CN1424584A - Magnetic separated immunoreaction optical inspecting device and method - Google Patents
Magnetic separated immunoreaction optical inspecting device and method Download PDFInfo
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- CN1424584A CN1424584A CN 02160691 CN02160691A CN1424584A CN 1424584 A CN1424584 A CN 1424584A CN 02160691 CN02160691 CN 02160691 CN 02160691 A CN02160691 A CN 02160691A CN 1424584 A CN1424584 A CN 1424584A
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Abstract
The present invention relates to an optical detecting apparatus for immunity reaction of magnetic separation type and detecting method thereof. The detecting apparatus consists chiefly of bottom plate optical wave-guide, immunity reaction pool and magnetic poles. The uses pack is used as a background matter by the magnetic particles with antibody. The content of antigen in a sample can be obtained through detecting the ratio of light intensities in the wave-guide before and after the immunity reaction of antigen-antibody or the variation of the critical angle of the whole reflection before and after the immunity reaction. In the method of the invention, because of the action of the magnetic poles, the magnetic particles in coordination with the resultant of the immunity reaction are absorbed to the bottom part of the immunity reaction pool so as to make the concentration of the solution (e.g. the concentration of the antigen) vary in the greatest.
Description
Technical field:
The present invention relates to a kind of magnetic divergence type immune response optical detection apparatus and detection method, be a kind of at magnetic particle surface adsorption antibody, and then the optical detection apparatus that carries out the immunoreactive qualitative and quantitative analysis of Ag-Ab, and utilize this novel detection device to carry out the method that immune response detects.
Background technology:
The immune response detection is the important subject in the biomedicine always, also is an important means in the fields such as molecular biology, basic medical research, clinical diagnosis, new drug development, Food Hygiene Surveillance and biological weapons war.The requirement that immune response is detected is specific detection by quantitative, and require the detection sensitivity height, sample size is little, testing process is rapid.At present, Ag-Ab immunoreaction measurement device real-time is mostly based on the absorption of measuring immune complex or optical detecting method, fluorescence immunoassay and the luminescence immunoassay of scattering.
The method (being single-phase immunoassay) of utilizing scattered light is a kind of straightforward procedure of washing of neither needing B-F to separate also not need, but the method for utilizing scattered light (comprising Rayleigh scattering and Mie scattering) exists detection sensitivity low and measure shortcoming such as low precision when measuring the material of low concentration.
Fluorescence immunoassay and luminescence immunoassay all are antigen and the antibody responses that utilizes stimulative substance or chemiluminescent substance mark, generation is marked with the immune complex of the antigen-antibody reaction of fluorescent material molecule, fluorescence by measuring the self-marker or luminous is measured the content of target material.These two kinds of methods all need the complex chemical treatment process with fluorescence or luminescent substance molecular labeling antigen or antibody.And, majority is heterogeneous immunoassay, this assay method must need B-F to separate, so that the immune complex (B) that antigen-antibody reaction takes place is separated with antigen that antigen-antibody reaction does not take place or antibody (F) and wash by a large amount of analytical procedures.
A kind of fluorescence immunoassay device is arranged, be that antibody is fixed on the surface of total reflection prism, then, antigen contained in the sample is attached on the antibody, by antigen-antibody reaction a kind of antibody of fluorescent material mark that utilizes is attached on this antigen more again by antigen-antibody reaction.Thereafter carrying out B-F separates to remove the unreacted antibody that utilizes the fluorescent material mark, then exciting light is imported in the total reflection prism and be strapped in the lip-deep Ag-Ab immune complex that is labeled of total reflection prism, thereby measure fluorescence by fluorescent material produced to excite.Though this method has been simplified the B-F detachment process,, still need complicated fluorescence labeling process, again because antibody is that to be fixed on completely reflecting mirror lip-deep, whenever carry out an immune response after, all to change completely reflecting mirror, use cost height, very flexible again.
Summary of the invention:
The objective of the invention is at the deficiencies in the prior art, a kind of novel magnetic divergence type immune response optical detection apparatus and detection method are provided, can realize real-time, sensitive and immunoassays accurately, need not fluorescence labeling, simplify the B/F detachment process.
For realizing such purpose, the basic structure of the magnetic divergence type immune response optical detection apparatus that the present invention proposes is made of base plate optical waveguide, immune response pond and magnetic pole, uses and is coated with the magnetic particle of antibody as reaction substrate.Because the effect of magnetic pole, magnetic particle synergetic immunity resultant of reaction are attracted to bottom, immune response pond, exist under the situation at limited solute, make solution concentration maximum the variation be taken place in the reaction tank bottom.By detecting ratio or the variation of the cirtical angle of total reflection before and after the immune response content that obtains antigen in the sample before and after the Ag-Ab immune response of light intensity in the waveguide.
Immune response of the present invention pond base plate is trapezoidal quartzy planar waveguide structure, forms reaction tank with top adhesive glass baffle plate all around.Optional one side in the baffle plate is opened a through hole perpendicular to this baffle plate at this face near the position at top around reaction tank, and one section glass tube of bonding in this through hole is as the inlet in immune response pond; Below the baffle plate of the reaction tank opposite side relative,, make liquid outlet according to the method for making inlet near the reaction tank bottom with inlet place baffle plate.Reaction tank base plate (being quartzy planar waveguide) is a trapezium structure, wherein can propagate black light, visible light and near infrared light, by adjusting suitable angle of light, in the upper and lower surface formation total reflection of waveguide.
Magnetic pole is made of magnet or hot-wire coil, the N utmost point and the S utmost point be positioned over respectively the immune response pond directly over and under, in use, can apply and remove magnetic field as requested.
The solution variations in refractive index of utilizing solution concentration to change and causing, adopting the ATR Optical detection method to measure solution concentration is a comparatively proven technique.The present invention continues this detection method of use, and the innovation part is to use magnetic particle, by means of the action of a magnetic field, exists under the situation at limited solute (for example antigen), makes solution concentration (for example antigen concentration) in the reaction tank bottom maximum variation take place.If do not use magnetic particle, then solute (for example antigen) is evenly dispersed in the solution.Both compare, and under the solute situation of using as much, the concentration change that the inventive method produces in the reaction tank bottom is much larger than the latter, and change of refractive also is like this.Consequently, the detection sensitivity of the inventive method is higher than the latter.
When using device of the present invention to carry out immunoassays, in reaction tank, drop into magnetic particle (for example magnetic particles such as permanent-magnet ferrite, barium ferrite, alloy magnetic powder and the rare earth permanent-magnetic material) solution that contains coated antibody earlier, apply magnetic field in the reaction tank bottom, magnetic particle carries absorption antibody thereon and is adsorbed to the sample cell bottom.Drop into the solution that contains antigen again, the Ag-Ab immune response takes place.Like this, great changes will take place for the solution refractive index of reaction tank bottom section, and the luminous energy of propagating in the waveguide is coupled into the solution in the reaction tank more, and therefore, the outgoing light intensity weakens from waveguide.In addition, because the variations in refractive index of reaction tank bottom causes the cirtical angle of total reflection of incident light to change.Therefore, utilize this two characteristics, can carry out the Ag-Ab immune response quantitative test of low concentration.After detecting end, remove magnetic field, increase setting-out cleaning reaction pond, device of the present invention can be used repeatedly.
Apparatus of the present invention have two kinds of detection approach, promptly detect the cirtical angle of total reflection or intensity of reflected light and solution change of refractive relation.Specify detection principle of the present invention below.
Total reflection when optically thinner medium (solution) transmits, may take place at two medium interfaces from optically denser medium (quartz waveguide) in light, and the condition that total reflection takes place is:
I wherein
cBe critical angle (the minimum incident angle of total reflection takes place), n
1And n
2It is respectively the refractive index of waveguide and solution.Shown in the formula (1), work as n
1＞n
2The time, i
cJust have real-valuedly, promptly require the solution refractive index n
2Less than waveguide index n
1Generally there are following relation in the refractive index of solution and its concentration:
n
2＝αC (2)
Wherein C is a strength of fluid, and α is the constant relevant with liquid property, and solution concentration C and critical angle i have been set up in formula (1) and (2)
cRelation:
By formula (1) and (3) as can be known, record the variation that the solution change of refractive is promptly known solution concentration, therefore, measure concentration and be summed up as the measurement refractive index.
Incident light is at the reflective light intensity I at interface
sWith the solution refractive index n
2Relation can calculate by Fresnel formula.In the Fresnel formula, light wave vertical direction amplitude reflectivity coefficient table is shown:
Wherein, i
1And i
2Be respectively incident angle and refraction angle.Reflective light intensity is:
I wherein
0It is incident intensity.The refractive index of solution and incident critical angle are one-to-one relationships, and we get a certain refractive index n of solution
2 0Pairing critical angle i
c 0Be fixing incident angle i
1, refraction angle i
2Can obtain by Si Naier formula (6).
n
1Sini
1=n
2Sini
2(6) combinatorial formula (4) (5) (6) can obtain light wave vertical direction amplitude component reflective light intensity I
sWith the solution refractive index n
2Relational expression
Pick-up unit of the present invention is simple in structure, uses planar waveguide in the bottom in immune response pond, and the incident angle of light of waveguide can be regulated, make light in waveguide, produce total reflection, and utilize magnetic separation technique, realized that real-time, sensitive, accurate and flexile immune response detects, and need not fluorescence labeling, the B/F detachment process is simple, and have higher precision, therefore, improved the use efficiency-cost ratio, have tangible economic benefit and social benefit, be beneficial to penetration and promotion and application.
Description of drawings
The structural representation of Fig. 1 magnetic divergence type of the present invention immune response optical detection apparatus.
Among Fig. 1,1, the base plate optical waveguide, 2, the immune response pond, 3, inlet, 4, liquid outlet, 5, magnetic pole, 6, condenser.
The magnetic particle that Fig. 2 will be coated with antigen is adsorbed on bottom, immune response pond.
After Fig. 3 antigen input generation immune response, wash free antigen.
Fig. 4 antigen-antibody response compound detects.
Fig. 5 cleans the immune response pond.
Fig. 6 light wave vertical direction amplitude component reflective light intensity and solution index of refraction relationship curve.
The relation curve of Fig. 7 solution refractive index and the cirtical angle of total reflection.
Embodiment
Below in conjunction with drawings and Examples technology implementation process of the present invention is described further.
As shown in Figure 1, the basic structure of pick-up unit of the present invention is made of base plate optical waveguide 1, immune response pond 2 and magnetic pole 5, reaction tank 2 bottoms link to each other with the base plate optical waveguide 1 of trapezium structure, reaction tank 2 a certain side shield tops have inlet 3, reaction tank on the other side 2 opposite side baffle plate bottoms have liquid outlet 4, the N utmost point of magnetic pole 5 and the S utmost point lay respectively under the reaction tank 2 and directly over, condenser 6 is positioned at 1 bright dipping place of base plate optical waveguide, places perpendicular to light direction.
In one embodiment of the invention, at first form system by structural drawing shown in Figure 1, testing process is:
1. antibody (for example rat immune globulin G) is coated on the magnetic particle, forms solution, the mixed solution of fixed volume is dropped in the reaction tank (2) by inlet (3).
2. add magnetic pole (5), the magnetic particle that then is coated with rat immune globulin G is attracted to reaction tank bottom (Fig. 2).
3. with fixed wave length (λ) and intensity (I
0) laser (polarization direction is perpendicular to the plane of incident light and reflected light decision) irradiation base plate optical waveguide, the adjustment incident angle is i
c 0, make light wave at light guide surface generation total reflection, at this moment incident intensity I
0With waveguide output intensity I
s 0Equate.Survey the waveguide output intensity I of this moment in condenser (6) back
s 0As light background (incident intensity).Record cirtical angle of total reflection i at this moment
c 0And calculating refractive index n
2 0
4. drop into the solution that contains antigen (for example mouse Lysozyme) of fixed concentration and volume in reaction tank, the reaction back washes antigen free in the solution with damping fluid.(Fig. 3)
5. detect the output intensity I of waveguide
s(Fig. 4).
6., then use light intensity I at this moment if use the reflective light intensity detection method
sDivided by light background I
0, use formula again
(7) calculate the solution refractive index.Fig. 6 has provided n
2 0=1.34, n
1=1.458, corresponding critical angle i
c 0The relation curve of the ratio of reflective light intensity and incident intensity and solution variations in refractive index in the time of=66.8 °.As seen, the solution refractive index can cause the violent decay of intensity of reflected light in the subtle change of 1.34-1.36 scope among the figure.Therefore, according to intensity of reflected light reduce can measure solution refractive index (concentration) variable quantity.If use cirtical angle of total reflection detection method, then changing the angle of light of this moment is i
c, make output light intensity at this moment equal incident intensity (light background), use formula (1) to calculate the solution refractive index again.Calculated curve is seen Fig. 7, the situation of having drawn two kinds of waveguide materials (refractive index is respectively 1.458 and 1.54) among the figure.
7. calculate antigen concentration in the solution with the solution refractive index substitution formula (3) that obtains.
8. after detecting end, remove magnetic pole (5), with High-Pressure Water reaction tank is cleaned (Fig. 5), this pick-up unit is reusable.
Claims (3)
1, a kind of magnetic divergence type immune response optical detection apparatus, it is characterized in that reaction tank (2) bottom links to each other with the base plate optical waveguide (1) of trapezium structure, have inlet (3) on the side plate of reaction tank (2), opposite side on the other side has liquid outlet (4), magnetic pole (5) is placed in the below in immune response pond (2) and top, and condenser (6) is placed in bright dipping place of quartzy base plate optical waveguide (1).
2, a kind of detection method of utilizing the said magnetic divergence type of claim 1 immune response optical detection apparatus, it is characterized in that earlier antibody sandwich being formed solution on magnetic particle, drop in the reaction tank (2), add magnetic pole (5), make magnetic particle be attracted to the reaction tank bottom, use laser radiation base plate optical waveguide (1) again, adjust incident angle, make light wave in light guide surface generation total reflection, survey waveguide output intensity at this moment in condenser (6) back as light background incident intensity, in reaction tank, drop into the solution that contains antigen then, the reaction back washes antigen free in the solution with damping fluid, detect the output intensity of waveguide,, and calculate antigen concentration in the solution according to the ratio calculation solution refractive index of reflective light intensity and incident intensity.
3, a kind of detection method of utilizing the said magnetic divergence type of claim 1 immune response optical detection apparatus, it is characterized in that earlier antibody sandwich being formed solution on magnetic particle, drop in the reaction tank (2), add magnetic pole (5), make magnetic particle be attracted to the reaction tank bottom, use laser radiation base plate optical waveguide (1) again, adjust incident angle, make light wave in light guide surface generation total reflection, survey waveguide output intensity at this moment in condenser (6) back as light background incident intensity, in reaction tank, drop into the solution that contains antigen then, the reaction back washes antigen free in the solution with damping fluid, changes laser incident angle, makes incident light that total reflection take place at this moment, calculate the solution refractive index according to twice total reflection angle difference, and calculate antigen concentration in the solution.
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| CN 02160691 CN1184482C (en) | 2002-12-30 | 2002-12-30 | Magnetic separated immunoreaction optical inspecting device and method |
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|---|---|---|---|
| CN 02160691 CN1184482C (en) | 2002-12-30 | 2002-12-30 | Magnetic separated immunoreaction optical inspecting device and method |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN101846690A (en) * | 2010-06-09 | 2010-09-29 | 中国科学院生态环境研究中心 | Microporous plate type washing-immune magnetic separation full-automatic integral machine |
| CN1947016B (en) * | 2004-04-28 | 2012-04-25 | 佳能株式会社 | Detector and detecting method |
| CN103344753A (en) * | 2013-07-24 | 2013-10-09 | 公安部第三研究所 | Device for achieving rapid detection of narcotic drug content based on magnetic immunoassay |
| CN104764724A (en) * | 2006-12-12 | 2015-07-08 | 皇家飞利浦电子股份有限公司 | Microelectronic sensor for detection of label particles |
| CN104807993A (en) * | 2015-04-23 | 2015-07-29 | 广东国际旅行卫生保健中心（广东出入境检验检疫局口岸门诊部） | Mycobacterium tuberculosis ESAT-6 protein detection kit, as well as preparation method and use method |
| CN110609009A (en) * | 2019-09-29 | 2019-12-24 | 张阳 | Sample pretreatment system suitable for terahertz specificity detection of biological sample and application |
| CN110832301A (en) * | 2018-05-30 | 2020-02-21 | 务实诊断有限公司 | Optical magneto-optical method for detecting biological and chemical substances |
| WO2020038235A1 (en) * | 2018-08-20 | 2020-02-27 | 上海攀颂生物科技有限公司 | High-flux biological, chemical and environmental detection system and method based on planar waveguide technology |
| CN111108252A (en) * | 2017-09-22 | 2020-05-05 | 骊住株式会社 | Toilet device |
| CN112213300A (en) * | 2019-07-09 | 2021-01-12 | 苏州宇测生物科技有限公司 | Molecular quantitative detection device |
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2002
- 2002-12-30 CN CN 02160691 patent/CN1184482C/en not_active Expired - Fee Related
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1947016B (en) * | 2004-04-28 | 2012-04-25 | 佳能株式会社 | Detector and detecting method |
| US11243199B2 (en) | 2006-12-12 | 2022-02-08 | Siemens Healthineers Nederland B.V. | Carrier for detecting label particles |
| CN104764724A (en) * | 2006-12-12 | 2015-07-08 | 皇家飞利浦电子股份有限公司 | Microelectronic sensor for detection of label particles |
| US9658219B2 (en) | 2006-12-12 | 2017-05-23 | Koninklijke Philips N.V. | Microelectronic sensor device for detecting label particles |
| US11402374B2 (en) | 2006-12-12 | 2022-08-02 | Siemens Healthineers Nederland B.V. | Method of detecting label particles |
| CN101846690A (en) * | 2010-06-09 | 2010-09-29 | 中国科学院生态环境研究中心 | Microporous plate type washing-immune magnetic separation full-automatic integral machine |
| CN101846690B (en) * | 2010-06-09 | 2012-11-28 | 中国科学院生态环境研究中心 | Microporous plate type washing-immune magnetic separation full-automatic integral machine |
| CN103344753A (en) * | 2013-07-24 | 2013-10-09 | 公安部第三研究所 | Device for achieving rapid detection of narcotic drug content based on magnetic immunoassay |
| CN104807993A (en) * | 2015-04-23 | 2015-07-29 | 广东国际旅行卫生保健中心（广东出入境检验检疫局口岸门诊部） | Mycobacterium tuberculosis ESAT-6 protein detection kit, as well as preparation method and use method |
| CN111108252A (en) * | 2017-09-22 | 2020-05-05 | 骊住株式会社 | Toilet device |
| CN110832301A (en) * | 2018-05-30 | 2020-02-21 | 务实诊断有限公司 | Optical magneto-optical method for detecting biological and chemical substances |
| CN110832301B (en) * | 2018-05-30 | 2022-05-27 | 务实诊断有限公司 | Optical magneto-optical method for detecting biological and chemical substances |
| WO2020038235A1 (en) * | 2018-08-20 | 2020-02-27 | 上海攀颂生物科技有限公司 | High-flux biological, chemical and environmental detection system and method based on planar waveguide technology |
| CN112213300A (en) * | 2019-07-09 | 2021-01-12 | 苏州宇测生物科技有限公司 | Molecular quantitative detection device |
| CN112213300B (en) * | 2019-07-09 | 2024-02-13 | 苏州宇测生物科技有限公司 | Molecular quantitative detection device |
| CN110609009A (en) * | 2019-09-29 | 2019-12-24 | 张阳 | Sample pretreatment system suitable for terahertz specificity detection of biological sample and application |
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|---|---|
| CN1184482C (en) | 2005-01-12 |
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