首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Head group modulated pH-responsive hydrogel of amino acid-based amphiphiles: Entrapment and release of cytochrome c and vitamin B-12
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Head group modulated pH-responsive hydrogel of amino acid-based amphiphiles: Entrapment and release of cytochrome c and vitamin B-12

机译:头基调节的基于氨基酸的两亲物的pH响应水凝胶:捕获和释放细胞色素c和维生素B-12

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摘要

The present study describes the rational design and synthesis of amino acid-based amphiphilic hydrogelators, which were systemically fine-tuned at the head group to develop pH-responsive hydrogels. To understand the basic structural requirements of a low molecular weight amphiphilic hydrogelator, 10 analogous amphiphiles based on L-phenylalanine and L-tyrosine with structurally related head group were synthesized. Among them, three with quaternary ammonium substitution at the head group formed transparent hydrogels at room temperature while others were unable to gelate water. To establish correlations between the head group architecture of the gelators and their supramolecular arrangements, a variety of spectroscopic and microscopic techniques were investigated that showed that a balance between hydrophilicity and hydrophobicity is required to achieve hydrogelation. Interestingly, the gelator with tyrosinate in its head group showed remarkable response toward external pH. All hydrogels including the pH-responsive one were used in the controlled and/or pH-triggered release of entrapped (with in hydrogels) vitamin B-12 and cytochrome c at different pHs. Since the hydrogels were formed at room temperature without heating, this could be very important during the entrapment of biomolecules such as proteins because of their heat sensitivity. At biological pH (7.4), the release of entrapped biomolecules from all three hydrogels was caused by diffusion through the gel structure, but at endosomal pH (similar to 5.5) and further lower pH, the release rate of biomolecules from the pH-responsive hydrogel with tyrosinate head group (pK(a) approximate to 7.2) increased by 9-10-fold compared to that observed at physiological pH, because of gel dissolution. Retention of the structure and activity of released biomolecule has established the prospect of the hydrogel as an efficient drug delivery vehicle.
机译:本研究描述了基于氨基酸的两亲性水凝胶剂的合理设计和合成,对它们进行了系统的微调以开发pH响应水凝胶。为了了解低分子量两亲性水凝胶剂的基本结构要求,合成了10种基于L-苯丙氨酸和L-酪氨酸的具有结构相关首基的类似两亲物。其中,三个在头部被季铵取代的化合物在室温下形成透明的水凝胶,而另一些则不能使水凝胶化。为了建立胶凝剂的头基结构与其超分子排列之间的相关性,研究了多种光谱和显微技术,这些技术表明实现亲水凝胶化需要亲水性和疏水性之间的平衡。有趣的是,头部带有酪氨酸盐的胶凝剂对外部pH表现出显着的响应。包括pH响应型在内的所有水凝胶均用于在不同pH下控制和/或通过pH触发释放(在水凝胶中)包埋的维生素B-12和细胞色素c。由于水凝胶是在不加热的情况下于室温下形成的,因此,由于其热敏感性,在包埋生物分子(如蛋白质)期间可能非常重要。在生物pH值(7.4)下,所有三种水凝胶的截留生物分子的释放是通过凝胶结构的扩散引起的,但是在内体pH(约5.5)以及更低的pH值下,生物分子从pH响应水凝胶的释放速率酪氨酸盐头部组(pK(a)约7.2)与生理pH值相比增加了9-10倍,这是因为凝胶溶解。保留释放的生物分子的结构和活性已经确立了水凝胶作为有效药物递送载体的前景。

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