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多糖制成的多层膜和膜的pH响应性

pH Responsiveness of Multilayered Films and Membranes Made of Polysaccharides.

作者信息

Silva Joana M, Caridade Sofia G, Costa Rui R, Alves Natália M, Groth Thomas, Picart Catherine, Reis Rui L, Mano João F

机构信息

3B's Research Group-Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence of Tissue Engineering and Regenerative Medicine , Avepark-Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco GMR, Portugal.

ICVS/3B's-PT Government Associate Laboratory , Braga/Guimarães, Portugal.

出版信息

Langmuir. 2015 Oct 20;31(41):11318-28. doi: 10.1021/acs.langmuir.5b02478. Epub 2015 Oct 7.

Abstract

We investigated the pH-dependent properties of multilayered films made of chitosan (CHI) and alginate (ALG) and focused on their postassembly response to different pH environments using a quartz crystal microbalance with dissipation monitoring (QCM-D), swelling studies, ζ potential measurements, and dynamic mechanical analysis (DMA). In an acidic environment, the multilayers presented lower dissipation values and, consequently, higher moduli when compared with the values obtained for the pH used during the assembly (5.5). When the multilayers were exposed to alkaline environments, the opposite behavior occurred. These results were further corroborated by the ability of this multilayered system to exhibit a reversible swelling-deswelling behavior within the pH range from 3 to 9. The changes in the physicochemical properties of the multilayer system were gradual and different from those of individual solubilized polyelectrolytes. This behavior is related to electrostatic interactions between the ionizable groups combined with hydrogen bonding and hydrophobic interactions. Beyond the pH range of 3-9, the multilayers were stabilized by genipin cross-linking. The multilayered films also became more rigid while the pH responsiveness conferred by the ionizable moieties of the polyelectrolytes was preserved. This work demonstrates the versatility and feasibility of LbL methodology to generate inherently pH stimulus-responsive nanostructured films. Surface functionalization using pH responsiveness endows several biomedical applications with abilities such as drug delivery, diagnostics, microfluidics, biosensing, and biomimetic implantable membranes.

摘要

我们研究了由壳聚糖(CHI)和藻酸盐(ALG)制成的多层膜的pH依赖性特性,并使用具有耗散监测功能的石英晶体微天平(QCM-D)、溶胀研究、ζ电位测量和动态力学分析(DMA),重点关注它们在组装后对不同pH环境的响应。在酸性环境中,与组装过程中使用的pH值(5.5)相比,多层膜呈现出较低的耗散值,因此具有更高的模量。当多层膜暴露于碱性环境时,情况则相反。该多层系统在pH值为3至9的范围内表现出可逆的溶胀-消溶胀行为,这进一步证实了上述结果。多层系统的物理化学性质变化是渐进的,且与单个溶解的聚电解质不同。这种行为与可电离基团之间的静电相互作用以及氢键和疏水相互作用有关。在pH值范围3-9之外,多层膜通过京尼平交联得以稳定。多层膜也变得更加刚性,同时保留了由聚电解质的可电离部分赋予的pH响应性。这项工作证明了层层自组装方法生成固有pH刺激响应性纳米结构薄膜的多功能性和可行性。利用pH响应性进行表面功能化赋予了药物递送、诊断、微流体、生物传感和仿生可植入膜等多种生物医学应用相关能力。

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