The system to provide the required pressure and vacuum for main unit operation consists of the
following. Pressurized air is regulated at 2.5 kg/cm
water droplets are removed by an air filter. An air drier is used to remove any remaining moisture before
it is supplied to the main unit. The pressure of the dry air is regulated at 1.6, 0.7, and 0.3 kg/cm
The vacuum (400 mmHg or higher) is adjusted to 300 mmHg by the bellows unit in the main unit.
A filter is provided on the bellows unit to prevent the needle in the bello w from accumulating dirt.
The outline of pneumatic control system is shown below.
2
by a relief valve in the pneumatic unit, any dust and
2
.
2-1February 5, 2009XE-series S/M
2.2USE OF PRESSURE AND VACUUM
Use of pressure and vacuum for the main unit are as follows.
TypeNameFunctions
Pressure2.5 kg/cm
1.6 kg/cm
0.7 kg/cm
0.3 kg/cm
VacuumSource VacuumAspiration of reagent and driving diaphragm pumps.
300 mmHgAspiration of waste to WC1
2
2
2
2
Driving master valves, air cylinders, and diaphragm pump (DP 5mL for
FCM (EPK) replenishment)
Sheath Flow forming for FCM
Draining waste chamber and driving of diaphragm pumps
Sheath Flow forming for RBC
2-2February 5, 2009XE-series S/M
2.3HYDRAULIC SYSTEM
WBC/RBC Block Diagram
RBC/HGB Block Diagram
2-3February 5, 2009XE-series S/M
2.4ANALYSIS PARAMETER
Analysis Block
Principle
Analysis
Channel
Information
Parameter
Analytical
Parameter
Reagent
Analysis Block
Principle
Analysis
Channel
Information
Parameter
RBC/PLTHGBIMI
Searth Flow DC Detection MethodColorimetricRF/DC
RBC/PLT ChannelHGB ChannelIMI Channel
PLT HistogramRBC
Histogram
PLT HCTRBCHGB-
MCV,MCH,MCHC,
MPV,PDW, P-
LCR
CELL P ACKII / SE SEATHIISULFOLYSERSTOMATOLYSER-IM
WBC/BASO
Channel
WBC/BASO
Scattergram
WBC#BASO
*2
%
BASO
#
RDW-SD/CV
WBC/RET
Flowcytometry by using Semi-Conductor Laser
4DIFF ChannelNRBC
Lymph
%
Lymph
#
4DIFF Scattergram
MONO
%
MONO
#
NEUT
%
NEUT
#
*1
EOSI
%
EOSI
#
IMI Scattergram
Channel
NRBC
Scattergra
*3
m
NRBC%
NRBC#
*5
RET
Channel
RET
Scattergra
*4
m
RET%
RET# PLT-
O
Analytical
Parameter
Reagent
STROMATOLYS
ER-FB
STROMATOLYSER-4D
Lysing solution/ Staining Dye (NEW)
STROMAT
OL YSER-
NR Lysing
solution/
Staining
Dye (NEW)
L/M/HFR,
IRF
RET
SERACHII
Diluent
solution/
Staining
Dye (NEW)
2-4February 5, 2009XE-series S/M
*1 4DIFF Scattergram*2 WBC/BASO Scattergram
*3 NRBC Scattergram*4 RET Scattergram
*5 IMI Scattergram
Figure 2-1 Scattergrams
2-5February 5, 2009XE-series S/M
2.5REAGENT SYSTEM
Figure 2-2 Reaction Chamber Construction
2-6February 5, 2009XE-series S/M
2.6ANALYSIS FLOW
2-7February 5, 2009XE-series S/M
2.7FCM DETECTOR BLOCK
NOTE:
Laser Diode is very sensitive to static electricity. Follow the instruction below
when you replace the Laser Diode.
- Remove jumper pin from the terminal on the Laser Diode AFTER connectÂing to PCB No. 2140. If the jumper pin is removed before connecting to
PCB No.2140, Laser Diode will be damaged.
- Do not disconnect the connector to the PCB No.2140.
In the worst case, the device inside the Lase r Diode will be destroyed.
The life of the Laser Diode is approx. 10,000 hours.
2-8February 5, 2009XE-series S/M
2.7.1Function
(1)Outline
Laser diode apply to samples in sheath flow generated flow cell. FCM Detector Block detects front
scattered light, side scattered light, and side fluorescence light from these samples. XE-2100 genÂerates two-dimensional scattergrams from these signals as follows.
Beam spot generating system consists of laser diode, collimator lens. Laser beam generated b y
laser diode is converted to parallel beam by collimator lens. This beam is collected by condenser
lens and applies to samples. Beam shape is as follows.
(3)Sheath flow system
Sheath flow is generated in the flow cell. Sample flows center of the flow cell.
(4)Front scattered light system
Front scattered light system consists of beam stopper and FSC condenser lens.
Beam stopper shade direct light from the laser diod e. FSC condenser lens collect the scattered
light of the sample.
(5)Dichroic mirror
Light below 640 nm wave length reflects to the side scattered light PMT.
2-9February 5, 2009XE-series S/M
(6)Side fluorescence light system
Side fluorescence light sy st em co nsis t s of int erference filter, PMT (Photo Multiplier Tube). The light
through dichroic mirror is filtered by interferenc e filter and fluorescence light over 660 nm wave
length is detected by PMT. Detected fluorescence light signal is amplified by pre-amplifier and
transmitted to main amplifier.
(7)Side Scattered light syst em
Side Scattered light system consists of ND filter (Neutral Density filter) and PMT.
The light through dichroic mirror is attenuated by ND filter and sca ttered light is detected by PMT.
Detected scattered light signal is amplified by pre-amplifier and transmitted to main amplifier.
(8)Temperature Control
FCM Detector block is heater controlled to maintain the optical stability.
(9)Cover switch
Cover switch is installed to prevent interference from the outer light and leakage of the laser beam.
If the cover is opened, XE-2100 stops laser radiation and massage is displayed.
2-10February 5, 2009XE-series S/M
2.8OPTICAL SYSTEM
2-11February 5, 2009XE-2100 S/M
2.9HYDRAULIC SEQUENCE DESCRIPTION
0- 5 sec
[WB aspiration, reagent chamber]
- SRV turns activating SV60 f or 0 - 0. 5 sec.
- Whole blood pump descend to aspirate diluent for 0 - 2.0 sec.
- SRV is rinsed (perimeter cleaning) by activating SV60 for 0 - 0.5.sec.
- WC2 is drained by activating SV 43 for 1.5 - 7.5 sec.
- WC3 is drained by activating SV 45 for 0.5 - 2.0 sec.
- SNR is replenished by activating SV8 for 0 - 3.0 sec.
[HGB]
- Solution in HGB flow cell is drained by activating SV36 for 3.0 - 3.8 sec.
- HGB Diluent DP dispense diluent into HGB flow cell for rinsing for 3.8 - 4.9 sec.
- SV 11 is activated to push the solution in the air mixing tubing to WC1.
2-12February 5, 2009XE-2100 S/M
2-13February 5, 2009XE-2100 S/M
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