Block polymer for full-degradable intravascular stent and preparation method of block polymer
A technology of block polymers and vascular stents, which is applied in the field of block polymers and preparations of fully degradable vascular stents, which can solve problems such as stent fracture, low melt strength, and difficult melt extrusion processing, and achieve the effect of improving degradation
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[0031] A method for preparing a block polymer for fully degradable vascular stents, comprising the following steps:
[0032] Step 1: The hydroxyl end group in the polylactic acid and carbonyldiimidazole (CDI) react in a solvent to obtain polylactic acid (PLA-CDI) whose end group is carbonylimidazole; the mole of the hydroxyl end group in the polylactic acid and carbonyldiimidazole The ratio is 1:1~1:5. The reaction temperature is from room temperature to 100°C, and the reaction time is from 5h to 24h. The mass concentration of polylactic acid in the solvent is 0.2g / mL-5g / mL. The reaction solvent is one or a mixture of two or more of chloroform, dichloromethane, tetrahydrofuran, hexafluoroisopropanol and acetone in any proportion.
[0033] After the reaction is completed, the purification process is as follows:
[0034] Pour the reaction solution into anhydrous ether or anhydrous methanol, suction filter to obtain the target polymer, and then further purify the target polyme...
Embodiment 1
[0048] A block polymer for fully degradable vascular stents was prepared according to the following steps:
[0049] Step 1: React polylactic acid (Mw=50000) with carbonyldiimidazole in a chloroform solution at room temperature for 24 hours to obtain a polylactic acid material whose end group is carbonylimidazole. The mass concentration of polylactic acid was 1 g / mL.
[0050] Wherein, the molar ratio of polylactic acid hydroxyl group to carbonyldiimidazole is 1:1, after the solvent is concentrated, it is poured into anhydrous methanol, and the polylactic acid material whose target end group is carbonylimidazole is obtained by suction filtration.
[0051] Step 2: React carbonyl imidazole polylactic acid and polycaprolactone (Mw=1000) in chloroform solution for 48 hours at 50°C to obtain a polylactic acid-polycaprolactone block polymer whose linking site is carbonate . Wherein the mass concentration of the polylactic acid of carbonylimidazole is 3g / mL. The molar ratio of polyl...
Embodiment 2
[0054]A block polymer for fully degradable vascular stents was prepared according to the following steps:
[0055] Step 1: React polylactic acid (Mw=80000) with carbonyldiimidazole in a chloroform solution for 24 hours at room temperature to obtain a polylactic acid material whose end group is carbonylimidazole. The mass concentration of polylactic acid is 0.5g / mL.
[0056] Wherein, the molar ratio of polylactic acid hydroxyl group to carbonyldiimidazole is 1:3, after the solvent is concentrated, it is poured into anhydrous methanol, and the polylactic acid material whose target terminal group is carbonylimidazole is obtained by suction filtration.
[0057] Step 2: React carbonyl imidazole polylactic acid and polycaprolactone (Mw=2000) in chloroform solution for 48 hours at 80°C to obtain a polylactic acid-polycaprolactone block polymer whose linking site is carbonate . Wherein the mass concentration of the polylactic acid of carbonylimidazole is 1 g / mL. The molar ratio of ...
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