Tianjin Key Laboratory of Biomedical Materials, Institute of Biomedical Engineering, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300192, PR China.
Tianjin Key Laboratory of Biomedical Materials, Institute of Biomedical Engineering, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300192, PR China.
Colloids Surf B Biointerfaces. 2018 Oct 1;170:163-171. doi: 10.1016/j.colsurfb.2018.06.008. Epub 2018 Jun 6.
Elucidation of the pathway of drug delivery and carrier degradation in vivo is essential for the fabrication of a feasible drug delivery system. Multispectral fluorescence imaging can track a drug delivery system simultaneously based on the separation of fluorescence at multiple wavelengths without interference. In this study, the Doxorubicin loaded genipin-crosslinked globin and PEI nanoparticles (Gb-G-PEI/Dox NPs) were designed as a dual fluorescent drug delivery system to track the drug release and carrier degradation process. Both confocal laser scanning microscopy and flow cytometric results showed that Gb-G-PEI/Dox NPs had a higher cellular uptake efficiency than Doxorubicin in the Bel-7402 cell line due to its small size and positively charged surface. The in vivo metabolism experiments tracked by the multispectral fluorescence imaging system elucidated the sustained drug release and carrier degradation process of the Gb-G-PEI/Dox NPs. Furthermore, the in vivo antitumor effects study by the bioluminescence imaging showed that Gb-G-PEI/Dox NPs reduced the tumor size most significantly on hepatoma-bearing nude mice. As a result, Gb-G-PEI/Dox NPs were demonstrated to be a highly efficient, feasible and visible drug delivery system for tumor therapy.
阐明药物在体内的传递途径和载体降解对于制造可行的药物传递系统至关重要。多光谱荧光成像是一种基于多波长荧光分离而无干扰的同时跟踪药物传递系统的方法。在本研究中,设计了载阿霉素的京尼平交联珠蛋白和聚乙烯亚胺纳米粒(Gb-G-PEI/Dox NPs)作为双荧光药物传递系统,以跟踪药物释放和载体降解过程。共聚焦激光扫描显微镜和流式细胞术结果表明,由于其小尺寸和带正电荷的表面,Gb-G-PEI/Dox NPs 在 Bel-7402 细胞系中的细胞摄取效率高于阿霉素。多光谱荧光成像系统跟踪的体内代谢实验阐明了 Gb-G-PEI/Dox NPs 的持续药物释放和载体降解过程。此外,生物发光成像的体内抗肿瘤效果研究表明,Gb-G-PEI/Dox NPs 对荷肝癌裸鼠的肿瘤大小的抑制作用最为显著。因此,Gb-G-PEI/Dox NPs 被证明是一种高效、可行且可视化的肿瘤治疗药物传递系统。