Department of Biological Sciences, Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan 45137-66731, Iran.
Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan 45137-66731, Iran.
ACS Appl Bio Mater. 2021 Apr 19;4(4):3547-3560. doi: 10.1021/acsabm.1c00068. Epub 2021 Mar 15.
Among common strategies for amyloid fibrillation inhibition, the use of naturally occurring polyphenols as an efficient therapeutic approach has attracted a growing body of attention. However, the poor water solubility and low bioavailability of these compounds have greatly restricted their clinical application in amyloid-related diseases. Thus, different types of formulations have been developed to overcome these limitations; among them, nanonization appears to be one of the most notable approaches. Herein, we show that the polyphenolic fraction of propolis (PFP), in the nanosheet form (PFP nanosheet), exhibits an improved capacity for amyloid fibrillation inhibition as well as clearance of preformed fibrils of bovine insulin. This increased efficiency is suggested to be related to the aqueous solubility and surface area enhancement as well as surface modifications upon undergoing the nanonization process, which can lead to strong binding with and trapping of protein at the surface of the nanosheets. On the basis of thioflavin T results, it is suggested that although PFP may modulate the fibrillation process via shortening of the lag phase, prolongation of the nucleation phase through interaction with and stabilizing monomeric species is the mechanism of action of PFP nanosheets. We propose that nanonization of natural small molecules can be considered as a powerful approach to improve their anti-amyloidogenic properties and overcome obstacles originating from poor water solubility and low bioavailability of drug candidates relating to neurodegenerative diseases. Taken together, the obtained results may suggest PFP nanosheets as a potential candidate for use against neurological disorders.
在抑制淀粉样纤维形成的常见策略中,使用天然存在的多酚作为一种有效的治疗方法引起了越来越多的关注。然而,这些化合物的水溶性差和生物利用度低极大地限制了它们在与淀粉样蛋白相关的疾病中的临床应用。因此,已经开发了不同类型的制剂来克服这些限制;其中,纳米化似乎是最引人注目的方法之一。在此,我们表明,蜂胶的多酚部分(PFP)以纳米片的形式(PFP 纳米片),表现出改善的淀粉样纤维抑制能力以及牛胰岛素原纤维的清除能力。这种提高的效率与纳米化过程中的水溶性和表面积增强以及表面修饰有关,这可以导致与蛋白质的强结合和在纳米片表面的捕获。根据硫黄素 T 的结果,尽管 PFP 可能通过缩短潜伏期来调节纤维形成过程,但通过与单体相互作用和稳定单体来延长成核阶段是 PFP 纳米片的作用机制。我们提出,天然小分子的纳米化可以被认为是提高其抗淀粉样蛋白特性的有效方法,并克服与神经退行性疾病相关的候选药物水溶性差和生物利用度低的障碍。总之,获得的结果可能表明 PFP 纳米片可作为治疗神经紊乱的潜在候选药物。