磁共振成像
磁性纳米粒子
材料科学
磁小体
体内
癌症研究
核磁共振
纳米颗粒
乳腺癌
癌症
纳米技术
医学
生物
磁铁矿
放射科
冶金
生物技术
内科学
物理
作者
Yunlei Zhang,Qianqian Ni,Chaoli Xu,Bing Wan,Yuanyuan Geng,Gang Zheng,Zhenlu Yang,Jun Tao,Ying Zhao,Jun Wen,Junjie Zhang,Shouju Wang,Yuxia Tang,Yanjun Li,Qirui Zhang,Li Liu,Zhaogang Teng,Guangming Lu
标识
DOI:10.1021/acsami.8b15838
摘要
Supersensitive magnetic resonance (MR) imaging requires contrast with extremely high r2 values. However, synthesized magnetic nanoparticles generally have a relatively low r2 relaxivity. Magnetosomes with high saturation magnetization and good biocompatibility have shown potential values as MR imaging contrast agents. Magnetosomes that target human epidermal growth factor receptor-2 (HER2) were prepared using genetic technology and low-frequency sonication. Anti-HER2 affibody of the ability to target HER2 was displayed on the membrane surface of the magnetosomes through the anchor protein MamC, allowing the bacterial nanoparticles to target tumors overexpressing HER2. The prepared nanoparticles exhibited a very high relaxivity of 599.74 mM–1 s–1 and better dispersion, and their ability to target HER2 was demonstrated both in vitro and in vivo. Also, the HER2-targeting magnetosomes significantly enhanced the MR imaging of orthotopic breast cancer models with or without HER2 expression using a 7.0 T scanner. In particular, tumors overexpressing HER2 demonstrated better MR imaging than HER2-negative tumors after intravenous administration of HER2-targeting magnetosomes, and the MR signals of the augmented contrast could be detected from 3 to 24 h. The magnetosomes did not cause any notable pathogenic effect in the animals. Therefore, we expect that noninvasive imaging of tumors using HER2-targeting magnetosomes has potential for clinical applications in the near future.
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