A kind of amphiphilic sericin polymer and its preparation method and application
A technology of sericin and polymers, which is applied in the direction of non-active components of polymer compounds, can solve the problems of sericin polymers with hydrophobic polypeptide chain segments that have not yet been seen, and achieve the effect of mild preparation conditions and excellent performance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] (1) Add the shredded silk cocoons into 0.02mol / L sodium carbonate solution and boil for 60min, filter to remove insoluble silk fibroin and other insoluble matter, put the filtrate into a cellulose dialysis bag with a molecular weight cut-off of 8000-14000Da, pure Dialysis in water for three days to remove ion salts, freeze-drying to obtain sericin.
[0033] (2) Under the protection of argon, dissolve the protected 2g of L-glutamic acid-γ-benzyl ester in tetrahydrofuran dehydrated by NaH, add 1.4g of trimeric phosgene, react at 55°C for 1h, and cool to At room temperature, tetrahydrofuran was distilled off under reduced pressure, and the obtained oil soluble matter was dissolved in 100 mL of ethyl acetate, washed with saturated aqueous sodium bicarbonate solution, the organic phase was separated, dried with anhydrous magnesium sulfate overnight, filtered to remove the desiccant, and decompressed The solvent was distilled off to obtain benzyl glutamic acid anhydride.
[...
Embodiment 2
[0037] (1) Dissolve 10 mg of the sericin-polybenzyl glutamate polymer in Example 1 (the mass ratio of benzyl glutamate anhydride to sericin is 1:1) in 1 mL of DMSO, Stir for 1 h, then drop it into 4 mL of deionized solution under magnetic stirring, put the mixed solution into a dialysis bag with a molecular weight cut-off of 3500, dialyze with deionized water at 25 °C for 24 h, dilute to 10 mL, pass through 0.45 μm Filter through a syringe filter and set aside for testing. The micelles loaded with Nile Red were prepared in a similar manner, except that 5 μg of Nile Red was added while dissolving sericin-polybenzyl glutamate.
[0038] figure 2 In the transmission electron microscope image, the micelles formed by Nile Red-labeled benzyl glutamate grafts of sericin in aqueous solution are uniformly dispersed, and the size is 80-100nm.
Embodiment 3
[0040] In vitro cell uptake experiment of loaded fluorescent agent micelles: culture breast cancer cells (MCF-7) to a density of 70-80% in a six-well plate, add the micelles loaded with Nile Red prepared in Example 2, in different At the time points, the accumulation ability of the micelles in the cells was observed with an inverted microscope. The result is as image 3 shown.
[0041] image 3 The process of nanomicelles (arrows) entering the cell is observed with a fluorescent inverted microscope: the upper image is white light imaging, and the lower image is 488nm green light excitation imaging. A, B, C, and D represent the results observed at time 1h, 2h, 4h, and 24h, respectively. image 3 It can be seen that the micelles loaded with Nile red drug were added to the MCF-7 cells for co-cultivation, and the observation results with an inverted microscope indicated that the micelles (arrows) could enter the cells within 1 hour, and still accumulated in the MCF-7 cells afte...
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