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Salt-Assisted Mechanistic Analysis of Chitosan/Tripolyphosphate Micro- and Nanogel Formation

机译:壳聚糖/三聚磷酸微和纳米凝胶形成的盐辅助机理分析

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Self-assembled micro- and nanogels are frequently prepared by mixing tripolyphosphate (TPP) with dilute chitosan solutions. Upon its addition, the TPP ionically cross-links the chitosan molecules into gel-like colloids that range from tens of nanometers to micrometers in diameter. These particles are biocompatible, mucoadhesive and, because they are easy to prepare under very mild conditions, attract widespread interest in the encapsulation of drugs, neutraceuticals. and other bioactive Davloads. Despite their broad use, however. their formation mechanism has remained largely obscured by the very fast kinetics of their self-assembly. To this end, we have tuned the TPP and monovalent salt (NaCl) concentrations to dramatically slow down this process (to occur on the time scale of days instead of milliseconds), and then probed the evolution in the size and morphology of micro- and nanogels during their formation. This revealed that the micro- and nanogel formation rates are extremely sensitive to NaCl and TPP concentrations, and that the formation process occurs in two stages: (1) formation of small primary nanoparticles and (2) aggregation of primary particles into larger, higher-order colloids that are obtained at the end of the ionotropic gelation process.
机译:自组装的微凝胶和纳米凝胶通常是通过将三聚磷酸盐(TPP)与稀释的壳聚糖溶液混合来制备的。加入后,TPP将壳聚糖分子离子交联成凝胶状胶体,其直径范围从几十纳米到微米。这些颗粒具有生物相容性,粘膜粘附性,并且由于它们很容易在非常温和的条件下制备,因此在药物,神经营养药物的封装方面引起了广泛的关注。和其他具有生物活性的Davload。尽管用途广泛。它们的形成机理在很大程度上仍被其自组装的快速动力学所遮盖。为此,我们已经调整了TPP和一价盐(NaCl)的浓度,以显着减慢该过程(发生在几天而不是毫秒的时间范围内),然后探究了微观和微观结构的大小和形态的演变。纳米凝胶形成过程中。这表明微凝胶和纳米凝胶的形成速率对NaCl和TPP浓度极为敏感,并且形成过程分为两个阶段:(1)形成小的初级纳米颗粒,以及(2)初级颗粒聚集成更大,更高的订购在离子化凝胶化过程结束时获得的胶体。

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