Urokinase adsorbent as well as preparation method and application thereof
A technology of urokinase and adsorbent, which is applied in the field of medical biology, can solve the problems of unsuitability for large-scale production, high cost, and low crude extraction yield of urokinase, and achieve low cost, low environmental protection pressure, and high crude extraction yield Effect
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Embodiment 1
[0047] Embodiment 1 A kind of urokinase adsorbent and preparation method thereof
[0048]Dry the silica gel in an oven at 125°C for 4 hours, add 100g of activated silica gel into a 1L three-necked reaction flask, add 400ml of toluene, 50ml of vinylmethyldiethoxysilane, reflux for 8h, filter, extract with ethanol, wash with water, and obtain the former Body 1, add precursor 1 and 400ml water into a 1L three-necked flask, add bromine dropwise until the aqueous solution just turns red, react at room temperature (25°C) for 30 minutes, filter and wash with water to obtain precursor 2, mix precursor 2 and 400ml of water was added to a 1L three-neck flask, 20g of p-aminobenzamidine hydrochloride was added to adjust the pH to 9, and the temperature was raised to 80°C for 8 hours. Cool down to 30°C, filter, extract with ethanol, wash with water, and spin dry to obtain the urokinase adsorbent.
Embodiment 2
[0050] A kind of urokinase adsorbent and preparation method thereof
[0051] Dry the silica gel in an oven at 120°C for 10 hours, add 100g of activated silica gel into a 1L three-necked reaction flask, add 350ml of methanol, 45ml of vinyltriisopropoxysilane, reflux for 6h, filter, extract with ethanol, and wash with water to obtain the precursor 1. Put the precursor 1 and 350ml of water into a 1L three-necked flask, add bromine dropwise until the aqueous solution just turns red, react at room temperature for 30 minutes at 25°C, filter and wash to obtain the precursor 2, mix the precursor 2 and 350ml of water Add it into a 1L three-necked flask, add 10g of p-aminobenzamidine hydrochloride, adjust the pH to 9, react at 60°C for 10 hours, cool down to 30°C, filter, extract with ethanol, wash with water, and dry to obtain the urokinase adsorbent .
Embodiment 3
[0053] A kind of urokinase adsorbent and preparation method thereof
[0054] Dry the silica gel in an oven at 160°C for 3 hours, add 100g of activated silica gel into a 1L three-necked reaction flask, add 450ml of ethanol, 55ml of vinyltriacetoxysilane, reflux for 10h, filter, extract with ethanol, and wash with water to obtain the precursor 1, Add precursor 1 and 450ml of water into a 1L three-necked flask, add bromine dropwise until the aqueous solution just turns red, react at room temperature for 30 minutes at 25°C, filter and wash with water to obtain precursor 2, add precursor 2 and 450ml of water to Add 30g of p-aminobenzamidine hydrochloride to a 1L three-necked flask, adjust the pH to 10, react at 90°C for 4 hours, cool down to 30°C, filter, extract with ethanol, wash with water, and dry to obtain the urokinase adsorbent.
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