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Sysmex XN-1000/2000 Technical Guide

F: | Au:FANS | DA:2026-09-23 | 8 Br: | 🔊 点击朗读正文 ❚❚ | Share:

Sysmex XN-1000/2000 Technical Guide

In the automation upgrade and daily operation of clinical hematology laboratories, the Sysmex XN series is a highly representative modular analysis platform. As standalone configurations, XN-1000 and XN-2000 correspond to single analysis module and dual analysis module architectures, respectively, providing high sample processing capabilities and clinical scalability within a limited footprint. For laboratory engineers, technical supervisors, and procurement personnel, understanding the module differences, channel principles, parameter systems, sample size requirements, quality control strategies, and common anomaly troubleshooting logic of the XN series can help them make more accurate judgments in equipment installation, method validation, daily maintenance, and troubleshooting.

System positioning and modular architecture

The core analysis modules of the XN series include XN-10 and XN-20. XN-1000 consists of one analysis module, while XN-2000 consists of two analysis modules. Both are independent XN configurations that can achieve a complete hematology testing menu in a small space. The XN-1000 has a maximum throughput of about 100 samples per hour, making it suitable for laboratories with relatively low daily workloads but wide clinical needs. The XN-2000 has a maximum throughput of about 200 samples per hour, making it suitable for laboratories with higher workloads and stricter requirements for continuous operation and result turnover.

An important feature of XN-2000 is automatic workload balancing between dual modules. Two analysis modules can allocate detection tasks based on actual sample loads, reducing the pressure on individual modules and improving overall efficiency. Meanwhile, XN-2000 also supports reagent sharing options, which have practical significance for reagent management, inventory control, and cost optimization. Its "common primary" design concept enables dual modules to complement each other, improve processing capabilities during peak hours, and retain a certain sample processing capability during single module maintenance or exceptions.

The difference between XN-20 module and XN-10 module mainly lies in their advanced channel and parameter capabilities. The WPC channel and HPC parameters are only available on XN-20. WPC is a precursor cell channel for white blood cells, which can be used to indicate abnormal populations of white blood cells such as lymphocytes and primitive cells; HPC is used for counting human progenitor cells and can assist in determining the timing of peripheral blood stem cell collection when additional software activation is required. For laboratories with blood tumors, stem cell transplantation, or special hematological needs, XN-20's scalability is more advantageous.

The XN series supports upgrading from XN-1000 to XN-2000. When the workload of the laboratory increases, an analysis module can be added on the basis of the original configuration without completely replacing the system. The entire XN series adopts universal software, with a consistent operating interface and logic, which can reduce retraining costs. This scalability enables the XN series to not only meet current needs, but also adapt to future clinical project increases and sample size growth.


Laser Flow Core Technology

The XN series uses fluorescence flow cytometry as the core technology for white blood cell classification, reticulocyte, platelet, progenitor cell, and humoral cell analysis. The wavelength of the laser beam is 633 nm. After irradiating the cells passing through the flow chamber, forward scattered light, lateral scattered light, and lateral fluorescence are generated. Forward scattered light reflects cell size information; Lateral scattered light reflects intracellular structural information; Lateral fluorescence reflects the type and quantity of nucleic acids and organelles. By collecting signals of different intensities, the instrument generates scatter maps for each measurement channel for cell classification and abnormal population indication.

The advantage of this technological approach is that different cell populations form relatively independent distribution regions on the scatter map. Taking WDF channel as an example, it can display populations such as lymphocytes, monocytes, eosinophils, neutrophils, basophils, immature granulocytes, and abnormal lymphocytes. The WNR channel is used for counting nucleated red blood cells and white blood cells, supporting direct measurement and correction of NRBC in CBC analysis. The WPC channel further prompts for abnormal lymphocytes, primitive cells, and progenitor cells, providing more information for hematological anomaly screening.

In addition to fluorescence flow cytometry, the XN series also uses hydrodynamic focusing DC detection method for RBC, HCT, and PLT-I impedance detection. Hemoglobin was measured using the cyanide free SLS method. This combination provides a stable technical foundation for the instrument in terms of cell counting, hemoglobin concentration, and platelet counting. For engineers, understanding that different channels correspond to different principles can help quickly identify the source of problems when results are abnormal. For RBC, HCT, PLT-I abnormalities, impedance testing, sheath flow, and sample status can be prioritized for inspection; If there are abnormalities in WBC classification, RET, PLT-F, BF, and HPC, the focus should be on checking the laser flow channel, fluorescent reagent, scatter plot distribution, and sample size.

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