Preparation method of controlled release hydrogel for tumor postoperative radiotherapy in combination with photothermal-photodynamic therapy
A combined therapy and photodynamic technology, which is applied in the direction of antineoplastic drugs, medical preparations with non-active ingredients, medical preparations containing active ingredients, etc., can solve the problems of clean tumor resection and tumor recurrence, and achieve convenient storage and experimentation. The operation process is simple and the effect of improving stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0033] 1) Take 1g silk, with 0.5% Na 2 CO 3 Under the condition that the bath ratio is 1:100, the silk is degummed twice in a water bath at 90°C, each time for 30 minutes, and rinsed three times with deionized water after each degumming to remove residual impurities;
[0034] 2) Prepare 500mL of 9.3M lithium bromide solution, and dissolve the silk in a water bath at 60°C under the condition of a bath ratio of 1:50 for 3 hours;
[0035] 3) Place the solution in step 2) at 4°C, and dialyze in deionized water in an 8000Da dialysis bag for 2 days;
[0036] 4) Dialyze the dialyzed solution in step 3) in a 8000Da dialysis bag at 4°C for 2 days in PBS solution;
[0037] 5) Concentrate the solution obtained in step 4) in an 8000Da dialysis bag in 20wt% polyethylene glycol at 4°C to obtain a 6wt% silk fibroin solution, which is sealed and placed in an environment of 1°C refrigerated for later use;
[0038] 6) Dissolve 0.5g of melanin in 10mL of deionized water, then take 1g of CuCl ...
Embodiment 2
[0046] 1) Take 1g silk, with 0.5% Na 2 CO 3 Under the condition that the bath ratio is 1:100, the silk is degummed twice in a water bath at 95° C. for 35 minutes each time, and rinsed three times with deionized water after each degumming to remove residual impurities;
[0047] 2) Prepare 500mL of 9.3M lithium bromide solution, and dissolve silk in a water bath at 60°C for 3.5 hours at a bath ratio of 1:50;
[0048] 3) Place the solution in step 2) at 4°C, and dialyze in deionized water in an 8000Da dialysis bag for 2 days;
[0049] 4) Put the dialyzed solution in step 3) in an 8000Da dialysis bag at 4°C and dialyze in PBS solution for 3 days;
[0050] 5) Concentrate the solution obtained in step 4) in an 8000Da dialysis bag at 4°C in 20wt% polyethylene glycol to obtain a 6wt% silk fibroin solution, which is sealed and placed in an environment at 4°C refrigerated for later use;
[0051] 6) Dissolve 0.5g of melanin in 10mL of deionized water, then take 1.25g of CuCl 2 2H 2...
Embodiment 3
[0059] 1) Take 1g silk, with 0.5% Na 2 CO 3 Under the condition that the bath ratio is 1:100, the silk is degummed twice in a water bath at 100°C, each time for 40 minutes, and rinsed three times with deionized water after each degumming to remove residual impurities;
[0060] 2) Prepare 500mL of 9.3M lithium bromide solution, and dissolve the silk in a water bath at 60°C under the condition of a bath ratio of 1:50 for 4 hours;
[0061] 3) Place the solution in step 2) at 4°C, and dialyze in an 8000Da dialysis bag in deionized water for 3 days;
[0062] 4) Put the dialyzed solution in step 3) in an 8000Da dialysis bag at 4°C and dialyze in PBS solution for 3 days;
[0063] 5) Concentrate the solution obtained in step 4) in an 8000Da dialysis bag in 20wt% polyethylene glycol at 4°C to obtain a 6wt% silk fibroin solution, which is sealed and placed in an environment of 5°C refrigerated for later use;
[0064] 6) Dissolve 0.5g of melanin in 10mL of deionized water, then take ...
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