CN202854150U - Poliovirus II type IgG antibody test card - Google Patents
Poliovirus II type IgG antibody test card Download PDFInfo
- Publication number
- CN202854150U CN202854150U CN 201220591855 CN201220591855U CN202854150U CN 202854150 U CN202854150 U CN 202854150U CN 201220591855 CN201220591855 CN 201220591855 CN 201220591855 U CN201220591855 U CN 201220591855U CN 202854150 U CN202854150 U CN 202854150U
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- poliovirus
- igg antibody
- control line
- fiberglass packing
- chromatographic film
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Abstract
The utility model discloses a poliovirus II type IgG antibody test card. The poliovirus II type IgG antibody test card comprises a gasket (7), and a sample pad (1), a glass fiber mat (2), a chromatography membrane (5) and an absorption pad (6) which are sequentially connected in horizontal direction and fixedly arranged on the gasket (7); color latex granules with marks are coated on the glass fiber mat (2); the chromatography membrane (5) is provided with a test line (3) formed by II type poliovirus antigens, and a contrast line (4) parallel to the test line; and the test line (3) is positioned between the sample pad (1) and the contrast line (4). The poliovirus II type IgG antibody test card can fast and effectively detect whether the poliovirus II type IgG antibody is generated in a human body inoculated with poliovirus vaccine, the detection is simple and convenient to operate, and the production cost is low.
Description
Technical field
The utility model belongs to technical field of immunoassay, particularly a kind of poliovirus II type IgG antibody test card for whether producing the II type IgG antibody of poliomyelitis virus in the human body behind the fast detecting inoculation polio vaccine.
Background technology
Adopt euzymelinked immunosorbent assay (ELISA) (commercial reagent box for detection of whether producing the poliomyelitis virus IgG antibody in the human body behind the inoculation polio vaccine at present more, poliovirus IgG TPPA kit (euzymelinked immunosorbent assay (ELISA))), the method is after the human serum with the immunity inoculation polio vaccine dilutes, be added in the microwell plate of coated poliovirus antigen, 37 ℃ hatch 1 hour after, washing for several times, add anti-human IgG enzyme labeling thing, again through washing, add the substrate colour developing, the size of OD value per sample, judgement is the IgG antibody that whether contains poliomyelitis virus in the human serum.
The technical matters that the method exists: 1, complex operation: test procedure is more.Serum to be checked or blood plasma need dilute, and the first two reactions steps need be carried out the several washing, and last microplate reader reads the OD value; 2, length consuming time: three steps (adding sample, enzyme mark thing, substrate) all need 37 ℃ and hatch in the process of the test, add wash time, and whole test needs 3 hours consuming time.
The utility model content
Technical problem to be solved in the utility model provides a kind of poliovirus II type IgG antibody test card, whether produce poliomyelitis virus II type IgG antibody behind its energy fast detecting inoculation polio vaccine in the human body, detect easy and simple to handlely, production cost is low.
The utility model solves the problems of the technologies described above the technical scheme that adopts: a kind of poliovirus II type IgG antibody test card comprises liner, sample pad, fiberglass packing, chromatographic film and absorption pad; Described sample pad, fiberglass packing, chromatographic film and absorption pad join with the horizontal direction order and are fixed on the described liner; And be coated with the colored latex particle of tape label on the described fiberglass packing; The test wire that is made of II type poliovirus antigen and the control line parallel with described test wire are set on the described chromatographic film; And described test wire is between sample pad and control line.
Polio (poliomyelitis) is to infect a caused class acute infectious disease by poliovirus (poliovirus).Poliovirus has three different serotypes, i.e. I type, II type and III type, and each type has different Strain.Polio vaccine is the mixing live vaccine of making through attenuation with the representative strain of three types.
Described test wire is that the II type poliovirus antigen with purifying is fixed on the described chromatographic film and forms.
In the technique scheme, described sample pad and absorption pad all adopt the material with water absorbing properties to be prepared from, and can be commercially available filter paper and make, and the preferred stronger qualitative filter paper of water absorbing properties is beneficial to detection like this, increases detection speed.Described chromatographic film is commercially available nitrocellulose filter, and nitrocellulose filter claims again the NC film, is used as the supporting body of C/T line in colloid gold test paper, also is immunoreactive nidus simultaneously.Nitrocellulose filter model 135s, 170s or the definition of 180s(take second as unit adopted: every 4cm film, what seconds the chromatography time of water is).Fiberglass packing is a kind of of fiberglass products.Glass fibre is a kind of Inorganic Non-metallic Materials of excellent performance.English former Glassfiber by name, composition is silicon dioxide, aluminium oxide, calcium oxide, boron oxide, magnesium oxide, sodium oxide molybdena etc.It is through high temperature melting, wire drawing, doff, the technique such as weave cotton cloth take glass bead or discarded glass as raw material, form at last various product, the glass fiber single filament diameter is from several microns to twenties microns, the 1/20-1/50 that is equivalent to a hairline, every bundle fiber precursor all is comprised of hundreds of even thousands of monofilament, usually as reinforcing material, electrically insulating material and heat-insulating material in the multiple material, circuit substrate etc. are widely used in the national economy every field.
Evenly be coated with the colored latex particle of tape label on the described fiberglass packing, colored latex particle generally adopts red latex particle, and colour developing obviously like this; The method of the enterprising row labels of latex particle is the routine techniques means in this area, and the inventor does not do at this and gives unnecessary details.The mark of colored latex particle band can be combined by the IgG antibody in human serum, is antigen on the test wire.
As preferably, described sample pad length is 18mm, and width is 4mm; Fiberglass packing length is 10mm, and width is 4mm; Described chromatographic film length is 25mm, and width is 4mm; Described absorption pad length is 18mm, and width is 4mm; Described liner length is 30mm, and width is 4mm, and thickness is 1 ~ 2mm.
As preferably, described fiberglass packing is the fiberglass packing of the colored latex particle that is coated with band staphylococcal protein A (Staphylococal Protein A, SPA) mark.Staphylococcal protein A is a kind of protein that separates from the aureus cell wall.Since SPA can with the Fc end combination of the IgG of people, mouse, rabbit etc., become a kind of extremely useful instrument on the immunology.Described control line is that SPA is fixed on the control line that forms on the chromatographic film.Described control line is corresponding with label.
As preferably, described fiberglass packing is the fiberglass packing that is coated with the colored latex particle of mouse-anti human IgG labeling of monoclonal antibody.Mouse-anti human IgG monoclonal antibody is a kind of preferably label.Described control line is that sheep anti-mouse igg antibody is fixed on the control line that forms on the chromatographic film.Sheep anti-mouse igg antibody claims again the sheep anti-mouse igg polyclonal antibody.Sheep anti-mouse igg (immunoglobulin (Ig)) polyclonal antibody in the quick antibody diagnostic products of colloidal gold method on nitrocellulose filter, with the monoclonal antibody generation specific immune response of colloid gold label and show certain color, form control line and carry out immunodiagnosis.
Detection principle of the present utility model is: detection of the present utility model is to finish under the promotion of chromatography effect.After blood serum sample is added on the sample pad, arrive fiberglass packing by the chromatography effect, IgG antibody in the blood serum sample is combined with the colored latex particle of mark and is formed in conjunction with particle, then further to chromatographic film, under the chromatography effect of chromatographic film, move forward in conjunction with particle, when containing the antibody of poliomyelitis virus in the serum (should produce this antibody after inoculating polio vaccine), be combined with corresponding test wire, the color lines that present particle, unconjugated particle can continue to move forward, and is combined the color lines that present particle with control line, namely shows two color lines of test wire and control line; When not containing the antibody of poliomyelitis virus in the serum; the antigen of particle and corresponding test wire can't in conjunction with, test wire does not develop the color, for the particle of combination can continue to move forward; be combined the color lines that present particle with control line, namely only show color line of control line.
Because rete is analysed speed, the colored latex particle of tape label is removable complete chromatographic film bar in a few minutes, at once can sentence read result, all develop the color such as test wire and control line, and serum antibody is positive; Only have line colour developing of control line, serum antibody is negative.
In sum, the beneficial effects of the utility model are:
(1) the poliomyelitis virus IgG antibody is the species specificity protection antibody that produces in the human body behind the inoculation polio vaccine.When only having this species specificity protection antibody in the human body, could when human body touches poliovirus, kill the virus neutralization not infected.The utility model poliovirus II type IgG antibody test card has solved and has had now for detection of the euzymelinked immunosorbent assay (ELISA) complex operation that whether produces poliomyelitis virus II type IgG antibody in the human body behind the inoculation polio vaccine, the defective of length consuming time; Simultaneously it can detect behind the inoculation polio vaccine whether produce poliomyelitis virus II type IgG antibody in the human body quickly and efficiently, detects easy and simple to handlely, and production cost is low.
When (2) the utility model uses, only need sample to be checked with physiological saline 1:1 dilution, directly be added on the sample pad of the present utility model and get final product, operate very easy; Sample is added on the utility model sample pad, and naked eyes were the Observable testing result in 10 minutes, judges about 15 minutes consuming time of whole detection, weak point consuming time.
(3) the utility model sample pad length is 18mm, and width is 4mm; Described fiberglass packing length is 10mm, and width is 4mm; Described chromatographic film length is 25mm, and width is 4mm; Described absorption pad length is 18mm, and width is 4mm; Described liner length is 30mm, and width is 4mm, and thickness is 1 ~ 2mm.This size specification, the detection efficiency when not only improving the utility model use, and make things convenient for the packing of product and transportation.
Description of drawings
Fig. 1 is the vertical view of embodiment 1;
Fig. 2 is the cut-open view of embodiment 1.
The corresponding component names of mark is among the figure: 1-sample pad, 2-fiberglass packing, 3-test wire, 4-control line, 5-chromatographic film, 6-absorption pad, 7-liner.
Embodiment
Below by specific embodiment, and by reference to the accompanying drawings, the technical solution of the utility model is described in further detail.
As illustrated in fig. 1 and 2, a kind of poliovirus II type IgG antibody test card, comprise liner 7, the main body of liner 7 is plastic mattress, the surface of plastic mattress is coated with adhesive sticker, along continuous straight runs fixedly has the sample pad 1(filter paper of water absorbing properties successively on the described liner 7, Shanghai gold mark Bioisystech Co., Ltd), fiberglass packing 2(Ahlstrom 8964 glasses, the outstanding Bioisystech Co., Ltd in Shanghai, model JY-J101), chromatographic film 5(nitrocellulose filter, Millipore company, model 135s) and have the absorption pad 6(filter paper of water absorbing properties, Shanghai gold mark Bioisystech Co., Ltd).
Described fiberglass packing 2 is for evenly being coated with red latex particle (the red polystyrene latex particle with the SPA mark, the outstanding Bioisystech Co., Ltd in Shanghai, model PSR030N) method that fiberglass packing, latex particle carry out mark is techniques well known, and therefore not to repeat here.
Described test wire 3 is that the II type poliovirus antigen (Beijing Institute of Biological Products Co., Ltd.) with the purifying of deactivation is fixed on the chromatographic film 5 and forms.
Described control line 4 is that SPA(is commercially available, Zhengzhou hundred basic Bioisystech Co., Ltd) be fixed on the chromatographic film 5 and form.Purifying II type poliovirus antigen, SPA fixing means are techniques well known, and therefore not to repeat here.
In the utility model, described sample pad 1, fiberglass packing 2, chromatographic film 5 and absorption pad 6 join with the horizontal direction order.Particularly, the mode that described sample pad 1, fiberglass packing 2, chromatographic film 5 and absorption pad 6 orders are joined is partly overlapping, that is: the tail end of sample pad 1 is overlapped on the fiberglass packing 2, the tail end of fiberglass packing 2 is overlapped on the head end of chromatographic film 5, and the head end of absorption pad 6 is overlapped on the tail end of chromatographic film 5.
Further, sample pad 1 length described in the utility model is 18mm, and width is 4mm; Described fiberglass packing 2 length are 10mm, and width is 4mm; Described chromatographic film 5 length are 25mm, and width is 4mm; Described absorption pad 6 length are 18mm, and width is 4mm; Described liner 7 length are 30mm, and width is 4mm, and thickness is 1 ~ 2mm.
Present embodiment is substantially the same manner as Example 1, its different piece only is: described fiberglass packing 2 is for evenly being coated with the fiberglass packing with the colored latex particle of mouse-anti human IgG labeling of monoclonal antibody, and described control line 4 forms for sheep anti-mouse igg antibody is fixed on the chromatographic film 5.
Present embodiment is substantially the same manner as Example 1, and its different piece only is: the mode that the order that described sample pad 1, fiberglass packing 2, chromatographic film 5 are connected with absorption pad is joined is that head and the tail connect and do not have overlapping.
Present embodiment is substantially the same manner as Example 3, its different piece only is: described fiberglass packing 2 is for being coated with the fiberglass packing with the colored latex particle of mouse-anti human IgG labeling of monoclonal antibody, and described control line 4 forms for sheep anti-mouse igg antibody is fixed on the chromatographic film 5.
When the utility model uses, only need sample to be checked with physiological saline 1:1 dilution, directly be added on the sample pad of the present utility model and get final product, operate very easy; Sample is added on the utility model sample pad, and naked eyes were the Observable testing result in 10 minutes, judges, all develops the color such as test wire 3 and control line 4, and serum antibody is positive; Only have 4 one line colour developings of control line, serum antibody is negative.About 15 minutes consuming time of whole detection, weak point consuming time.
Above-described embodiment is a kind of better embodiment of the present utility model, is not to any pro forma restriction of the utility model, also has other variant and remodeling under the prerequisite that is no more than the technical scheme that claim puts down in writing.
Claims (4)
1. a poliovirus II type IgG antibody test card comprises liner (7), it is characterized in that, also comprises sample pad (1), fiberglass packing (2), chromatographic film (5) and absorption pad (6); Described sample pad (1), fiberglass packing (2), chromatographic film (5) and absorption pad (6) join with the horizontal direction order and are fixed on the described liner (7); And be coated with the colored latex particle of tape label on the described fiberglass packing (2); Described chromatographic film (5) is upper to arrange the test wire (3) that is made of II type poliovirus antigen and the control line (4) parallel with described test wire; And described test wire (3) is positioned between sample pad (1) and the control line (4).
2. poliovirus II type IgG antibody test card according to claim 1 is characterized in that described sample pad (1) length is 18mm, and width is 4mm; Described fiberglass packing (2) length is 10mm, and width is 4mm; Described chromatographic film (5) length is 25mm, and width is 4mm; Described absorption pad (6) length is 18mm, and width is 4mm; Described liner (7) length is 30mm, and width is 4mm, and thickness is 1 ~ 2mm.
3. poliovirus II type IgG antibody test card according to claim 1, it is characterized in that, described fiberglass packing (2) is for being coated with the fiberglass packing (2) with the colored latex particle of SPA mark, and described control line (4) is fixed on the upper control line that forms of chromatographic film (5) for SPA.
4. poliovirus II type IgG antibody test card according to claim 1, it is characterized in that, described fiberglass packing (2) is for being coated with the fiberglass packing (2) with the colored latex particle of mouse-anti human IgG labeling of monoclonal antibody, and described control line (4) is fixed on the upper control line (4) that forms of chromatographic film (5) for sheep anti-mouse igg antibody.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 201220591855 CN202854150U (en) | 2012-11-09 | 2012-11-09 | Poliovirus II type IgG antibody test card |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 201220591855 CN202854150U (en) | 2012-11-09 | 2012-11-09 | Poliovirus II type IgG antibody test card |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN202854150U true CN202854150U (en) | 2013-04-03 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 201220591855 Expired - Lifetime CN202854150U (en) | 2012-11-09 | 2012-11-09 | Poliovirus II type IgG antibody test card |
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| Country | Link |
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| CN (1) | CN202854150U (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108287237A (en) * | 2018-01-13 | 2018-07-17 | 中国医学科学院医学生物学研究所 | A kind of pre-coated detection method of II type D antigens of poliovirus and its detection kit and application |
-
2012
- 2012-11-09 CN CN 201220591855 patent/CN202854150U/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108287237A (en) * | 2018-01-13 | 2018-07-17 | 中国医学科学院医学生物学研究所 | A kind of pre-coated detection method of II type D antigens of poliovirus and its detection kit and application |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CX01 | Expiry of patent term | ||
| CX01 | Expiry of patent term |
Granted publication date: 20130403 |