Preparation method, product and application of antibacterial bone promoting composite coating on surface of PET fiber
A composite coating, fiber surface technology, used in coatings, medical science, prostheses, etc., can solve problems such as poor hydrophilicity and poor osteoconductivity, and achieve high biosafety, good biocompatibility, The method is simple and effective
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Embodiment 1
[0027] The PET fiber material was soaked in absolute ethanol, and ultrasonically treated for 30 min to remove the impurities adhered to the surface of the material. After the material was taken out, it was repeatedly washed with a large amount of ultrapure water to remove residual ethanol, and dried at room temperature. A 5 wt% sodium hydroxide solution was prepared, the PET material was soaked in it, and boiled for 1 h. The material was repeatedly washed with a large amount of ultrapure water until the pH value was about 7, and then dried at 60 °C to obtain a PET fiber material with a carboxyl-terminated end group.
[0028] Soak the above-treated PET material in 0.2 M morpholineethanesulfonic acid (MES) buffer solution with pH=5.5 for 2 h, and then add 0.2 M 1-ethyl-3-(3-dimethylaminopropyl ) carbodiimide hydrochloride (EDC) and 10 mM N-hydroxysuccinimide (NHS), stirred and activated at room temperature for 3 h. Dilute acetic acid with ultra-pure water to a dilute acetic ac...
Embodiment 2
[0031] The PET fiber material was soaked in absolute ethanol, and ultrasonically treated for 30 min to remove the impurities adhered to the surface of the material. After the material was taken out, it was repeatedly washed with a large amount of ultrapure water to remove residual ethanol, and dried at room temperature. A 5 wt% sodium hydroxide solution was prepared, the PET material was soaked in it, and boiled for 1 h. The material was repeatedly washed with a large amount of ultrapure water until the pH value was about 7, and then dried at 60 °C to obtain a PET fiber material with a carboxyl-terminated end group.
[0032] Soak the above-treated PET material in 0.2 M morpholineethanesulfonic acid (MES) buffer solution with pH=5.5 for 2 h, and then add 0.2 M 1-ethyl-3-(3-dimethylaminopropyl ) carbodiimide hydrochloride (EDC) and 10 mM N-hydroxysuccinimide (NHS), stirred and activated at room temperature for 3 h. Dilute acetic acid with ultra-pure water to a dilute acetic ac...
Embodiment 3
[0035] The PET fiber material was soaked in absolute ethanol, and ultrasonically treated for 30 min to remove the impurities adhered to the surface of the material. After the material was taken out, it was repeatedly washed with a large amount of ultrapure water to remove residual ethanol, and dried at room temperature. A 5 wt% sodium hydroxide solution was prepared, the PET material was soaked in it, and boiled for 1 h. The material was repeatedly washed with a large amount of ultrapure water until the pH value was about 7, and then dried at 60 °C to obtain a PET fiber material with a carboxyl-terminated end group.
[0036] Soak the above-treated PET material in 0.2 M morpholineethanesulfonic acid (MES) buffer solution with pH=5.5 for 2 h, and then add 0.2 M 1-ethyl-3-(3-dimethylaminopropyl ) carbodiimide hydrochloride (EDC) and 10 mM N-hydroxysuccinimide (NHS), stirred and activated at room temperature for 3 h. Dilute acetic acid with ultra-pure water to a dilute acetic ac...
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