Graphical '/> Targeting property and toxicity of a novel ultrasound contrast agent microbubble carrying the targeting and drug-loaded complex FA-CNTs-PTX on MCF7 cells
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Targeting property and toxicity of a novel ultrasound contrast agent microbubble carrying the targeting and drug-loaded complex FA-CNTs-PTX on MCF7 cells

机译:针对MCF7细胞上携带靶向和药物载体复合FA-CNTS-PTX的新型超声造影剂微泡的靶向性和毒性

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Graphical abstractDisplay OmittedHighlights?A novel ultrasound contrast agent microbubbles carrying the targeting and drug-loaded complex FA-CNTs-PTX was obtained.?The ultrasound contrast agent microbubbles with FA-CNTs-PTX had the cytotoxicity and targeting on MCF7 cells.?The targeting drug-loaded complex FA-CNTs-PTX was inserted into the film shell of the Span-PEG microbubbles filled with N2.AbstractThe application of ultrasound contrast agents not only is confined to the enhancement of ultrasound imaging but also has started to be used as a drug system for diagnosis and treatment. In this paper, Span60 and PEG1500 were used as membrane materials, and a new targeting and drug-loading multifunctional ultrasound contrast agent microbubble enveloping the FA-CNTs-PTX complex was successfully prepared by acoustic cavitation. With the breast cancer cell line MCF7 as the research target, the effects of the microbubble with FA-CNTs-PTX on the proliferation and toxicity of MCF7 cells were studied using a CCK-8 and AO/EB double-staining method. The influences of the microbubbles with FA-CNTs-PTX on the cellular morphology and apoptosis period of the MCF7 cells were detected using an inverted fluorescence microscope. The apoptosis of MCF7 cells induced by the microbubbles with FA-CNTs-PTX was investigated with flow cytometry and an annexin and PI double staining fluorescence quantitative analysis. The results indicated that the ultrasound contrast agent microbubble with FA-CNTs-PTX remarkably inhibited the proliferation of MCF7 cells, which was mainly controlled by the drug loading rate and the nanometer size of the microbubbles. Moreover, the proliferative inhibition rate of the microbubbles with FA-CNTs-PTX was related to the cell apoptosis period of MCF7 cells. Its inhibition degree on the proliferation of MCF7 cells was higher than that of the hepatoma HepG2 cells. The apoptosis rate of MCF7 cells induced by the microbubbles with FA-CNTs-PTX was higher than that of normal human umbilical vein endothelial cells (HUVECs), and the microbubbles with FA-CNTs-PTX could target the MCF7 cells.]]>
机译:<![cdata [ 图形抽象 显示省略 突出显示 获得了一种新的超声造影剂,携带靶向靶向和药物加载的复杂FA-CNTS-PTX。 <标签> 超声波AST代理微泡与FA-CNTS-PTX有细胞毒性和靶向MCF7细胞。 将靶向药物装载的复杂fa-cnts-ptx插入填充n 2 抽象 超声造影剂的应用不仅限于超声成像的增强,而且已经开始用作药物系统诊断和治疗。在本文中,SPAN60和PEG1500用作膜材料,通过声学空化成功地制备了封装FA-CNT-PTX复合物的新靶向和药物装载多功能超声造影剂微泡。通过乳腺癌细胞系MCF7作为研究靶标,使用CCK-8和AO / EB双染色方法研究了微泡与FA-CNTS-PTX对MCF7细胞增殖和毒性的影响。使用倒置荧光显微镜检测微泡与FA-CNTS-PTX对MCF7细胞的细胞形态和凋亡时段的影响。用流式细胞术研究微泡和PI双染色荧光定量分析研究了用FA-CNTS-PTX诱导的Microbubbls诱导的MCF7细胞的凋亡。结果表明,与FA-CNTS-PTX的超声造影剂微泡显着抑制MCF7细胞的增殖,其主要由药物负载率和微泡的纳米尺寸控制。此外,与FA-CNTS-PTX的微泡的增殖抑制率与MCF7细胞的细胞凋亡期有关。其对MCF7细胞增殖的抑制程度高于肝癌HepG2细胞的程度。用Fa-CNTS-PTX诱导的MCF7细胞的凋亡率高于正常人脐静脉内皮细胞(HUVEC)的细胞凋亡率高于CNTS-PTX的微泡可以靶向MCF7细胞。 ]]>

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