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一种用于铜(II)抗癌金属药物的 POSS 药物输送系统,在针对黑素瘤细胞的选择性应用中。

An engineered POSS drug delivery system for copper(II) anticancer metallodrugs in a selective application toward melanoma cells.

机构信息

Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, Av. Prof. Lineu Prestes 748, 05508-000 São Paulo, SP, Brazil.

EPSRC National EPR Facility, Department of Chemistry and Photon Science Institute, University of Manchester, Oxford Road, M13 9PL, Manchester, UK.

出版信息

Dalton Trans. 2024 Jul 30;53(30):12567-12581. doi: 10.1039/d4dt00535j.

Abstract

In this work, a polyhedral silsesquioxane (POSS) was used as an engineered drug delivery system for two oxindolimine-copper(II) anticancer complexes, [Cu(isaepy)] and [Cu(isapn)]. The interest in hybrid POSS comes from the necessity of developing materials that can act as adjuvants to improve the cytotoxicity of non-soluble metallodrugs. Functionalization of POSS with a triazole ligand (POSS-atzac) permitted the anchorage of such copper complexes, producing hybrid materials with efficient cytotoxic effects. Structural and morphological characterizations of these copper-POSS systems were performed by using different techniques (IR, NMR, thermogravimetric analysis). A combination of continuous-wave (CW) and pulsed EPR (HYSCORE) spectroscopies conducted at the X-band have enabled the complete characterization of the coordination environment of the copper ion in the POSS-atzac matrix. Additionally, the cytotoxic effects of the loaded materials, [Cu(isapn)]@POSS-atzac and [Cu(isaepy)]@POSS-atzac, were assessed toward melanomas (SK-MEL), in comparison to non-tumorigenic cells (fibroblast P4). Evaluation of their nuclease activity or ability to facilitate cleavage of DNA indicated concentrations as low as 0.6 μg mL, while complete DNA fragmentation was observed at 25 μg mL. By using adequate scavengers, investigations on active intermediates responsible for their cytotoxicity were performed, both in the absence and in the presence of ascorbate as a reducing agent. Based on the observed selective cytotoxicity of these materials toward melanomas, investigations on the reactivity of these complexes and corresponding POSS-materials with melanin, a molecule that contributes to melanoma resistance to chemotherapy, were carried out. Results indicated the main role of the binuclear copper species, formed at the surface of the silica matrix, in the observed reactivity and selectivity of these copper-POSS systems.

摘要

在这项工作中,采用多面体倍半硅氧烷(POSS)作为两种吲哚啉铜(II)抗癌配合物[Cu(isaepy)]和[Cu(isapn)]的工程药物传递系统。对杂化 POSS 的兴趣源于开发能够作为佐剂发挥作用的材料的必要性,以提高非溶性金属药物的细胞毒性。用三唑配体(POSS-atzac)对 POSS 进行功能化,允许锚定这些铜配合物,从而产生具有有效细胞毒性作用的杂化材料。通过使用不同的技术(IR、NMR、热重分析)对这些铜-POSS 系统进行结构和形态学表征。在 X 波段进行的连续波(CW)和脉冲 EPR(HYSCORE)光谱学的组合,使我们能够完全表征铜离子在 POSS-atzac 基质中的配位环境。此外,还评估了负载材料[Cu(isapn)]@POSS-atzac 和[Cu(isaepy)]@POSS-atzac 的细胞毒性作用,与非致瘤细胞(成纤维细胞 P4)相比,对黑色素瘤(SK-MEL)的影响。评估其核酸酶活性或促进 DNA 切割的能力表明,浓度低至 0.6 μg mL 时,就会观察到完全的 DNA 片段化。通过使用适当的清除剂,在没有和作为还原剂的抗坏血酸存在的情况下,对负责其细胞毒性的活性中间体进行了研究。基于这些材料对黑色素瘤的选择性细胞毒性,对这些配合物及其相应的 POSS 材料与黑色素的反应性进行了研究,黑色素是导致黑色素瘤对化疗产生抗性的一种分子。结果表明,在观察到的这些铜-POSS 系统的反应性和选择性中,形成于二氧化硅基质表面的双核铜物种起着主要作用。

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