Asymmetric magnetic mesoporous silica rod supporting chemotherapeutic and gene drugs and application thereof to tumor diagnosis and treatment
A silica rod and silica technology, which is used in gene therapy, drug combination, antitumor drugs, etc., to achieve good biocompatibility, improve therapeutic effect, and enhance the effect of nuclear magnetic imaging.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0040] (1) In 34mL diethylene glycol (DEG) solution, add 0.576g PAA and 0.13g FeCl 3 , stirred and heated to 250°C under the protection of nitrogen, after 20 minutes, 2.8mL of 80°C sodium hydroxide (NaOH) diethylene glycol solution (0.1g / mL) was added, and the reaction product was magnetically separated after stirring for 1 hour. Washed with water and dried to prepare spherical magnetic ferrite nanoparticles (Fe 3 o 4 ).
[0041] (2) Fe 3 o 4 Disperse in deionized water, add 50mg CTAB, add 0.5mL ammonia water after ultrasonication for 40 minutes, stir and heat to 40°C, slowly add 15uL TEOS dropwise, stir and react for 20 minutes; separate and purify the reaction product to obtain asymmetric magnetic mesoporous dioxide silicon rods. Disperse it in 100mL0.5% ammonium nitrate ethanol solution, stir and heat to reflux three times to remove CTAB. The obtained spherical magnetic ferrite nanoparticles have a diameter of 100nm, a mesoporous silica rod with a rod length of 200nm,...
Embodiment 2
[0046] (1) In 50mL diethylene glycol (DEG) solution, add 0.8g PAA and 0.2g FeCl 3 , stirred and heated to 250°C under the protection of nitrogen. After 20 minutes, 4.0mL of 80°C sodium hydroxide (NaOH) diethylene glycol solution (0.1g / mL) was added, stirred and reacted for 1 hour, and the reaction product was magnetically separated, washed with water, and dried to prepare spherical magnetic ferrite nanoparticles. Particles (Fe 3 o 4 ).
[0047] (2) Fe 3 o 4 Disperse in deionized water, add 50mg CTAB, add 1mL ammonia water after ultrasonication for 40 minutes, stir and heat to 40°C. 25uL TEOS was slowly added dropwise, and the reaction was stirred for 20 minutes; the reaction product was separated and purified to obtain asymmetric magnetic mesoporous silica rods. Disperse it in 100mL0.5% ammonium nitrate ethanol solution, stir and heat to reflux three times to remove CTAB. The obtained spherical magnetic ferrite nanoparticles have a diameter of 100nm, a mesoporous silica...
Embodiment 3
[0052] (1) In 50mL diethylene glycol (DEG) solution, add 0.6g PAA and 0.15g FeCl 3 , stirred and heated to 250°C under the protection of nitrogen. After 20 minutes, 3.0mL of 80°C sodium hydroxide (NaOH) diethylene glycol solution (0.1g / mL) was added, stirred and reacted for 1 hour, and the reaction product was magnetically separated, washed with water, and dried to prepare spherical magnetic ferrite nanoparticles. Particles (Fe 3 o 4 ).
[0053] (2) Fe 3 o 4 Disperse in deionized water, add 40mg CTAB, add 0.8mL ammonia water after ultrasonication for 40 minutes, stir and heat to 40°C. 50uL TEOS was slowly added dropwise, and the reaction was stirred for 20 minutes; the reaction product was separated and purified to obtain asymmetric magnetic mesoporous silica rods. Disperse it in 100mL0.5% ammonium nitrate ethanol solution, stir and heat to reflux three times to remove CTAB. The obtained spherical magnetic ferrite nanoparticles have a diameter of 100nm, a mesoporous sil...
PUM
Property | Measurement | Unit |
---|---|---|
length | aaaaa | aaaaa |
specific surface area | 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