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Background Information
COBI-CD
cobas e 411
Revision history
Order numbers
Edition notice
Intended use
Copyrights
Trademarks
Manual
Template
Version
Version
1.0
3.0
Language
Order number
English
French
German
Italian
Portuguese
Spanish
Instrument approvals
The cobas e 411 analyzer meets the requirements stated in Directive 98/79/EC of the
European Parliament and the Council of the European Union (EU) on in vitro
diagnostic medical devices. Furthermore, the cobas e 411 analyzer is manufactured
and tested according to International Standard IEC 61010-1, 2nd edition, Safety
requirements for electrical equipment for measurement, control and laboratory use,
Part 1: General requirements. This International Standard is equivalent to the
national standards Underwriters Laboratories (UL) 61010-1 2nd edition for the USA,
and CAN/CSA C22.2 No. 61010-1:2004 for Canada. Compliance is demonstrated by
the following marks:
Issued by Underwriters Laboratories, Inc. (UL) for Canada and the USA.
US
The purchase of this product allows the purchaser to use it solely for detection by ECL
Technology for human in vitro diagnostic uses. No general patent or other license of
any kind other than this specific right of use from purchase is granted hereby. This
product may not be used by purchaser to conduct life science research and/or
Roche Diagnostics
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cobas e 411
Contact addresses
Manufacturer
Authorized Representative
Roche Diagnostics
COBI-CD Version 1.0
cobas e 411
Conventions used
Visual cues are used to help you quickly locate and interpret information in this
manual. This section explains formatting conventions used in this manual.
Symbols
Used for
Procedural step
List item
Cross-reference
Call up of screen
Note
Caution
Warning
Laser Radiation
Biohazard
Abbreviations
Definition
ANSI
CBT
CCITT
CE
Conformit Europenne
CLAS 2
CLIA
COBI-CD
CSA
Roche Diagnostics
4
cobas e 411
Abbreviation
Definition
dBA
DIL
diluent
EC
European Community
ECL
electrochemiluminescence
EMC
electromagnetic compatibility
EN
european standard
FIFO
HCFA
IEC
IS
IVD
KVA
LDL
LIS
LLD
MSDS
NCCLS
PC/CC
ProCell/CleanCell
QC
quality control
REF
SD
standard deviation
S/R
sample/reagent
SVGA
TPA
tripropylamine
UL
Roche Diagnostics
COBI-CD Version 1.0
cobas e 411
Abbreviation
Definition
VDE
Roche Diagnostics
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cobas e 411
Table of contents
Revision history
Contact addresses
Conventions used
Table of contents
2
3
4
7
Quality control
5 Quality control concept
Mechanical theory
Part D
D-5
Part A
Index
Part E
1 Mechanical theory
Introduction
Preparative operations
Test protocols
Assay sequence
Workflow and throughput
Operation flow in analysis
Detailed assay sequence
Dilution steps
Pretreatment steps
Analyzer status conditions
Measurement technology
A-5
A-6
A-7
A-8
A-11
A-13
A-14
A-21
A-22
A-23
Index
E-3
Part B
2 ECL technology
Test principles
B-5
B-10
Part C
3 Test principles
Test principles
C-5
4 Reagent concept
Introduction
Data transfer media
Data transfer rules
Reagents for cobas e 411 analyzer tests
Product labeling
Data links
Calibration
Master calibration
Lot calibration
Reagent pack calibration
Difference between lot and reagent calibration
Calibration procedures
Calibration stability
Calibration validation
Calibration assessment
Calibration of quantitative assays
Calibration of qualitative assays
Result calculation for qualitative assays
C-15
C-15
C-16
C-16
C-18
C-19
C-21
C-22
C-23
C-23
C-24
C-25
C-26
C-26
C-27
C-30
C-33
C-33
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Roche Diagnostics
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Mechanical theory
cobas e 411
1 Mechanical theory
Table of contents
Mechanical theory
This chapter provides an overview of the mechanical theory of the cobas e 411
analyzer. The assay sequence and operational flow are described, as well as dilution
steps.
In this chapter
Chapter
Introduction .................................................................................................................. 31
Preparative operations .................................................................................................. 32
Test protocols ................................................................................................................. 33
Assay sequence ............................................................................................................... 34
Run operation .......................................................................................................... 34
First incubation at 37 C ................................................................................... 34
Pipetting of additional reagent ........................................................................ 34
Second incubation at 37 C ............................................................................... 35
Pipetting of additional reagent (pretreatment assays) .................................... 35
Third incubation at 37 C (pretreatment assays) ............................................. 35
Aspirating the reaction mixture ....................................................................... 35
Cleaning the measuring cell ............................................................................. 35
Finalization ........................................................................................................ 35
Workflow and throughput ............................................................................................ 37
Effects of test combinations on throughput ......................................................... 37
9-minute tests only ............................................................................................ 37
18-minute tests only .......................................................................................... 37
Combination of 9- and 18-minute tests ........................................................... 37
27-minute tests only .......................................................................................... 38
Combination of 18- and 27-minute tests ......................................................... 38
Typical test durations .............................................................................................. 38
Operation flow in analysis ............................................................................................ 39
Detailed assay sequence ................................................................................................ 40
Preoperational steps ............................................................................................... 40
Dispensation of reagent 1, reagent 2, and sample (disk system) .......................... 41
Dispensation of reagent 1, reagent 2, and sample (rack system) .......................... 43
First incubation ....................................................................................................... 44
Microbead preparation ........................................................................................... 45
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Table of contents
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1 Mechanical theory
Introduction
Introduction
The cobas e 411 analyzer automates the immunoassay reactions utilizing
electrochemiluminescence (ECL). The individual test steps and how the system
performs the necessary procedures are described here.
e For information on ECL immunoassay reaction methods, see Chapter 2 ECL technology.
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Preparative operations
Preparative operations
Once the analyzer is switched on, the initialization process starts. During
initialization, the mechanisms are reset to their home positions.
e Figure A-1 shows the run preparation process for the cobas e 411 hardware.
Start
First order?
Were reagents
exchanged?
No
Yes
Counting
AssayTips and
AssayCups
barcode
Volume
check for
ProCell and
Have 90 or more
minutes passed since
CleanCell
No
Clearing the
incubator and
the AssayTip
and AssayCup
Yes
trays
Microbeads mixing
Is the inventory
sufficient?
Short
(item)
45-xx-01
Enough
Preparation cycle
Scheduling
First sipping
First pipetting
Resume cycle
Pipetting continues
Sipping continues
Figure A-1
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Test protocols
Test protocols
There are 28 test protocols that can be used on the analyzer. These protocols are
predefined by Roche Diagnostics for each test and cannot be changed by the operator.
No.
0
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
...
63
Step 0
Inc 0
R0 S
R0 S
R0 S
R0 S
R0 S -> DL1 R0
R0 S -> DL1 R0
R0 S -> DL1 R0
R0 S -> DL1 R0
PS S
PS S
PS S
PS S
RM S
RM S
RM S
RM S
RM S -> DL1 RM
RM S -> DL1 RM
RM S -> DL1 RM
RM S -> DL1 RM
i0
i0
i0
i0
i0
i0
i0
i0
i0
i0
i0
i0
PS1 PS2 S
PS1 PS2 S
i0
i0
Table A-1
Step 1
Inc 1
B R1 R2 S
B R1 S
R1 R2 S
R1 S
B R1 R2 DL
B R1 DL
R1 R2 DL
R1 DL
B R1 R2 DL
B R1 DL
R1 R2 DL
R1 DL
B R1 R2
B R1
R1 R2
R1
B R1 R2 DL
B R1 DL
R1 R2 DL
R1 DL
B R1 R2 DL
B R1 DL
R1 R2 DL
R1 DL
R1 R1
R1 R2
R2 R2
R1 R2
R1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
i1
(Reserve)
Step 2
Inc 2
R2
B
B R2
i2
i2
i2
R2
B
B R2
i2
i2
i2
R2
B
B R2
i2
i2
i2
R2
B
B R2
i2
i2
i2
R2
B
B R2
i2
i2
i2
R2
B
B R2
i2
i2
i2
B
B R2
i2
i2
Det.
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D
D'
D'
D'
D'
D'
D'
D'
D'
Test protocols
R1 = Reagent 1
R2 = Reagent 2
B = Beads (microbeads in the assay reagent pack)
RO = Universal diluent (special reagent pack)
PS = Pretreatment solution (for assays such as B12, Folat, and Anti-HBc)
RM = Pretreatment for IgM
S = Sample/calibrator/control
DL = Diluted sample
D = Detection with magnet drive
D' = Detection without magnet drive
I = Incubation
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Assay sequence
Assay sequence
An immunological ECL test is made up of various pipetting steps, at least one
incubation period and a measurement step. Generally at least three test components
(sample, reagent and microbeads) are pipetted into an AssayCup. After the
appropriate incubation period, the reaction mixture is aspirated into the measuring
cell where the measurement process takes place. Each of the required pipetting cycles
is performed within a defined period (42 seconds).
The number of pipetting steps, as well as the make up of the reaction mixture are
dependent on the test method (1 or 2 step test). For some methods, predilution with
diluent and/or pretreatment with a special reagent is necessary. Thus the number of
pipetting steps is increased.
The following steps apply in principle to all methods. The sequence of the individual
processes differ from test to test.
Run operation
After the appropriate test selections for patient samples are made in the software,
operation is started according to the predetermined test protocol for each assay
selected. Initially, at least one reagent (R1 or R2) and the sample or microbeads (M)
are aspirated one after another by the S/R probe. After each aspiration, the outside of
the S/R probe AssayTip is cleaned at the rinse station. The sample and reagents are
dispensed into a new AssayCup and the AssayTip is ejected into the solid waste tray.
For some tests that require sample dilution or pretreatment, diluent or pretreatment
reagent is pipetted together with sample into an AssayCup. An aliquot of the diluted/
pretreated sample is then dispensed with reagent into a second AssayCup. Therefore,
certain tests with predilution/pretreatment may require two or more AssayCups.
e For more information on dilution, see Dilution steps on page A-21.
First incubation at 37 C
The incubation times are 4.5 or 9 minutes long, depending on the test. Some tests
require only two incubation periods, whereas tests that include pretreatment can
require three incubation periods. During the incubation step(s) the immune complex
products are formed.
Pipetting of additional reagent
Some assays (usually those with more than one incubation step) require additional
reagent pipetting. As in the initial reagent pipetting step, a new AssayTip is picked up
before reagent aspiration. The S/R probe AssayTip is washed at the rinse station after
each liquid aspiration. The liquid is then dispensed into the corresponding AssayCup
where the sample and other liquids were dispensed in the first pipetting step. The
probe rises while dispensing the reaction mixture back into the AssayCup, thereby
mixing the solution and accelerating the reaction in the AssayCup. The AssayTip is
discarded into the solid waste tray when pipetting is complete.
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Assay sequence
Second incubation at 37 C
If necessary, a second incubation step (4.5 or 9 minutes) occurs.
If using a pretreatment assay, the second incubation is similar to that described above
for First Incubation at 37 C.
Pipetting of additional reagent (pretreatment assays)
For pretreatment assays, reagent pipetting is similar to that described above for
Pipetting of additional reagent occurs.
Third incubation at 37 C (pretreatment assays)
If necessary, a third incubation step (9 minutes) occurs for pretreatment assays.
Aspirating the reaction mixture
In this process, the sipper probe first aspirates ProCell (tripropylamine solution,
TPA) to prepare the measuring cell. Then, the sipper probe aspirates the reaction
mixture from the AssayCup and transfers it to the measuring cell. The sipper probe is
washed at the rinse station and ProCell is aspirated again to rinse away the unbound
constituents of reagent and sample. Next, the ECL reaction in the measuring cell
occurs.
Cleaning the measuring cell
Once the measurement is complete, the measuring cell is cleaned with CleanCell and
prepared for a new measurement process.
It takes 42 seconds (one pipetting cycle) from the aspiration of the reaction mixture
by the sipper probe until the measuring cell is filled with ProCell and ready for the
next sample.
Finalization
Thirty minutes after documentation of the last result, the sipper pipetter flushes
system water through the sipper probe, and then fills the measuring cell with ProCell
before the analyzer returns to Standby mode.
After this procedure, every 30 minutes the waste pump of the S/R rinse station runs
for 2 seconds (waste consumption approximately 12 mL). This procedure stops if the
operation switch is switched off.
e Figure A-2 shows the finalization process for the cobas e 411 hardware.
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Assay sequence
Last sipping
Finalization
Pipetter prime
Sipper prime
Standby
Figure A-2
Finalization process
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Workflow and throughput
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9 minutes
Thyroid
18 minutes
27 minutes
Fertility
hCG
Cardiac
CK-MB, Troponin T,
Myoglobin
CK-MB, Troponin T,
Myoglobin, Digoxin,
Digitoxin, proBNP
Oncology
Infectious disease
HBsAg, anti-HBs,
anti-HBc IgM(a)
anti-HAV IgM *
Anti-HAV, Anti, HBe,
HBeAg, HIV Antigen,
HIV combi
anti-HBc
Anemia
Ferritin
Diabetes
Bone
Other
IgE
Table A-2
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Operation flow in analysis
Pre-start inspection
Switch on
(Initialization and Standby)
Check alarm button
Pre-routine operation
Routine operation
Calibration and control
Rerun
Assigned
-----------------------------------------------------Results
Sampling Stop
(Finalization, Stop, and Standby)
Maintenance
Switch off
(a)
Figure A-3
Operational process
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Preoperational steps
When Start is pressed from Standby mode, the following preoperational steps occur:
1. The analyzer resets all mechanisms to their respective home positions and accesses
the data disk. Next, the S/R pipetter primes the S/R probe.
2. The gripper checks for an AssayTip in position number 1 of the AssayTip trays. If
this position is empty, the gripper remembers where it last left off and checks that
position. If this position is empty, the gripper considers the whole tray empty and
the Inventory screen is updated accordingly.
If the analyzer is in S. Stop, the gripper remembers where it last left off and checks for an AssayTip
in that position.
3. During the AssayTip check, the S/R probe is checked for the presence of an
AssayTip. The probe moves to the AssayTip eject station and performs the
movements to eject an AssayTip. If an AssayTip is present, it is ejected.
4. After the AssayTip check is complete, the AssayCups are checked in the same
manner. During the cup check, the analyzer finishes priming the probes.
5. Next, the gripper checks the last three of the five positions on the pipetting
station. If an AssayCup is present, the analyzer goes through the following cup
disposal sequence:
a) The gripper places an AssayTip in position 1 of the pipetting station.
b) The S/R probe picks up the AssayTip, descends into the AssayCup, and
aspirates any liquid.
c) The AssayCup is discarded, while the S/R probe moves to the rinse station and
dispenses any aspirated liquid.
d) The AssayTip is washed and then discarded.
6. The gripper moves to the incubator, where it checks all 32 incubator positions. If
an AssayCup is present, the gripper moves the AssayCup to position 5 on the
pipetting station and uses the same procedure listed in step 5 to discard the
AssayCup.
7. The S/R probe AssayTip is discarded after all the incubator positions are checked.
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Detailed assay sequence
R1 aspiration position
Figure A-4
R2 aspiration position
5. The S/R probe moves from its Standby position to the R1 aspiration position.
While activating liquid level detection, the probe descends until it is 2 mm below
the reagent surface and aspirates 50 L of R1.
While the probe is aspirating R1, the gripper puts another AssayTip in position 1
of the pipetting station.
6. If the S/R probe does not detect liquid as it descends, no reagent aspiration can
occur, and an alarm is generated.
7. After R1 aspiration, the S/R probe rises and moves to the rinse station. To prevent
the aspirated R1 from coming into contact with the water in the rinse station, the
probe aspirates 10 L of air. The rinse station externally washes the AssayTip.
8. During step 7, the reagent rotor rotates until the TSH reagent pack is in the R2
position.
9. The S/R probe moves from the rinse station to the R2 aspiration position while
aspirating another 10 L of air. This air layer prevents R1 from mixing with R2.
While activating liquid level detection, the probe descends until it is 2 mm below
the reagent surface and aspirates 50 L of R2. While the probe is aspirating R2, the
gripper moves an AssayCup to position 5 of the pipetting station.
e See Figure A-4 for the location of the R2 aspiration position.
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10. Upon completion of R2 aspiration, the S/R probe rises and moves to the rinse
station. To prevent the aspirated R2 from coming into contact with the water in
the rinse station, the probe aspirates another 10 L of air. The rinse station
externally washes the AssayTip.
11. After R2 aspiration, the reagent rotor rotates until the TSH reagent pack is at the
cap open/close mechanism. The mechanism moves out and closes the caps.
12. The S/R probe moves from the rinse station to the sampling position while
aspirating another 10 L of air. While activating liquid level detection, the probe
descends until it is 2 mm below the sample surface and aspirates 50 L of sample.
During sample aspiration, clot detection is activated.
A
A
Sampling position
Figure A-5
13. The S/R probe moves from the sampling position to position 5 of the pipetting
station. The probe descends until the tip reaches 2 mm below the calculated level
of the reaction mixture surface and dispenses the sample, R2, and R1. The probe's
downward displacement is determined by calculating the volume of the reaction
mixture for the sample and using downward-displacement tables in the software.
The probe does not rise during dispensation.
e See Figure A-5 for the location of the sampling position for disk systems.
14. After dispensation, the S/R probe moves to the tip eject position and ejects the
AssayTip.
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Detailed assay sequence
components section in the Analyzer components chapter of the cobas e 411 analyzer
Operators Manual.
3. As the rack incrementally moves on the B-Line, the rack barcode reader scans all
five rack positions and rack ID. When scanning is complete, position 1 of the rack
is in the sampling position.
4. The S/R probe moves to position 1 of the pipetting station, descends to obtain the
AssayTip, rises, and returns to its Standby position.
5. During this time, the reagent rotor rotates until the TSH reagent pack is at the
cap-open/close mechanism. The mechanism moves forward and opens the caps
on the reagent pack. The disk rotates again to move the TSH reagent to the R1
position.
e See Figure A-4 on page A-15 for details of the R1 and R2 aspiration positions.
6. The S/R probe moves from its Standby position to the R1 aspiration position.
While activating liquid level detection, the probe descends until it is 2 mm below
the surface of the reagent and aspirates 50 L of R1.
e See Figure A-4 for the location of the R1 aspiration position.
While aspirating R1, the gripper puts another AssayTip in position 1 of the
pipetting station.
7. If the S/R probe does not detect liquid during descent, no reagent aspiration can
occur, an alarm is generated.
8. After R1 aspiration, the S/R probe rises and moves to the rinse station. To prevent
the aspirated R1 from contacting the water in the rinse station, the probe aspirates
10 L of air. The rinse station externally washes the AssayTip.
9. During step 8, the reagent rotor rotates until the TSH reagent pack is in the R2
position.
10. The S/R probe moves from the rinse station to the R2 position while aspirating
another 10 L of air. This air layer prevents R1 from mixing with R2. While
activating liquid level detection, the probe descends until it is 2 mm below the
surface of the reagent and aspirates 50 L of R2. While aspirating R2 the gripper
moves an AssayCup to position 5 of the pipetting station.
e See Figure A-4 for the location of the R2 aspiration position.
11. Upon completion of R2 aspiration, the S/R probe rises and moves to the rinse
station. To prevent the aspirated R2 from coming into contact with the water in
the rinse station, the probe aspirates another 10 L of air. The rinse station
externally washes the AssayTip.
12. After R2 aspiration, the reagent rotor rotates until the TSH reagent pack is at the
cap-open/close mechanism. The mechanism moves out and closes the caps.
13. The S/R probe moves from the rinse station to the sampling position while
aspirating another 10 L of air. While activating liquid level detection, the probe
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Sampling position
Figure A-6
14. The S/R probe moves from the sampling position to position 5 of the pipetting
station. The probe descends until the tip reaches 2 mm below where the calculated
level of the reaction mixture surface should be and dispenses the sample, R2, and
R1. The probe's downward displacement is determined by calculating the volume
of the reaction mixture for the sample and using downward-displacement tables
in the software. The probe does not rise during dispensation.
e See Figure A-6 for the location of the sampling position for rack systems.
15. After dispensation, the S/R probe moves to the tip eject position and ejects the
AssayTip.
First incubation
1. The gripper picks and transports the cup containing the reaction mixture from
the pipetting station to the incubator.
2. The cup is incubated at 37 C for 9 minutes.
3. During incubation, the analyzer continues to perform operations for other test(s)
or sample(s), if necessary.
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Detailed assay sequence
Microbead preparation
Before the first incubation is completed, the TSH microbeads are mixed to facilitate
their aspiration and dispensation.
1. The reagent rotor rotates until the TSH reagent pack is at the reagent cap-open/
close mechanism. The mechanism moves out and opens the cap. The disk moves
the reagent pack to the mixing position.
2. The mixer moves over the reagent rotor and descends into the microbeads to 1.4
mm above the bottom of the bottle.
3. The mixer stirs the microbeads to obtain a homogeneous suspension.
4. During the mixing, the gripper obtains a fresh AssayTip and transports it to
position 2 of the pipetting station.
5. When mixing is complete, the mixer rises and returns to the rinse station where it
descends and rotates in the rinse station for washing.
6. At the same time, the reagent rotor rotates the TSH reagent pack to the microbead
pipetting position.
Second incubation
1. The gripper picks the cup containing the mixed reaction mixture and returns it to
the incubator.
2. The cup is incubated at 37 C for 9 minutes.
3. During incubation, the analyzer continues to perform operations for other test(s)
or sample(s), if necessary.
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Measurement process
1. The gripper picks and transports the cup that has completed its second incubation
from the incubator to the aspiration station.
2. The sipper probe moves to the aspiration station and descends into the cup.
3. When the sipper probe detects the reaction mixture in the cup, it aspirates 150 L.
4. After aspiration, the sipper probe rises, aspirates 10 L of air, and moves to the
sipper rinse station to descend for rinsing.
5. The gripper grasps the cup from the aspiration station, transports it to the cup
disposal opening, and discards the cup.
6. The sipper probe is rinsed.
7. The sipper probe rises and moves to the ProCell position, descends into the bottle
and aspirates ProCell in a set aspiration/dispensation sequence. The immune
complexes are magnetically captured on the working electrode, but unbound
reagent and sample are washed away by ProCell.
e For additional information on the measuring cell, see Chapter 2 ECL technology.
principles.
9. The sipper probe rises and moves to the CleanCell position and aspirates 20 L of
air. The probe then descends into the CleanCell bottle and aspirates reagent. This
procedure is repeated eight times. The alternatating flow of air and cleaning
solution washes the measuring cell. During this washing process, a voltage is
applied between the electrodes, which aids in the cleaning process.
10. The sipper probe moves to the sipper rinse station, aspirates 20 L of air, and
descends into the rinse station for washing.
11. Finally, the sipper probe rises and moves to the ProCell bottle. The probe
descends into the bottle and aspirates 500 L of ProCell. Next, the probe aspirates
90 L of ProCell and moves to the rinse station. At the rinse station, the probe
dispenses 35 L to flush the probe and prepare it for the next sample. During the
aspirations of the ProCell, a sequence of voltages is applied three times to prepare
the electrodes for the next measurement.
One cycle of the measurement process consumes approximately 2 mL each of ProCell
and CleanCell.
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Dilution steps
While the analyzer is in operation, the solid waste tray periodically shakes for
1.5 seconds.
While the analyzer is in Standby, the reagent rotor turns 90 every 30 minutes.
While the analyzer is in Standby, the rinse stations for the S/R probe and sipper
probe are switched on for 2 seconds every 30 minutes.
Microbeads undergo a long mix when starting from Standby and then every 90
minutes until pipetting starts.
Microbeads undergo a short mix and then a short mix every 60 minutes for each
reagent pack.
Dilution steps
The following is a description of how an assay with a dilution is performed, including
the number of AssayTips and AssayCups used in the process.
Assay with one-step dilution
(1:2, 1:5, 1:10) AssayTip 1 ~ diluent (wash)* + sample
AssayTip 1
AssayTip 2
AssayTip 3
AssayCup 1
AssayCup 2 (1st incubation)
AssayCup 2 (2nd incubation)
Detection
Table A-3
Dilution steps for an assay with one-step dilution (1:2, 1:5, 1:10)
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Pretreatment steps
AssayTip 2
AssayTip 3
AssayTip 4
AssayTip 1
AssayCup 1
R1 (wash)* + R2 (wash)*
+ diluted sample from AssayCup 2
AssayCup 3
(1st incubation)
M (wash)*
AssayCup 3
(2nd incubation)
Diluent (wash)*
+ diluted sample from AssayCup 1
AssayCup 2
Detection
Table A-4
Pretreatment steps
In certain test protocols, pretreatment reagent is added before R1, R2, or M, as
summarized in the following table.
Pretreatment assay
AssayTip 1
AssayCup 1
(1st incubation)
AssayTip 2
AssayCup 1
(2nd incubation)
AssayTip 3
M (wash)* + R2
+ reaction mixture in AssayCup 1
AssayCup 1
(3rd incubation)
Detection
Table A-5
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1 Mechanical theory
Analyzer status conditions
BC card scan
This status is seen when a barcode card scan is initiated from the Control Definition
or Calibration Data screens.
Finalization
This is the status of the analyzer when it is between the status conditions S. Stop and
Standby.
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Finalization maint.
This status occurs when Finalization Maintenance is initiated from the Maintenance
screen.
Initialization
This status is seen when the cobas e 411 analyzer is switched on, or when Start is
pressed from Standby.
M. Cell preparation
Measuring cell (M. Cell) preparation occurs when this function is initiated from the
Maintenance screen.
Operation
This is the status during which the cobas e 411 analyzer performs its routine
operations.
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1 Mechanical theory
Analyzer status conditions
Rack clear
Rack clear status occurs when the corresponding function is initiated from the
Maintenance screen. This function clears any remaining racks on the A-, B- or CLines.
Reagent scan
This status is seen when a reagent scan is initiated from the Inventory screen.
S. Stop-S. Scan
The analyzer is in S. Stop and a sample scan is requested from the Status screen, or S is
pressed while the analyzer is in S. Stop.
Sample scan
This status occurs when a sample scan is initiated from the Status screen.
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Standby
The analyzer is not performing any operations.
Stop
This status occurs when Stop is pressed or when a Stop alarm condition exists. If an
alarm exists, take the appropriate measures to resolve the problem.
System reset
A system reset is initiated from the Maintenance screen.
Roche Diagnostics
A-26
Measurement technology
cobas e 411
2 ECL technology
Table of contents
ECL technology
In this chapter
Chapter
Roche Diagnostics
COBI-CD Version 1.0
B-3
cobas e 411
2 ECL technology
Table of contents
Roche Diagnostics
COBI-CD Version 1.0
B-4
cobas e 411
2 ECL technology
ECL measuring principles
The chemiluminescent reactions that lead to the emission of light from the
ruthenium complex are triggered electrically, rather than chemically. This is achieved
by applying a voltage to the immunological complexes (including the ruthenium
complex) that are attached to streptavidin-coated microbeads. The advantage of
electrically initiating the chemiluminescent reaction is that the entire reaction can be
precisely controlled.
O
O
N
N
Ru
N
2+
N
N
Figure B-1
Roche Diagnostics
COBI-CD Version 1.0
B-5
2 ECL technology
cobas e 411
Photon
Diffusion
Magnetic
microbead
TPA
-H+
TPA+
TPA
ee-
Figure B-2
Electrode
to Figure B-2.
In turn, the ruthenium complex also releases an electron at the surface of the
electrode thus oxidizing to form the Ru(bpy)33+ cation. This ruthenium cation is the
second reaction component for the following chemiluminescent reaction with the
TPA radical.
e For further information on the ECL reaction at the electrode surface, refer to Figure B-3.
Roche Diagnostics
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cobas e 411
2 ECL technology
ECL measuring principles
Electrode
surface
TPA+
e-
-H+
TPA
Ru(bpy) 3+
3
TPA
e-
e2+
Ru(bpy)3
ground
state
Ru(bpy)3
excited
state
2+
Photon
(620 nm)
Figure B-3
TPAo and Ru(bpy)33+ react with one another, whereby Ru(bpy)33+ is reduced to
Ru(bpy)32+ and at the same time forms an excited state through energy transfer. This
excited state is unstable and decays, with emission of a photon at 620 nm to its
original state. The reaction cycle then starts again. The tripropylamine radical reduces
to by-products that do not affect the chemiluminescence process. TPA is used up and
therefore must be present in excess. The reaction is controlled by diffusion of the TPA
and the amount of ruthenium complex present. As TPA in the electrical field is
depleted, the signal strength (light) is slowly reduced once the maximum is reached.
Although TPA is depleted during measurement, the ruthenium ground-state
complex is continually regenerated. This means that the ruthenium complex can
perform many light-generating cycles during the measurement process. This has an
inherent amplification effect that contributes to the sensitivity of the technology.
Many photons can be created from one antigen-antibody complex.
Roche Diagnostics
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2 ECL technology
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1500
350,000
1200
300,000
900
250,000
200,000
600
150,000
300
100,000
50,000
0
0.00
Figure B-4
0
0.20
0.40
0.60
0.80
1.00
1.20
Time [s]
The dotted line indicates the voltage at the electrode used to generate the ECL signal.
The solid line is the actual light output measured by the photomultiplier detector.
Roche Diagnostics
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cobas e 411
2 ECL technology
ECL measuring principles
F
G
H
I
J
O
Screw
Counter electrode
Optical window
Distance washer
Top cell
Cell gap
Gasket
O-ring
Diaphram
Reference electrode
Outlet fitting
Working electrode
Inlet fitting
Cell body
M Movable magnet
Figure B-5
The temperature is maintained at 28C . Three operating steps are performed in the
measuring cell:
o
Bound/free separation
Using a magnet, the streptavidin microbeads that are coated with antigenantibody complexes are uniformly deposited on the working electrode. A system
buffer (ProCell) is used to wash the particles on the working electrode and to flush
out the excess reagent and sample materials from the measuring cell.
ECL reaction
To initiate the ECL reaction, the magnet is removed and a voltage is applied to the
electrode. The microbeads that are coated with antigen-antibody complexes are
deposited onto the electrode. The light emission is measured with a
Roche Diagnostics
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2 ECL technology
cobas e 411
photomultiplier. The system then uses the corresponding signals for the
calculation of results.
o
F
G
A
E
B
Photomultiplier
antibody complex
C
Counter electrode
Flow channel
Magnet
Working electrode
Figure B-6
The extremely stable nonisotopic label means that you can use convenient liquid
reagents.
The applicability of the technique to detect all analytes provides a solid platform
for menu expansion.
Roche Diagnostics
B-10
Test principles
cobas e 411
3 Test principles
Table of contents
Test principles
This chapter provides an overview of the immunology test principles used by the
cobas e 411 analyzer.
In this chapter
Chapter
Roche Diagnostics
COBI-CD Version 1.0
C-3
cobas e 411
3 Test principles
Table of contents
Roche Diagnostics
COBI-CD Version 1.0
C-4
cobas e 411
3 Test principles
Test principles
Test principles
Three test principles are available on the cobas e 411 analyzer:
o
Bridging principle to
determine IgG and IgM
Analyte
ECL label
Antibody
Surface of paramagnetic microbead
Streptavidin-biotin
binding
Figure C-1
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3 Test principles
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Test principles
Competitive principle
This principle is applied to analytes of low molecular weight, such as free
triiodothyronine (FT3).
e Refer to Figure C-2 on page C-7 for an illustration of the competitive principle.
In the first step, sample and a specific anti-T3 antibody labeled with a ruthenium
complex are combined in an assay cup.
After the second incubation, the reaction mixture containing the immune
complexes is transported into the measuring cell. The immune complexes are
magnetically captured on the working electrode, but unbound reagent and sample
are washed away by ProCell.
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3 Test principles
Test principles
COMPETITIVE PRINCIPLE
FIRST REACTION
SECOND REACTION
LIGHT REACTION
Signal (light)
TPA
ECL
Concentration
Antigen
Figure C-2
antibody
Biotinylated
Streptavidin-coated
antigen
microbead
TPA Tripropylamine
Competitive principle
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3 Test principles
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Test principles
Sandwich principle
The sandwich principle is applied to higher molecular weight analytes, such as
thyroid-stimulating hormone (TSH).
e Refer to Figure C-3 on page C-9 for an illustration of the sandwich principle.
In the first step, the patient sample is combined in an AssayCup with a reagent
containing biotinylated TSH antibody and a ruthenium-labeled TSH-specific
antibody in an assay cup. During a 9-minute incubation step, antibodies capture
the TSH present in the sample.
After the second incubation, the reaction mixture containing the immune
complexes is transported into the measuring cell; the immune complexes are
magnetically entrapped on the working electrode, and the unbound reagent and
sample are washed away by ProCell.
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3 Test principles
Test principles
SANDWICH PRINCIPLE
FIRST REACTION
Serum constituents
SECOND REACTION
LIGHT REACTION
Signal (light)
TPA
ECL
Concentration
Antigen
Figure C-3
antibody
Biotinylated
Streptavidin-coated
antibody
microbead
TPA Tripropylamine
Sandwich principle
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3 Test principles
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Test principles
Bridging principle
The bridging principle is similar to the sandwich principle, except that the assay is
designed to detect antibodies (for example, IgG, IgM, and IgA), not antigens. This is
accomplished by including biotinylated and ruthenium-labeled antigens in the
reagents for which the targeted antibody has affinity.
e Refer to Figure C-4 on page C-11 for an illustration of the bridging principle.
In the first step, serum antibodies bind with the biotinylated and rutheniumlabeled antigens to form an immune complex.
After the second incubation, the reaction mixture containing the immune
complexes is transported into the measuring cell; the immune complexes are
magnetically entrapped on the working electrode, and the unbound reagent and
sample are washed away by ProCell.
In the ECL reaction, the conjugate is a ruthenium based derivative and the
chemiluminescent reaction is electrically stimulated to produce light. The amount
of light produced is directly proportional to the amount of analyte in the sample.
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3 Test principles
Test principles
BRIDGING PRINCIPLE
FIRST REACTION
Serum
constituents
SECOND REACTION
LIGHT REACTION
Signal (light)
TPA
ECL
Concentration
Figure C-4
Serum
antibodies
TPA Tripropylamine
Streptavidin-coated
microbeads
Bridging principle
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3 Test principles
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Test principles
Roche Diagnostics
C-12
cobas e 411
4 Reagent concept
Table of contents
Reagent concept
This chapter provides an overview of all types of reagents used on the cobas e 411
analyzer system. It describes the various reagent containers used, and also provides an
overview of the system-related reagent management, explaining processes such as
how the system registers new reagents, and how it monitors reagent consumption.
In this chapter
Chapter
Introduction ................................................................................................................. 15
Data transfer media ....................................................................................................... 15
Data transfer rules ......................................................................................................... 16
Reagents for cobas e 411 analyzer tests ........................................................................ 16
Diluents .................................................................................................................... 16
System reagents ........................................................................................................ 17
Calibrators and controls .......................................................................................... 17
Reagent packs .......................................................................................................... 17
Product labeling ............................................................................................................ 18
Data links ...................................................................................................................... 19
Calibration .................................................................................................................... 21
Master calibration ......................................................................................................... 22
Lot calibration ............................................................................................................... 23
Reagent pack calibration ............................................................................................... 23
Difference between lot and reagent calibration .......................................................... 24
Calibration procedures ................................................................................................ 25
Calibration stability ....................................................................................................... 26
Calibration validation ................................................................................................... 26
Calibration assessment .................................................................................................. 27
Missing values .......................................................................................................... 27
Monotony of curve (quantitative assays only) ....................................................... 27
Slope (qualitative assays only) ................................................................................ 27
Calibration factor (quantitative assays only) ......................................................... 28
Minimum signal ...................................................................................................... 29
Minimum/maximum signal (qualitative assays only) .......................................... 29
Minimum difference (quantitative assays only) ................................................... 29
Minimum acceptable difference (qualitative assays only) .................................... 29
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Table of contents
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4 Reagent concept
Introduction
Introduction
Elecsys reagent packs (cobas e packs) have a special 2D (two-dimensional) barcode.
This allows fully automatic registration and management of reagent information. The
advantage of this barcode is that manual entry or additional monitoring is not
necessary. The ready-to-use liquid reagents are loaded into one of the 18 positions on
the reagent rotor. Reagents are available for analysis after their barcodes are scanned.
The handling of calibrators and Roche Diagnostics controls is similar to that of
reagents. Some calibrators are supplied ready to use. Lyophilized controls and some
calibrators must be prepared and transferred into the appropriate container. For
quantitative assays, calibrator and control information is stored on 2D barcode cards.
For qualitative assays, all information necessary for calibration is encoded on the
barcoded labels.
Reagent pack
BlankCell
Assay
page C-19.
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If the reagent pack was produced after the CalSet (calibrator set), the target values
from the reagent pack have priority and are used for generating the calibration
curve.
If the reagent pack was produced before the CalSet, data followed by target values
from the calibrator card are used for generating the calibration curve.
Thyroid
Fertility
Cardiac
Oncology
Infectious disease
Anemia
Diabetes
Bone
Other
e For more information, see User access levels in the Software description section of the
online Help.
Diluents
For most tests where dilution may be necessary, use Universal Diluent or MultiAssay
as diluent. However, some testsincluding Anti-HAV, Estradiol, Progesterone, and
NSE (neuron-specific enolase )require specific diluents.
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4 Reagent concept
Reagents for cobas e 411 analyzer tests
e For information on required diluents and recommended dilution factors, refer to the
System reagents
The cobas e 411 analyzer uses the following system reagents:
Reagent
Use
Bottle size
ProCell
o
o
o
o
380 mL
CleanCell
o
o
Cleaning of the tubing system and of the measuring cell after every measurement
Conditioning of the electrodes
380 mL
SysClean
o
o
Sodium hypochlorite solution used for cleaning of the measuring cells (every two weeks).
SysClean is not stored on the instrument.
100 mL
SysWash
o
o
o
o
500 mL
Table C-1
insert.
To get information about what calibrator and controls are currently needed for
calibration or QC, print a Calibration/QC Load List from the software.
Reagent packs
The principal reagent container for the cobas e 411 is the cobas e pack.
e For additional information on the packaging and barcoding of reagents, see the Product
labeling section in the System overview chapter of the cobas e 411 analyzer Operators
Manual.
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Product labeling
Figure C-5
Reagent pack
A cobas e pack is a reagent pack that consists of three separate, capped reagent
containers. The cobas e 411 can open and close these caps automatically. There is an
individual reagent pack available for each test.
Product labeling
Each reagent pack is equipped with a barcode label. The barcode label contains
reagent, control, and calibration information. The reagent barcode labels are in a
unique format. The symbology uses portable data files (PDF) and is called PDF417.
Traditional linear barcodes serve as a link to relevant information stored in a
database. However a PDF417 is a two-dimensional, stacked barcode encoded to
contain an entire data record. The large amount of data that can be encoded allows all
instrument settings to be included, as well as the master calibration curve and
additional information for the assay. From this master calibration curve and from the
operator 2-point calibration, the analyzer derives the update of the master calibration
curve.
Every PDF417 symbol (barcode) contains two error detection codewords that are
used like the check digit in linear barcode symbologies to detect decode errors and
verify that all data has been read and decoded accurately. Additionally, PDF417
provides error correction in the event that portions of the symbol have been
damaged, destroyed or are unreadable. (a)
It is a combination of this error detection and error correction that ensures a reliable
barcode. There should only be a small number of exceptional cases when barcodes are
so badly damaged that the analyzer cannot read them. If the barcode cannot be read
(a) 1. Itkin S, Martell J. A PDF417 Primer: A Guide to Understanding Second Generation Barcodes and
Portable Data Files. Bohemia, NY: Symbol Technologies, Inc; 1992:17-18.
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4 Reagent concept
Data links
and the reagent lot has previously been used by the analyzer, you can manually enter
the 15-digit number found on the reagent barcode label into the software.
Data links
This following table illustrates the information that may be encoded on the barcode
labels. Background colors are used to indicate calibration links that exist between
information on separate barcodes.
The exact information encoded onto the barcode labels is not detailed here, as this
information is propriety to Roche Diagnostics. Items that are not directly linked are
mapped within the cobas e 411 software or user interface.
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Data links
Reagent Pack
Calibrator
Calibrator vial
Control
Control vial
Diluent
barcode
barcode card
barcode
barcode card
barcode
barcode
Test number
Test number
Test number
Test number
(space for 28
different tests (test
number, target
values and ranges
in %)
Lot number:
calibrator (space
for 5 different
calibrator control
values)
Lot number:
calibrator
Lot number:
calibrator
Lot number:
reagent pack
Lot number:
reagent pack (space
for 10 different
reagent pack lots
and calibrator
target values)
Reagent pack:
bottle number
Calibrator vial
number
Test lot ID
(only for ID-assays
or assays where
calibrators are
within the reagent
pack package)
Test lot ID
Test lot ID
Calibrator levels
Calibrator level
number
Lot number:
control (space for
10 different control
lot target values)
Test number
Control vial
number
Test lot ID
Test lot ID
Control level
number
Lot number:
control
Lot number:
control
Rodbard
parameters
Calibration
validation criteria
Calibrator
identification
Expiry date
Table C-2
Expiration date
Control
identification
Control number
Control number
Expiration date
Expiration date
e For further information about reagent checklists, see Reagents, calibrators, and controls in
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4 Reagent concept
Calibration
Calibration
Calibration is required to determine the concentration of an unknown substance as
accurately as possible. For this, a master calibration curve is generated at Roche
Diagnostics during production of the reagent and is encoded in the 2D barcode of the
appropriate reagent pack. This information is then transferred to the analyzer. At the
customer site, the analyzer generates an update of the master curve by measuring two
calibrators under routine laboratory conditions.
Master Calibration
performed by Roche Diagnostic
Figure C-6
Data Carrier
Calibration
with two calibrators
Calibration procedure
The calibration curve produced from the barcoded master calibration and the
measured calibration is specific to each reagent lot and, in some cases, to an
individual reagent pack. The condition of the analyzer and the reagents influence the
system-specific calibration. The result of a calibration is validated automatically by
the analyzer and can be further validated by the operator.
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Master calibration
Master calibration
The following diagram illustrates how measurement accuracy can be increased by
combining the calibration results from a lot calibration of master calibrators
produced by Roche Diagnostics (RD) with the information encoded in the 2D
barcode:
Accuracy
RD Production
Effort
RD Development
Customer
Figure C-7
Calibration concept
A reference standardization curve utilizing master test kit reagents and certified
reference standard material [for example, World Health Organization (WHO)
reference material] is measured at Roche Diagnostics. This curve uses 10 to 12 points
(n = 10 to 12). The reference standard curve is the basis for the production of master
calibrators.
A lot-specific master calibration curve (n = 5 or 6) is measured at Roche Diagnostics
using lot-specific test kit reagents and master calibrators. The shape of the lot-specific
master curve is characterized by a four-parameter Rodbard function. The data
characterizing this curve are stored in the lot-specific reagent barcode. Lot-specific
calibrator assigned values (CalSet assigned values) are read off the lot-specific master
calibration curve and are encoded in the barcode label of the reagent pack.
At the customer site, the calibration results from two calibrators that were measured
under routine conditions are mathematically combined with the encoded data from
the 2D barcode. From this combination, the system determines a lot calibration or
reagent pack calibration from which the concentration of measured samples is
reliably calculated.
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4 Reagent concept
Lot calibration
Lot calibration
A lot calibration (L-Calib) is a calibration performed with a fresh reagent pack that
has not been on the analyzer longer than 24 hours and for which all calibration
validation criteria are acceptable. Reagent-specific calibrators are used to update two
of the four Rodbard curve-defining parameters. This adjusts the curve to match the
original lot-specific calibration curve.
The lot calibration is valid for all other reagent packs of the same lot, provided these
reagent packs were stored as specified in the package insert and have not been on the
analyzer for longer than seven days.
e For further information, see Calibration factor (quantitative assays only) on page C-28.
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Reagent pack
acceptable
acceptable
acceptable
(system-released)
Lot calibration
Calibration
same lot
Figure C-8
Controls and
samples
Roche Diagnostics
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4 Reagent concept
Calibration procedures
Calibration procedures
The following table contains examples of the procedures to be followed for various
scenarios when more than one reagent pack is used for one assay:
Example case
Procedure
Controls are measured daily for each reagent pack. If a control is measured out of
range for all four reagent packs:
o
o
o
o
Controls are measured daily for each reagent pack. If a control is measured out of
range for all of the reagent packs:
o
o
o
Table C-3
Controls are measured daily for each reagent pack. If a control is measured out of
range for one of the new reagent packs, the reagent pack is calibrated and
controlled. This reagent pack is assigned a reagent pack calibration as the reagent
pack has been on board > 24 h.
Controls are measured daily for each reagent pack. If a control is measured out of
range for one of the new reagent packs, the reagent pack is calibrated and
controlled. This reagent pack is assigned a lot calibration (if all calibration criteria
are within the limits) as the reagent pack has been on board for < 24 h.
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Calibration stability
Calibration stability
The stability of calibration is determined by two factors:
o
For many assays, a reagent pack will be used within seven days. In this situation, it is
not necessary to renew the calibration for the new reagent pack. In this case, the lot
calibration can be used for all other new reagent packs for a period as recommended
in the Calibration Frequency section of the package insert. After that period, a new lot
calibration is recommended.
If the reagent is kept on the analyzer for more than seven days, it is recommended that
the calibration be renewed. This renewal of the calibration can be repeated as needed
until the on-analyzer open stability of the reagent is exceeded (for example, two
months).
start
low thro
u
ghpu t
time
ut
roughp
high th
Figure C-9
calibration recomended
every 28 days
Calibration workflow
Calibration can be performed more frequently if required. This may be because of local regulations,
or before performing specific types of test.
Calibration validation
The calibration of a test can be easily identified on the Calibration > Status screen.
If the test is highlighted in red, this indicates that both of the calibrator measurements
have failed or the calibration factor is outside the range 0.9-1.2 . There is no red
highlighting if the calibration was successful.
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4 Reagent concept
Calibration assessment
Calibration assessment
The quality criteria of a calibration are displayed on the Working Information
window in the Calibration menu.
All calibrations are automatically checked for:
o
Missing values
Monotony of curve
Slope
Calibration factor
Minimum/maximum signal
Deviation of duplication
System error
Target
Cutoff
Borderline
Missing values
Duplicate determinations of two calibrators are used to adjust the master calibration
curve stored on the reagent pack barcode. Therefore, you must have a minimum of
n-1 values for all calibrator replicates measured (n = total number of calibrator
replicates. For any current Elecsys assay, this number totals 4.). Currently, all Elecsys
reagents use only two calibrators. This box can accommodate up to five calibrators.
Check to see if any alarms occurred during calibration that may have caused the
missing values. Treat any questionable calibration according to laboratory policy.
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4 Reagent concept
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Calibration assessment
The calibration factor criterion is used only in validating reagent pack calibration (R-Cal).
The calibration factor is set to 1 at each new lot calibration. The following reagent
pack calibrations are compared with the last measured lot calibration. The calibration
factor is the ratio between the calibrator signals (difference of CalSet 1 and CalSet 2)
of the lot and reagent pack calibration. The calibration factor is only used as a
calibration validation criteria and not used for sample calculation.
The following formulae show the relationship between lot calibration and reagent
pack calibration:
t1
Calibration factor for each Lot calibration = ---- = 1
t1
CalSet 1 signal (standardization) CalSet 2 signal (standardization)
t 1 = -----------------------------------------------------------------------------------------------------------------------------------------------------------------------actual CalSet 1 l signal actual CalSet 2 l signal
CalSet 1 signal (standardization) CalSet 2 signal (standardization)
t r = -----------------------------------------------------------------------------------------------------------------------------------------------------------------------actual CalSet 1r signal actual CalSet 2 r signal
t1
actual CalSet 1r signal actual CalSet 2 r signal
Calibration factor for Reagent pack calibration = ---- = --------------------------------------------------------------------------------------------------------------------------tr
CalSet 1 l signal CalSet 2 l signal
Example:
Reagent calibration
Lot calibration
This simplified formula is only valid when the same calibrator concentrations are used for the
reagent pack and lot calibration. If these calibrator concentrations are different, the calibration
signals of the standardization have to be considered.
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4 Reagent concept
Calibration assessment
Minimum signal
The measured signal of the calibrator replicate must be above the minimum value.
Values are test dependent and are encoded in the reagent barcode. Currently, all
Elecsys reagents use only two calibrators. This table can accommodate up to five
calibrators.
Check to see if any alarms occurred during calibration that may have caused a
calibrator replicate to have an unacceptable minimum signal. Treat any questionable
calibration according to your laboratory policy.
Deviation of duplication
The deviation of duplicate measurements is a check of the signal values for each
replicate of a calibrator. If the difference between the duplicate measurements is too
great, the appropriate calibrator is flagged. The signal values are used to calculate the
mean value of the duplicate measurements.
System errors
A hardware error occurred during a calibrator measurement. If either 1 (Cal 1) or 2
(Cal 2) is displayed in this box, the result is a failed calibration.
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Cal.
The actual measurement signal levels of Cal 1 and Cal 2, used to calculate the mean
value of the duplicate measurements. Two measurements are taken:
1. Signal
The actual signal level of the first measurement of Cal 1 or Cal 2. The mean of the first
and second measurements is used in the calculation of the calibration curve.
2. Signal
The actual signal level of the second measurement of Cal 1 or Cal 2. The mean of the
first and second measurements is used in the calculation of the calibration curve.
Rodbard function
The calibration function used by the system is encoded in the 2D barcode on the
appropriate reagent pack. The calculations are performed automatically by the
analyzer, including the correction for samples diluted by the analyzer.
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4 Reagent concept
Calibration of quantitative assays
Rodbard function
The relation between the measured signal and the corresponding analyte
concentration is given the following equation:
Equation C-1
ad
y = -------------------c- + d
1 + --x-
b
Sample concentration
a , b ,c , d
Signal
Parameters b and c define the shape of the curve and parameters a and d define the
position of the curve.
Under the controlled conditions of automation on the analyzer, the shape of the
calibration curve is very stable and, therefore, it is possible to calibrate this nonlinear
function with only two calibrators and the information of the shape parameters b and
c. The curve position parameters a and d are calculated with each calibration. Such a
calibration is called 2-point calibration.
The following inverse formula is used to determine the sample concentration based
on its signal.
1/c
Equation C-2
a y
x = b --------- y d-
Signal
a , b ,c , d
Sample concentration
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y = bx+a
Signal
Concentration
a ,b
Calibrations using a linear calibration curve are always performed using two
calibrators.
The following inverse formula is used to determine the sample concentration based
on its signal.
Equation C-4
ya
x = ----------b
Sample concentration
a ,b
Signal
1
--- = b x + a
y
Signal
Concentration
a ,b
Calibrations using a linear reciprocal calibration curve are always performed using
two calibrators.
The following inverse formula is used to determine the sample concentration based
on its signal.
Equation C-6
1ay
x = -----------------by
Sample concentration
a ,b
Signal
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Calibration of qualitative assays
S Cutoff
Cutoff value
S POS
S NEG
A ,B ,C
S eff
Cutoff Index = ----------------S Cutoff
Cutoff Index
Cutoff index
S eff
S Cutoff
If the effective signal of the measurement S eff equals the cutoff signal of the
calibration S Cutoff , the cutoff index CutoffIndex equals 1. For effective signals being
lower or higher than the cutoff signal, the cutoff index is smaller or larger than 1,
respectively.
In order to evaluate the reactivity of a sample, the 2D barcode contains defined limit
values. If the cutoff indices, which were calculated from the effective signals, lie
between the lower limit (LL) and the upper limit (UL), no decision can be made
regarding the reactivity or non-reactivity of the sample (borderline).
The test result is evaluated as follows, depending on the test principle (sandwich tests
show a positive slope, and competitive tests show a negative slope).
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Result
Reactive
Cutoff Index UL
Cutoff Index LL
Nonreactive
Borderline
Table C-4
The analyzer automatically calculates the cutoff based on the measurement of Cal1
and Cal2. The results of a sample is given either as reactive, nonreactive, or
borderline, as well as in the form of a cutoff index.
For sandwich assays:
o
Roche Diagnostics
C-34
Quality control
cobas e 411
This chapter provides a brief overview of the assignment of control target values for
the cobas e 411 analyzer.
In this chapter
Chapter
Roche Diagnostics
COBI-CD Version 1.0
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cobas e 411
Roche Diagnostics
COBI-CD Version 1.0
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Case 2
Advantage
Disadvantage
The recovered value can have another level within the given range.
For example, 105% for reagent lot 1 and 94% for reagent lot 2.
The controls are out of the target range: > +/- 1 SD for this reagent lot
The target values of the controls are on the reagent pack barcode, which means the
specific target values for reagent lots exist and the control values on the control card
are not valid. As a consequence, an extra information sheet is put inside the reagent
kit indicating the re-assigned values and the new values are stated on the reagent pack
barcode.
Advantage
Disadvantage
Priority 3: Control barcode card or data downloaded from cobas Link (under development)
This means once a target value of a control is entered manually this value is valid as long as the
customer uses a new control lot. If the customer deletes this control on the QC Install screen and
scans the control barcode card once again, then the manual input is no longer valid.
Roche Diagnostics
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Due to the priority rules with a new reagent lot, the target value of a control will not
be taken from the control barcode card or the reagent barcode if the target value has
been entered manually for this assay.
The main point of each standardization action is to receive the same human serum
recovery independent of the reagent lot. Multi-analyte controls are spiked, stripped
and preserved and unfortunately, do not always react in the same way.
Roche Diagnostics
D-6
Index
cobas e 411
Index
Index
A
Abbreviations, 4
Analyzer cycles
automatic, A-21
Approvals, instrument, 2
Aspiration
reaction mixture, A-9
Assay principles
bridging principle, C-10
competitive principle, C-6
sandwich principle, C-8
Assay sequence, A-8, A-14
B
Barcode
calibration information, C-19
Borderline range, C-30
Bridging principle, C-10
C
Calibration
barcode information, C-19
curve, C-21
data links, C-19
factor, C-28
introduction, C-21
master, C-22
procedures, C-25
qualitative assays, C-33
quality criteria, C-27
quantitative assays, C-30
reagent pack, C-23, C-24
signal level, C-30
stability, C-26
validation, C-26
Calibration assessment, C-27
Calibration quality criteria
borderline, C-30
calibration factor, C-28
calibration signal level, C-30
cutoff, C-30
deviation of duplicate, C-29
minimum acceptable difference in calibrator signal,
C-29
minimum difference, C-29
minimum signal, C-29
minimum/maximum signal, C-29
missing values, C-27
monotony, C-27
slope, C-27
system errors, C-29
target, C-30
Cleaning
measuring cell, A-9
Competitive principle, C-6
Contact addresses, 3
Control target value assignment
Roche controls, D-5
Copyrights, 2
Cutoff value, C-30
D
Data links
calibration, C-19
Deviation of duplicate calibration measurement, C-29
E
ECL (electrochemiluninescence)
advantages of, B-10
assay principles, C-5
measuring cell, B-9
measuring principles, B-5
reaction, B-6
signal generation, B-8
F
Finalization, A-9
Flow
operation, A-13
Function
linear calibration, C-32
linear reciprocal calibration, C-32
Rodbard, C-31
I
Immunology calibration
calibration validation, C-26
lot calibration, C-23, C-24
master calibration, C-22
procedures, C-25
qualitative assays, C-33
quality criteria, C-27
quantitative assays, C-30
reagent pack calibration, C-23, C-24
stability, C-26
Incubation
first, A-8, A-18
second, A-9, A-19
third, A-9
Initialization process, A-6
Instrument
approvals, 2
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COBI-CD Version 1.0
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Index
Intended use, 2
L
Labeling
product, C-18
License, 2
Linear calibration function, C-32
Linear reciprocal calibration function, C-32
Lot calibration, C-23
M
Master calibration, C-22
Master calibration curve, C-21
Measurement
preparations, A-20
reaction mixture, A-9
Measurement process, A-20
Measuring cell
cleaning, A-9
description, B-9
Measuring principles
ECL (electrochemiluninescence), B-5
Microbead
aspiration, A-19
dispensation, A-19
preparation, A-19
Minimum acceptable difference in calibrator signal,
C-29
Minimum calibrator signal, C-29
Minimum difference in calibrator signal, C-29
Minimum/maximum signal, C-29
Missing calibration values, C-27
Monotony of calibration curve, C-27
O
Operation flow, A-13
Operators Manual
conventions used, 4
version, 2
cobas e 411
Reagent concept
introduction, C-15
Reagent pack calibration, C-23, C-24
Reagent pipetting
additional, A-8
pretreatment assays, A-9
Result calculation
qualitative assays, C-33
Rodbard function, C-31
Ruthenium complex, B-5
S
Sandwich principle, C-8
Scaling factor, C-30
Sequence
assay, A-8
Signal detection and conversion, A-21
Slope of calibration curve, C-27
Software
version, 2
Symbols, 4
System errors during calibrator measurement, C-29
T
Target value of calibrator, C-30
Test principles
bridging principle, C-10
competitive principle, C-6
overview, C-5
sandwich principle, C-8
Test protocols, A-7
Throughput
effects of test combinations, A-11
workflow, A-11
Trademarks, 2
TSH microbeads
preparation, A-19
W
Workflow, A-11
Patents, 2
Preoperational steps, A-14
Product labeling, C-18
Protocols
test, A-7
Q
Qualitative assays
calibration, C-33
result calculation, C-33
R
Reaction mixture
aspiration, A-9
measurement, A-9
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