NIR-II imaging probe and preparation method and application thereof
An imaging probe and probe technology, applied in the field of in vivo fluorescence imaging of cells, can solve the problems of inability to identify the boundary between tumor and healthy tissue, increase in recurrence and death, blurred edge of tumor site, etc., to reduce non-specific cell phagocytosis, The effect of prolonging blood circulation, high luminescence performance and photostability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0026] A NIR-II approach for tumor imaging and image-guided surgery.
[0027] S1. Put the mesenchymal stem cells in 25×25cm 2 culture flask with MSCM mesenchymal stem cell medium at 37 °C, CO 2 Cultivate under the condition of 5% concentration, until the cells grow to 80%-90%, about 5×10 6 , discard the culture medium, add 5ml of CP@mSiO with a concentration of 50μg / ml diluted with low-sugar DMEM incomplete medium 2 -PEG, incubated for 18-22h;
[0028] S2. Digest the cells with 2ml of 0.25% trypsin-EDTA solution for 1-2min, pay attention to observe the shape of the cells, and stop the digestion until the cells are completely detached; add 2-3ml of the medium to stop the digestion, mix the cell suspension Transfer to a 15ml centrifuge tube, centrifuge at 1000r for 5min, discard the supernatant waste liquid after centrifugation, add 500μl PBS to the cells, gently pipette, and resuspend the cells;
[0029] S3. Gently pipette the cell suspension evenly with a 1ml syringe, draw...
Embodiment 2
[0041] A NIR-II approach for tumor imaging and image-guided surgery.
[0042] S1. Put the mesenchymal stem cells in 25×25cm 2 culture flask with MSCM mesenchymal stem cell medium at 37 °C, CO 2 Cultivate under the condition of 5% concentration, until the cells grow to 80%-90%, about 5×10 6 , discard the culture medium, add 5ml of 50μg / ml diluted with low-sugar DMEM incomplete medium, and incubate for 18-22h;
[0043] S2. Digest the cells with 2ml of 0.25% trypsin-EDTA solution for 1-2min, pay attention to observe the shape of the cells, and stop the digestion until the cells are completely detached; add 2-3ml of medium to stop the digestion, mix well and suspend the cells Transfer the solution to a 15ml centrifuge tube, centrifuge at 1000r for 5min, discard the upper waste solution after centrifugation, add 500μl PBS to the cells, gently pipette, and resuspend the cells;
[0044] S3. Gently pipette the cell suspension evenly with a 1ml syringe, draw 200 μl of the cell suspe...
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