Gao Di, Gao Jinbiao, Xu Ming, Cao Zhong, Zhou Luyao, Li Yingqin, Xie Xiaoyan, Jiang Qing, Wang Wei, Liu Jie
Department of Biomedical Engineering, School of Engineering, Sun Yat-sen University , Guangzhou, Guangdong 510006, China.
Department of Medical Ultrasonics, Institute of Diagnostic and Interventional Ultrasound, The First Affiliated Hospital of Sun Yat-sen University , Guangzhou, Guangdong 510080, China.
Mol Pharm. 2017 Apr 3;14(4):984-998. doi: 10.1021/acs.molpharmaceut.6b00761. Epub 2017 Mar 21.
For successful gene therapy, it is imperative to accumulate therapeutic gene in tumor tissues followed by efficiently delivering gene into targeted cells. Ultrasound irradiation, as a noninvasive and cost-effective external stimulus, has been proved to be one of the most potential external-stimulating gene delivery strategies recently in further improving gene transfection. In this study, we developed tumor-targeting ultrasound-triggered phase-transition nanodroplets AHNP-PFP-TNDs comprising a perfluorinated poly(amino acid) CF-PAsp (DET) as a core for simultaneously loading perfluoropentane (PFP) and nucleic acids, and a polyanionic polymer PGA-g-PEG-AHNP as the shell for not only modifying the surface of nanodroplets but also introducing an anti-Her2/neu peptide (AHNP) aiming to targeted treatment of Her2-overexpressing breast cancer. The results showed the average diameter of AHNP-PFP-TNDs was below 400 nm, nearly spherical in shape. The modification of PGA-g-PEG-AHNP not only increased the serum stability of the nanodroplets but also improved the affinity between nanodroplets and Her2-overexpressing breast cells. Both intratumor and intravenous injection of AHNP-PFP-TNDs into nude mice bearing HGC-27 xenografts showed that the gene transfection efficiency and the ultrasound contrast effect were significantly enhanced after exposed to the ultrasound irradiation with optimized ultrasound parameters. Therefore, this targeting nanodroplets system could be served as a potential theranostic vector for tumor targeting ultrasound diagnosis and gene therapy.
对于成功的基因治疗而言,在肿瘤组织中积累治疗性基因并随后将基因有效递送至靶细胞至关重要。超声辐照作为一种非侵入性且具有成本效益的外部刺激手段,最近已被证明是进一步提高基因转染效率的最具潜力的外部刺激基因递送策略之一。在本研究中,我们开发了肿瘤靶向性超声触发相变纳米液滴AHNP-PFP-TNDs,其包含全氟聚(氨基酸)CF-PAsp(DET)作为同时负载全氟戊烷(PFP)和核酸的核心,以及聚阴离子聚合物PGA-g-PEG-AHNP作为外壳,不仅用于修饰纳米液滴的表面,还用于引入抗Her2/neu肽(AHNP)以靶向治疗Her2过表达的乳腺癌。结果表明,AHNP-PFP-TNDs的平均直径低于400nm,形状近乎球形。PGA-g-PEG-AHNP的修饰不仅提高了纳米液滴的血清稳定性,还改善了纳米液滴与Her2过表达乳腺细胞之间的亲和力。将AHNP-PFP-TNDs瘤内注射和静脉注射到携带HGC-27异种移植瘤的裸鼠体内均显示,在以优化的超声参数进行超声辐照后,基因转染效率和超声造影效果均显著增强。因此,这种靶向纳米液滴系统可作为一种潜在的用于肿瘤靶向超声诊断和基因治疗的诊疗载体。