Method for detecting surface enhanced Raman scattering of cancer cells based on self-assembled material
A surface-enhanced Raman, self-assembly technology, applied in the field of analytical chemistry, to achieve the effect of homogeneous assembly structure
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Embodiment 1
[0056] Preparation of gold nanoparticles and gold nanorod probes
[0057] It is similar to the steps of preparing gold nanoparticles and gold nanorod probes in the patent applied by the applicant: a method for preparing self-assembled materials with surface-enhanced Raman activity, application number 101010605799.9, to prepare the gold nanoparticles required by this patent Probes for rods and gold nanoparticles.
[0058] 1) Preparation of gold nanoparticle probes
[0059] Add 95mL of water to a clean Erlenmeyer flask, then add 5mL of chloroauric acid with a concentration of 2g / L to the water, heat, boil, then add 2.5mL of trisodium citrate solution with a mass concentration of 1%, and stir while heating , the color of the solution changed from light yellow to red, and the reaction lasted for 6-8 minutes to allow the trisodium citrate to settle completely. Finally, the solution was cooled to room temperature, diluted to 100 mL, and stored at 4°C to obtain gold nanoparticles wi...
Embodiment 3
[0075] Example 3 Self-assembly of gold nanorod probes and gold nanoparticle probes
[0076] Gold nanoparticles assemble around gold nanorods to form satellite-like assembly structures
[0077] Take 2 μL of modified whole-body modified gold nanorods and 10 μL of modified gold nanoparticles, add 12 μL of 0.01M Tris-HCl with pH 7.5, 0.01% SDS, and 20 mM KCl hybridization buffer, mix well, and shake at room temperature. Shake the reaction for 12h.
[0078] Gold nanoparticles assemble around the sides of gold nanorods
[0079] Take 2 μL of modified side-modified and end-blocked gold nanorods and 9 μL of modified gold nanoparticles, add 11 μL of 0.01M Tris-HCl at pH 7.5, 0.01% SDS, and 20 mM KCl hybridization buffer, and mix well. The reaction was shaken at room temperature for 12h.
[0080] End-face assembly of gold nanoparticles and gold nanorods
[0081] Take 3 μL of modified gold nanorods with modified end faces and side-blocked sides and 3 μL of modified gold nanop...
Embodiment 4
[0084] Example 4 Hela cell culture
[0085] The cancer cells used in this patent are Hela cells. Hela cell processing from flask to 96-well plate:
[0086] Remove the old medium in the culture flask, add 2 mL of pH 7.4 0.01M phosphate buffer to each culture flask, shake the culture flask slightly left and right, and then remove the phosphate buffer.
[0087] Then add 1mL of 0.25% trypsin digestion solution to each culture flask and digest for 3min.
[0088] The added tryptic solution was removed.
[0089] Add 2 mL of DMEM medium (provided by Shanghai Hufeng Biotechnology Co., Ltd.), and gently pipette several times until the cells on the wall of the culture flask are dispersed into the medium.
[0090] Add the above-prepared cell culture solution into the cell culture plate, and add 100 μL to each well.
[0091] Then the above cell culture plate was placed in the culture condition of 37°C, 5% CO 2 Cultivate in a constant temperature incubator for 12 h.
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