Immunochromatographic test kit for extracting and measuring sugar chain antigens and capable of controlling analyte development
A technology of immunochromatography and sugar chain antigen, which is applied in the field of immunochromatography kits, can solve the problems of decreased sensitivity, non-expansion of samples, and occurrence of non-specific reactions.
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Embodiment 1
[0104] Examples of immunochromatographic test strips for group A hemolytic streptococci
[0105] The following nitrites, solid acidic agents, and neutralizing agents were used as the nitrites, solid acidic agents, and neutralizing agents.
[0106] Nitrite (liquid reagent) 3.0M sodium nitrite
[0107] Solid acidic reagent (impregnated in immunochromatographic test piece) 1.0M citric acid
[0108] Neutralization reagent (impregnated in the immunochromatographic test piece) 3.0M Tribasic (Trizma BASE).
[0109] 1. Immobilization of Anti-Streptococcus pyogenes (Group A β-hemolytic Streptococcus) Antibody on Nitrocellulose Membrane (Support)
[0110] Prepare the liquid in which anti-Streptococcus pyogenes antibody was diluted and anti-rabbit IgG antibody, and apply anti-Streptococcus pyogenes antibody linearly on the sample pad side of the nitrocellulose membrane lined with a PET film, and apply anti-Streptococcus pyogenes antibody linearly on the side of the absorption band, res...
Embodiment 2
[0128] The immunochromatography test piece of Example 1 was placed in a test device case (resin case for storing the immunochromatography test piece). The solution containing only 3.0M Na nitrite solution was used as a control, and Triton X-100, benzalkonium chloride, benzethonium chloride, phosphoric acid, sodium hydroxide, NALC, NaCl, PVA, BSA, and NaBr were prepared according to Table 1. The recorded concentration was added to the solution of each condition of 3M Na nitrite solution. Using a negative human nasal fluid sample known to cause a non-specific reaction, a sample was prepared from a Na nitrite solution to which Na nitrite solution and the above-mentioned substances were added (Solution 4: Sample 1) to prepare a sample. 75 µL of the prepared sample was added dropwise, and the judgment was made 5 minutes later.
[0129] As a result, compared with the control condition without addition, under any conditions, the development start time can be shortened, and band dete...
Embodiment 3
[0133] Put the immunochromatographic test piece of Example 1 into the casing of the test device. (1) 2M Na nitrite solution (PVA-free), (2) 2M Na nitrite + 0.5% PVA were prepared as Na nitrite solution. Specimens were prepared by preparing specimens from respective Na nitrite solutions in which live bacteria of Streptococcus pyogenes were added to human throat swab specimens. 75 µL of the prepared sample was added dropwise, and the judgment was made 5 minutes later.
[0134] As a result, in the presence of PVA, the development start time is shortened, and in the case of a positive sample, positive determination can be made from an earlier time period, and the band coloration at the determination time of 5 minutes also becomes faster. Concentrated results. In addition, in the case of test-negative samples, the frequency of non-specific reactions decreased by about 4% (Table 2).
[0135] [Table 2]
[0136]
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