Preparation and use of injectable isopropyl acrylamide tripolymer as thrombus material and its use
A technology of isopropylacrylamide terpolymer and n-propylacrylamide, which is applied in the field of vascular embolization materials and can solve the problems of unfavorable injection and high concentration
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Embodiment 1
[0026] 65.86 ml of n-propylamine after water removal was dissolved in 160 ml of tetrahydrofuran, and 32.47 ml of acryloyl chloride was added dropwise under magnetic stirring in an ice-water bath. After the reaction is complete, remove the generated amine salt by vacuum filtration, and remove tetrahydrofuran by rotary evaporation to obtain liquid n-propylacrylamide (NPAAm).
[0027] Dissolve 1.8106g of isopropylacrylamide, 1.8106g of n-propylacrylamide and 0.1065ml of vinylpyrrolidone in 80ml of deionized water; pass nitrogen gas for 30min under magnetic stirring, add 0.0268g of potassium persulfate and 0.0149g of tetramethylethylenediamine ml; the temperature was controlled in a water bath at 20°C, and the reaction was carried out under nitrogen protection for 8 hours. After the reaction, the mixed solution was put into a dialysis bag for purification (molecular weight cut-off 5000), and the water was changed every 12 hours. After 5 days of dialysis, freeze-dried to obtain PNI...
Embodiment 2
[0035] The synthesis of monomer n-propylacrylamide is the same as in Example 1.
[0036] Dissolve 0.9053g of isopropylacrylamide, 1.3579g of n-propylacrylamide and 0.0532ml of vinylpyrrolidone in 46ml of deionized water; pass nitrogen gas for 30min under magnetic stirring, add potassium persulfate 0.0166g and tetramethylethylenediamine 0.0092 ml; the temperature was controlled in a water bath at 20°C, and the reaction was carried out under nitrogen protection for 8 hours. After the reaction, the mixed solution was put into a dialysis bag for purification (molecular weight cut-off 5000), and the water was changed every 12 hours. After 5 days of dialysis, freeze-dried to obtain PNINAVP of 16:24:1.
[0037] Proton NMR spectrum detection: an appropriate amount of sample is dissolved in deuterated water (D 2 O) in, record on NMR spectrometer Varian UNITY plus 400 1 H-NMR spectrum, such as figure 2 shown.
[0038] DSC detection: Weigh a certain amount of copolymer to prepare a ...
Embodiment 3
[0044] The synthesis of monomer n-propylacrylamide is the same as in Example 1.
[0045] Dissolve 0.9053g of isopropylacrylamide, 0.4526g of n-propylacrylamide and 0.0532ml of vinylpyrrolidone in 28ml of deionized water; pass nitrogen gas for 30min under magnetic stirring, add potassium persulfate 0.0101g and tetramethylethylenediamine 0.0056 ml; the temperature was controlled in a water bath at 20°C, and the reaction was carried out under nitrogen protection for 8 hours. After the reaction, the mixed solution was put into a dialysis bag for purification (molecular weight cut-off 5000), and the water was changed every 12 hours. After 5 days of dialysis, freeze-dried to obtain PNINAVP of 16:8:1.
[0046] Proton NMR spectrum detection: an appropriate amount of sample is dissolved in deuterated water (D 2 O) in, record on NMR spectrometer Varian UNITY plus 400 1 H-NMR spectrum, such as figure 2 shown.
[0047] DSC detection: Weigh a certain amount of copolymer to prepare a s...
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