†School of Chemistry and Molecular Engineering, ‡School of Pharmaceutical Sciences, and §School of Public Health, Zhengzhou University, 100 Kexue Avenue, Zhengzhou 450001, PR China.
ACS Appl Mater Interfaces. 2015 Mar 18;7(10):5736-47. doi: 10.1021/am507898z. Epub 2015 Mar 3.
In this study, a new type of magnetic tumor-targeting PEGylated gold nanoshell drug delivery system (DOX-TSMLs-AuNSs-PEG) based on doxorubicin-loaded thermosensitive magnetoliposomes was successfully obtained. The reverse-phase evaporation method was used to construct the magnetoliposomes, and then gold nanoshells were coated on the surface of it. The DOX-TSMLs-AuNSs-PEG delivery system was synthesized after SH-PEG2000 modification. This multifunction system was combined with a variety of functions, such as radiofrequency-triggered release, chemo-hyperthermia therapy, and dual-mode magnetic resonance/X-ray imaging. Importantly, the DOX-TSMLs-AuNSs-PEG complex was found to escape from endosomes after cellular uptake by radiofrequency-induced endosome disruption before lysosomal degradation. All results in vitro and in vivo indicated that DOX-TSMLs-AuNSs-PEG is a promising effective drug delivery system for diagnosis and treatment of tumors.
在这项研究中,成功获得了一种基于载多柔比星热敏磁脂质体的新型磁性肿瘤靶向聚乙二醇化金纳米壳药物递送系统(DOX-TSMLs-AuNSs-PEG)。采用逆相蒸发法构建磁脂质体,然后在其表面包覆金纳米壳。经过 SH-PEG2000 修饰后合成了 DOX-TSMLs-AuNSs-PEG 递药系统。该多功能系统结合了多种功能,如射频触发释放、化疗-热疗和双模式磁共振/X 射线成像。重要的是,在细胞摄取后,通过射频诱导的内涵体破坏,DOX-TSMLs-AuNSs-PEG 复合物在溶酶体降解之前从内涵体中逃逸。体外和体内的所有结果表明,DOX-TSMLs-AuNSs-PEG 是一种很有前途的用于肿瘤诊断和治疗的有效药物递送系统。
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