Antagonistic peptide, copolymer thereof, nano-assembly as well as preparation methods and applications of antagonistic peptide, copolymer and nano-assembly
A nano-assembly and antagonistic peptide technology, applied in the field of medicine, can solve the problems of IR780 such as poor water solubility, limited action distance, and short action time of singlet oxygen, so as to improve the anti-tumor effect, inhibit the escape process, and improve the utilization rate.
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Embodiment 1
[0054] Example 1 Synthesis of M-APP
[0055] (The structure of the M-APP polypeptide is: Mercaptopropionic acid-L-Met-PLGLVG-DPPA-1)
[0056] The preparation process of M-APP is as follows:
[0057] First carry out resin swelling, soak 10 grams of Rink amide AM Resin (resin substitution degree is 0.35mmol / g) with 200mL methylene chloride for 15 minutes, wait for the resin to swell, and remove the methylene chloride. Next, remove the amino protection, add 200mL hexahydropyridine / DMF solution, use nitrogen agitation, and react twice at room temperature for 5 minutes and 15 minutes, and wash the resin with DMF after the reaction. Add a small amount of resin to the color detector and heat at 100°C for 3 minutes. The color of the solution and resin should be blue or red, which means the reaction is complete. It can be judged that the amino Fmoc protection has been removed. Then, carry out the condensation reaction, add 2 times the number of moles of Fmoc-D-Phe-OH and HBTU, di...
Embodiment 2
[0060] Example 2 Molecular synthesis of IR780-M-APP
[0061] IR780 was precisely weighed with an analytical balance, dissolved in anhydrous N,N-dimethylformamide (DMF) solvent, and placed in a round bottom flask. Weigh M-APP (prepared according to the method described in Example 1), dissolve it in anhydrous DMF, add it to the DMF solution of IR780 being stirred, and add triethylamine (TEA), and react under argon protection and room temperature For 48 hours, the ratio of the amount of IR780, M-APP and TEA was 5:1:20. After the reaction, dimethyl sulfoxide was dialyzed to remove anhydrous DMF and unreacted IR780, dialyzed overnight, followed by methanol dialyzed to remove dimethyl sulfoxide, evaporated under reduced pressure to remove methanol in the solution, and vacuum dried overnight to obtain IR780- M-APP product. The structure identification of IR780-M-APP is as follows: figure 1 B and figure 1 C shows:
[0062] 1. In-flight mass spectrometry (ESI-TOF-MS):
[0063]...
Embodiment 3
[0066] Example 3 Preparation of IR780-M-APP NPs
[0067] Accurately weigh 2 mg of IR780-M-APP, dissolve it in 500 μL of methanol, and place it in a round-bottom flask; sonicate, add 2 mL of membrane-passed water into the methanol solution of IR780-M-APP, and continue to sonicate (ultrasonic conditions: 100W, 30min) Form nano-aggregates and evaporate under reduced pressure to obtain a nanoparticle solution of IR780-M-APP, that is, nano-preparation IR780-M-APP NPs. The TEM results are as follows figure 2 As shown, the morphology of the prepared IR780-M-APP NPs was shown to be nanoparticle morphology, confirming the successful preparation of the formulation.
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