Fabrication of Covalently Crosslinked and Amine-Reactive Microcapsules by Reactive Layer-by-Layer Assembly of Azlactone-Containing Polymer Multilayers on Sacrificial Microparticle Templates.

Eric M Saurer, Ryan M Flessner, Maren E Buck, David M Lynn
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Abstract

We report on the fabrication of covalently crosslinked and amine-reactive hollow microcapsules using 'reactive' layer-by-layer assembly to deposit thin polymer films on sacrificial microparticle templates. Our approach is based on the alternating deposition of layers of a synthetic polyamine and a polymer containing reactive azlactone functionality. Multilayered films composed of branched poly(ethylene imine) (BPEI) and poly(2-vinyl-4,4-dimethylazlactone) (PVDMA) were fabricated layer-by-layer on the surfaces of calcium carbonate and glass microparticle templates. After fabrication, these films contained residual azlactone functionality that was accessible for reaction with amine-containing molecules. Dissolution of the calcium carbonate or glass cores using aqueous ethylenediamine tetraacetic acid (EDTA) or hydrofluoric acid (HF), respectively, led to the formation of hollow polymer microcapsules. These microcapsules were robust enough to encapsulate and retain a model macromolecule (FITC-dextran) and were stable for at least 22 hours in high ionic strength environments, in low and high pH solutions, and in several common organic solvents. Significant differences in the behaviors of capsules fabricated on CaCO(3) and glass cores were observed and characterized using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). Whereas capsules fabricated on CaCO(3) templates collapsed upon drying, capsules fabricated on glass templates remained rigid and spherical. Characterization using EDS suggested that this latter behavior results, at least in part, from the presence of insoluble metal fluoride salts that are trapped or precipitate within the walls of capsules after etching of the glass cores using HF. Our results demonstrate that the assembly of BPEI/PVDMA films on sacrificial templates can be used to fabricate reactive microcapsules of potential use in a wide range of fields, including catalysis, drug and gene delivery, imaging, and biomedical research.

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通过在人工微粒模板上反应性逐层组装含氮内酯的聚合物多层来制造共价交联胺活性微胶囊
我们报告了利用 "反应 "逐层组装技术在牺牲微粒模板上沉积聚合物薄膜,制造共价交联胺反应空心微胶囊的情况。我们的方法基于合成多胺和含有反应性氮内酯官能团的聚合物的交替沉积层。我们在碳酸钙和玻璃微粒模板表面逐层制作了由支化聚(乙烯亚胺)(BPEI)和聚(2-乙烯基-4,4-二甲基氮内酯)(PVDMA)组成的多层薄膜。制作完成后,这些薄膜含有可与含胺分子反应的残余氮内酯官能团。分别使用乙二胺四乙酸(EDTA)或氢氟酸(HF)水溶液溶解碳酸钙或玻璃芯,可形成空心聚合物微胶囊。这些微胶囊足以封装和保留模型大分子(FITC-葡聚糖),并且在高离子强度环境、低pH值和高pH值溶液以及几种常见有机溶剂中至少能稳定存在22小时。使用扫描电子显微镜(SEM)和能量色散 X 射线光谱(EDS)观察和表征了在 CaCO(3) 和玻璃芯上制造的胶囊在行为上的显著差异。在 CaCO(3) 模板上制作的胶囊在干燥时会塌陷,而在玻璃模板上制作的胶囊则保持坚硬和球形。利用 EDS 进行的表征表明,后一种行为至少部分是由于存在不溶性金属氟化物盐造成的,这些盐在使用 HF 蚀刻玻璃核心后被截留或沉淀在胶囊壁内。我们的研究结果表明,在牺牲模板上组装 BPEI/PVDMA 薄膜可用于制造活性微胶囊,在催化、药物和基因递送、成像和生物医学研究等广泛领域具有潜在用途。
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来源期刊
Journal of Materials Chemistry
Journal of Materials Chemistry 工程技术-材料科学:综合
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1.5 months
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