Laboratory of Molecular Imaging and Nanomedicine, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health , Bethesda, Maryland 20892, United States.
Department of Chemistry, University of Utah , 315 South 1400 East, Room 2020, Salt Lake City, Utah 84112, United States.
J Am Chem Soc. 2017 Nov 8;139(44):15940-15949. doi: 10.1021/jacs.7b09224. Epub 2017 Oct 27.
Despite the well-known anticancer activity of mono- and multinuclear platinum complexes, studies of the antitumor performances of platinum-based supramolecular coordination complexes are rare. Herein, we report on the synthesis of a four-armed amphiphilic copolymer, Pt-PAZMB-b-POEGMA, containing a metallacycle M, in which the tetraphenylethene derivative acts as an aggregation-induced emissive fluorescent probe for live cell imaging and the 3,6-bis[trans-Pt(PEt)]phenanthrene (PhenPt) is an anticancer drug. This copolymer was further self-assembled into nanoparticles of different sizes and vesicles depending upon the experimental conditions. The impacts of the morphology and size of the assemblies on their endocytic pathways, uptake rates, internalization amounts, and cytotoxicities were investigated. The self-assemblies were further employed to encapsulate doxorubicin (DOX) to achieve a synergistic anticancer effect. Controlled drug release was also realized via amphiphilicity changes and was driven by a glutathione-induced cascade elimination reaction. The DOX-loaded nanoparticles of around 50 nm in size exhibited an excellent antitumor performance as well as a low systemic toxicity, due to an enhanced permeability and retention effect.
尽管单核和多核铂配合物具有众所周知的抗癌活性,但对基于铂的超分子配位配合物的抗肿瘤性能的研究却很少。在此,我们报告了一种四臂两亲性嵌段共聚物 Pt-PAZMB-b-POEGMA 的合成,其中金属配合物 M 包含四苯乙烯衍生物,其作为用于活细胞成像的聚集诱导发射荧光探针,3,6-双[顺式-Pt(PEt)]菲咯啉(PhenPt)是一种抗癌药物。该共聚物进一步自组装成不同尺寸的纳米颗粒和囊泡,这取决于实验条件。研究了组装体的形态和尺寸对其细胞内吞途径、摄取率、内化量和细胞毒性的影响。进一步将自组装体用于包封阿霉素(DOX)以实现协同抗癌作用。通过两亲性变化和谷胱甘肽诱导的级联消除反应驱动,实现了受控药物释放。由于增强的渗透性和保留效应,尺寸约为 50nm 的载 DOX 纳米颗粒表现出优异的抗肿瘤性能和低系统毒性。