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Time-resolved fluorescent immunochromatographic test strip, kit and preparation method for detecting myo

An immunochromatographic test paper and time-resolved technology, which is applied in the field of medical testing, can solve the problems of affecting microprotein activity, narrow linear range, and affecting results, etc., and achieve the effects of being suitable for large-scale production, simple preparation method, and convenient clinical use

Active Publication Date: 2019-11-08
RAYBIOTECH INC GUANGZHOU
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] 2. Gold standard method - this method is fast, simple and easy to observe, but the sensitivity of qualitative detection is not high
[0008] 3. Transmission immunoturbidimetry——This method is simple, fast, and can be automated, and is suitable for batch detection. However, the methodology and clinical application of immunoturbidimetry still need further verification
Various test strips and instruments based on immunochromatography, chromatography and dry chemistry techniques will affect the activity of microproteins in the matrix due to differences in temperature, humidity and pH, thereby affecting the results
The methodological flaws of some POCT instruments, such as poor sensitivity and repeatability, and narrow linear range, are only used for reference in emergencies or emergencies, and need to be sent to the laboratory for re-examination if necessary.
[0011] The current immunofluorescence chromatography device uses the reflection method to detect the fluorescent signal on the porous membrane. The fluorescence detector captures the specific antibody modified by the fluorescent dye on the surface of the porous membrane, but cannot detect the fluorescent signal inside the porous membrane, which leads to the detection of Sensitivity drop

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] Example 1 Time-resolved immunochromatographic test strip for detecting MYO

[0040] A time-resolved immunochromatographic test strip for detecting MYO of this embodiment includes a bottom liner, and a sample pad, a binding pad, a coating film and absorbent paper which are sequentially arranged on the bottom liner, and the binding pad is coated MYO monoclonal detection antibody (Raybiotech.) labeled with fluorescent microspheres, the coating film includes a detection zone and a control zone arranged in parallel and spaced 0.5 cm apart from each other, the detection zone is close to the binding pad, and the control zone Close to the absorbent paper, the detection area is coated with a MYO monoclonal capture antibody that recognizes a single epitope (self-produced, prepared by using well-known techniques in the art), and the control area is coated with a goat anti-mouse IgG antibody.

[0041] In this embodiment, the coating film is a nitrocellulose film of chemically cross-link...

Embodiment 2

[0048] Example 2 Time-resolved immunochromatography kit for detecting MYO

[0049] The time-resolved fluorescence immunochromatography kit for detecting MYO of this embodiment, the kit includes: the test strip, the plastic cartridge, and the buffer bag described in embodiment 1; the test strip is contained in the plastic cartridge Inside, the buffer solution bag is located at the corners of the plastic card housing, close to the sample pad of the test strip, and a round hole is left on the surface of the buffer solution bag for needling.

[0050] In this embodiment, the reagent strip is immersed in a PBS buffer containing 0.5% BSA, 0.05% Tween 20, and 0.1-1% reducing agent. The buffer solution is a 0.01-0.1% reducing agent added to the ordinary phosphate solution to reduce the free peroxidase in the specimen. The reducing agent is reduced glutathione or ascorbic acid.

[0051] When the time-resolved fluorescence immunochromatographic kit for detecting MYO of the present invention i...

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Abstract

The invention discloses a time-resolved immunochromatographic test strip for detecting MYO, a kit and a preparation method thereof. The test strip comprises a bottom substrate, a sample pad, a binding pad, A coated membrane and absorbent paper, the binding pad is coated with MYO monoclonal detection antibody labeled with fluorescent microspheres, the coated membrane includes a detection area and a control area arranged in parallel and spaced apart from each other, and the detection area is coated with a recognition The MYO monoclonal capture antibody of a single epitope, the control area is coated with goat anti-mouse IgG antibody; the coating membrane is a nitrocellulose membrane combined with a polymer, and the polymer has a wavelength of less than 450nm with 10% The light transmittance below is a material that has a light transmittance of 95% or more at a wavelength of 500nm or more. The test strip of the invention can be used for rapid quantitative detection, the test result is accurate and reliable, the sensitivity is high, the preparation method is simple, the method is suitable for large-scale production, and it has positive significance for the quantitative detection of MYO.

Description

Technical field [0001] The present invention belongs to the technical field of medical testing. Specifically, the present invention relates to a time-resolved fluorescence immunochromatographic test strip for quantitative detection of MYO, a kit and a preparation method thereof. Background technique [0002] Myoglobin (Myoglobin, MYO) is a kind of oxygen-bound heme protein, mainly distributed in the myocardium and skeletal muscle tissue, accounting for about 0.1%-0.2% of the total muscle. The muscles of diving mammals such as whales, seals and dolphins are so rich in myoglobin that they make their muscles brownish red. Because myoglobin stores oxygen, these animals can be underwater for a long time. In acute myocardial injury, MYO is the first to be released into the blood. About 2-3 hours after the onset of symptoms, Mb in the blood can exceed the upper limit of normal, reaching a peak in 9-12 hours, and returning to normal after 24-36 hours. It can increase 1.5h after infarct...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N33/68G01N33/577G01N33/558G01N21/64
CPCG01N21/6408G01N21/6486G01N33/577G01N33/68G01N33/6887G01N33/54387G01N21/64
Inventor 徐部灼宋旭东黄若磐
Owner RAYBIOTECH INC GUANGZHOU
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