Surface enhanced Raman scattering immunochromatography test paper strip and preparation method and application
An immunochromatographic test paper and surface-enhanced Raman technology, which is applied in the field of spectrum and immunological detection and detection, can solve the problems of cumbersome steps, affecting sensitivity, narrow emission spectrum, etc., and achieve stable production process, wide application range and safe operation Effect
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Embodiment 1
[0045] The preparation and application of the SERS immunochromatographic test strip for rapid detection of divalent cadmium ions comprises the following steps:
[0046] (1) Preparation of gold nanoflowers: After adding 0.2mL of chloroauric acid (25mM) to 10mL of HEPES (20mM, pH 7.4), let it stand for 30 minutes, and the color of the liquid changes from colorless to blue, indicating that gold nanoflowers The flower preparation was successful.
[0047] (2) Preparation of gold-core silver-shell nanoflowers: 40 μL of NaOH (0.1M) and 30 μL of ascorbic acid (0.1M) were added to 1 mL of gold nanoflowers, and after stirring, 400 μL of AgNO 3 (10mM). After half an hour of reaction, when the nanoparticles turned red, it meant that the gold-core silver-shell nanoflowers were successfully prepared.
[0048] (3) Preparation of gold-core silver-shell nanoflower-labeled antibody: 0.2 μL of tetramercaptobenzoic acid (20 mM) was added to 1 mL of gold-core silver-shell nanoflower. After stan...
Embodiment 2
[0058] The preparation and application of the SRES immunological test strip for rapid detection of hemoglobin comprises the following steps:
[0059] (1) Preparation of gold nanoflowers: Add 0.2mL of chloroauric acid (25mM) to 10mL of HEPES (20mM, pH7.4), let it stand for 30 minutes, and the color of the liquid changes from colorless to blue, indicating that gold nanoflowers The flower preparation was successful.
[0060] (2) Preparation of gold-core silver-shell nanoflowers: 40 μL of NaOH (0.1M) and 30 μL of ascorbic acid (0.1M) were added to 1 mL of gold nanoflowers, and after stirring, 400 μL of AgNO3 (10 mM) was added. After half an hour of reaction, when the nanoparticles turned red, it meant that the gold-core silver-shell nanoflowers were successfully prepared.
[0061] (3) Preparation of gold-core silver-shell nanoflower-labeled antibody: 0.2 μL of tetramercaptobenzoic acid (20 mM) was added to 1 mL of gold-core silver-shell nanoflower. After standing at room tempera...
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