocol programming, it is the only UDxx pack number to use for this protocol. Special Reagent Packs for User Defined Assays (please order from Ortho Clinical Diagnostics; not available from Microgenics) UD01 Packs (Empty) 1 BOX/6PKS UD02 Packs (Empty) 1 BOX/6PKS UD03 Packs (Empty) 1 BOX/6PKS UD04 Packs (Empty) 1 BOX/6PKS UD05 Packs (Empty) 1 BOX/6PKS UD06 Packs (Empty) 1 BOX/6PKS UD07 Packs (Empty) 1 BOX/6PKS UD08 Packs (Empty) 1 BOX/6PKS UD09 Packs (Empty) 1 BOX/6PKS UD10 Packs (Empty) 1 BOX/6PKS Calibration Frequency It is recommended that recalibration occur after reagent pack change, after calibrator lot change, after performance of monthly instrument maintenance and as required following quality control procedure. Sample Preparation To maintain good repeatability of the timing of the pre-treatment steps, it is recommended that Tacrolimus samples not be prepared or run in batches greater than 10 samples at a time. Follow the CEDIA Tacrolimus Assay Sample Preparation as described in the package insert. CuveTip Exp time has been reduced to 10 minutes to increase priority and reduce delay in while running these samples. It is suggested that these samples be run when the MicroTip module is not heavily loaded. Page 2 of APPS, Rev 1
3 Ortho Clinical Diagnostics VITROS 5600, 5,1 FS, and 4600 System Parameters CEDIA Tacrolimus Assay Configure Assay Full Assay Name: _Tacrolimus Version Date: 9/15/2010 Short Assay Name: TAC Assay Model Type: 2 Point Rate Fluid Type: Wh Blood Template: *2Pt R1 S R2 Cal Model Type: Linear Calibrator Bottles: _2 Reagent Reps per Cal :_2 Reagent Lot Information Edit Dilution Parameters On Board Stability:_3_ Days Diluent: _None _ Standard Dilution Factor:_1.0_ Reagent Lot Num. Kit Lot Reflex Dilution:_OFF_ Dilution Factor: _1.0_ Shelf Exp. Date: Kit Exp Date Reduction Factor: _1.0 Edit Result Parameters Units: ng/ml Reference Interval: 5.0 to 20.0 Significant Digits: _3_ Precision Digits:_3_ Supplementary: 0.0 to _ User Adjusted Parameters Reportable Range: 2.0 to 30.0 Slope: 1.0 Intercept: 0.0 (More Assay Parms) Edit 2 Pt Rate Additional Parameters CuveTip Exp Time: 10_ Temp Sens :_No Initial Abs. Limits: 0.20_ to _2.70_ Second Abs. Limits: 0.20_ to 2.70_ Antigen Excess Factor: 9.0 Edit Protocol Parameters Step Volume Pack ID Seconds Wavelength 1. Reagent 160 ul UDxx /A 2. Incubation Sample 28 ul 4. Incubation Reagent 60.0 ul UDxx /B 6. Incubation Read 575 nm 8. Incubation Read 575 nm Page 3 of APPS, Rev 1
4 Ortho Clinical Diagnostics VITROS 5600, 5,1 FS and 4600 System Parameters, continued CEDIA Tacrolimus Assay Edit Calibration Parameters Bottle # Dil Factor Cal Rep Resp Range Calibrator Lot: Cal Kit lot 1 _ Cal value: _per cal lot 2 _ Cal Value: _per cal lot (More Cal Parms) Edit Linear or Logit/Log Additional Parameters Monotonicity: _Increase Max Resp High: _3.00 Min. Resp. High: _3.00 Cal Fit Goodness Limit: _0.990_ Max Resp. Low: _ 3.00 Min Resp. Low: _ 3.00 Edit Triple Read Parameters Reportable Conc. Triple Read Limit Reportable Min.: Critical Conc.: % Reportable Max.: % Comments: Please see important assay and analyzer notes on page 2. Page 4 of APPS, Rev 1
5 VITROS Precision Tests for within-run and total precision, evaluated with packaged reagents, controls and calibrators, yielded the following results (N=80/level): Controls Control 1 Control 2 Control Mean (ng/ml) Within-Run SD (ng/ml) Within-Run CV (%) Total SD (ng/ml) Total CV (%) ,1 FS/4600* Mean (ng/ml) Within-Run SD (ng/ml) Within-Run CV (%) Total SD (ng/ml) Total CV (%) VITROS Accuracy and Correlation Forty (40) whole blood samples were assayed using the CEDIA Tacrolimus Assay on the Ortho Clinical Diagnostics VITROS 5600, Ortho Clinical Diagnostics VITROS 5,1 FS and Hitachi 917 analyzers. A Deming s linear regression analysis yielded the following: 5600 = 1.02 (Hitachi 917) + 1.0, with a correlation coefficient of ,1 FS/4600* = 1.00(Hitachi 917) + 1.1, with a correlation coefficient of *Analytical processing hardware and software algorithms on the VITROS 4600 Chemistry System are desinged to the same specifications as those applied to the VITROS 5,1 Chemistry System. Assay performance on the VITROS 4600 System has been demonstrated to be comparable to that on the VITROS 5,1 FS System. All performance characteristics for the VITROS 5,1 FS System are therefore applicable to the VITROS 4600 System Thermo Fisher Scientific, Inc. All rights reserved. VITROS is a trademark of Ortho Clinical Diagnostics. All other trademarks are the property of Thermo Fisher Scientific and its subsidiaries. Page 5 of APPS, Rev 1
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