Hollow gold nanoparticle-DNA composite base and preparation method thereof
A gold nanoparticle, composite substrate technology, applied in Raman scattering, material excitation analysis, etc., can solve the problems of different adsorption properties, quantitative analysis limitations, etc., to achieve simple preparation method, good chemical stability, and increased Raman scattering intensity. Effect
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[0034] A method for preparing a hollow gold nanoparticle-DNA composite substrate, the method comprising the following steps:
[0035] (1) Design the probeDNA single strand shown in SEQ ID NO.1 and the reporterDNA single strand shown in SEQ ID NO.2.
[0036] probeDNA is 5'-acatagcacattcgaggtag-3';
[0037] reporterDNA is 5'-ctacctcgaatgtgctatgt-3';
[0038] (2) Assembling a first hollow gold nanolayer with a uniform and dense monolayer on the Si substrate;
[0039] Firstly, hollow gold nanospheres are prepared, which can be proposed by Kobayashi et al. (Y. Kobayashi; M. Horie; M. Konno; B.R. Gonzalez; L. Marzan, J. Phys. Chem. B, 2003(107), 7420.) method, or proposed by L.J. Wan et al. (H.P. Liang; L.J. Wan; C.L. Bai; L. Jiang; Gold Hollow Nanospheres: Tunable Surface Plasmon Resonance Controlled by Interior-Cavity Sizes. J. Phys. Chem. B 2005(109), 7795-7800) method to prepare hollow gold nanoparticles with different sizes and wall thicknesses, and the preparation process i...
Embodiment 1
[0048]In this example, a single-layer hollow gold nanoparticle-DNA layer structure, ie, a Si / HGN-DNA structure, was prepared, and a Raman activity test was performed.
[0049] Design samples Si / HGN-probeDNA-probeDNA (non-complementary paired DNA single strand) and Si / HGN-probeDNA-reporterDNA (complementary paired DNA single strand) structures.
[0050] Saltify probeDNA and reporterDNA separately: Mix 900μL of PBS solution with pH=7.1, 100μL of 0.1% sodium dodecyl sulfate and 10μL of 1mmol / LprobeDNA (or 10μL of 1mmol / L reporterDNA), and let the mixed solution stand for 6h followed by salinization. The salinization process is as follows: add equal volumes of NaCl solution with increasing concentration to the mixed solution in 5 times, and add 100 μL of NaCl solution each time; the concentration of NaCl solution in the first drop is 2mol / L, and the concentration gradient of NaCl solution is 0.05mol / L; after adding NaCl solution for 5 times, the NaCl concentration in the final s...
Embodiment 2
[0054] In this example, a double-layer hollow gold nanoparticle layer is prepared, and the interlayer is a composite material of a DNA layer, that is, a Si / HGN-DNA-HGN structure, and a Raman activity test is performed:
[0055] Connect reporterDNA to hollow gold nanoparticles in hydrosol: mix 500 μL of PBS solution with pH=7.1, 100 μL of 0.1% sodium dodecyl sulfate, 10 μL of 1 mmol / L reporterDNA and 400 μL of gold hollow sphere hydrosol, and statically Set aside for 6h to carry out salinization. The salinization process is as follows: add equal volumes of NaCl solution with increasing concentration to the mixed solution in 5 times, and add 100 μL of NaCl solution each time; the concentration of NaCl solution in the first drop is 2mol / L, and the concentration gradient of NaCl solution is 0.05mol / L; after adding NaCl solution for 5 times, the NaCl concentration in the final solution was 0.7mol / L. The mixture was left to stand for 24 hours and then centrifuged at a speed of 700...
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