负载有吡罗替尼的曲妥珠单抗功能化 SK-BR-3 细胞膜包裹介孔二氧化硅纳米粒子用于 HER-2 阳性乳腺癌的靶向治疗

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Xing Liu, Wenwen Shen
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引用次数: 0

摘要

本研究制备了负载吡罗替尼的曲妥珠单抗功能化SK-BR-3细胞膜包裹介孔二氧化硅纳米颗粒(Tra-CM-MSN-PYR),用于HER2阳性乳腺癌的靶向治疗。透射电子显微镜(TEM)表征显示,MSN具有球形形态和介孔通道,Tra-CM-MSN的结构是成功包覆在MSN表面的细胞膜(CM)层。细胞摄取实验表明,FITC标记的Tra-CM-MSN能被SK-BR-3乳腺癌细胞摄取,这说明Tra-CM-MSN与CM-MSN和MSN相比具有良好的靶向能力。体内成像实验表明,FITC 标记的 Tra-CM-MSN 在肿瘤组织中有显著积累,进一步证明了 Tra-CM-MSN 具有卓越的靶向特性。细胞凋亡实验表明,Tra-CM-MSN-PYR 能明显抑制 SK-BR-3 乳腺癌细胞的增殖。体内动物实验结果也表明,Tra-CM-MSN-PYR 能明显抑制肿瘤生长。这些结果表明,Tra-CM-MSN-PYR 未来有可能用作 HER2 阳性乳腺癌的靶向疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Trastuzumab-functionalized SK-BR-3 cell membrane-wrapped mesoporous silica nanoparticles loaded with pyrotinib for the targeted therapy of HER-2-positive breast cancer

Trastuzumab-functionalized SK-BR-3 cell membrane-wrapped mesoporous silica nanoparticles loaded with pyrotinib for the targeted therapy of HER-2-positive breast cancer
In this study, the trastuzumab-functionalized SK-BR-3 cell membrane-wrapped mesoporous silica nanoparticles loaded with pyrotinib (Tra-CM-MSN-PYR) were prepared for targeted therapy of HER2-positive breast cancer. Transmission electron microscopy (TEM) characterization showed that MSN had a spherical morphology with mesoporous channels and that the structure of Tra-CM-MSN was a cell membrane (CM) layer successfully coated on the surface of MSN. A cellular uptake assay demonstrated that FITC-labeled Tra-CM-MSN were taken up by SK-BR-3 breast cancer cells, which illustrated that Tra-CM-MSN had good targeting ability compared with CM-MSN and MSN. In vivo imaging experiments demonstrated significant accumulation of FITC-labeled Tra-CM-MSN in tumor tissues, further proving that Tra-CM-MSN have superior targeting properties. Cell apoptosis experiments suggested that Tra-CM-MSN-PYR significantly inhibited the proliferation of SK-BR-3 breast cancer cells. The results of in vivo animal experiments also showed that Tra-CM-MSN-PYR significantly inhibited tumor growth. These results indicate that Tra-CM-MSN-PYR has potential application as a targeted therapy for HER2-positive breast cancer in the future.
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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
自引率
0.00%
发文量
32
审稿时长
24 days
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