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用于治疗侵袭性孤儿癌的细胞毒性 Cu(II)和 Ru(III)化合物传递的标记胶束:设计和生物学体外数据。

Labelled micelles for the delivery of cytotoxic Cu(II) and Ru(III) compounds in the treatment of aggressive orphan cancers: Design and biological in vitro data.

机构信息

Department of Surgical, Oncologic and Gastroenterological Sciences, University of Padova, Via Giustiniani 2, 35128 Padova, Italy; Department of Chemical Sciences, University of Padova, Via F. Marzolo 1, 35131 Padova, Italy.

Department of Chemical Sciences, University of Padova, Via F. Marzolo 1, 35131 Padova, Italy.

出版信息

J Inorg Biochem. 2020 Dec;213:111259. doi: 10.1016/j.jinorgbio.2020.111259. Epub 2020 Oct 2.

Abstract

A recent study on our metal-dithiocarbamato complexes pointed out the antiproliferative properties and the druglikeness of some new patented derivatives. In this work, the best compounds have been encapsulated in micellar nanocarriers, being also carbohydrate-functionalized on their hydrophilic surface to investigate the possibility of a cancer-selective delivery. In particular, the nonionic block copolymer Pluronic® F127 (PF127) has been chemically modified with sugars and the derivatives characterized by means of NMR spectroscopy and FT-IR spectrophotometry. Then, the two selected complexes (β-[Ru(PipeDTC)]Cl (PipeDTC = piperidine dithiocarbamate) and [Cu(ProOMeDTC)] (ProOMeDTC = L-proline methyl ester dithiocarbamate)), have been loaded into the hydrophobic core of PF127 micelles and cancer-targeting counterparts. These nanoformulations have been studied for their dimensions (DLS, TEM) and stability, and tested for their cytotoxicity against aggressive human cancer cell lines. The in vitro results were paralleled with mechanistic studies through Confocal Laser Scanning Microscopy and xCELLigence analysis.

摘要

最近一项关于我们的金属-二硫代氨基甲酸盐配合物的研究指出了一些新的专利衍生物的抗增殖特性和类药性。在这项工作中,最好的化合物已被包裹在胶束纳米载体中,并在其亲水表面上进行碳水化合物功能化,以研究癌症选择性递药的可能性。具体而言,非离子嵌段共聚物 Pluronic® F127(PF127)已用糖进行化学修饰,并通过 NMR 光谱和 FT-IR 分光光度法对衍生物进行了表征。然后,将两种选定的配合物(β-[Ru(PipeDTC)]Cl(PipeDTC=哌啶二硫代氨基甲酸盐)和[Cu(ProOMeDTC)](ProOMeDTC=L-脯氨酸甲酯二硫代氨基甲酸盐))负载到 PF127 胶束的疏水核中和癌症靶向对应物中。这些纳米制剂已针对其尺寸(DLS、TEM)和稳定性进行了研究,并针对其对侵袭性人类癌细胞系的细胞毒性进行了测试。体外结果通过共聚焦激光扫描显微镜和 xCELLigence 分析与机制研究相平行。

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