CS-400 Service Manual
CS-400 Service Manual
Product compositionThe analytical part (host), operation part (computer system), the
result output part (printer), accessories and consumables.
Product applicable scope: used for quantitative analysis of serum, plasma, urine,
cerebrospinal fluid and other clinical chemical constituents of sample.
R2 stirring mechanism
R2 reagent disk
1.2
CS-400 auto-chemistry analyzer working speed means the one at which it reaches
constant speed 400 tests / hour of single / double-reagent item, whose working period is 9
seconds. Instrument overall structure adopts the "4 -disk + three-probe + two-stirring rod",
specifically, a sample disk, one reaction disk, two reagent disks, 2 reagent probes for
adding R1 and R2 respectively, a sample probe for sampling, 2 stirring rods for mixing
R1,R2 respectively. "Grating + diode array" approach is adopted in optical measurement
mechanism for real-time optical collection of reaction cup. The rinsing mechanism 7-stop
11-step automatically rinsing the reaction cup is carried out in test process.
1-2-1 The Structure of Analyzer
Sample disk
Barcode window
50
20
34
QC position
Barcode window
Reaction disk
probe mechanism
Probe mechanism3
1sample probe, 2 reagent probes
High-precision digital liquid detector
Stirring mechanism2
High-speed hollow cup motor
Surface high-intensity Teflon coating
ISE unit3SIPDILIS
Colorimetric unit3 samplereagent R2reagent R1
Colorimetric cup original rinsing liquid box
1.3
Function Overview
Name
main function
R1probe unit
R2 probe unit
Reagent
unit
R1
disk
Reagent
unit
R2
disk
Reagent R1 stirring
unit
Reagent R2 stirring
unit
Optical
groupware
system
Auto-rinsing unit
ISE unitoptional
barcode
10
Figure 1 i
A well grounded power supply socket is a must. (Socket at least with one 20 A and three 5A).
Large electrical appliance such as air condition, refrigerator, even cannot use the same
electrical wire as analyzer.
11
! Warning:
Input voltage should conform to requirement. 6KVA-line UPS power supply is advised.
! warning
Normal running and accuracy of result can not be guaranteed if instrument works beyond
the requirements mentioned above. Please use air conditioner if the temperature or
humidity can not meet the requirement above.
The heat generated in the work process by the instrument will be emitted the rear of the
instrument, so good ventilation should be kept well and ventilation equipment can be
adopted if necessary, but direct air current is avoided, or inaccuracy of instrument test may
be caused.
Make sure the installation place, space, electrical environment, installation room
temperature and purified water equipment can conform to requirements
Make sure instrument installation tools needed are complete and reagent and QC liquid are
enough.
Please check the prepared items according to packing list when open the package; please
write them down on the check report if any missing.
12
Place instrument in applicable position, and mount with computer host, display and printer.
Adjust instrument level, and check whether the injection pump wires are loose or not after
open the left and right cover board of instrument.
Infuse CS-alkaline detergent into instrument rinsing box, and infuse CS-anti-bacterial
detergent into the 45th position of R1, R2 reagent disks.
cUnplug the cork of the two hoses connecting to cooling system water tank as figure 3 shows
13
dInfuse purified water into low water level hose till the purified water flows out of the
high level hose.
eSwitch on the main power. After several minutes,
into low water level hose till the purified water flows out of the high level hose again,
requiring 3L water.
fReplug the rubber cork and mount the left front cover board of the instrument.
Check the up and down flexibility of reagent probe and sample probe.
Get through pure water machine, computer host and display and analytical unit power
supply, and enter CS auto-chemistry analyzer systematic application software. Initial user
name: 001, initial password: 001.
14
of test should be
2.8
15
3.1
3.1.1
Performance Index
characteristics
Wavelength
range
Grating
rear spectrophotometry system,
Simultaneous photometric processing of 12
wavelengths within the range340 380 405
450 480 505 546 570 600 660
700 750nm
Wavelength
precision
2nm
Reaction
temperature
370.1
Test item
Sample system
standard specification
Measuring
method
Measuring
speed
Sample disk
and position
Sample type
16
Sample
volume
235ul0.1l Incremental
Test tube 10mm75mm 10mm100mm
Sample cup
specification
13mm75mm13mm100mm(1 mm)
Standard cup 14mm37mm(1 mm)
Sample system
Remaining
sample
volume
Sample
probe
Sample
probe rinsing
Sample liquid
level sensor
Barcode
info.
Reagent system
Reagent disk,
reagent
position
Reagent
volume
20350ul1l
Reagent
bottle
specification
Reagent
remaining
volume
(incremental)
20mL 70mL
17
Reagent
probe
Reagent
probe rinsing
Reagent
storage
temperature
Reagent liquid
level sensor
Reagent system
Barcode
info.
Reaction system
Reaction cup
mode
Discrete
Reaction cup
optical path
6mm
Reaction cup
quantity
Reaction time
Reaction
liquid
volume
150450ul
Light source
Absorbance
range
03.3ABS
QC
Automatical
rinsing
QC interval, monthly QC
Automatically rinsing reaction cup, reagent probe,
sample probe, stirring rod.
18
Stirring
system
interface
Printer
Data system
Connecting
LIS/HIS
system
weight
Approximate
Dimensions
Instrument system
PowerVA
2000VA
Water
consumption
25L/h
Power supply
Installation
requirement
3.1.2
Using
environment
300Kg
220V/230V50Hz/60Hz2000VA
System storage temperature:0 40
volatility <2/Hstorage humidity:30%RH
80%RH non-condensing at working,
temperature:15
30
volatility<2/H
Testing speed
NoteDue to the different specific conditions, sometimes equipment processing capacity will be
lower than 400 tests / hour.
Test conditions
Retest
after
prediluted
sample
Use
avoiding
cross
contamination function
R1 and R4 items or R2 and
R3
items
are
used
simultaneously in testing.
19
Test Flow
3.2
Stop automatically
Rinse reaction cup
Tested completely
stir
1min
plus
21s
13min 3os
Add reagent 4
stir
Add reagent 3
stir
Add reagent 2
stir
Add reagent 1
Add sample
Assimilate water
3min plus27s
18s
More then72s
15min
3min
9s
9min 18s
20
3.2.2
3.2.2.1
R4
e. Rise from sample test tube and rotate to above reaction disk
f. Discharge quantitive volume of R1 and R4
g. Rotate to above rinsing bath
(next periodic movement sequence)
3.2.2.3
The same to R1
3.2.2.4
21
3.2.2.5
A track includes total 120 reaction cups in reaction disk, and rotates in a fixed way when
testing. The reaction cup always rotates and stops 3 times counterclockwise, total 2237
2=61 rotation and stop sequence 22372patches, in every working period, 9
seconds elapsed. 122 patches are passed in two working periods within 18 seconds.
figure 3-2 Position of reaction disk and probe
Rinsing mechanism
Reset point
Photoelectric
detection
62,R1 stirring po
63,R4 stirring pos
Sample probe
R1, R4 Probe
60 R1 Pipetting
61 R4 Pipetting
Reference position
Reagent probe 2.3
Stirring rod
number
Outer circle figure: No. of reactioninner circle figure: No. of mechanism position;
Sample position: No. 1 position; reagent 1,4 probes: No.60,61 position; stirring at
NO.62,63 position; reagent 2,3 probes: No. 31 position, stirring: No. 33 position; reaction
cup rinsing mechanism: No. 10110310510710911711 position.
Reaction cup stops at No. 101 position after reaction disk resetting. The sequence of
reaction cup rinsing and sampling:
162364566768 591209 minutes60times
612634656678 119609 minutes60times
22
3.2.3
figure 3-3
Rotati
Rotationa
l
l
direction
f
4 4
times 1
cell
blank
measurement.
1 stop, 3 pass.
Above figure shows that seven steps are needed when rinsing reaction cuvette. (four times
cell blank test is added) , therefore, to finish rinsing one reaction cuvette, 11 steps are
needed
23
3.2.4
Photometry in the entire process is adopted. In 15-minute reaction time, the continuous
determination of the absorbance of reaction solution is carried out. Reaction disk rotates 1
plus 2 pitches, about 18 seconds, absorbance values are measured out when the 120
reaction cups passing optical axis of the photometer one by one.
Each reaction Cup in 3-minute reaction time was measured 10 times (10 photometric
points), 4-minute reaction time was measured 13 times (13 photometric points), 5-minute
reaction time was measured 16 times (16 photometric points), 10-minute reaction time was
measured 33 times (33 photometric points), 15-minute reaction time was measured 49
times (49 photometric points).
Detector
(340-750nm)
12
wavelength
fixed
Reacti
on
lamp
cuvett
e
Figure 3-4
Photometer
Light starting from the light source was focused by the lens, and passed the reaction cup
first, and then was disparted by concave grating. After spectrophotometry, each
wavelength were received by 12 fixed photoelectric sensor simultaneously, and were
amplified 12 amplifier, after Log transformation to derive the rate of change of absorbance
or absorbance. When dual-wavelength testing is used, the concentration value is
calculated by the difference of the main and sub-wavelength absorbance or that of
absorbance change rate, and therefore dual-wavelength testing can not only compensate
the blood lipid, hemolytic, jaundice sample test, but also compensate on the result
impacted by voltage changes, so that measurement is more accurate, more stable.
24
4.3
4.3.1
Sample/reagent probe unit includes sample probe, No. 1 sample probe(R1) and No.2
sample probe (R2), which are called 3-probe component.
Sample probe can realize the assimilation from the sample test tube and sampling into
reaction cup. No. 1 sample probe(R1) and No.2 sample probe (R2) can realize the
assimilation from the reagent bottle and adding reagent into reaction cup.
In addition, main function of 3-probe component: liquid level detecting and bump-proof in
movement process, sample probe block detecting function.
Other subsidiary function includes mechanical limit, power-down self-locking function.
3-probe component working position
1. sample probe component rinsing bathsample
positionreaction disk/ISE sampling position
disk
assimilating
disk
assimilating
Probe drive mechanism plays a key role of reagents and samples adding. The way of
probe are only up-down and circular moving, so two step motors are necessary to drive.
4.3.2
Probe up-down
weight block
Probe up-down
guide slider
Reagent 1, reagent 2 and sample probe drive mechanism in addition to different probe
turning angles, namely the corner mechanical limit block tablets different, the other
structures are identical.
25
figure 4-2
Rotating motor
mounting hole
Guide
movements
long hole
Up-down
motor
mounting
hole
Probe
rotating
knight head
Rotating probe drive ratio 12:34, using 0.9 stepper motor and 8 segment controller.
Control accuracy can achieve 0.0398.
Up-down main gear driver diameter is 19.1mm, the 60mm for the perimeter, also using 0.9
stepper motor and 8 segment controller. Up-down control accuracy can achieve
0.01875mm.
26
4.4
4.4.1
Function Introduction
The main function of rotating mechanism is bearing of the sample warehouse, reagent
warehouse and reaction disk, and drive it to rotate, so that sample, reagent carried in
reaction cup rotate to the designated location to finish sampling, mixing and other work.
Reagent disk 1, reagent disk 2, the sample disk and reaction disk mechanisms are classified
as turntable mechanism. Meeting the requirements of functionality and performance
simultaneously, in order to improve the craftwork of product, the four disks are designed as the
same frame structure.
motor-driven
2, reagent turntable: The reagents storehouse, disk rotating bracket, step motor-driven
components
3, the reaction disk turntable: reaction plate, the reaction cup, incubation bath, disk rotating
bracket, step motor-driven components
Figure 4-3 Disk rotating bracket
Mandrel
Storehouse
t
fixing
S/Driving seat
Zero light sensor
Reagent disc 1 and disc 2 are same the structure , and the sample disk drive structure and
the drive transmission ratio are the same with reagent disc.
27
Driven gear
System transmission ratio is 10:1.Because of using 0.9 step motor with 8 segment driver
circuit, the wheel rotation accuracy can achieve 0.01125 .
Connecting loop of
disk cover
28
45 teeth of reagent
code disk
4.5
4.5.1
Cooling mechanism
Function Introduction
R1 and R2 with two refrigerated reagent disk, adopting semiconductor refrigeration, the
temperature maintains at 6 degrees -10 degrees, 45 reagent positions for each reagent
disk respectively(the 45th fixed position for placing phosphor-free CS-anti-bacterial
cleaning liquid in each disk)
29
4.5.2
Figure 4-7 reagent cooling storehouse reagent box rack assembly configuration
Equipped
temperature-keeping
cooling storehouse
with
reagent
30
Gear drive is adopted to reaction disk due to the relatively high positioning precision.
Fixing pin
Colorimetric cup
rotating rack
Driven gear
Driving gear
motor vibrator
cuvette
cuvette install pin
Locking screw of
colorimetric cup rack
6 sets of colorimetric
31
R1 stirring rod
rinsing bath
R1 probe rinsing
bath
Optical
window
Circular constant
temperature water
outlet
Spilling outlet of
incubation bath
Circular constant
temperature water
inlet
Figure 4-11 reaction disk with incubation bath components assembly configuration
Incubation bath
Phosphor-free
detergent inlet
Figure 4-12 reaction disk and optical system components assembly configuration
Optical system
32
4.6
Stirring unit
4-6-1
function introduction
Stir and mix reagent after adding it
Reagent 1, reagent 2 agencies are identical in addition to the mixing angle of rotation,
namely the code disk is different.
4-6-2
Stirring mechanism
up-down motor
Stirring mechanism
up-down slider
Rotating mechanism of stirring and rotating arm adopts the direct drive way of
step motor output axle, using 8 segment drive circuit of 0.9 motor, and the control
accuracy can achieve 0.1125 . The largest angle is limited by the open angle of
rotatation code disk mechanical limit. And positioning is determined separately by
the left and right light sensors.
Figure 4-14 stirring up-down driver configuration
Stirring mechanism
up-down light
sensor
Stirring mechanism
up-down motor
Curve axle and curve handle drive is adopted by stirring up-down mechanism .
33
Up-down linear
sliding axle
Up-down
guide axle
Up-down
slider
Because of mixing body movements are used by way of the crankshaft crank,
so the movements of the positioning accuracy at different locations different.
Landing and taking-off between the location of the speed of the highest, lowest
accuracy, and precision at both ends of the highest, the lowest speed.
Electrical axis from the axis of the slider bearings the size of 16.5mm, crank in
horizontal position, the landing position accuracy of 0.032mm.
Due to curve axle and curve handle drive is adopted by stirring up-down
mechanism, the up-down positioning precision are different at different position.
The speed is the highest and precision is lowest at the middle, however the
precision is highest and speed is lowest at the two ends.
The size of Motor axis from the axis of the slider bearings is 16.5mm, when
curve handle locates horizontally; the up-down position precision is 0.032mm.
Figure 4-16
Up-down
slider
Up-down
slider
34
4.7
4.8
Figure 4-17
Rinsing probe
rack of
colorimetric cup
Up-down
step motor
Rinsing probe of
colorimetric cup
Up-down slider
35
4.9
Rack
Rack includes the main rack, electrical, gas liquid valve and water tanks and
other racks.
Standing
supporting board
Main worktable
board
Cable leading
groove
Isolating
standing
board
Adjusting foot
All-directional
caster
Water-proof cover
board
Electrical
box
control
Cooling controller
Isolated
transformer
Power switch
rack
Electric rack is mainly consisted of control panel box, power rack and
waterproof board and such parts.
36
Water inlet
Vacuum tank
Figure 4-21 Valve rack, gear pump rack and the main rack assembly.
37
figure 4-22
Pressure gauge
Vacuum exhausting
tank
Magnetic pump
4.10
Optical system
CS-400 adopts advanced flat field grating photometer. Concave holographic grating
photometer is today's domestic and foreign advanced optical system with simple
structure, high optical efficiency, and signal to noise ratio and measurement speed
of machine have greatly been improved, compact photometer dimension, stable
performance, long life, and such highlighting advantage, achieving the requirements
such as multi-wavelength, multi-item simultaneously testing at high speed,
multi-wavelength (12) simultaneously collecting signals, a relatively large aperture,
good imaging quality and post-spectrophotometry.
Photoelectirc
cable array
Water-cooled
light source
Diaphragm
Log applifier
38
5.1
2.
Sampling subsystem uses three probes plus two stirring rods and three
injectors. The sampling injector uses 100uL, and the two reagent
injectors use 500uL.
3.
The inner and outer wall cleaning of three probes and two stirring rods
uses barotropic driving.
4.
Cleaning bath: five cleaning bathes plus waste liquor in the reagent
storehouse, together with the flooding waste liquor in the reaction disk
are seven kinds of routine waste liquor.
5.
The reaction cup cleaning uses the way named 7-stop 11-step.
6.
7.
Waste liquor: use plastic hollow main pipe whose inside diameter is 20
to 30 mm, and the wall thickness is 3 to 5 mm. The installation of the
main waste liquor pipe is height limited, and it requires the height is
helpful to the waste liquor entering the low concentration liquid buffer
vessel by its self-weight. As to the high concentration waste liquid, it is
providing liquid level sensor interface and outboard high concentration
waste liquid barrel.
8.
9.
10.
The vacuum degree for vacuum pump assimilating is between -28k and
-35kPa.
11.
The inner and outer wall cleaning of three probes uses independent
solenoid valves while the two stirring rods use one solenoid valve
together.
39
5.2
Figure 5-1
40
Figure 5-2
1, when the low water level float detects out the signal, open the inlet valves
SV8, and water tank begins to be infused water until the high water level float
detects out signal, then turn off SV8 to stop the water. Influent flow is as follows:
Alarm of low water
level check
influent water
Alarm of
Stop influent
water
2, when the low water level float did not detect out signal, the water tank heater
began to work, and temperature control started. Magnetic pump began to work
simultaneously.
3, Output water pressure of water tank is controlled by the magnetic pump and fixed
damper regulator. Magnetic pump head is 8 / 11 m. Control water pressure is around
0.8kgf/cm2.
4, The outlet of tank water leads directly to the cleaning and incubation bath; the
other output water through gear pump supercharger to the pressure 1kgf/cm2 to 3
line probe mechanisms to rinse inner wall and pipeline, with exhausting device of
probe liquid line.
5, SV13 valve remains closed status so as not to affect water pressure during the
normal use of instrument. Only in the implementation of the maintenance of water
tanks, open SV13 valve, at the same time, time switch of SV8 inlet valve to empty
impurities in a water tank.
6, when abnormality occurs to the high and low water level floats, possibly water
tank remains the status of inputting water. When the water tank is full of water, SV8
not shut down, tank outflow water spills out from the overflow pipe into the waste
liquid barrel through waste liquid pipe.
41
1.In the system, two reagent disks as well as standard and QC sample need to be
cooled in the environment from four to ten degrees centigrade. Water is used to
exchange temperature and transfer heat.
2. the system also adopts the semiconductor refrigeration mode which is better for
environmental protection and convenient for maintenance than the traditional.
3.each refrigeration unit is made of four groups of same semiconductor refrigeration
module string by parallel connection. Each module is constituted by one piece of
Peltier (semiconductor refrigeration), one water cooling block and one radiator.
4.the refrigeration power of each module is about 80W, the total 320W. Radiation
adopts pyrotub wind-cooled heat pipe to radiate. The single power is 150W.
5.the refrigeration warehouse shell with two reagent disks adopts stainless steel
structure, and the cold water flows into it from the bottom and flows out from the top
through circumvolution circulation, thus the warehouse interlayer is full of cold water
and its temperature is even.
42
6.the refrigeration volume of sample disk is small and the refrigeration area is
formed by aluminum cylinder, so the aim of refrigeration can be achieved by
circulating stainless steel tube. The whole circulation process is finished by magnetic
pump with a head 2.7m.
7. sluice water tank can check temperature and water level. The scope of
temperature is from 5 to 15 degrees centigrade above zero.
8.the refrigeration water tank is complete closed.
When adding water, it should be added from the inlet tube at the bottom by filler.
About 1.5 litter is added into water tank or flowing-out water from the top of water
tank observed (the two water-changing nozzle should be above the water tank,
water-changing tube is mainly used to exhaust). Here, turn on the main power
supply and the refrigeration system starts to work. Then the water level will drop,
water should be added continuously until the exhausting tube reflows out water.
When working stably, there is no change with the water level of exhausting tube, and
the two water-changing tube plugs should be installed. If there is no leakage, the
system water changing has been finished.
When spouting the water, please turn off the main power supply, pull out the two
water-changing tube plugs and contain water with container. The total water volume
is approximately four litters.
43
1, Open the inlet valve SV10 and turn off outlet valves SV16 to infuse water into
incubation bath, simultaneously with reagent R1 and R2 probes adding
phosphor-free anti-bacterial rinsing liquid to the incubation bath, liquid level detector
determining whether to stop water.
2, Turn off outlet valve and inlet valve, and start the water circulation magnetic
pump and temperature controller. In order to improve the adjusting performance of
the PID temperature controller in high temperature environment, the system is
added the cooling device through the water tank to get a small amount of
temperature cooled.
3, Turn off magnetic pump and temperature controller, open the drain valve SV16,
time to turn off the drain valve when the incubation bath is draining.
44
Figure 5-5 probe internal and external walls rinsing and sample probe block check liquid line.
1, Opening the valves SV1 and SV41 simultaneously can get the inner wall of
sample probe rinsed; open valve SV2 or SV3 to carry out reagent probe R1 or R2
internal wall cleaning. Probe position should be at the top of the corresponding
cleaning trough when cleaning so that waste liquid can get out of the instrument.
2Open the valve SV4SV5SV9 or SV6 to rinse the external walls of sample,
reagent R1, R2 or 2 stirring rods. Each stirring rod has one corresponding valve
respectively. Fixing pressure adjusting piston is adopted to every external wall
rinsing pipeline to avoid rinsing water spilling out of rinsing bath.
3, valve SV1 pressure testing and the valve SV41 constitutes series structure, not
only completing the sample probe cleaning of the inner wall, but also completing the
block detection of probe, which does not affect the accuracy of assimilating and
discharging liquid volume of a small amount of sample.
4. The block detection must be implemented when probe is cleaned. Turn off valve
SV1 after the cleaning, Detect pressure, and probe is completely blocked or partially
blocked if the pressure value change is the same or smaller than the range value.
And previous added sample should be deserted and alarm is issued. Turn off SV1
and SV41 when probe assimilates and discharges sample.
45
46
3, There is a device on the vacuum tank to eliminate air bubbles with liquid, gas
separating bottle.
4, vacuum liquid discharging, having concentrated and diluted liquid passages,
consists of the valves SV21, SV30, SV31 and concentrated, diluted liquid
separating bottles. Concentrated liquid means reaction liquid, including relatively
concentrated sample and reagent of patients, requiring separate collection.
5, when the colorimetric cup cleaning mechanism descends, turn off valves SV30
and SV31 first, and then open the valve SV21. It tarts assimilating sample under the
vacuum pressure, and the liquid of colorimetric cup will be discharged after a short
period of time when the rinsing mechanism arrives at the bottom of Colorimetric
Cup.
6, cleaning mechanism begins to add cleaning solution and ionized water, turn off
valve SV21 after the addition is completed, and then open valves SV30 and SV31.
At this time, the waste liquid discharged into isolating bottle outflows by its gravity.
7, cleaning liquid and ionized water adding is completed by the five valves SV42,
SV43, SV14, SV15 and SV11 which are timed. Because the vacuum liquid
discharging begins to work simultaneously when adding liquid to discharge
redundant liquid, the liquid will not spill outside colorimetric cup.
8, SV12 and SV14 valves are responsible for adding cleaning liquid. Before adding
or after the previous adding, open the valve SV12, but SV14 valve is at COM and
NO conduction status (power off status). Because there is a one-way valve in the
3-way top pipeline, cleaning fluid flows into the middle pipeline of the SV12 and
SV14 valves, and time valve SV12, cleaning liquid will remain in pipeline. Open
SV14 valve when adding, cleaning liquid will be added into colorimetric cup through
single way valve under the pressure. About 70ul cleaning liquid is consumed every
time.
Figure 5-7 ISE liquid line
47
Hardware configuration
6.1
PC
ISE
module
A/D
module
R2
module
R1
module
Sample
module
Reation
module
and
R2 adding mechanism
R2 reagent disk
R1 adding mechanism
R1 reagent disk
Sampling mechanism
Sample disk
stirring mechanism
Rinsing mechanism
Reaction disk
48
6.2
Security Note:
At working, touching hardware panel with hand or any other objects is forbidden.
In order to dismount panels, operation is only allowed when cut off power (220V, AC).
6.3
Description
Electrical
panel No.
tanks
2, two
5Solenoid valveSV6SV11SV12SV14SV15
SV21SV30SV31SV42SV43
6Alkaline cleaning liquid level monitoring
1, communication with the main control board
2, reagent 1 probe mechanism control
Reagent 1 disk
Circuit board
49
5, buzzer control
Reagent 2 disk
Circuit board
Sample disk
Circuit board
ISE
Circuit board
AD board
Cooling board
50
Circuit connecting
Board
Level
detecting
board
ISE
Preamp
board
Mother board
51
6.4
52
53
54
Solid
board
relay
12V switch
NES-35-12
55
56
57
58
59
60
6.5
61
6.6.3 Reaction disk/ sample disk / reagent 1 disk / reagent 2 disk/ ISE board function
The main function of circuit boards of three disks are to receive the main control
board's instruction to complete the reaction disk, the sample disk, reagent 1 disk, reagent
2 disk, ISE circuit board work, the specific functions as follows:
Each CPU communicates with the main control board to receive instruction;
Each CPU outputs control order of each executive unit;
to receive the sensor signals and other status of implementation unit;
sent to the main control board If alarm occurs,
6.6.4
62
type
NET-50B
Output voltage
DC 5V,0.6-5A;12V0.2-2.5A;-12V,0.1-0.7A
Output wattage
50W
Output set
3sets
Temperature
range
Input voltage
-20+60
85-264VAC/120-370VDC
size
129*98*38mm
Warranty period
2years
manufacturing
location
Guangzhou
Series
type
NES-15-12
Output voltage
DC 12V,0-1.3A
Output wattage
15W
Output set
1set
Temperature range
-20+60
Input voltage
85-264VAC(120-370VDC)
size
79*51*28mm
Warranty
period
manufacturing location
2 years
Guangzhou
63
Series
type
NES-15-5
Output voltage
DC 5V,0-3A
Output wattage
15W
Output set
1set
Temperature range
-20+60
Input voltage
85-264VAC(120-370VDC)
size
79*51*28mm
Warranty
period
manufacturing location
2 years
Guangzhou
Series
PFC series
type
SP-500-24
Output voltage
DC 24V,020A
Output wattage
500W
Output set
1set
Temperature range
0+40
Input voltage
88264VAC
size
170*120*93mm
Warranty
period
manufacturing location
2 years
Guangzhou
64
Series
type
NES-35-12
Output voltage
DC 12V,0-3A
Output wattage
35W
Output set
1set
Temperature range
-20+60
Input voltage
85-264VAC(120-370VDC)
size
99*97*36mm
Warranty
period
manufacturing location
2 years
Guangzhou
65
Tools
66
Figure 6-1
3. To observe whether the injection pump is leaking,
If so, check the leakage causes, and check the pipeline and connector timely.
67
Caution:
Make sure liquid flow catheter was not bent and flows smoothly.
Otherwise, it may result in that poor waste water spills from the cover
panel of analysis part, even the serious damage of analysis part.
68
Warning:
Please be careful to avoid hands from being scratched
Biological contamination danger:
In operation, please put on gloves, work cloths, and put on protective
glasses for the best.
Do not dispose the gauze used to clean sample probe at your own will,
please follow the relevant provisions for proper disposal.
Lift the rotating arms of sample and reagent probes by hands to the top
position, and rotate them to the top of sample or reagent storehouse for
convenient operation.
Caution:
When cleaning, do not touch directly the sample
surface to prevent probe scratch; avoid too much hand
force to prevent deformation of the sample probe.
69
Note:
Acidic and alkaline cleaning liquid can be used
alternatively, for instance, acidic cleaning liquid is used
at previous time maintenance, use alkaline cleaning
liquid at this time maintenance.
Wipe the external walls of sample and reagent probes lightly with cotton
stick moisturized with alcohol, especially the point of probe, until no
impurities left at all.
Wipe sample and reagent probes with the gauze dipped with deionized
water
After cleaning, lift the rotating arms of sample and reagent probes to the top
position, and rotate the rotating arm of sample probe to locate the sample
probe above the rinsing bath of sample and reagent probes.
Caution:
After cleaning the surface of a sample probe, please
make sure sample probe must be rotated to the top of
sample probe rinsing bath.
Switch on the power of analysis part and wait 30 seconds, enter the
"maintenance - routine maintenance" column to implement instrument
resetting", the system will automatically reset the sample and reagent
probes and rinse them with deionized water.
70
Lift the stirring rod by hands to the its top position, and rotate its rotating
arm to the above a position for convenient operation.
Caution:
When cleaning, do not touch the sample surface directly to
prevent probe scratch; avoid too much hand force to prevent
deformation of the sample probe.
Note:
Acidic and alkaline cleaning liquid can be used alternatively,
for instance, acidic cleaning liquid is used at previous time
maintenance, use alkaline cleaning liquid at this time
maintenance.
Wipe the surface of stirring rod lightly with cotton stick moisturized with
alcohol, especially the point of probe, until no impurities left at all.
Wipe stirring rod with the gauze dipped with deionized water
After cleaning, lift the rotating arms stirring rod to the top position, and
rotate the rotating arm of stirring rod to locate the stirring rod to the top of
the rinsing bath of stirring rod.
Switch on the power of analysis part and wait 30 seconds, enter the
"maintenance - routine maintenance" column to implement instrument
resetting", the system will automatically reset the sample and reagent
probes and rinse them with deionized water.
71
Caution:
Do not gaze scanning laser light, or it may cause eyes injury
Remove the reagent and sample disk covers, and then remove the sample
and reagent disks.
Wipe the scanning glass window lightly with gauze dipped with deionized
water.
Switch on the analysis part and wait 30 seconds, the system will reset
automatically.
Mount sample disk, tighten disk fixing screws clockwise and cover it.
72
Warning:
Please be careful to avoid being scratched by
sample probe.
Biological contamination danger:
In operation, please put on gloves, work cloths, and put on
protective glasses for the best.
Do not dispose the gauze used to clean sample
probe at your own will, please follow the relevant
provisions for proper disposal.
Mount sample disk, tighten disk fixing screws clockwise and cover it.
73
Warning:
Please be careful to avoid being scratched by
sample probe.
Biological contamination danger:
In operation, please put on gloves, work cloths, and put on
protective glasses for the best.
Do not dispose the gauze used to clean sample
probe at your own will, please follow the relevant
provisions for proper disposal.
Lift the rotating arm of sample probe by hands to the its top position, and
rotate its rotating arm to keep sample probe away from rinsing bath for
convenient operation.
Clean the inside and appearance of sample probe rinsing bath with clean
cotton stick.
After cleaning, lift the rotating arm of sample probe to the top position, and
rotate the rotating arm of stirring rod to locate the sample probe to the top
of the rinsing bath of sample probe.
Caution
After the work of sample probe surface rinsing, please
make sure to rotate the sample probe to the top of
sample probe rinsing bath.
5
Switch on the power of analysis part and wait 30 seconds, enter the
"maintenance - routine maintenance" column to implement instrument
resetting", the system will automatically reset the sample and reagent
probes and rinse them with deionized water.
74
Warning:
Please be careful to avoid being scratched by
sample probe.
Biological contamination danger:
In operation, please put on gloves, work cloths, and put on
protective glasses for the best.
Do not dispose the gauze used to clean sample
probe at your own will, please follow the relevant
provisions for proper disposal.
Lift the stirring arm to the top position by hand to one side of rinsing bath.
Remove the three screws of cooling unit and remove the cooling unit.
Remove the dustproof from the cooling unit and rinse it with water and dry
it.
figure
75
Caution
Please use consumables recommended by Dirui company, using other
consumables may cause system performance degradation.
Do not touch the light source lamp shell surface and lens in front of the
light source lamp by hand, because it may change the characteristics
of the light source. If you accidentally make noodle stained with filth,
absorbent cotton dipped by absolute alcohol can be used to clean it.
Turn off the system main power, so that the light source box and light
source lamp will be cooled for at least 15 minutes.
Warning:
High-temperature light source lamp and light box will
cause burn. Operation is carried out only after the light
source and light source lamp are cooled.
76
Loosen the two screws fixing light source seat to remove halogen lamp.
Mount a new halogen lamp according to the above opposite steps; pay
attention to tighten the screws. The cooling rubber hose in the lamp room
can not be twisted and down-lead can not be loosed or cocked.
Remount the reaction disk, the reaction cup and rinsing mechanism;
switch on the power supply of analysis part. After standby mode,
single-click Next in System maintenance window; infuse purified water
into reaction groove. After instrument standby mode, execute light quantity
check function. Check the back of halogen lamp if the light quantity
conforms to the requirement to start test.
77
Lift the rotating arm of sample probe by hands to its top position, and rotate
its rotating arm to keep sample probe away from rinsing bath for
convenient operation.
Hold shell claw of probe rotating arm with fingers and lift to remove.
78
warning
Carefully place dismounted sample probe and prevent it
scratching human body and sample probe damage.
Note
Take out sample probe from the rotating arm and be careful
to operate to avoid the damage of probe point caused by
touching rotating arm.
Note
Sample probe is precisely processed to ensure the sample adding
precision. If the probe point is damaged or bent, checking sample
probe is a must, or no guarantee can be made for test precision. Please
refer to "Error! Reference source not found. Error! Reference source
not found." for specific check of sample probe.
7.8.2 Clean sample probe/reagent probe
Warning
Please be careful to avoid being scratched by sample probe.
Biological contamination danger:
In operation, please put on gloves, work cloths, and put on protective
glasses for the best.
Do not dispose the gauze used to clean sample probe at
your own will, please follow the relevant provisions for
proper disposal.
Caution
Sample probe is precisely processed to ensure the sample adding
precision. If the probe point is damaged or bent, checking sample
probe is a must, or no guarantee can be made for test precision.
Please refer to "Error! Reference source not found. Error! Reference
source not found." for specific check of sample probe.
79
Lift the rotating arm of sample probe by hands to its top position, and rotate
its rotating arm to keep sample probe away from rinsing bath for
convenient operation.
Infuse about 1ml alkaline detergent of 0.5% (V / V) sodium hypochlorite or
84 disinfectant into rinsing bath for 10 minutes.
3
4
Lift the rotating arm of sample probe by hands to its top position, and rotate
its rotating arm to keep sample probe above the rinsing bath of sample
probe.
Caution
Please rotate the sample probe to the top of sample probe
rinsing bath after clean rinsing bath of sample probe.
80
Warning
Please be careful to avoid being scratched by sample probe.
Any touch is forbidden except at the knurling of it only by hand when
checking, and prevent any scratch on the flat part of stirring part.
Biological contamination danger:
In operation, please put on gloves, work cloths, and put on protective
glasses for the best
Please deal with removed stirring rod properly.
Caution
Please use consumables recommended by Dirui company, using other
consumables may cause system performance degradation.
Prepare a new stirring rod and wipe the flat part of it with gauze or cotton
stick dipped with cleaning liquid, and then wipe it with gauze dipped with
deionized water.
Lift the rotating arm of stirring rod by hands to its top position, and rotate its
rotating arm for convenient operation.
81
Caution
When pulling out stirring rod, make sure the direction of
force is vertical to that of axis of rotating arm. Lateral force
may damage the axis or stirring rod.
4
Prepare a new stirring rod, and wipe the front of the stirring rod with gauze
dipped with 2% CS-antibacterial cleaning liquid.
When mounting new stirring rod, insert stirring rod till the bottom of motor
axis and tighten it with M2 screw.
Caution
When inserting stirring rod, make sure the direction of force is
vertical to that of axis of rotating arm. Lateral force may
damage the axis or stirring rod.
Pushing the stirring rod completely
After stirring rod check, visually check whether stirring rod and its rotating
arm are vertical with each other.
If not vertical, return to step 5 and remount the stirring rod.
If vertical, continue to next.
Lift the rotating arm of stirring rod by hands to its top position, and rotate its
rotating arm to the top of its rinsing bath.
Caution
Please make sure to rotate stirring rod to its rinsing bath top
after mount it.
Switch on the power of analysis part and wait 30 seconds, enter the
"maintenance - routine maintenance" column to implement instrument
resetting", the system will automatically reset the sample probe and rinse it
with deionized water. Observe the outflow of sample probe.
82
Warning
Please be careful to avoid being scratched by sample probe.
Place each probe and pole into proper position for convenient.
Biological contamination danger:
In operation, please put on gloves, work cloths, and put on protective
glasses for the best
Please deal with removed reaction cup properly which is broken.
Caution
Please use consumables recommended by Dirui company, using other
consumables may cause system performance degradation.
Switch
off
instrument
83
Rotate reaction disk by hand and remove the reaction cup sequently. Take out
reaction cup while rotating it.
Rinse the new reaction cup dipped in with water; rinse inside and outside of
reaction and no scratch is allowed.
Rotate reaction disk by hands, and mount new reaction cup on reaction disk
and check the six sets reaction cups simultaneously.
Mount reaction disk with the opposite steps and make sure the fixing screw of
reaction disk is tight.
84
Analysis principle
The assay mode of Auto-Chemistry Analyzer is based on the Beer-Lambert law that the
material selective absorption light
The main principle is: When monochromatic light with specific wavelength passes
through the cuvette with sample, the monochromatic light absorbency and sample liquid
concentration are varies directly as the distance which is passed through sample liquid by
light:
I0
= b c
It
A Absorbency of the light when passing through liquid
A = lg 1/T = lg
Solution layer thickness (b): Optical path, which is fixed by instrument. Molar absorption
coefficient () is the correlation coefficient of the wavelength, solution and solution
temperature. Linear relationship is displayed between solution thickness and absorbency
when in stable temperature and single wavelength value is given on the reagent bottle by
factory
If the sample liquid adequate distribution, interaction between liquid and incidence
monochromatic light only happens during absorbing process. No fluorescence, disperse and
photochemical appear. No interaction between substances in the solution while absorbing
process. The absorbency possess conducts nature, and this condition conforms to the
Beer-Lambert law
85
8.2
Method
Photometry point
L 0 0 0
1-point
Assay
AL + AL 1
2
1LM49
B1 + B 2 + B 3
3
( AM + AM 1 ) k ( AL + AL 1 )
2
L M 0 0
B1 + B 2 + B 3
3
AM + AM 1 AL + AL 1
2
2
t
L M 0- 0
2-point
Rate Assay
Formula
B1 + B 2 + B 3
3
1L49
2-point
assay
Cell
blank
Remark
L
M
1LM49
L M 0 - 0
Rate
Assay
1LM49
B1 + B 2 + B 3
3
AM-L
L +2M
Fist half
1-point
&
Rate Assay
L 0 0 0
1 M NL P
Q49
B1 + B 2 + B 3
3
AL + AL 1
2
86
Second half
MNPQ
1 M NL P
Q49
B1 + B 2 + B 3
3
AQ- P-kAN -M
M+2N P+2Q
Fist half
L 0 0 0
3-point dual
item
B1 + B 2 + B 3
3
AL + AL 1
2
B1 + B 2 + B 3
3
( AN + AN 1 ) k ( AM + AM 1 )
2
1LMN49
Second half
MN00
1LMN49
Fist half
L M 0 - 0
3LMNP49
Rate
B
Assay
(mode 1 )
B1 + B 2 + B 3
3
AM-L
L +2M
An p
wavelength
Second half
NP00
3LMNP49
B1 + B 2 + B 3
3
N+2P
diffe
Two conditions
AnpkALmsame
wavelength as the second
half
Fist half
Rate
B
Assay
(mode 2 )
L M 0 0
3LMNPQ
R49
B1 + B 2 + B 3
3
AM-L
B1 + B 2 + B 3
3
A(R-Q)kA(P-N)
L +2M
Second half
N P Q R
3LMNPQ
R49
N+2P Q+2R
87
L,m,n,p,q,r
: Photometric points
Rn
B1B 2B 3
(B1,B2,B3 )/3
Ax
A(m-L)
points L and M
k
a
k=
S + Rj
j =1
b
S + Ri
i =1
Sample volume
Rj Ri
Note 1: The 5 th Photometric point wont be Stirred after adding reagent 2. Stirring
when the reaction disk pauses after rotates one circle plus 2 pitches
Note 2: liquid in the reaction cuvette should be more than or equal to 150 ul, less
than or equal to 450ul.
Note 3: Do input 0 if the photometric point is not used.
88
8.3
Endpoint assay
Endpoint assay means the reaction takes a period time. Due to reaction balance constants
are big, all substrates (tested) are transformed into product when reaction reaches balance,
and no increase (decrease) of reaction solution absorbance will occur, and the degree of
absorbance increase (decrease) and the concentration of tested substance is directly
proportional. This assay is call endpoint assay or balance assay more accurately, which is
the ideal assay mode.
The endpoint assay is not sensitive to small changes (such as enzyme amount, pH,
temperature, etc.) as long as this change does not affect the balance in certain time.
A
b
Cell blank
Time
89
Absorbance 02A
range
endpoint assay
Optical path 10mm
sample
10uL
1250uL
Mixing
reagent A:B50:1
storage
37
incubation 10min
10min
0
550nmblank pipe
5mA equals to 1umol/L
Linearity
300umol/L18mg/dL
range
Unit
1umol/L0.0585mg/dL
89.6umol/L0.425A
conversion
Adult5.119umol/L0.31.1mg/dL
Baby20200umol/L1.212mg/dL
Main 550nmsub 660nm
Absorbance
02A
range
Optical path
10mm
sample
4uL
Mixing
285days stable
storage
3730, 25
incubation
5min6min , 8min
5min
0
520nmblank pipe
0.42mA equals to1umol/L
Linearity
1.5mmol/L25mg/dL
range
0.72mmol/L0.302A
Unit
1mmol/L16.8mg/dL
conversion
child0.120.33mmol/L2.05.5mg/dL
Male0.210.43mmol/L3.57.2mg/dL
female0.150.36mmol/L2.56.0mg/dL
urine 14.944.6mmol/L250750mg/dL
90
8.4
2-point assay
2-point assay (fixed time assay) is also called first class dynamics assay, which means the
reaction speed is in direct proportion to the simple power of substrate concentration in
specified time, namely v=k[S]. Due to the reduction of substrate, the whole reaction speed
is decreasing gradually, which reflects the decrease (increase) of absorbance and
decrease of speed. Because reaction time to reach balance is very long, , it can be
monitored at any time theoretically, but because of the complexity of serum ingredient and
much reaction, therefore, it takes a certain period of time to enter in stable reaction phase.
Figure 8-2
Absorbance
Cell blank
Time
Time
2-point assay
8.5
Rate assay
Rate assay, also known as zero-class dynamics assay, refers to the reaction rate is directly
proportional to the zero power of substrate concentration, which has nothing to do with the
substrate concentration. Hence, the reactants can generate a certain product at constant
speed throughout the reaction process, resulting in even decrease or increase of
absorbance of measured solution at a wavelength, and the decrease or increase speed (
A / min) is directly proportional to the activity or concentration of the tested substance
(catalytic material). Dynamics assay is also called as the continuous monitoring assay,
mainly used for the measurement of enzyme activity.
In fact, because substrate concentration can not be big enough, with the reaction
proceeding, the reaction is no longer zero class when substrate is consumed to a certain
extent, Therefore, zero-class dynamics assay is targeted at a specific period in terms of
time; Because reaction time to reach balance is very long, , it can be monitored at any time
theoretically, but because of the complexity of serum ingredient and much reaction,
therefore, it takes a certain period of time to enter in stable reaction phase. So all reagent
manufactures have strict requirements to the two periods
Dynamics assay is based on the changes between specified photometric points to obtain
the absorbance concentration or activity value.
Metering point in accordance with the input form, dynamics method can be divided into
single-band and dual-band dynamics assay.
91
Absorbance
Time
Example 3ALT/GPT Alanine aminotransferase IFCC
wavelength
Main 340nm
Test mode
Reagent
Single
reagent
temperature
reaction
Rate assay
1200uL250uL
4 reagent 1and 1reagent 2
sensitivity
calibration
Reference
value
3730, 25
60s delaymeasure 60
120s
0.30mA/min equals to
1.0U/L
Absorbance
range
Optical path
sample
Mixing
storage
incubation
0
02A
10mm
15uL
285days stable
5min
340nmblank pipe
Linearity
450U/L7.5ukat/L
range
Unit
1U/L16.6710-3ukat/L
conversion
Female<31U/L<0.52ukat/L
37Male<40U/L<0.67ukat/L
Calculating method