Polyethylene glycol-dipeptide-antitumour drug complex and use thereof
An anti-tumor drug, polyethylene glycol technology, used in anti-tumor drugs, drug combinations, pharmaceutical formulations, etc., can solve problems such as limited effect and reduced half-life of conjugates
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Embodiment 1
[0037] The preparation of the activated PEG-X-Y of embodiment 1, X-Y is Val-Cit
[0038] Synthesized by conventional amide condensation reaction, the easily available mPEG-NHS (the average molecular weight of PEG is 4kD) and the dipeptide (Val-Cit) according to the feeding ratio of 2:1, adding pH7.5 phosphate, HEPES or Tris-HCl and other buffer solutions were dissolved, the reaction temperature was 25° C., stirred slowly for 60 minutes, and 5 times the molar amount of PEG of glycine was added to terminate the reaction. The mPEG-Val-Cit molecular complex can be obtained after dialysis purification and lyophilization. Then use conventional EDC and NHS reagents to activate the terminal carboxyl group of the mPEG-Val-Cit molecular complex to obtain mPEG-Val-Cit-NHS.
Embodiment 2
[0039] The preparation of the activated PEG-X-Y of embodiment 2, X-Y is Ala-Lys
[0040] Synthesized by conventional amide condensation reaction, the readily available mPEG-NHS and dipeptide (Ala-Lys) are dissolved in buffers such as phosphate, HEPES or Tris-HCl at pH 7.5 at a feed ratio of 2:1 , the reaction temperature was 25° C., the mixture was stirred slowly for 60 minutes, and glycine with 5 times the molar amount of PEG was added to terminate the reaction. The mPEG-Ala-Lys molecular complex can be obtained after dialysis purification and lyophilization. Then use conventional EDC and NHS reagents to activate the terminal carboxyl group of the mPEG-XX molecular complex to obtain mPEG-Ala-Lys-NHS.
Embodiment 3
[0041] The preparation of the activated PEG-X-Y of embodiment 3, X-Y is Val-Lys
[0042] It is synthesized by conventional amide condensation reaction, and the readily available mPEG-NHS and dipeptide (Val-Lys) are dissolved in buffers such as phosphate, HEPES or Tris-HCl at pH 7.5 at a feed ratio of 1:1. , the reaction temperature was 25° C., the mixture was stirred slowly for 60 minutes, and glycine with 5 times the molar amount of PEG was added to terminate the reaction. The mPEG-Val-Lys molecular complex can be obtained after dialysis purification and lyophilization. Then, conventional EDC and NHS reagents are used to activate the terminal carboxyl group of the mPEG-Val-Lys molecular complex to obtain mPEG-Val-Lys-NHS.
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