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用于与青蒿琥酯联合治疗的聚乙二醇包封组蛋白去乙酰化酶抑制剂药物复合纳米颗粒

Polyethylene Glycol-Encapsulated Histone Deacetylase Inhibitor Drug-Composite Nanoparticles for Combination Therapy with Artesunate.

作者信息

Goswami Upashi, Kandimalla Raghuram, Kalita Sanjeeb, Chattopadhyay Arun, Ghosh Siddhartha Sankar

机构信息

Centre for Nanotechnology, Department of Chemistry, and Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati 781039, India.

Drug Discovery Lab, Institute of Advanced Study in Science and Technology, Guwahati 781035, Assam, India.

出版信息

ACS Omega. 2018 Sep 30;3(9):11504-11516. doi: 10.1021/acsomega.8b02105. Epub 2018 Sep 20.

Abstract

Combination drug therapy has become an effective clinical practice for cancer treatment because of low cytotoxicity by the synergistic effect of each medicine. Luminescent Au nanoclusters (Au NCs) were formulated into spherical polyethylene glycol (PEG)-Au NC-encapsulated drug-sodium butyrate (NaB) composite nanoparticles (PEG-Au NC-NaB-NPs) in the presence of PEG and NaB. Their effect on cancer cells was investigated using bio imaging, unravelling the mechanism of the endocytosis pathway and combination therapeutic interventions with a plant-based antimalarial drug artesunate (ART). PEG-Au NC-NaB-NPs showed bright red luminescence in the lysosomal compartment of the cells upon uptake predominantly through a caveolae-mediated pathway. Combination of PEG-Au NC-NaB-NPs with ART displayed enhanced therapeutic activity at a reduced dose compared to its individual doses and revealed heightened synergistic activity as identified from the combination index. The mechanism of synergism revealed elevated generation of reactive oxygen species with both NaB and ART, which disrupts mitochondrial membrane potential as evident from JC-1 staining. Remarkably, the histone deacetylase (HDAC) assay and terminal deoxynucleotidyl transferase dUTP nick end labeling assay enlightened the role of NaB and ART in HDAC inhibition and DNA fragmentation, respectively. Thus, induction of apoptosis with the synergistic effect of both NaB and ART with its meticulous mechanism makes it a promising tool for combinational cancer therapy. In vivo activity of the NPs was evaluated on Daltons lymphoma ascites bearing mice, which exhibited significant reduction of tumor volume and viable tumor cells with a prolonged life span.

摘要

由于每种药物的协同作用导致细胞毒性较低,联合药物疗法已成为一种有效的癌症临床治疗方法。在聚乙二醇(PEG)和丁酸钠(NaB)存在的情况下,将发光金纳米团簇(Au NCs)制备成球形的聚乙二醇包裹金纳米团簇-包封药物-丁酸钠(NaB)复合纳米颗粒(PEG-Au NC-NaB-NPs)。使用生物成像研究了它们对癌细胞的作用,揭示了内吞途径的机制以及与植物性抗疟药物青蒿琥酯(ART)的联合治疗干预。PEG-Au NC-NaB-NPs在被细胞摄取后,主要通过小窝介导的途径在细胞的溶酶体区室中显示出明亮的红色荧光。与单独给药相比,PEG-Au NC-NaB-NPs与ART联合使用时,在降低剂量的情况下显示出增强的治疗活性,并且从联合指数可以看出协同活性增强。协同作用机制表明,NaB和ART均会增加活性氧的生成,从JC-1染色可以明显看出这会破坏线粒体膜电位。值得注意的是,组蛋白脱乙酰酶(HDAC)测定和末端脱氧核苷酸转移酶dUTP缺口末端标记测定分别揭示了NaB和ART在HDAC抑制和DNA片段化中的作用。因此,NaB和ART两者的协同作用诱导细胞凋亡及其精细的机制使其成为联合癌症治疗的有前途的工具。在携带道尔顿淋巴瘤腹水的小鼠上评估了纳米颗粒的体内活性,结果显示肿瘤体积和存活肿瘤细胞显著减少,寿命延长。

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