Ureter rack tube made of absorbable material
A technology of ureteral stents and absorbent materials, which can be applied to devices with tubular structures in the human body, medical science, and prostheses. It can solve problems such as low molecular weight, difficulty in developing practical products, and fast absorption, so as to reduce pain and Burden, good for imaging and development, good biocompatibility
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Embodiment 1
[0019] Example 1 Preparation of ε-caprolactone-DL-lactide copolymer: 50 grams each of dehydrated and purified ε-caprolactone and DL-lactide were placed in a 500ml reaction bottle, and then 0.01% The stannous octoate catalyst was reacted under vacuum conditions at 150°C for 6 hours to obtain an elastic polymer, which was dissolved in acetone and precipitated in ethanol, and the precipitate was dried in a vacuum desiccator for 48 hours to obtain Elastomer material. The molecular weight of the product is 300,000, and the ε-caprolactone unit in the ε-caprolactone-lactide copolymer accounts for 49.6% as determined by the NMR C13 spectrum. The glass transition temperature was determined to be 3°C.
[0020] The ε-caprolactone-lactide copolymer synthesized above was extruded in an extruder at a temperature of 100-135°C. The outer diameter of the formed ureteral stent was 2.8mm, the inner diameter was 1.9mm, and the appearance of the pipe was transparent.
Embodiment 2
[0021] Example 2 Put 65 grams of dehydrated and purified ε-caprolactone and 35 grams of DL-lactide into a 500ml reaction bottle, then add 0.01% stannous octoate catalyst, and react under vacuum conditions at 150°C After 7 hours, an elastic copolymer was obtained. The copolymer was dissolved in acetone, precipitated in ethanol, and the precipitate was dried in a vacuum desiccator for 48 hours to obtain an elastomer material. The molecular weight is 480,000. The glass transition temperature was determined to be -8°C.
[0022] The ε-caprolactone-DL-lactide copolymer synthesized above was extruded in an extruder at a temperature of 145°C. The outer diameter of the formed ureteral stent was 2.8 mm, the inner diameter was 1.9 mm, and the appearance of the tube was transparent.
Embodiment 3
[0023] Example 3 Preparation of ε-caprolactone-L-lactide copolymer: 65 grams of dehydrated and purified ε-caprolactone and 35 grams of L-lactide were placed in a 500ml reaction flask, and then 0.01 % stannous octoate catalyst, reacted under vacuum condition and 150 ℃ for 5 hours, obtained the multipolymer of elasticity, this multipolymer was dissolved in acetone, precipitated in ethanol, and the precipitate was dried in a vacuum drier for 48 hours. Obtain an elastomeric material. The molecular weight is 100,000. The glass transition temperature was determined to be -9°C.
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