Preparation method for poly(ethylene glycol) modified recombinant human interleukin-2
A technology of polyethylene glycol and human interleukin, applied in the field of preparation of recombinant human interleukin 2, can solve the problems of poor uniformity of coupling products and large loss of activity, etc., achieve high antiviral activity, simple steps, easy quality control and scale-up The effect of production
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[0015] The embodiment of the present invention provides a preparation method of polyethylene glycol-modified recombinant human interleukin-2, comprising the following steps:
[0016] S01 activates mPEG with an activator to obtain mPEG activated molecules;
[0017] S02 reacts the mPEG activated molecule with recombinant human interleukin 2 in a buffer solution with a pH of 7.5-9.0, then adds a glycine solution to terminate the reaction, and separates and purifies the reaction product.
[0018] Specifically, the monomethoxypolyethylene glycol (Methoxy Polyethylene Glycol), referred to as mPEG, used in step S01 is a kind of polyethylene glycol, which has good water solubility, wettability, lubricity, physiological inertness, Non-irritating to the human body, mild in nature.
[0019] In a preferred embodiment, the molecular weight of mPEG used in step S01 is between 10kDa~100kDa, more preferably between 10kDa~50kDa, more preferably 10kDa~30kDa.
[0020] In this step S01, the act...
Embodiment 1
[0038] The molecular weight of mPEG used in this example is 10 kDa, and the activator is succinic anhydride and N-hydroxysuccinimide. The specific operation steps are as follows:
[0039] 1. mPEG activation
[0040] Dissolve mPEG in dioxane, add an appropriate amount of succinic anhydride so that the molar amount of succinic anhydride is slightly more than that of mPEG, use pyridine as a catalyst, and reflux at 100°C for 4 hours. After the reaction solution was cooled, anhydrous diethyl ether was added under vigorous stirring until the precipitation no longer appeared, and then stirred in an ice bath for 30 min. After filtration, the resulting precipitate was dissolved in dichloromethane, and the insoluble matter was removed by filtration again. Anhydrous ether was added to the filtrate until no precipitation occurred, and then stirred in an ice bath for 15 min. The precipitate was filtered again and dried in vacuo. The dry product and N-hydroxysuccinimide were dissolved in...
Embodiment 2
[0046] The molecular weight of mPEG used in this example is 20kDa, and the activator is succinic anhydride and N-hydroxysuccinimide. The specific operation steps are as follows:
[0047] 1. mPEG activation
[0048] Dissolve mPEG in dioxane, add an appropriate amount of succinic anhydride to make the molar amount more than that of mPEG, use pyridine as a catalyst, and reflux at 0°C for 24h. After the reaction solution was cooled, anhydrous diethyl ether was added under vigorous stirring until the precipitation no longer appeared, and then stirred in an ice bath for 30 min. After filtration, the resulting precipitate was dissolved in dichloromethane, and the insoluble matter was removed by filtration again. Anhydrous ether was added to the filtrate until no precipitation occurred, and then stirred in an ice bath for 15 min. The precipitate was filtered again and dried in vacuo. The dry product is mixed with N-hydroxysuccinimide and dissolved in dimethylformamide (DMF), and th...
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