School of Chemistry, Northeast Normal University, Changchun, PR China.
Dalton Trans. 2011 Oct 14;40(38):9789-94. doi: 10.1039/c1dt10565e. Epub 2011 Aug 30.
A novel strategy was utilized to develop a stable probe based on thiolated poly(ethylene glycol) (SH-PEG) and polyacrylic acid (PAA) functionalized gold nanorods (GNRs), following the attachment of an anti-cancer drug, doxorubicin (DOX), to obtain PAA-PEG-GNRs@DOX assemblies. Importantly, the obtained probe as a novel drug-delivery and fluorescent imaging agent for simultaneous imaging of and drug delivery to prostate cancer cells has also been demonstrated. In addition to designing PAA-PEG-GNRs that passively target tumor cells for cancer-fighting drug therapy, GNRs are also regarded as hyperthermia agents for photokilling cancer cells, so that the tumor would be attacked on two fronts simultaneously.
采用一种新策略,基于巯基化聚乙二醇(SH-PEG)和聚丙烯酸(PAA)功能化的金纳米棒(GNRs)开发了一种稳定的探针,随后将抗癌药物阿霉素(DOX)连接到该探针上,得到 PAA-PEG-GNRs@DOX 组装体。重要的是,所得到的探针作为一种新型的药物递释和荧光成像剂,可同时对前列腺癌细胞进行成像和药物递释,也已得到了证实。除了设计能够被动靶向肿瘤细胞的 PAA-PEG-GNRs 以进行抗癌药物治疗外,GNRs 还被视为光热治疗剂,用于光杀死癌细胞,从而使肿瘤能够同时受到两种方式的攻击。