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通过用异双功能聚(乙二醇)/聚丙交酯嵌段共聚物进行涂层处理对功能化聚丙交酯的表面表征。

Surface characterization of functionalized polylactide through the coating with heterobifunctional poly(ethylene glycol)/polylactide block copolymers.

作者信息

Otsuka H, Nagasaki Y, Kataoka K

机构信息

Department of Materials Science, Graduate School of Engineering, University of Tokyo, Hongo 7-3-1, Tokyo 113-8656, Japan.

出版信息

Biomacromolecules. 2000 Spring;1(1):39-48. doi: 10.1021/bm990005s.

Abstract

An AB-type block copolymer composed of alpha-acetalpoly(ethylene glycol) (PEG) as the hydrophilic segment and polylactide (PLA) as the hydrophobic segment was synthesized and utilized to construct a functionalized PEG layer possessing a reactive aldehyde group at the free end of the tethered PEG chain by simple coating on polylactide substrates. Detailed characterization of the functionalized PEGylated surfaces was done from the physicochemical (contact angle and zeta potential) as well as the biological (protein adsorption) point of view to highlight their potential utility as biofunctional interfaces. The amount of protein adsorption was inversely correlated with the degree of water structuring around the PEG molecules, which facilitates the formation of a strongly bound water film to increase the surface hydration. For these surfaces investigated, the extent of surface hydration was more important in determining the materials biocompatibility rather than the actual PEG molecular weight, as evidenced by an extremely low receding contact angle directly related to the adhesive energy of a water molecule. Furthermore, the contact angle relaxation less than a few minutes proved to be determinant for the receding contact angle and resultant hysteresis, caused by rearrangement of the hydrophilic PEG component. Aldehyde groups were confirmed to be present at the tethered PEG chain end using an electron spin resonance probe and can be derivatized with bioactive molecules with amino or hydrazide functionality. The functionalized PEG layer thus prepared on a biodegradable polylactide surface has both nonfouling and ligand-binding properties and may have promising utility as engineered biomaterials including tissue engineering scaffolds.

摘要

合成了一种AB型嵌段共聚物,其由α-缩醛聚(乙二醇)(PEG)作为亲水链段和聚丙交酯(PLA)作为疏水链段组成,并通过在聚丙交酯基底上简单涂覆,用于构建在连接的PEG链的自由端具有反应性醛基的功能化PEG层。从物理化学(接触角和zeta电位)以及生物学(蛋白质吸附)的角度对功能化聚乙二醇化表面进行了详细表征,以突出其作为生物功能界面的潜在用途。蛋白质吸附量与PEG分子周围的水结构程度呈负相关,这有利于形成强结合水膜以增加表面水合作用。对于所研究的这些表面,表面水合程度在决定材料的生物相容性方面比实际的PEG分子量更重要,这一点通过与水分子的粘附能直接相关的极低后退接触角得到证明。此外,由亲水性PEG组分的重排引起的接触角弛豫在几分钟以内被证明对后退接触角和由此产生的滞后现象起决定性作用。使用电子自旋共振探针证实连接的PEG链末端存在醛基,并且可以用具有氨基或酰肼功能的生物活性分子进行衍生化。因此在可生物降解的聚丙交酯表面上制备的功能化PEG层具有抗污和配体结合特性,并且作为包括组织工程支架在内的工程生物材料可能具有广阔的应用前景。

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