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Magnetic particle luminescence micro-fluidic chip for multi-marker detection and detection device

A microfluidic chip, multi-marker technology, applied in measurement devices, fluid controllers, laboratory containers, etc., can solve the problems of reducing the accuracy of test results, easy cross-influence of magnetic particles, etc., to avoid mutual influence. Cross-influence, the effect of improving accuracy

Pending Publication Date: 2020-01-03
SHENZHEN HUAMAIXINGWEI MEDICAL TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The embodiment of the present invention provides a magnetic particle light-emitting microfluidic chip and a detection device for multi-marker detection, aiming to solve the problem that the magnetic particles are easy to cross-interact with each other when detecting the existing magnetic particle light-emitting microfluidic chip, which greatly reduces the detection results. problem of accuracy

Method used

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  • Magnetic particle luminescence micro-fluidic chip for multi-marker detection and detection device
  • Magnetic particle luminescence micro-fluidic chip for multi-marker detection and detection device
  • Magnetic particle luminescence micro-fluidic chip for multi-marker detection and detection device

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Embodiment 1

[0025] refer to Figure 1 to Figure 4 , the first embodiment provides a magnetic particle luminescence microfluidic chip for multi-marker detection, including: a top plate 1, the top plate 1 is provided with at least one sample adding part 11, a mixing area 12 interconnected with the sample adding part 11, And a plurality of labeling ligands arranged in the mixing area 12, each labeling ligand is different from each other; the bottom plate 2 arranged on the top plate 1, the bottom plate 2 includes a guide area 21 that communicates with the mixing area 12, and the guide area 21 The reaction zone 22 communicated with each other, a plurality of detection zones communicated with the reaction zone 22, the cleaning liquid storage part 24 and the luminescent liquid storage part 25 communicated with the detection zone; the reaction zone 22 is provided with a plurality of magnetic particle ligands, magnetic The particle ligands include magnetic particles and ligands, and the magnetic p...

Embodiment 2

[0034] On the basis of the first embodiment, at least one of the core-to-mass ratio, the mass and the volume of the magnetic particles in the second embodiment is different. Each magnetic particle ligand is placed in the reaction zone 22, and the external magnet moves, which can drive the magnetic particles to move. By controlling the moving speed of the magnet, when the moving speed of the magnet is fast, it drives the magnetic particles with large nuclear-to-mass ratio, high mass or large volume to move; when the moving speed of the magnet is slow, it drives the magnetic particles with small nuclear-to-mass ratio and mass. Smaller or smaller magnetic particles move. Therefore, the moving speed of the magnet can be controlled, and the magnetic particles matching the moving speed can be driven to move, even if other magnetic particles will move, but there is a channel between the reaction area 22 and the detection area, only the movement of the magnet Only magnetic particles ...

Embodiment 3

[0036] On the basis of Embodiment 1, positive electrodes and negative electrodes are respectively provided on both sides of the detection area channel in Embodiment 3, figure 1 The positions of the positive and negative electrodes are shown, as figure 1 The "+" sign shown is the position of the positive electrode, as in figure 1 The shown "-" is the position of the negative electrode. Of course, in other embodiments, the positive electrode and the negative electrode may also be located at other positions, which will not be repeated here. The isoelectric point of each magnetic particle is different, and the isoelectric point refers to the pH value when the surface of the magnetic particle is not charged. Each magnetic particle ligand is placed in the reaction zone 22, and the external magnet moves, which can drive the magnetic particles to move. After the magnet drives the magnetic particles from the reaction zone 22 to the detection zone, the magnets are withdrawn. Since the...

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Abstract

The invention belongs to the technical field of micro-fluidic chip luminescence immunoassay, and particularly relates to a magnetic particle luminescence micro-fluidic chip for multi-marker detectionand a magnetic particle luminescence micro-fluidic detection device. The magnetic particle luminescence micro-fluidic chip comprises a top plate and a bottom plate, wherein the top plate is provide with at least one sample adding part, a mixing region communicated with the sample adding part, and a plurality of labeled ligands arranged in the mixing region; the bottom plate comprises a flow guideregion communicated with the mixing region, a reaction region communicated with the flow guide region, a plurality of detection regions communicated with the reaction region, a cleaning liquid storagepart communicated with the detection region, and a luminescent liquid storage part; a plurality of magnetic particle ligands are arranged in the reaction region, and magnetic particles of each magnetic particle ligand are different from the ligands; a cleaning liquid is arranged in the cleaning liquid storage part, and a luminescent liquid is stored in the luminescent liquid storage part; and anair pump is arranged on the top plate and is used for driving the sample in the sample adding part to flow through the mixing region. Since the plurality of detection regions are arranged, mutual cross influence of the magnetic particles can be avoided, and the precision of a detection result is greatly improved.

Description

technical field [0001] The invention belongs to the technical field of luminescence immunodetection of microfluidic chips, and in particular relates to a magnetic particle luminescence microfluidic chip for multi-marker detection and a detection device. Background technique [0002] At present, there are two main development trends in in vitro diagnosis (IVD): one is automation and integration, that is, using fully automated, highly sensitive large-scale instruments and equipment in the central laboratory supporting large hospitals to achieve high-precision disease analysis and diagnosis ; Another kind of miniaturization and bedside, that is, through a small and simple handheld device, to achieve rapid on-site analysis and diagnosis. However, small hospitals have insufficient funds and small sample sizes, and are not suitable for purchasing expensive large-scale equipment. As a result, the rapid detection equipment used in most hospitals at this stage is mainly test strips ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N33/543G01N33/532
CPCG01N33/54326G01N33/532G01N33/54366B01L3/502715B01L2200/0689B01L2200/16B01L2300/042B01L2300/0663B01L2300/0819B01L2300/0867B01L2300/087B01L2300/0883B01L2400/043
Inventor 王东江荣香李泉
Owner SHENZHEN HUAMAIXINGWEI MEDICAL TECH CO LTD