A preparation method of α-helical epitope/dox double-template molecularly imprinted fluorescent nanoparticles
An epitope, fluorescent nanotechnology, applied in non-active ingredients medical preparations, medical preparations containing active ingredients, antitumor drugs, etc., can solve the problems of complex preparation process, achieve high specific surface area, excellent fluorescence properties, the effect of enhancing recognition specificity
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Embodiment 1
[0027] A method for preparing α-helical epitope / DOX double-template molecularly imprinted fluorescent nanoparticles, specifically comprising the following steps:
[0028]1) Preparation of silicon nanoparticles, take 0.318g trisodium citrate and add 8mL glycerol, add 2mL 3-aminopropyltriethoxysilane (APTES) under the protection of argon, the above reaction is carried out in a microwave reactor, 15min Finally, silicon nanoparticles (Si NPs) are obtained;
[0029] 2) Purification of silicon nanoparticles: add 8 mL of silicon nanoparticles to 12 mL (0.5 mol / L) dilute hydrochloric acid, take the molecular cut-off of the dialysis bag to be 1000 for dialysis, change the water once every 8 hours, and change the water 3 times in total. The time is 24h overnight to obtain purified silicon nanoparticles (Si NPs);
[0030] 3) Add 6 mL of purified silicon nanoparticles to 40 mL of ethanol solution, add 0.667 mL of ammonia, add 0.8 mL of tetraethoxysilane (TEOS), and react at room temperat...
Embodiment 2
[0038] A preparation method of α-helical epitope / DOX double-template molecularly imprinted fluorescent nanoparticles, the synthesis steps are basically the same as in Example 1, the difference is: step 1) take 0.315g trisodium citrate and add 8mL glycerine alcohol.
[0039] The results of the final preparation of double-template conformational epitope-imprinted nanoparticles and the application of MIPs@DOX are similar to those in Example 1.
Embodiment 3
[0041] A preparation method of α-helical epitope / DOX double-template molecularly imprinted fluorescent nanoparticles, the synthesis steps are basically the same as in Example 1, the difference is: step 1) take 0.32g trisodium citrate and add 8mL glycerine alcohol.
[0042] The results of the final preparation of double-template conformational epitope-imprinted nanoparticles and the application of MIPs@DOX are similar to those in Example 1.
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