Polydopamine-zwitterionic polymer anti-adhesion coating modification method and application thereof
A technology of zwitterion and polydopamine, which is applied in the field of polymer materials and medical implants, can solve the problems that it is difficult to achieve the effect of resisting long-term and chronic foreign body reactions, and achieve the avoidance of initiator residues, good biocompatibility, and biological good compatibility
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Embodiment 1
[0032] Example 1. This embodiment uses the electrode as a medical implant to illustrate the method for modifying the electrode with polydopamine-zwitterionic polymer anti-adhesion coating:
[0033] 1. In an ice bath, dissolve 1.89 g of dopamine hydrochloride (DA·HCl), 4.52 g of tert-butyldimethylsilyl chloride (TBDMS) and 3.4 g of imidazole in 30 ml of dichloromethane (DCM) solution. After the reaction ceased exothermic, the ice bath was removed. Next, the reaction was continued for 2 hours at 25° C. under nitrogen. The precipitate in the reacted mixed solution was removed by centrifugation, the supernatant was extracted and extracted to separate the organic phase, and then concentrated by rotary evaporation. The concentrated solution was purified by silica gel chromatography (dichloromethane:methanol=4:1), and then the purified solution was concentrated and vacuum-dried for 8 hours to obtain an intermediate product in the form of a yellow oily liquid. The reaction process ...
Embodiment 2
[0042] Example 2. This embodiment uses polyetheretherketone (PEEK) as a medical implant to illustrate the method for modifying the surface of PEEK with polydopamine-zwitterionic polymer anti-adhesion coating:
[0043] 1. 2.27g of dopamine hydrochloride (DA·HCl), 5.42g of tert-butyldimethylsilyl chloride (TBDMS) and 4.08g of imidazole were dissolved in 30ml of chloroform solution and reacted at 0°C. Next, the reaction was continued for 2 hours at 25° C. under nitrogen. The precipitate in the reacted mixed solution was removed by centrifugation, the supernatant was extracted and extracted to separate the organic phase, and then concentrated by rotary evaporation. The concentrated solution was purified by silica gel chromatography (dichloromethane:methanol=8:1), and then the purified solution was concentrated and vacuum-dried for 10 hours to obtain an intermediate product. The reaction process is as follows:
[0044]
[0045] 2. Dissolve 2.85g of the intermediate product an...
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