Amphiphilic superparamagnetism magnetic resonance contrast medium and preparation method thereof
A magnetic resonance contrast agent and superparamagnetic technology, which is applied in the direction of nuclear magnetic resonance/magnetic resonance imaging contrast agent, etc., can solve the problems of low coefficient and cannot be suitable for advanced magnetic resonance imaging, etc., and achieves good dispersion, scientific research and compatibility. The effect of convenient clinical application and good biocompatibility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] The preparation method of the amphiphilic superparamagnetic magnetic resonance contrast agent provided in this embodiment, the specific operation is as follows:
[0034] Add 2mmol of iron triacetylacetonate and 1mmol of manganese acetylacetonate into 30ml of tetraethylene glycol; perform anhydrous and oxygen-free operation, heat the reaction system under the protection of an inert gas, and when the temperature rises to 120°C, keep the reaction for 2 hours; then continue Heat up, when the temperature rises to 210°C, keep warm for 2 hours; then continue to heat up, when the temperature rises to 295°C, keep warm for 2 hours; the reaction is completed, naturally cool to room temperature, centrifuge, wash the precipitate with absolute ethanol , dried under vacuum at 25°C for 15 hours to obtain black MnFe coated with tetraethylene glycol molecules. 2 o 4 Nanoparticles.
[0035] Weigh the surface of the above-made MnFe coated with polyol molecules 2 o 4 15 mg of nanopartic...
Embodiment 2
[0047] The preparation method of the amphiphilic superparamagnetic magnetic resonance contrast agent provided in this embodiment, the specific operation is as follows:
[0048] Add 2mmol of iron triacetylacetonate and 1mmol of manganese acetylacetonate into 10ml of tetraethylene glycol; perform anhydrous and oxygen-free operation, heat the reaction system under the protection of an inert gas, and when the temperature rises to 100°C, keep the reaction for 3 hours; then continue Heat up, when the temperature rises to 200°C, keep warm for 3 hours; then continue to heat up, when the temperature rises to 285°C, keep warm for 3 hours; the reaction is completed, naturally cool to room temperature, centrifuge, wash the precipitate with absolute ethanol , dried under vacuum at 25°C for 15 hours to obtain black MnFe coated with tetraethylene glycol molecules. 2 o 4 Nanoparticles.
[0049] Weigh the surface of the above-made MnFe coated with polyol molecules 2 o 4 15 mg of nanopartic...
Embodiment 3
[0052] The preparation method of the amphiphilic superparamagnetic magnetic resonance contrast agent provided in this embodiment, the specific operation is as follows:
[0053] Add 2mmol of iron triacetylacetonate and 1mmol of manganese acetylacetonate into 50ml of tetraethylene glycol; perform anhydrous and oxygen-free operation, heat the reaction system under the protection of an inert gas, and when the temperature rises to 140°C, keep the reaction for 1 hour; then continue Heat up, when the temperature rises to 220°C, keep warm for 1 hour; then continue to heat up, when the temperature rises to 305°C, keep warm for 1 hour; the reaction is completed, naturally cool to room temperature, centrifuge, wash the precipitate with absolute ethanol , dried under vacuum at 25°C for 15 hours to obtain black MnFe coated with tetraethylene glycol molecules. 2 o 4 Nanoparticles.
[0054] Weigh the surface of the above-made MnFe coated with polyol molecules 2 o 4 15 mg of nanoparticles a...
PUM
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