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Chitosan microgels obtained by on-chip crosslinking reaction employing a microfluidic device

机译:通过使用微流体装置的芯片上交联反应获得的壳聚糖微凝胶

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In the present work, we report on the preparation of microgels of chitosan crosslinked with sodium tripolyphosphate (TPP) employing the microfluidics technique (MF). To achieve this, several flow focusing geometries were designed and tested. As a first step, a two-inlet flow focusing geometry was employed to emulsify chitosan and the crosslinking reaction was carried out offchip. This procedure did not allow separating the resulting chitosan microgels due to an incomplete crosslinking reaction. A crosslinking reaction on-chip was studied as an alternative. A four-inlet flow focusing geometrywas designed in which three dispersed phases, chitosan 0.25% (w/v), TPP 0.05% (w/v) and acetic acid 1% (v/v) and an continuous phase mineral oil + Span 80 (3% w/v) were employed. The flow rates for the continuous phase were varied from 6.7 to 11.7 μL/min and chitosan microgels were successfully obtained with average diameters from 68 to 42 μm. The average size of the microgels outside the MF device decreased up to ~21% with respect to their size inside the MF device due to partial expulsion of water from the microgels when complete gelation occurred.
机译:在本工作中,我们报告了使用微流控技术(MF)制备与三聚磷酸钠(TPP)交联的壳聚糖微凝胶的方法。为了实现这一目标,设计并测试了几种流动聚焦几何形状。第一步,采用两入口流动聚焦几何形状来乳化壳聚糖,并在芯片外进行交联反应。由于不完全的交联反应,该程序不允许分离所得的壳聚糖微凝胶。研究了片上交联反应作为替代方案。设计了一种四入口流动聚焦几何结构,其中三个分散相分别为:壳聚糖0.25%(w / v),TPP 0.05%(w / v)和乙酸1%(v / v)和连续相矿物油+ Span 80 (3%w / v)被使用。连续相的流速从6.7到11.7μL/ min不等,成功获得了壳聚糖微凝胶,平均直径为68到42μm。相对于其在MF装置内部的尺寸,MF装置外部的微凝胶的平均尺寸降低了约21%,这是由于当发生完全胶凝时水从微凝胶中部分排出。

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