A method to enhance the luminescent properties of double-stranded DNA-protected silver nanoclusters
A technology of silver nanoclusters and luminescence properties, applied in the field of nanomaterials, can solve the problems of low fluorescence quantum yield and limited application, etc.
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Embodiment 1
[0024] Silver nanoclusters protected by double-stranded DNA were prepared according to the literature method (Analyst, 2017, 142, 800-807): the DNA sequence 5′-TTTAAATAATATCCCCTTAATCCCC-3′ of the template strand containing the complementary strand (TTTAAATAATAT is the complementary segment, CCCTTAATCCCC is the protected silver nanocluster The template segment of the cluster) and the complementary strand DNA sequence 5'-GGGGTGGGGTGGGGTGGGATATTTATTTAAA-3' containing G bases (ATATTATTTAAA is a complementary segment, GGGGTGGGGTGGGGTGGG is a G base-rich segment) to prepare DNA-protected silver nanoclusters, Specific steps are as follows:
[0025] Method: Weigh silver nitrate (AgNO 3 ) 17.0mg, add 20mL distilled water to configure 5mmol / L silver nitrate mother liquor for later use (keep away from light); weigh 358mg disodium hydrogen phosphate (Na 2 HPO 4 12H 2 O) add 50mL water configuration 20mmol / L disodium hydrogen phosphate solution; Then weigh 156mg sodium dihydrogen phosph...
Embodiment 2
[0027] Establish the quantitative relationship between the silver nanoclusters protected by double-stranded DNA and BSA: the silver nanocluster solution protected by double-stranded DNA prepared in Example 1 was diluted to 10 times the volume with phosphate buffer solution, and the concentration was 1.0×10 -6 mol / L solution; take 1mL of this solution, add BSA mother liquor to it respectively, so that the final concentration of BSA is 0~140×10 -6 mol / L (0, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 120, 140×10 -6 mol / L), and after 4min, use a fluorescence spectrometer (Shimadzu, Japan, RF-5301PC) to record the fluorescence emission spectra (excitation wavelength 470nm) of the silver nanocluster solution in response to different concentrations of BSA. Such as figure 1 As shown, with the increase of BSA concentration, its fluorescence emission peak at 555nm is gradually enhanced and blue-shifted to 522nm, and the intensity is enhanced from 12 at 555nm to 70 at 522nm, which is abou...
Embodiment 3
[0029] The silver nanocluster solution protected by double-stranded DNA prepared in Example 1 was diluted to 10 times volume with phosphate buffer solution to form a concentration of 1.0×10 -6 mol / L solution, take 12 parts of 1mL of the solution, add BSA mother liquor to it, so that the final concentration is 10×10 -6 mol / L; 4min later, add trypsin stock solution to each portion to make the final concentration of 0-80ng / μL (0, 5, 10, 15, 20, 25, 30, 40, 50, 60, 70, 80ng / μL), after 5min, use a fluorescence spectrometer to record the fluorescence emission spectra of the mixed solution of double-stranded DNA-protected silver nanoclusters and BSA in response to different concentrations of trypsin (excitation wavelength is 470nm). Such as image 3 As shown, with the increase of trypsin concentration, the fluorescence emission peak intensity at 522nm gradually increased, the intensity increased from 35 at 522nm to 120 at 545nm, about 3.5 times stronger, and red shifted to 545nm. S...
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