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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Surface modification with well-defined biocompatible triblock copolymers Improvement of biointerfacial phenomena on a poly(dimethylsiloxane) surface
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Surface modification with well-defined biocompatible triblock copolymers Improvement of biointerfacial phenomena on a poly(dimethylsiloxane) surface

机译:用明确定义的生物相容性三嵌段共聚物进行表面改性改善聚二甲基硅氧烷表面上的生物界面现象

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摘要

To improve interfacial phenomena of poly(dimethylsiloxane) (PDMS) as biomaterials, well-defined triblock copolymers were prepared as coating materials by reversible addition-fragmentation chain transfer (RAFT) controlled polymerization. Hydroxy-terminated poly(vinylmethylsiloxane-co-dimethylsiloxane) (HO–PVlDmMS–OH) was synthesized by ring-opening polymerization. The copolymerization ratio of vinylmethylsiloxane to dimethylsiloxane was 1/9. The molecular weight of HO–PVlDmMS–OH ranged from (1.43 to 4.44) × 104, and their molecular weight distribution (Mw/Mn) as determined by size-exclusion chromatography equipped with multiangle laser light scattering (SEC-MALS) was 1.16. 4-Cyanopentanoic acid dithiobenzoate was reacted with HO–PVlDmMS–OH to obtain macromolecular chain transfer agents (macro-CTA). 2-Methacryloyloxyethyl phosphorylcholine (MPC) was polymerized with macro-CTAs. The gel-permeation chromatography (GPC) chart of synthesized polymers was a single peak and Mw/Mn was relatively narrow (1.3–1.6). Then the poly(MPC) (PMPC)–PVlDmMS–PMPC triblock copolymers were synthesized. The molecular weight of PMPC in a triblock copolymer was easily controllable by changing the polymerization time or the composition of the macro-CTA to a monomer in the feed. The synthesized block copolymers were slightly soluble in water and extremely soluble in ethanol and 2-propanol.Surface modification was performed via hydrosilylation. The block copolymer was coated on the PDMS film whose surface was pretreated with poly(hydromethylsiloxane). The surface wettability and lubrication of the PDMS film were effectively improved by immobilization with the block copolymers. In addition, the number of adherent platelets from human platelet-rich plasma (PRP) was dramatically reduced by surface modification. Particularly, the triblock copolymer having a high composition ratio of MPC units to silicone units was effective in improving the surface properties of PDMS.By selective decomposition of the Si–H bond at the surface of the PDMS substrate by irradiation with UV light, the coating region of the triblock copolymer was easily controlled, resulting in the fabrication of micropatterns. On the surface, albumin adsorption was well manipulated.
机译:为了改善作为生物材料的聚二甲基硅氧烷(PDMS)的界面现象,通过可逆的加成-断裂链转移(RAFT)控制的聚合反应,制备了定义明确的三嵌段共聚物作为涂料。通过开环聚合反应合成了羟基封端的聚(乙烯基甲基硅氧烷-共二甲基硅​​氧烷)(HO-PVlDmMS-OH)。乙烯基甲基硅氧烷与二甲基硅氧烷的共聚比为1/9。 HO-PVlDmMS-OH的分子量为(1.43至4.44)×104,通过配备多角度激光散射(SEC-MALS)的尺寸排阻色谱法测定的分子量分布(Mw / Mn)为1.16。 4-氰基戊酸二硫代苯甲酸酯与HO–PVlDmMS–OH反应,得到大分子链转移剂(大分子CTA)。将2-甲基丙烯酰氧基乙基磷酰胆碱(MPC)与大型CTA聚合。合成聚合物的凝胶渗透色谱(GPC)图为一个峰,Mw / Mn相对较窄(1.3-1.6)。然后合成了聚(MPC)(PMPC)–PVlDmMS–PMPC三嵌段共聚物。通过改变进料中单体的聚合时间或大分子CTA的组成,可以容易地控制三嵌段共聚物中PMPC的分子量。合成的嵌段共聚物微溶于水,极易溶于乙醇和2-丙醇。表面改性通过氢化硅烷化进行。将该嵌段共聚物涂覆在PDMS膜上,该PDMS膜的表面用聚(氢甲基硅氧烷)预处理。通过用嵌段共聚物固定化,有效改善了PDMS膜的表面润湿性和润滑性。另外,通过表面修饰显着减少了来自富含人血小板的血浆(PRP)的粘附血小板数量。特别是,具有高MPC单元与有机硅单元组成比的三嵌段共聚物可有效改善PDMS的表面性能。通过用紫外线照射PDMS基材表面的Si-H键选择性分解,涂层三嵌段共聚物的区域容易控制,从而形成微图案。在表面上,白蛋白吸附得到了很好的控制。

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