Fast preparation method of biological affinity copper nanometer cluster
A technology of copper nanoclusters and physical properties, which is applied in the field of nanomaterial preparation, can solve the problems of low quantum yield of copper nanoclusters, poor light stability, and long synthesis time, and achieve light stability, good biophilicity, and improved stability Effect
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Embodiment 1
[0029] Mix 20mmol / L copper sulfate solution and 20mg / mL bovine serum albumin solution at a volume ratio of 1:5, adjust the pH of the solution to 12 with 1.0mol / L sodium hydroxide solution, and stir at room temperature for 5min to obtain purple copper - bovine serum albumin complex; dropwise add 0.1mol / L of H at a speed of 20D / min 2 o 2 15mL, incubated at 55°C for 1h to obtain a light yellow copper nanocluster solution, which was stored in a refrigerator at 4°C; pipette 600μL of the prepared copper nanocluster solution into a centrifuge tube, and add 100μL of Hg 2+ Shake well, incubate at room temperature for 10 min, and then test the fluorescence intensity on a fluorescence spectrophotometer with excitation wavelength and emission wavelength of 320nm and 420nm, respectively. Calculate Hg according to the fluorescence emission peak intensity and substitute the linear regression equation 2+ content, resulting in Hg 2+ The detection limit was 4.7×10 -12 mol / L. The relative s...
Embodiment 2
[0031] Mix 20mmol / L copper nitrate solution and 15mg / mL bovine serum albumin solution at a volume ratio of 1:5, adjust the pH of the solution to 12 with 1.0mol / L potassium hydroxide solution, and stir at room temperature for 3 minutes to obtain purple copper - bovine serum albumin complex; add 1.0 mol / L of H dropwise at a speed of 10D / min 2 o 2 1.5 mL, incubated at 55°C for 1 hour to obtain a light yellow copper nanocluster solution, which was stored in a refrigerator at 4°C; pipette 600 μL of the prepared copper nanocluster solution into a centrifuge tube, and add 100 μL of Hg 2+ Shake well, incubate at room temperature for 20 minutes, and then test the fluorescence intensity on a fluorescence spectrophotometer with excitation and emission wavelengths of 320nm and 420nm, respectively. Calculate Hg according to the fluorescence emission peak intensity and substitute the linear regression equation 2+ content, resulting in Hg 2+ The detection limit was 5.2×10 -12 mol / L. The...
Embodiment 3
[0033] Mix 20mmol / L copper chloride solution and 50mg / mL bovine serum albumin solution at a volume ratio of 2:3, adjust the pH of the solution to 12 with 1.0mol / L potassium hydroxide solution, and stir at room temperature for 3min to obtain purple Copper-bovine serum albumin complex; drop 0.1mol / L of H at a speed of 20D / min 2 o 2 20mL, incubated at 70°C for 0.5h to obtain a light yellow copper nanocluster solution, which was stored in a refrigerator at 4°C; pipette 800μL of the prepared copper nanocluster solution, and add 200μL of Hg 2+ Put the standard solution or sample solution in a centrifuge tube, shake well, incubate at room temperature for 30 minutes, and then test the fluorescence intensity on a fluorescence spectrophotometer with excitation wavelength and emission wavelength of 340nm and 428nm, respectively. Calculate Hg according to the fluorescence emission peak intensity and substitute the linear regression equation 2+ content, resulting in Hg 2+ The limit of d...
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