CN101750498A - Magnetic immunochromatographic test strip for detecting hepatitis B e antigen and preparation method thereof - Google Patents
Magnetic immunochromatographic test strip for detecting hepatitis B e antigen and preparation method thereof Download PDFInfo
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- CN101750498A CN101750498A CN 200910236334 CN200910236334A CN101750498A CN 101750498 A CN101750498 A CN 101750498A CN 200910236334 CN200910236334 CN 200910236334 CN 200910236334 A CN200910236334 A CN 200910236334A CN 101750498 A CN101750498 A CN 101750498A
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Abstract
The invention relates to a magnetic immunochromatographic test strip for detecting hepatitis B e antigen in blood and a preparation method thereof. The magnetic immunochromatographic test strip introduces the magnetic micro-particle immunochromatographic technology into the hepatitis B e antigen detection, and the test strip is assembled by sequentially mutually sticking a coating film, a magnetic particle pad combined with hepatitis B e antibody, a sample pad and a water-absorbing pad on a substrate in a staggered manner and then covering a transparent plastic sealing film on the upper layer. A hepatitis B e antigen detection line and a quality control line are pre-coated on the coating film. The magnetic immunochromatographic test strip has the advantages of simple operation, high sensitivity, good specificity and the like.
Description
Technical field
The invention belongs to field of medical examination, particularly relate to a kind of magnetic immuno-chromatographic test paper strip that detects hepatitis B virus e antigen and preparation method thereof.
Background technology
Hepatitis B is caused that by hepatitis type B virus (HBV) HBV is a kind of genomic enveloped virus of partially double stranded cyclic DNA that comprises, and belongs to Hepadnaviridae.When virus is duplicated in liver cell, can disturb the function of liver, immune system activation produces a series of special reactions with antagonism and elimination infectiousness factor immediately.As a kind of result of pathologic damage, liver is inflamed.The HBV that continues infects the serious pathology result who causes and comprises: chronic liver function is incomplete, cirrhosis and hepatocellular carcinoma (HCC).
HBeAg occurs with hepatitis b surface antigen positive simultaneously or thereafter in hepatitis b virus infected back, and the peak period of HBsAg in blood also is the peak period of HBeAg.The positive explanation of HBeAg hepatitis type B virus is duplicated active in vivo, and infectiousness is strong, and HBeAg can turn out cloudy earlier before HBsAg turns out cloudy.If the HBeAg lasting masculin, it is hepatitis b virus infected then can to develop into chronic continuation.
Present HBeAg etiological diagnosis technology mainly comprises enzyme linked immune assay (ELISA), chemiluminescence (CLIA), immunochromatographic method (collaurum or latex particle method), and these methods all have characteristics and applicable object separately.
ELISA and CLIA method are generally to use detection technique in the present clinical immunoassay, but the reaction time is longer relatively, and all need microplate reader or light-emitting appearance and wash complex apparatus such as plate machine and incubator, detect before can't satisfying clinical emergency treatment art, the requirement of direction of medication usage has also limited the application at some different medical units before rescuing.Collaurum or latex particle are the quick detection test paper bar of representative, and shortcoming is that the result needs visual inspection, be subjected to the influence of observer's subjective judgement easily, and sensitivity is lower.
(Mgnetic ImmunoChromatographic Test MICT) is a kind of single part of fast quantification detection technique that occurs in recent years to magnetic immuno-chromatographic.It is to replace traditional label (collaurum, latex particle etc.) to carry out immunochromatography with supperparamagnetic particles (superPMPs), measures the content that magnetic field intensity is come the spike testing sample by detecting.This technology is compared with conventional art has following advantages: a. used magnetic detecting instrument adopts the solid phase element, and miniaturized design is had a style of one's own, independent operating, and volume is little, and is easy and simple to handle; B. the high 10-100 of all kinds of range estimation quick diagnosis of remolding sensitivity method doubly; C. reading is quick, can measure the nearly data of 6 site of analysis in 15 seconds; D. linear range can reach and be linear in the scope of 4 concentration numbers magnitudes; E. the super-paramagnetism nano particulate can not decayed in time by polymer coating.This technology has been inherited traditional immunochromatographic method (collaurum, latex particle etc.) easy to be quick, the advantage of single part of operation, it is low to have remedied traditional immunochromatography technique sensitivity again, can only be qualitative, shortcoming that can not be quantitative is current real-time test (Point of CareTest, the POCT) advanced person of technical development representative.
Mark magnetic particle commonly used at present is a super paramagnetic particle (superPMPs), do not have any magnetic in the absence of externally-applied magnetic field, only just can show magnetic adding under the action of a magnetic field, the super paramagnetic particle of commercialization all passes through finishing, greatly facilitate labeling process, mark is easy, good reproducibility.
Summary of the invention
Purpose of the present invention promptly is that the magnetic immuno-chromatographic technology is applied in the HBeAg immunoassay.With the HBeAb covalent coupling on super paramagnetic particle, the HBeAb bag is made detection line as catching solid phase on nitrocellulose filter, carry out the detection of sample according to routine immunization chromatography ratio juris, detect, can realize detecting rapidly and sensitively in conjunction with simple and easy to do magnetism detector, present technique both can single part detect, also can batch detection, and can provide quantitative result immediately, surveying instrument is simple and reliable, easy and simple to handle, convenient and practical.
For reaching above-mentioned purpose, technical scheme of the present invention is as follows: with coated film, in conjunction with HBeAb magnetic mat of particles, sample pad, adsorptive pads, stick on the base plate successively interlaced 2mm, cover the transparent plastic diaphragm seal then on the upper strata and make, be coated with the HBeAb detection line on the wherein said coated film in advance, and pre-bag is by two nature controlling lines that resist.
The base plate of selecting for use is the transparent plastic base plate, and coated film is the nitrocellulose filter of 35mm width, and the adsorptive pads of selecting for use is a cellulose membrane, and the magnetic mat of particles is a fiberglass packing, and sample pad is the pretreated cellulose membrane of process sample pad treating fluid.Described sample pad treating fluid is the polyvinyl alcohol (PVA) (PVP) that contains 1%-5% casein (casein) and 0.1%-1%, and the 0.02M of 0.01-0.2% Tween-20 (Tween-20), the phosphate buffered solution of pH7.0-7.6 (PBS).
Detect the preparation method of the magnetic immuno-chromatographic test paper strip of hepatitis B virus e antigen, may further comprise the steps:
The preparation of A, magnetic particle: selecting diameter for use is the super paramagnetic particle of 50-300nm, the mode of using carbodiimide (EDC) and succinimide (NHS) covalent coupling with two anti-marks to the magnetic particle, with HBeAb with 1: 3-1: 10 ratio (volume ratio) is mixed with two anti-mark magnetic particles;
B, use quantitative liquid-jet device to be sprayed on the magnetic mat of particles magnetic particle for preparing with the amount of 25 μ l/cm-50 μ l/cm;
The preparation of C, coated film: use bag to be cushioned liquid respectively with HBeAb and the two anti-concentration that are diluted to 0.5-2mg/m, use quantitative liquid-jet device respectively with the two being interval on the nitrocellulose filter with 0.5-1.0cm, dry the back and in confining liquid, soak after 10 minutes, add drying agent and seal up for safekeeping standby in 25-35 ℃ of oven dry 8 hours;
The processing of D, sample pad: sample pad is put into sample pad Treatment Solution immersion treatment take out 25-35 ℃ of oven dry 8 hours after 1 hour;
The assembling of E, test strips: interlaced successively 2mm sticks coated film, magnetic mat of particles, sample pad, adsorptive pads on the transparent plastic base plate, covers the transparent plastic diaphragm seal then on the upper strata, obtains test paper plate, and the width cutting promptly obtains test strips as requested.
The preparation of HBeAb-magnetic particle in the described steps A: use the 50mM that contains 0.1%Tween-20, the sodium-acetate buffer washing magnetic particle of pH4.5-5.0, adding EDC and NHS makes the two final concentration be 20mmol, room temperature reaction 1 hour, use contains the 50mM of 0.1%Tween-20, adding two was anti-after the sodium-acetate buffer of pH4.5-5.0 fully washed the magnetic particle, making two anti-molecule ratios with the magnetic particle is 5: 1 (mol ratio), room temperature reaction 3 hours, add the 0.02M that contains 0.5%BSA, the PBS room temperature sealing of pH7.0-7.6 30 minutes; Washing magnetic particle uses and contains 1%PVP, 1%Casein, 0.5%Tween-20, the boric acid of the 50mM pH8.2-9.0 of 5% sucrose is preserved damping fluid and is redissolved the magnetic particle, with HBeAb with 1: 3-1: 10 ratio (volume ratio) is mixed with two anti-mark magnetic particles, and 4 ℃ of preservations are standby;
Among the described step B, the spraying method of magnetic particle is: use quantitative spray film device evenly to be sprayed on the glass fibre with the amount of 50 μ l/cm the magnetic particle for preparing, add drying agent after the freeze drying and seal up for safekeeping standby.
Among the described step C, the preparation method of coated film is: be cushioned liquid (0.02M PB with bag, pH7.0-7.6) the HBeAb dilution is 0.5mg/ml, two anti-dilutions are 1mg/ml, use quantitative spray film device with the amount of 1 μ l/cm with the two with the interval spray printing of 0.6cm on nitrocellulose filter, room temperature is dried after 30 minutes and to be soaked in confining liquid after 10 minutes in 25-35 ℃ of oven dry 8 hours, adds drying agent and seals up for safekeeping standby.
Compare with traditional quick detection test paper bar, the present invention has the following advantages:
1) by on the magnetic particle, introducing two anti-systems, makes the preparation process of test strips simplify greatly, be fit to large-scale production.
2) the utilization magnetism detector carries out result's interpretation, carries out yin and yang attribute according to the magnetic detection value ratio of detection line and nature controlling line and judges, has avoided subjectivity, and the result accurately, reliably.
The present invention is easy and simple to handle, be fit to large-scale production, detect required portable set and also go on the market, therefore can be widely used in applying unit in enormous quantities such as hospital, blood station, epidemic prevention station, health check-up and short run or single part of applying units such as some blood sampling scenes, rural area and basic unit clinic.
Description of drawings
Fig. 1 detects the magnetic immuno-chromatographic test paper strip structural representation of hepatitis B virus e antigen for the present invention.
Detect magnetic immuno-chromatographic test paper strip of hepatitis B virus e antigen and preparation method thereof for further specifying the present invention, describe especially exemplified by following embodiment, this embodiment is in order to explain rather than limit by any way the present invention.
Embodiment
The magnetic immuno-chromatographic test paper strip of hepatitis B virus e antigen in the detection blood of the present invention, as shown in Figure 1, this test strips is magnetic mat of particles, sample pad, the adsorptive pads of pasting coated film on interlaced successively 2mm ground on the base plate, combining HBeAb, and in upper strata covering transparent plastic diaphragm seal, the test strips that assembles.
In specific embodiment, the HBeAb that adopts is a commercialization antibody.Utilize the double antibody sandwich method principle to detect the sample of HBeAg; when containing HBeAg in the sample to be measured; the HBeAb combination of combination on antigen meeting elder generation and the magnetic particle; carrying out along with the chromatography effect; bond moves forward and arrives the HBeAb bag by line T place; antigen can accumulate in the T place with coated antibody in conjunction with forming the double-antibody sandwich compound once more; in addition; in the time of can not continuing to move ahead arrival nature controlling line C in conjunction with HBeAb-magnetic particle, thereby the magnetic particle aggregation appears in two anti-can combinations at C line place with the HBeAb on the magnetic particle equally on the coated film.Entire reaction was carried out in 30 minutes fully, general reaction can be used magnetic immuno-chromatographic instrument Card Reader after 15 minutes, T line and C line all can produce corresponding magnetic signal value, calculate the ratio of T/C, get final product the yin and yang attribute of result of determination according to default boundary ratio.Whole Card Reader, calculating, with the process sequencing fully of preset bounds value comparison, magnetism detector can directly provide the yin and yang attribute result.
The preparation method of the magnetic immuno-chromatographic test paper strip of hepatitis B virus e antigen sees following example in the detection blood of the present invention:
Embodiment 1
Detect the magnetic immuno-chromatographic test paper strip of hepatitis B virus e antigen in the blood and the preparation method of paper box
The test strips of present embodiment and the preparation method of paper box may further comprise the steps:
The preparation of A, antibody: select commercial HBeAb for use, to 20mM, the PBS of pH7.2 (pH7.0-7.6 all is suitable for), 4 ℃ of dialysed overnight are standby.
The preparation of B, coated film:
Bag is cushioned the preparation of liquid: the phosphate buffer of 0.02M pH 7.2 (PBS) is cushioned liquid for bag, and the rearmounted 4 ℃ of preservations of 0.22 μ m filtering with microporous membrane degerming are standby, two weeks of the term of validity.
The preparation of confining liquid: contain the phosphate buffer (PBS) of the 0.02M pH7.2 (pH7.0-7.6 all is suitable for) of 0.5%BSA, it is standby that 0.22 μ m filtering with microporous membrane degerming is placed on 4 ℃ of preservations, one week of the term of validity.
The preparation of coated film: be cushioned liquid (PB of 0.02M pH7.2 (pH7.0-7.6 all is suitable for)) with bag the HBeAb dilution is 0.5mg/ml, two anti-dilutions are 1mg/ml, use quantitative spray film device with the amount of 1 μ l/cm with the two with the even spray printing in the interval of 0.6cm on 3.5cm width nitrocellulose filter, room temperature is dried after 30 minutes in the confining liquid (PBS that contains the 0.02M pH7.2 (pH7.0-7.6 all is suitable for) of 0.5%BSA,) in 25-35 ℃ of oven dry 8 hours, the adding drying agent was sealed up for safekeeping standby after 10 minutes in middle immersion.
The preparation of C, magnetic particle:
The preparation of sodium-acetate buffer: with distilled water and sodium acetate and glacial acetic acid secure ph is 4.7 (pH4.5-5.0 all is suitable for), concentration is the acetate buffer solution of 50mM, adding Tween-20 is that 4 ℃ of preservations are standby after 0.1%, the 0.22 μ m filtering with microporous membrane degerming to final concentration, two weeks of the term of validity.
Boric acid is preserved the preparation of damping fluid: use distilled water, boric acid and borax preparation pH are 8.5 (pH8.2-9.0 all is suitable for), and final concentration is the borate buffer of 50mM, add PVP, Casine, Tween-20, sucrose, final concentration is respectively 1%, 1%, 0.5%, 5%, 0.22 4 ℃ of preservations are standby after the degerming of μ m filtering with microporous membrane, one week of the term of validity.
The preparation of HBeAb magnetic particle: use 50mM pH4.7 (pH4.5-5.0 all is suitable for) the sodium-acetate buffer washing magnetic particle that contains 0.1%Tween-20; adding EDC and NHS makes the two final concentration be 20mmol; room temperature reaction 1 hour; fully adding two behind the washing magnetic particle resists; making two anti-molecule ratios with the magnetic particle is 5: 1 (mol ratio); room temperature reaction 3 hours; the PBS that adds the 0.02M pH7.2 (pH7.0-7.6 all is suitable for) that contains 0.5%BSA; room temperature sealing 30 minutes; washing magnetic particle; use contains 1%PVP; 1%Casein, 0.5%Tween-20, the boric acid of the 50mmolpH8.5 of 5% sucrose (pH8.2-9.0 all is suitable for) preserve damping fluid redissolution magnetic particle; with HBeAb with 1: 3-1: 10 ratio (volume ratio) is mixed with two anti-mark magnetic particles, and 4 ℃ of preservations are standby.
The spraying of D, magnetic particle and freeze-drying
That uses BioDot spray film instrument nozzle specially usedly evenly is sprayed at the magnetic particle handled well the amount with 50 μ l/cm on the 0.8cm width fiberglass packing, the frozen overnight drying, add drying agent seal up for safekeeping standby,
The processing of E, sample pad
1.8cm width sample pad is put into sample pad Treatment Solution immersion treatment take out 25-35 ℃ of oven dry 8 hours after 1 hour.
The sample pad treating fluid is the PBS solution that contains the PVA of 1%-5%Casein and 0.1%-1% and the 0.02M pH7.2 of 0.01-0.2%Tween-20 (pH7.0-7.6 all is suitable for).
The assembling of F, test strips and cutting
Following all operations all must carry out in temperature 20-25 ℃ the room in humidity less than 20%.
The assembling of test paper plate: use as requested that 3.5cm is the wide coated film of BioDot LM5000 type assembling instrument, 2.5cm wide thieving paper, the magnetic mat of particles that 0.8cm is wide, the wide sample pad of 1.8cm are assembled on the 9.8cm width transparent plastic base plate, stick upper strata transparent plastic cover plate, be assembled into test paper plate.
Cutting of test strips: use BioDot CM4000 type cutting cutter that the test paper plate that assembles is cut into the wide finished product test strips of 0.5cm.
The assembling of G, test card
The single part test strips of well cutting of the present invention is placed in the draw-in groove on the plastic bottom card, covers loam cake, use card press machine up and down two plastic clips compress, guarantee that whole test strips is in tensioned state.Adding the drying agent room temperature seals up for safekeeping standby.
H, determine the 2 D code information of this batch
The name of an article: HBeAg magnetic detection card
Batch: on the assembling date of test card, form is: Year/Month/Day, XXXX/XX/XX
Determining of yin and yang attribute interpretation standard: get 100 parts confirm HBeAg samples (power all has), 500 parts at random sample use this batch test card to detect, use the magnetism detector testing result, calculate the T1/C value of each test card, the T2/C value, use statistical method computation of mean values and standard deviation, determine: T/C＜0.1, T/C＞0.2 is positive, is gray area between the two.
The printing of I, two-dimension code is pasted
With in the above-mentioned 2 D code information input two-dimension code printer and print, two-dimension code is pasted on the ad-hoc location of test card, use two-dimension code paste position detecting device to inspect 2% at random by random samples and guarantee that two-dimension code pastes errorless.
J, finished product packing
The single part test card and that the posts two-dimension code drying prescription of being responsible for a task until it is completed is sealed in the aluminium foil bag, 100 person-portions are that a packing places in the packing box, and a instructions of a box and 1 bottle of 10ml dress chromatography damping fluid are promptly made paper box, this paper box keeps in Dark Place in room temperature, and the shelf-life is 18 months.The chromatography buffer formulation is: 1%Tween-20, and 0.5%Triton X-100,1%NP-40,0.05%NaN3, the PBS of 20mmol pH7.2 (pH7.0-7.6 all is suitable for).
Embodiment 2
The using method of test card of the present invention
1, application of sample
From packing box, take out single part test card, tear the aluminium foil strip packing, test card is placed on the smooth desktop, get 50 μ l sample serum with micropipettor and add in the well on the card, add 50 μ l chromatography damping fluids again, wait question response to carry out 15 minutes.
2, measurement and result output
The MICT detector is started shooting in advance, test card is inserted the card inserting mouth of detector, the operation instrument, instrument can read the 2 D code information on the card automatically and measure, and prints measurement result immediately, and the yin and yang attribute result can show in print result.
Claims (9)
1. magnetic immuno-chromatographic test paper strip that detects hepatitis B virus e antigen (HBeAg), it is characterized in that: this test strips is to stick on coated film, the magnetic mat of particles that combines hepatitis B e antibody (HBeAb), sample pad, adsorptive pads on the base plate successively interlacedly, cover the transparent plastic diaphragm seal then on the upper strata and assemble, be coated with hepatitis B virus e antigen detection line " T " and nature controlling line " C " on the wherein said coated film in advance.
2. coated film according to claim 1 is characterized in that: described film is a nitrocellulose filter.
3. coated film according to claim 1 is characterized in that: the material of the quilt that wraps is that HBeAb and two resists.
4. magnetic mat of particles according to claim 1 is characterized in that: the pad that is adopted is a fiberglass packing.
5. magnetic mat of particles according to claim 1 is characterized in that: the magnetic particle that is adopted is super paramagnetic particle, and coupling has HBeAb on this magnetic particle.
6. according to the HBeAb immune magnetic particle described in the claim 6, it is characterized in that: described HBeAb immune magnetic particle preparation is earlier with two anti-being coupled on the magnetic particle, with HBeAb and two anti-connections of magnetic particle mark, form magnetic particle-two and resist-the HBeAb compound again.
7. according to claim 3,5,6 described HBeAb, it is characterized in that: described HBeAb can be monoclonal antibody, polyclonal antibody.
8. anti-according to two described in the claim 3, it is characterized in that: described two anti-should pairings with the HBeAb antibody that is connected on the magnetic particle.
9. according to the magnetic particle described in the claim 5,6, it is characterized in that: described magnetic particle grain size is at 50-300nm.
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| CN 200910236334 CN101750498A (en) | 2009-10-16 | 2009-10-16 | Magnetic immunochromatographic test strip for detecting hepatitis B e antigen and preparation method thereof |
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| CN 200910236334 CN101750498A (en) | 2009-10-16 | 2009-10-16 | Magnetic immunochromatographic test strip for detecting hepatitis B e antigen and preparation method thereof |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103048454A (en) * | 2012-12-18 | 2013-04-17 | 苏州浩欧博生物医药有限公司 | Nanometer magnetic particle chemiluminescence detection kit for hepatitis B virus e antigen as well as preparation method thereof and detecting method thereof |
| CN103293295A (en) * | 2013-05-07 | 2013-09-11 | 上海爱纳玛斯医药科技有限公司 | Magnetic biological probe and test strip for detecting hepatitis B virus (HBV) and preparation method and using method of biological probe |
| WO2015070750A1 (en) * | 2013-11-16 | 2015-05-21 | 成都领御生物技术有限公司 | Test strip card |
| WO2015070749A1 (en) * | 2013-11-16 | 2015-05-21 | 成都领御生物技术有限公司 | Test strip card |
| WO2015070703A1 (en) * | 2013-11-13 | 2015-05-21 | 成都领御生物技术有限公司 | Test strip card |
| CN106290824A (en) * | 2016-10-19 | 2017-01-04 | 中国科学院电子学研究所 | Two-parameter fan-shaped immunity magnetosphere analysis strip |
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2009
- 2009-10-16 CN CN 200910236334 patent/CN101750498A/en active Pending
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103048454A (en) * | 2012-12-18 | 2013-04-17 | 苏州浩欧博生物医药有限公司 | Nanometer magnetic particle chemiluminescence detection kit for hepatitis B virus e antigen as well as preparation method thereof and detecting method thereof |
| CN103048454B (en) * | 2012-12-18 | 2015-08-26 | 苏州浩欧博生物医药有限公司 | Nano magnetic particulate chemistry luminescent assay kit of a kind of hepatitis B virus e antigen and preparation method thereof |
| CN103293295A (en) * | 2013-05-07 | 2013-09-11 | 上海爱纳玛斯医药科技有限公司 | Magnetic biological probe and test strip for detecting hepatitis B virus (HBV) and preparation method and using method of biological probe |
| WO2015070703A1 (en) * | 2013-11-13 | 2015-05-21 | 成都领御生物技术有限公司 | Test strip card |
| WO2015070750A1 (en) * | 2013-11-16 | 2015-05-21 | 成都领御生物技术有限公司 | Test strip card |
| WO2015070749A1 (en) * | 2013-11-16 | 2015-05-21 | 成都领御生物技术有限公司 | Test strip card |
| CN106290824A (en) * | 2016-10-19 | 2017-01-04 | 中国科学院电子学研究所 | Two-parameter fan-shaped immunity magnetosphere analysis strip |
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Owner name: BEIJING KEMEI BIOLOGICAL TECHNOLOGY CO., LTD. Free format text: FORMER OWNER: KEMEI DONGYA BIOLOGICAL TECHNOLOGY CO., LTD., BEIJING Effective date: 20111024 |
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Application publication date: 20100623 |