Targeted tumor MRI with gadobutrol-loaded anti-HER2 immunoliposomes

被引:4
作者
Chen, Weicui [1 ]
Liu, Bo [1 ]
Chen, Jun [1 ]
Liu, Guoqing [1 ]
Liu, Xian [1 ]
机构
[1] Guangdong Prov Hosp Chinese Med, Dept Radiol, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Breast cancer; HER2; immunoliposomes; molecular imaging; magnetic resonance imaging (MRI); CONTRAST AGENTS; RELAXIVITY; LIPOSOMES; NANOPARTICLES;
D O I
10.1177/0284185116664225
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background Immunoliposomes have been used to deliver MR contrast agents to cancer tissue by targeting tumor associated antigens, thus enabling the visualization of biological processes at the cellular level. Purpose To develop and evaluate the feasibility of specific HER2 targeted liposomal MR contrast agent. Material and Methods Gd-loaded anti-HER2 immunolipomes (Gd-ILs) and non-targeted PEGylated liposomes (Gd-NTLs) were prepared and characterized. Tumor bearing animals were randomized into three groups: Gd- ILs, Gd- NTLs and gadobutrol. Animals were imaged prior and 5, 15, 60, 120 and 180min after i.v. injection of different contrast agents. The signal intensity enhancement percentage, signal- to- noise ratio and contrast- to -noise ratio was used to qualify tumor enhancement of different groups. After imaging, tumors were excised for histological examination. Results Invivo dynamic MR images, the specific targeted contrast agent bound to tumor tissue and result in a gradual and persisting enhancement for at least 3 hours in mice bearing tumor xenografts, reaching a maximum of 87.7% enhancement after 120min post-injection. Gd-ILs demonstrated superior tumor enhancement over control non target contrast agent and gadobutrol in HER2 overexpressing tumors at 60, 120 and 180min post- injection. The SNR and CNR of Gd-ILs in the tumors were significantly greater than that of Gd-NTLs at 60, 120, 180min post- injection. Conclusion The results indicate the feasibility of Gd-ILs providing prolonged circulation, specific tumor enhancement and cancer cell recognition as targeted contrast agent.
引用
收藏
页码:573 / 580
页数:8
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