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基于多孔磁铁纳米球的联合化疗-磁-光热乳腺癌治疗。

Combined chemo-magnetic field-photothermal breast cancer therapy based on porous magnetite nanospheres.

机构信息

Department of Nanotechnology, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.

Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran.

出版信息

Sci Rep. 2020 Apr 3;10(1):5925. doi: 10.1038/s41598-020-62429-6.

Abstract

The efficacy of different modalities of treating breast cancer is inhibited by several limitations such as off-targeted drug distribution, rapid drug clearance, and drug resistance. To overcome these limitations, we developed Lf-Doxo-PMNSs for combined chemo-MF-PTT. The PMNSs were synthesized by hydrothermal method and their physicochemical properties were examined by FE-SEM, TEM, DLS, TGA, XRD investigations. The cytotoxicity of as-synthesized NPs against 4T1 cells was carried out by MTT and flow cytometry assays. Afterwards, the anti-cancer activities of as-synthesized Lf-Doxo-PMNSs on the tumor status, drug distribution and apoptosis mechanism were evaluated. The anti-cancer assays showed that Lf-Doxo-PMNSs significantly suppressed the cancer cell proliferation and tumor weight by prolonging drug availability and potential drug loading in tumor cells; whereas they showed a minimum cytotoxicity against non-cancerous cells. Likewise, combined chemo-MF-PTT using Lf-Doxo-PMNSs displayed the highest anti-cancer activity followed by combined chemo-PTT and combined chemo-MF therapy based on altering the apoptosis mechanism. Therefore, these results showed that combined chemo-MF-PTT based on Lf-Doxo-PMNSs can be used as a promising therapeutic platform with potential targeted drug delivery and high loading capacity features as well as reducing cancer drug resistance.

摘要

不同模式治疗乳腺癌的疗效受到多种限制,例如药物靶向分布不佳、药物快速清除和耐药性。为了克服这些限制,我们开发了Lf-Doxo-PMNSs 用于联合化疗-MF-PTT。PMNSs 通过水热法合成,并通过 FE-SEM、TEM、DLS、TGA、XRD 研究检查其物理化学性质。通过 MTT 和流式细胞术测定法测定合成 NPs 对 4T1 细胞的细胞毒性。之后,评估了合成的 Lf-Doxo-PMNSs 对肿瘤状态、药物分布和细胞凋亡机制的抗癌活性。抗癌测定表明,Lf-Doxo-PMNSs 通过延长药物在肿瘤细胞中的有效时间和潜在药物载量,显著抑制了癌细胞的增殖和肿瘤重量;而对非癌细胞的细胞毒性最小。同样,基于改变凋亡机制,使用 Lf-Doxo-PMNSs 的联合化疗-MF-PTT 显示出最高的抗癌活性,其次是联合化疗-PTT 和联合化疗-MF 治疗。因此,这些结果表明,基于 Lf-Doxo-PMNSs 的联合化疗-MF-PTT 可以用作一种有前途的治疗平台,具有潜在的靶向药物递送和高载药能力的特点,同时降低癌症耐药性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ba/7125194/52ff094f1f37/41598_2020_62429_Fig1_HTML.jpg

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