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Formation of multilayered biopolymer microcapsules and microparticles in a multiphase microfluidic flow

机译:在多相微流中形成多层生物聚合物微胶囊和微粒

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摘要

This paper reports the development of a scalable continuous microfluidic-based method for the preparation of multilayered biopolymer microcapsules and microparticles, with a size range of 1 to 100 μm, in a single-layered polydimethylsiloxane-based device. This new approach has been utilised to produce polyethylene oxide (PEO)-based microparticles, layered with subsequent stage wise coatings of polylactide-based block copolymers and polyvinylpyrrolidone. The production process was shown to allow for on-chip encapsulation of protein and vitamin molecules in the biopolymer micro particles, without any further handling after collection from the device. We have studied the release profiles in the case of model molecules of distinctive molecular weights, namely, vitronectin, horse radish peroxidase, and vitamin B12. We compared the release properties of the microparticles to those from macro-gels of the same materials prepared off-chip. The results indicated that the microparticles have definitively different molecular weight cut-off characteristics, likely due to a denser microstructure within the microparticles compared to the bulk hydrogels. This difference suggests that significant benefits may exist in the use of this method to produce layered biopolymer microparticles in achieving improved controlled release and encapsulation.
机译:本文报道了一种可扩展的基于连续微流体的方法的发展,该方法用于在单层聚二甲基硅氧烷基器件中制备尺寸范围为1至100μm的多层生物聚合物微胶囊和微粒。该新方法已被用于生产基于聚环氧乙烷(PEO)的微粒,并在其后的聚丙交酯基嵌段共聚物和聚乙烯吡咯烷酮的逐步涂层上进行分层。已表明,该生产过程可将蛋白质和维生素分子芯片封装在生物聚合物微粒中,而从设备中收集后无需任何进一步处理。我们已经研究了具有独特分子量的模型分子,即玻连蛋白,辣根过氧化物酶和维生素B12的释放曲线。我们将微粒的释放性能与芯片外制备的相同材料的大凝胶的释放性能进行了比较。结果表明,微粒具有截然不同的分子量截留特性,这可能是由于与本体水凝胶相比,微粒内的致密微观结构。这种差异表明,使用该方法生产层状生物聚合物微粒可能会带来明显的好处,以实现改进的控释和包封。

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