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首页> 外文期刊>Molecular pharmaceutics >Insights into the Cellular Uptake, Cytotoxicity, and Cellular Death Modality of Phospholipid-Coated Gold Nanorods toward Breast Cancer Cell Lines
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Insights into the Cellular Uptake, Cytotoxicity, and Cellular Death Modality of Phospholipid-Coated Gold Nanorods toward Breast Cancer Cell Lines

机译:探讨磷脂涂覆的金纳米棒对乳腺癌细胞系的细胞吸收,细胞毒性和细胞死亡模态的见解

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摘要

Gold nanorods (GNRs) have gained pronounced recognition in the diagnosis and treatment of cancers driven by their distinctive properties. Herein, a gold-based nanosystem was prepared by utilizing a phospholipid moiety linked to thiolated polyethylene glycol, 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-IV-PEG-SH, as a surface decorating agent. The synthesized phospholipid-PEG-GNRs displayed good colloidal stability upon exposure to the tissue culture medium. Cytotoxicity of phospholipid-PEG-GNRs was investigated toward MCF-7 and T47D breast cancer cells using sulforhodamine B test. The results revealed that phospholipid-PEG-GNRs demonstrated high cytotoxicity to MCF-7 cells compared to T47D cells, and minimal cytotoxicity to human dermal fibroblasts. The cellular uptake studies performed by imaging and quantitative analysis demonstrated massive internal- ization of phospholipid-coated GNRs into MCF-7 cells in comparison to T47D cells. The cellular death modality of cancer cells after treatment with phospholipid-PEG-GNRs was evaluated using mitochondrial membrane potential assay (JC-1 dye), gene expression analysis, and flow cytometry study. The overall results suggest that phospholipid-modified GNRs enhanced mainly the cellular apoptotic events in MCF-7 cells in addition to necrosis, whereas cellular necrosis and suppression of cellular invasion contributed to the cellular death modality in the T47D cell line upon treatment with phospholipid-PEG-GNRs. The phospholipid-coated GNRs interact in a different manner with breast cancer cell lines and could be considered for breast cancer treatment.
机译:金纳米棒(GNRS)在诊断和治疗因其独特性质驱动的癌症诊断和治疗中获得了明显的识别。在此,通过利用与硫化聚乙二醇,1,2-羟基酰基-N-甘油-3-磷乙胺-IV-PEG-SH连接的磷脂部分来制备基于金的纳米系统,作为表面装饰性药剂。合成的磷脂-PEG-GNR在暴露于组织培养基时显示出良好的胶体稳定性。使用苏尔磺胺胺B试验研究了磷脂-PEG-GNRS的细胞毒性。结果表明,与T47D细胞相比,磷脂-PEG-GNRs对MCF-7细胞进行了高细胞毒性,并对人皮肤成纤维细胞的最小细胞毒性。通过成像和定量分析进行的蜂窝摄取性研究表明与T47D细胞相比,通过成像和定量分析表现出磷脂涂覆的GNR的大量内部。使用线粒体膜电位测定(JC-1染料),基因表达分析和流式细胞术研究评价用磷脂-PEG-GNRS治疗后癌细胞的细胞死亡模态。整体结果表明,除坏死外,磷脂改性的GNR主要增强了MCF-7细胞中的细胞凋亡事件,而细胞坏死和细胞侵袭的抑制在用磷脂 - 钉治疗后T47D细胞系中的细胞死亡方式有助于细胞死亡方式-GNRS。磷脂涂覆的GNRs以不同的方式与乳腺癌细胞系相互作用,可以考虑乳腺癌治疗。

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