CT imaging contrast agent and preparation method thereof
A technology of CT imaging and contrast agent, which is applied in the preparation of X-ray contrast agent, etc., which can solve the problems of weak X-ray absorption of iodine contrast agent, difficulty in obtaining important information of lesions, and inability to observe lesions for a long time, achieving a good absorption coefficient , good biocompatibility, and uniform shape
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0040] 1) Get 0.19, 0.38, 1.9, 3.8ml iohexol solution (300mg I / ml), be dissolved in 22ml ultrapure water respectively, stir evenly;
[0041] 2) Add 3 mL of chloroauric acid solution (0.01M), and stir at room temperature for 10 minutes to obtain a reaction precursor solution;
[0042] 3) Pour the reaction precursor solution into a polytetrafluoroethylene-lined stainless steel reaction kettle, and react at 120°C for 1.5h;
[0043] 4) The reaction system was naturally cooled to room temperature. Centrifuge twice at a speed of 4000 rpm to separate the synthesized gold nanoparticles from excess iohexol in the solution, and then wash twice with ultrapure water.
[0044] The scanning electron micrograph of the product obtained under the conditions of iohexol 0.19, 0.38, 1.9, 3.8ml is as follows figure 1 shown.
[0045] The ultraviolet diagram of the product obtained under the conditions of iohexol 0.19, 0.38, 1.9, 3.8ml is as follows figure 2 shown.
Embodiment 2
[0047] 1) Get 0.38ml iohexol solution (300mg I / ml), be dissolved in 22ml ultrapure water respectively, stir;
[0048] 2) Add 3 mL of chloroauric acid solution (0.01M), and stir at room temperature for 10 minutes to obtain a reaction precursor solution;
[0049] 3) Pour the reaction precursor solution into a polytetrafluoroethylene-lined stainless steel reaction kettle, and react at 120°C for 1.5h;
[0050] 4) The reaction system was naturally cooled to room temperature. Centrifuge twice at a speed of 4000 rpm to separate the synthesized gold nanoparticles from excess iohexol in the solution, and then wash twice with ultrapure water.
[0051] The scanning electron microscope image of the prepared iohexol-wrapped icosahedral gold nanoparticles is shown in image 3 shown.
[0052] The transmission electron microscope image of the prepared iohexol-wrapped icosahedral gold nanoparticles is shown in Figure 4 shown.
Embodiment 3
[0054] 1) Get 0.38ml iohexol solution (300mg I / ml), be dissolved in 22ml ultrapure water respectively, stir;
[0055] 2) Add 3 mL of chloroauric acid solution (0.01M), and stir at room temperature for 10 minutes to obtain a reaction precursor solution;
[0056] 3) adjusting the reaction precursor solution to pH=7 with Na(OH);
[0057] 4) Pour the reaction precursor solution with pH=7 into a polytetrafluoroethylene-lined stainless steel reaction kettle, and react at 120°C for 1 hour;
[0058] 5) The reaction system was naturally cooled to room temperature. Centrifuge twice at a speed of 4000 rpm to separate the synthesized gold nanoparticles from excess iohexol in the solution, and then wash twice with ultrapure water.
[0059] The scanning electron microscope image of the prepared iohexol-wrapped spherical gold nanoparticles is as follows: Figure 5 shown.
PUM
Property | Measurement | Unit |
---|---|---|
Particle size | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com