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Laponite/PEG 接枝聚合物纳米复合薄膜和具有抗污染性能的聚合物刷。

Nanocomposite Films of Laponite/PEG-Grafted Polymers and Polymer Brushes with Nonfouling Properties.

机构信息

Institute for Materials & Surface Technology, University of Applied Sciences , 24149 Kiel, Germany.

Cell Culture Laboratory, Clinic of Dentistry, University of Kiel , 24118 Kiel, Germany.

出版信息

Langmuir. 2017 Jul 11;33(27):6739-6750. doi: 10.1021/acs.langmuir.7b00534. Epub 2017 Jun 27.

Abstract

We explore the suitability of nanocomposite thin films based on laponite nanomaterial and grafted antiadhesive polymers as transparent nonfouling surfaces. For this purpose, two polymers were chosen: a linear poly(ethylene glycol) (PEG) silane, 2-[methoxy(polyethyleneoxy)propyl]-trimethoxysilane), and thermoresponsive poly(oligo ethylene glycol)-methyl ether-methacrylate (POEGMA) brushes. PEG silane was grafted on the laponite nanoparticles in solution yielding homogeneous and transparent thin films via a dip coating procedure on glass and silicon substrates. POEGMA was grafted on laponite-(3-Aminopropyl)trimethoxysilane (APTMS) nanocomposite films that were processed similarly to PEG-silane using atom transfer radical polymerization (ATRP). Film characterization with, among others, Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), and atomic force microscopy (AFM) attests to successful grafting of the polymers to the laponite nanoparticles. In particular, evidence of basal plane expansion of laponite with increasing silane concentration are obtained using XRD, while patent morphological changes are revealed with AFM. The results are discussed in terms of the different grafting sites on laponite and compared with literature. While LP-PEG-silane is easily applied to a surface from a precursor solution via a dip coating procedure LP-APTMS-OEGMA requires lots more chemicals, a thorough control of reaction parameters, and longer reaction time in order to generate films with the desirable properties. We therefore also addressed the antifouling properties of the films. These were tested together with control samples of bare glass and laponite thin films for 30 days in an algae container. More tests were conducted with fibroblast cell cultures. Our preliminary results show that grafting of PEG containing polymers and polymer brushes alters the properties of the laponite films from fouling to nonfouling surfaces. As a first estimate, the adhesion of particles (diatoms, algae, etc.) to surfaces is reduced by approximately 85% in the case of LP-PEG-silane and up to 92% in the case of LP-APTMS-POEGMA, in comparison to the control surfaces. Furthermore, practically no cell adhesion on such surfaces could be observed.

摘要

我们探索了基于纳米级蒙脱土纳米材料和接枝抗粘聚合物的纳米复合薄膜作为透明防污表面的适用性。为此,选择了两种聚合物:线性聚乙二醇(PEG)硅烷 2-[甲氧基(聚氧乙烯基)丙基]-三甲氧基硅烷)和温敏性聚(聚乙二醇)甲基醚甲基丙烯酸酯(POEGMA)刷。PEG 硅烷在溶液中接枝到蒙脱土纳米颗粒上,通过在玻璃和硅衬底上的浸涂工艺得到均匀透明的薄膜。POEGMA 接枝到蒙脱土-(3-氨丙基)三甲氧基硅烷(APTMS)纳米复合薄膜上,采用原子转移自由基聚合(ATRP)以类似的方式处理 PEG 硅烷。通过傅里叶变换红外(FT-IR)光谱、X 射线衍射(XRD)和原子力显微镜(AFM)等手段对薄膜进行了表征,证明了聚合物成功接枝到蒙脱土纳米颗粒上。特别是,通过 XRD 获得了随着硅烷浓度增加蒙脱土基面膨胀的证据,而 AFM 则揭示了明显的形态变化。结果根据蒙脱土上的不同接枝位点进行了讨论,并与文献进行了比较。虽然 LP-PEG-silane 可以很容易地从预聚物溶液通过浸涂工艺涂覆到表面上,但 LP-APTMS-OEGMA 需要更多的化学品、更严格的反应参数控制和更长的反应时间,才能生成具有所需性能的薄膜。因此,我们还研究了薄膜的抗污性能。这些薄膜与裸玻璃和蒙脱土薄膜的对照样品在藻类容器中进行了 30 天的测试。还进行了更多的成纤维细胞培养测试。我们的初步结果表明,接枝含 PEG 的聚合物和聚合物刷可以将蒙脱土薄膜的性质从易污染转变为不易污染的表面。作为初步估计,与对照表面相比,LP-PEG-silane 情况下颗粒(硅藻、藻类等)的粘附减少了约 85%,而 LP-APTMS-POEGMA 情况下减少了 92%。此外,在这些表面上几乎观察不到细胞粘附。

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