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A hyperbolic calibration quantitative immunochromatographic detection method

An immunochromatographic detection, calibration and quantification technology, which is applied in the field of hyperbolic calibration and quantitative immunochromatography detection, can solve the problems of complex process and uncertain dilution ratio, and achieve the effect of saving operation and improving detection efficiency.

Active Publication Date: 2018-06-29
ANBIO XIAMEN BIOTECHNOLOGY CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The existing detection technology needs to dilute high-concentration samples to a certain multiple before testing. Due to the different nature of each item, the dilution multiple is uncertain, and it is necessary to try different dilution ratios to determine the best dilution multiple for accurate quantitative detection. , the process is more complex

Method used

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  • A hyperbolic calibration quantitative immunochromatographic detection method
  • A hyperbolic calibration quantitative immunochromatographic detection method
  • A hyperbolic calibration quantitative immunochromatographic detection method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0064] C-reactive protein hyperbolic calibration quantification

[0065] The pure C-reactive protein standard was serially diluted to obtain the following concentrations:

[0066] 0mg / L, 0.5mg / L, 1mg / L, 2.5mg / L, 10mg / L, 25mg / L, 50mg / L, 100mg / L, 110mg / L, 110mg / L, 125mg / L, 150mg / L, 175mg / L, 200mg / L.

[0067] The concentration of C-reactive protein to be tested is unknown.

[0068] Take equal amounts of different concentrations of C-reactive protein and the C-reactive protein to be tested and drop them on the test strips respectively.

[0069] The test strip is provided with a binding pad, a detection line and a control line.

[0070] The binding pad is coated with a first antibody labeled with a fluorescent marker and capable of binding to C-reactive protein;

[0071] The detection line is coated with a second antibody immobilized on the detection line which is different from the antigen epitope bound by the first antibody;

[0072] The control thread is coated with C-react...

Embodiment 2

[0100] Hyperbolic Calibration Quantification of Hepatitis B Surface Antibody

[0101] The pure hepatitis B surface antibody standard version was serially diluted to obtain the following concentrations:

[0102] 0mIU / ml, 50mIU / ml, 100mIU / ml, 250mIU / ml, 500mIU / ml, 1000mIU / ml, 2500mIU / ml, 5000mIU / ml, 7500mIU / ml, 10000mIU / ml, 15000mIU / ml, 20000mIU / ml, 25000mIU / ml ml.

[0103] The concentration of hepatitis B surface antibody to be tested is unknown.

[0104] Take equal amounts of hepatitis B surface antibody of different concentrations and the hepatitis B surface antibody to be tested and drop them on the test strips respectively.

[0105] The test strip is provided with a binding pad, a detection line and a control line.

[0106] The binding pad is coated with a first antigen labeled with a fluorescent marker and capable of binding to the hepatitis B surface antibody;

[0107] The detection line is coated with a second antigen immobilized on the detection line which is differ...

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Abstract

The invention relates to the technical field of biomedical detection, and specifically relates to a dual-curve calibration quantitative immunochromatography detection method. The method comprises the following steps: individually reacting a sample of a substance to be detected and gradiently diluted standards of the substance with equal reactants, measuring the signal values representing the reaction intensities; taking the concentration of the substance as the horizontal coordinate and the signal value intensities as the vertical coordinate to establish a coordinate system, substituting the signal values corresponding to standards with different concentrations into the coordinate system, drawing a fitting curve, cutting the fitting curve into two sections from the inflection point of the curve, namely a front calibration curve corresponding to low concentrations of the substance and a rear calibration curve corresponding to high concentrations of the substance; according to the signal intensities of a control line, estimating the content of the substance, and then substituting the corresponding signal value into different curves to know the definite protein concentration. The provided method has the advantages that a sample of a substance to be detected does not need to be diluted before quantitative analysis and detection, and the method is suitable for the detection of precious samples or massive samples.

Description

technical field [0001] The invention relates to the technical field of biomedical detection, in particular to a hyperbolic calibration quantitative immunochromatographic detection method. Background technique [0002] The hook effect is the HOCK effect, which refers to the phenomenon of false negatives caused by the inappropriate ratio of antigen and antibody. The excess of antibodies is called the prozone effect, and the excess of antigen is called the posterior zone effect, collectively referred to as the HOCK effect. [0003] When an antigen-antibody reacts specifically, the amount of the conjugate produced is related to the concentration of the reactant. Regardless of adding different amounts of antigen to a certain amount of antibody, or adding different amounts of antibody to a certain amount of antigen, it can be found that the strongest reaction occurs only when the molecular ratio of the two is appropriate. By adding increasing amounts of the corresponding antigen ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N33/558
CPCG01N33/558
Inventor 江应玲肖江群王保丹钟乾兴
Owner ANBIO XIAMEN BIOTECHNOLOGY CO LTD