Efficient porous superparamagnetic fluoride ion dual fluorescence detection probe and preparation method thereof
A technology for detecting probes and superparamagnetism, applied in fluorescence/phosphorescence, chemical instruments and methods, measuring devices, etc. Toxicity and other issues, to achieve excellent superparamagnetic properties, good cell permeability, and low cytotoxicity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0104] Embodiment 1 hydrophilic Fe 3 o 4 Synthesis of cores, organosilane-functionalized carbon dots (SiCDs) in dilute solutions and autofluorescent markers (Fe 3 o 4 @mSiO 2 -SiCDs) preparation
[0105] 1. Hydrophilic Fe 3 o 4 The synthesis of the core includes the following steps:
[0106] (1) 0.325g anhydrous FeCl 3 and 0.4g of trisodium citrate were dissolved in 40mL of ethylene glycol, and magnetically stirred until an orange-yellow solution was formed;
[0107] (2) Under magnetic stirring, add 3 g of sodium acetate until a uniform yellow-brown solution is obtained, transfer the solution to a 50 mL Teflon-lined autoclave, and keep it at 200 ° C for 10 h; cool to room temperature Finally, the black product was separated by magnetic force, washed 5 times with ethanol, washed 1 time in deionized water, and dried in vacuum at 40 °C to obtain hydrophilic Fe 3 o 4 core.
[0108] 2. The synthesis of organosilane functionalized carbon dots (SiCDs) dilute solution, comp...
Embodiment 2
[0117] Example 2 DTPA anhydride and magnetic nanoparticles coated with fluorescent silica (Fe 3 o 4 @mSiO 2 -SiCDs@DTPA-Ni 2+ , FSMN) preparation
[0118] 1, the preparation process of diethylenetriaminepentaacetic acid (DTPA) anhydride is as follows figure 1 As shown, it specifically includes the following steps:
[0119] (1) 33.7g of diethylenetriaminepentaacetic acid (DTPA) was added to a 250mL round bottom flask containing 40mL of pyridine, and then 33mL of acetic anhydride was added;
[0120] (2) Pass N 2 Dissolved oxygen was removed, and the solution was vigorously stirred (1000 rpm) at 70°C for 24 hours to obtain DTPA anhydride;
[0121] (3) Wash DTPA anhydride twice in excess acetic anhydride, then wash three times in excess ether, and dry in vacuum to obtain diethylenetriaminepentaacetic dianhydride.
[0122] 2. Fluorescent silica-coated magnetic nanoparticles (Fe 3 o 4 @mSiO 2 -SiCDs@DTPA-Ni 2+ , FSMN) preparation method, comprises the following steps:
...
Embodiment 3
[0126] Example 3 Synthesis of pure carbon dots (NCDs) and fluoride ion dual fluorescent detection probes (Fe 3 o 4 @mSiO 2 -SiCDs@DTPA-Ni 2+ -NCDs, FSMN-NCDs) preparation
[0127] 1. The preparation process of pure carbon dots (NCDs) is as follows: figure 2 As shown, it specifically includes the following steps:
[0128] (1) Mix 20 mL of deionized water with 0.84 g of trisodium citrate, transfer it to a 50 mL polytetrafluoroethylene-lined hydrothermal reactor, and react at a constant temperature of 200 ° C for 5 h;
[0129] (2) After cooling, add ammonia solution and react at 200°C for another 10 hours, dialyze the obtained yellow-brown solution in a dialysis bag, soak it in 1000mL deionized water, and stir it with gentle magnetic force (200~600rpm) at the same time overnight;
[0130] (3) After adjusting the pH value to 6, the NCDs solution was obtained.
[0131] 2. Fluoride ion dual fluorescent detection probe (Fe 3 o 4 @mSiO 2 -SiCDs@DTPA-Ni 2+ -NCDs, the prepar...
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | aaaaa | aaaaa |
particle diameter | aaaaa | aaaaa |
diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information

- R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com