Xue Xiangdong, Xu Jing, Wang Paul C, Liang Xing-Jie
Chinese Academy of Sciences (CAS) Center for Excellentce in Nanoscience and CAS Key Laboratory for Biological Effects of Nanomaterials & Nanosafety, National Center for Nanoscience and Technology, No. 11 Beiyitiao, Zhongguancun, Beijing, China 100190; University of Chinese Academy of Sciences, Beijing, China 100049.
Chinese Academy of Sciences (CAS) Center for Excellentce in Nanoscience and CAS Key Laboratory for Biological Effects of Nanomaterials & Nanosafety, National Center for Nanoscience and Technology, No. 11 Beiyitiao, Zhongguancun, Beijing, China 100190.
J Mater Chem C Mater. 2016 Apr 14;4(14):2719-2730. doi: 10.1039/C5TC03651H. Epub 2016 Jan 27.
Nanopharmaceuticals possess a myriad of advantages for disease treatment, not only in delivering therapeutic agents, but also in deciphering their innate intracellular or subcellular behaviours, providing detailed diagnostic and prognostic information, quantifying treatment efficacy and designing better therapeutics. To evaluate the subcellular behaviour of nanopharmaceuticals, colourful fluorescence is the most potential technique, because it is capable of painting the subcellular detail in three dimensions with high resolution. Furthermore, the fluorescence is switchable, and thus the subcellular details can be lightened specifically without the undesirable background. However, most nanopharmaceuticals lack a fluorescent report group, and its introduction requires extra steps. Moreover, the introduced fluorescent groups can suffer from concentration quenching or aggregation-caused quenching (ACQ) when they are embedded in nanopharmaceuticals at a high concentration. The unique aggregation-induced emission (AIE) effect provides a straightforward solution. The aromatic cores of AIE molecules are always hydrophobic and do not undergo the ACQ effect even at high concentrations. Hence, AIE molecules can be directly introduced as building blocks to provide the driving force for the self-assembly of nanopharmaceuticals and can allow us to develop label-free, ACQ-free and luminescent nanopharmaceuticals that can simultaneously implement drug delivery and subcellular behaviour evaluation. This review presents different types of AIE molecules-based nanopharmaceuticals and their biological properties and applications for imaging subcellular behaviours, including the drug releasing process, metabolism of nanopharmaceuticals, subcellular distributions of drug and carriers, and therapeutic effect. With detailed acquaintance of these subcellular behaviours, we anticipate that the research we discuss in this review can inspire other scientists to develop next generation nanopharmaceuticals that can be guided by fluorescence imaging and thus can realize concisely controllable drug delivery.
纳米药物在疾病治疗方面具有众多优势,不仅体现在递送治疗剂上,还在于解析其内在的细胞内或亚细胞行为、提供详细的诊断和预后信息、量化治疗效果以及设计更优的治疗方法。为了评估纳米药物的亚细胞行为,彩色荧光是最具潜力的技术,因为它能够以高分辨率在三维空间中描绘亚细胞细节。此外,荧光是可切换的,因此亚细胞细节可以被特异性照亮而无不良背景。然而,大多数纳米药物缺乏荧光报告基团,其引入需要额外步骤。而且,当引入的荧光基团以高浓度嵌入纳米药物中时,可能会遭受浓度猝灭或聚集诱导猝灭(ACQ)。独特的聚集诱导发光(AIE)效应提供了一个直接的解决方案。AIE分子的芳香核通常是疏水的,即使在高浓度下也不会发生ACQ效应。因此,AIE分子可以直接作为构建块引入,为纳米药物的自组装提供驱动力,并使我们能够开发出无标记、无ACQ且发光的纳米药物,这些纳米药物能够同时实现药物递送和亚细胞行为评估。本综述介绍了不同类型的基于AIE分子的纳米药物及其生物学特性,以及用于亚细胞行为成像的应用,包括药物释放过程、纳米药物的代谢、药物和载体的亚细胞分布以及治疗效果。通过详细了解这些亚细胞行为,我们预计本综述中讨论的研究能够激发其他科学家开发下一代可由荧光成像引导的纳米药物,从而实现精确可控的药物递送。