Shurpik Dmitriy N, Makhmutova Lyaysan I, Usachev Konstantin S, Islamov Daut R, Mostovaya Olga A, Nazarova Anastasia A, Kizhnyaev Valeriy N, Stoikov Ivan I
A. M. Butlerov Chemical Institute, Kazan Federal University, Kremlevskaya, 18, 420008 Kazan, Russia.
Institute of Fundamental Medicine and Biology, Kazan Federal University, Kremlevskaya, 18, 420008 Kazan, Russia.
Nanomaterials (Basel). 2021 Apr 8;11(4):947. doi: 10.3390/nano11040947.
In this work, we have proposed a novel universal stimulus-sensitive nanosized polymer system based on decasubstituted macrocyclic structures-pillar[5]arenes and tetrazole-containing polymers. Decasubstituted pillar[5]arenes containing a large, good leaving tosylate, and phthalimide groups were first synthesized and characterized. Pillar[5]arenes containing primary and tertiary amino groups, capable of interacting with tetrazole-containing polymers, were obtained with high yield by removing the tosylate and phthalimide protection. According to the fluorescence spectroscopy data, a dramatic fluorescence enhancement in the pillar[5]arene/fluorescein/polymer system was observed with decreasing pH from neutral (pH = 7) to acidic (pH = 5). This indicates the destruction of associates and the release of the dye at a pH close to 5. The presented results open a broad range of opportunities for the development of new universal stimulus-sensitive drug delivery systems containing macrocycles and nontoxic tetrazole-based polymers.
在这项工作中,我们提出了一种基于十取代大环结构(柱[5]芳烃)和含四氮唑聚合物的新型通用刺激敏感纳米级聚合物体系。首先合成并表征了含有大的、良好离去基团对甲苯磺酸酯和邻苯二甲酰亚胺基团的十取代柱[5]芳烃。通过去除对甲苯磺酸酯和邻苯二甲酰亚胺保护基,高产率地获得了含有能够与含四氮唑聚合物相互作用的伯氨基和叔氨基的柱[5]芳烃。根据荧光光谱数据,在柱[5]芳烃/荧光素/聚合物体系中,随着pH从中性(pH = 7)降至酸性(pH = 5),观察到荧光显著增强。这表明在接近pH = 5时缔合物被破坏且染料被释放。所呈现的结果为开发包含大环和无毒四氮唑基聚合物的新型通用刺激敏感药物递送系统开辟了广泛的机会。