ADVIA Chemistry XPT System

Formula budućnosti. Danas.

Zahtevi laboratorije i zaposlenih su u kontinuiranom porastu. Da biste opstali ispred ovih rastućih zahteva, potreban vam je sistem za biohemiju koji je jednostavan za upotrebu, koji održava rad i donosi moćniju produktivnost i veću efikasnost.
The ADVIA® Chemistry XPT System je dizajniran za stalni rad i brze, tačne rezultate. Raspolaže naprednim softverom i VeriSmart® tehnologijom koja obezbežuje precizno testiranje i pouzdane rezultate koji ispunjavaju vaša očekivanja.
General Chemistry
Alanine Aminotransferase (ALT)1
Alanine Aminotransferase (P5P)1
Albumin (BCP)1
Alkaline Phosphatase (AMP)1
Aspartate Aminotransferase1
Aspartate Aminotransferase (P5P)1
Bilirubin, Direct
Bilirubin, Total
Calcium (Arsenazo)1
Calcium (CPC)1
Carbon Dioxide, Enzymatic3
Creatine Kinase
Creatinine, Enzymatic
Gamma-Glutamyltransferase (GGT)
Glucose (Hexokinase)1
Glucose (Oxidase)1
HDL Cholesterol
Lactate Dehydrogenase (L-P)
Lactate Dehydrogenase (P-L)
LDL Cholesterol
Pancreatic Amylase
Total Iron Binding Capacity (TIBC)
Total Protein1
Total Protein (Urine/CSF)
Urea Nitrogen1
Uric Acid1

Specific Proteins
α1- Acid Glycoprotein
α-1 Antitrypsin
Antistreptolysin O
Apolipoprotein A1
Apolipoprotein B
β2 Microglobulin
CardioPhase® high-sensitivity CRP
Complement C3
Complement C4
C-Reactive Protein (CRP)
CRP, Wide Range (wr-CRP)
Cystatin C
Immunoglobulin A (IgA)
Immunoglobulin G (IgG)
Immunoglobulin M (IgM)
Rheumatoid Factor (RF)
Hemoglobin A1c

Drugs of Abuse/Toxicology
Barbiturates (Serum)
Benzodiazepines (Serum)
Cannabinoids (THC)
Cocaine Metabolite
Creatinine Specimen Validity Test2
Methadone Metabolites (EDPP)
Nitrite Specimen Validity Test2
Oxidant Specimen Validity Test2
pH Specimen Validity Test2
Specific Gravity Specimen Validity Test2
Tricyclic Antidepressants

Therapeutic Drug Monitoring (TDM)
Valproic Acid

Product Specifications
System Description Fully random and continuous access, discrete processing clinical chemistry system with batch run capability
Test Throughput Up to 2400 tests/hour: 1800 tests/hour photometric, 600 tests/hour ISE
Assays Onboard 59 assays, including 3 ISE (Na, K, Cl)
Sample Handling
Sample Tubes 5 mL, 7 mL, and 10 mL tubes; 1 mL and 2 mL sample cups; user-defined containers
Sample Tray 84 sample positions; positive sample identification
Validated Sample Types Serum, plasma, urine, whole blood, and CSF, assay-dependent
Sample Integrity Control Qualitative check for hemolysis, lipemia, and icterus; clot detection, flagging, and management; short-sample
detection, flagging, and management
STAT Handling 84 positions, not dedicated; STAT samples are processed with priority
Auto-repeat Testing Automatic repeat testing from the retained prediluted sample or original sample
Sample Dilution Automatic dilution up to 1:5625 from retained prediluted sample or original sample
Auto-reflex Testing Automatic ability to perform additional tests based on results of first test or test combination
Primary Sample Probe Liquid-level sensing, crash protection, clot/clog detection, liquid-surface verification
Sample Carryover Prevention Automated wash; additional automated sample probe washes programmable for greater prevention
Sample Throughput Up to 200 tubes per hour with ISE use; faster without ISE use
Bar Codes
Sample Bar Codes Up to 20 digits; Interleaved 2 of 5, Code 39, Code 128, Codabar; A, B, and special characters (.-+/*$%)
Micro-volume Technology
Automatic Sample Predilution Samples typically diluted 1:5 (30 μL sample + 120 μL saline generates up to 15 tests results);
retained for auto-repeat, auto-reflex, or auto-dilution until results are available
Predilution Tray 120 dilution cuvettes
Sample Volume per Test 2–30 μL of prediluted sample, equating to 0.4–6.0 μL of original sample per test (varies by assay)
Average Reagent Volume 80–120 μL per test, assay-dependent
Reaction Area
Reaction Cuvettes 340 reusable optical-grade plastic cuvettes
Reaction Bath Inert fluorocarbon oil circulation system, 37°C
Photometer 14 fixed wavelengths (340, 410, 451, 478, 505, 545, 571, 596, 658, 694, 751, 805, 845, and 884 nm)
Light Source 12V, 50W halogen lamp, cooled by forced water circulation
Assay Result Calculations Endpoint (EPA), rate reaction (RRA), 2-point rate (2PA), constant rate analysis (CRA), and immunoassay
analysis (IMA) methodologies; prozone checking; substrate depletion check; results available as completed
Reaction Times 3, 4, 5, and 10 minutes; extended reaction times 15 and 21 minutes
Automatic Correction Sample blank, cuvette blank, measurement point change, sample volume change in re-assay
Point Forwarding Can automatically extend linearity to measure samples over assay range
Assay Technology Potentiometric, photometric, turbidimetric
Reagent Handling
Reagent Tray 2 trays, (R1=60 and R2 =56 positions), refrigerated between 6°C and 13°C (43°F–55°F)
Reagent Capacity Onboard 56 photometric assays
Test Capacity Onboard 40,000 photometric tests average; over 100,000 photometric tests with the use of concentrated reagents
Reagent Containers 20, 40, 70 mL reagent wedges
Reagent Integrity Control Bar-code reagent identification; automatic inventory tracking and flagging; calibration and control validity
tracking and flagging; reagent onboard stability tracking and flagging; reagent expired/reagent low flagging
Onboard Stability Up to 60 days, depending on assay
Reagent Dilutions Capability to dilute concentrated reagents onboard
Open-system Capability
Channels 200 assay channels; includes 50 channels for user-defined applications
Ion-selective Electrodes (ISE)
ISE Indirect simultaneous measurement of Na+, K+, Cl-
ISE Sample Volume 22 μL original sample for all three tests
Electrode Expected Use Life 30,000 samples or 3 months, whichever occurs first
Throughput Rate Up to 600 tests/hour; 200 tubes/hour
Validated Calibration Interval Up to 60 days, tracked by software
Auto-calibration User-defined time interval or with new reagent container
Auto-QC User-defined test count interval or with auto-calibration
View Calibration Graphical display of calibration curves
QC Data Graphical display of QC; real-time/QC monitoring; Advanced QC package includes Levey-Jennings plots,
Westgard rules, and RiliBÄK rules; 125,000 control results can be stored, archivable to removable media
Calibration/Control Tray 61 refrigerated positions for calibrators, controls, and diluents
User Interface/Data Management
Monitor 22-inch (55.9 cm) diagonal high-resolution LCD touchscreen with adjustable height
Operating System Microsoft® Windows® 7
System Documentation Operator manual, quickstart guide, and online help
Data Storage 500,000 active plus 500,000 historical test results; can archive to removable media
Onboard Maintenance Logs Yes
Host Interface TCP/IP bidirectional
Host Query ASTM; system requests work order or batch of work orders from host
Remote Access and Service Siemens Remote Service via 1000BASE-T Ethernet port
Removable Media
Removable Media DVD, CD-RW, or USB
General Specifications
Power Requirements 200–240V at 50/60 Hz, 3 kVA consumption
Water Requirements CLSI® Clinical Laboratory Reagent Water or equivalent connected directly to a pressurized water source
Maximum Water Consumption 40 liters (10.6 gallons) per hour
Drain Requirements Minimum of 40 liters (10.6 gallons) per hour
Dimensions With monitor: 149 (h) x 177 (w) x 99 (d) cm; 59 (h) x 70 (w) x 39 (d) inches
Without monitor: 134 (h) x 177 (w) x 99 (d) cm; 53 (h) x 70 (w) x 39 (d) inches
Weight 725 kg (1598 lb)
Compliance Complies with international environmental, health, and safety standards, including CE and RoHS
Noise Emission Less than 62 dB
Processing Heat Output 5374 BTU/hour
Ambient Temperature 18°–30°C (64°-86°F)
Ambient Humidity 20–80% noncondensing