J Biomed Nanotechnol. 2019 Sep 1;15(9):1897-1908. doi: 10.1166/jbn.2019.2833.
With the advance in nanomedicine, diagnostic and therapeutic nanoscale prodrugs have been rapidly developed in the field of cancer treatment. In this study, we constructed an enzyme-responsive polymer-paclitaxel (PTX) prodrug with a biocompatible saccharide-containing polymer backbone through the reversible addition-fragmentation chain transfer (RAFT) polymerization. A near-infrared fluorescent molecule (pheophorbide a) and magnetic resonance imaging (MRI) contrast agent (gadolinium-tetraazacyclododecanetetraacetic acid) were further conjugated onto the copolymer backbone to impart the ability of multimode imaging and tracing, forming the final diagnosis and treatment polymeric prodrug. This prodrug was amphiphilic and was able to self-assemble into uniform-size nanoparticles (80.1 nm). With the specific catalysis of enzymes, the anti-cancer drug, PTX, in the nanoparticles could be effectively released to kill cancer cells. The results of near-infrared fluorescence imaging and MRI showed that the diagnostic prodrug was preferentially concentrated at the tumor site compared with the free imaging reagents, suggesting improved and durable tumor imaging effects, which are beneficial for precise cancer diagnosis. The tumor growth in the mice could be effectively retarded after the administration of the prodrug. The tumor almost completely disappeared till the final treatment, and the tumor inhibition rate was as high as 96.4%. Immunohistochemical analysis indicated that the high anti-tumor effects might be attributed to the result that the prodrug not only induced the apoptosis of tumor cells, but also inhibited the formation of new blood vessels in the tumor environment. Therefore, this theranostic prodrug, which is based on the saccharide-containing polymer, holds potency for the development of a robust nanoscale platform for the diagnosis and treatment of cancer.
随着纳米医学的发展,诊断和治疗性纳米尺度前药在癌症治疗领域得到了迅速发展。在本研究中,我们通过可逆加成-断裂链转移(RAFT)聚合,构建了一种具有生物相容性糖基聚合物主链的酶响应性聚合物-紫杉醇(PTX)前药。进一步将近红外荧光分子(原卟啉 IX)和磁共振成像(MRI)造影剂(钆-四氮杂环十二烷四乙酸)共轭到共聚物主链上,赋予其多模式成像和示踪能力,形成最终的诊断和治疗聚合物前药。该前药具有两亲性,能够自组装成均一尺寸的纳米颗粒(80.1nm)。在酶的特异性催化下,纳米颗粒中的抗癌药物 PTX 能够有效释放,从而杀死癌细胞。近红外荧光成像和 MRI 的结果表明,与游离成像试剂相比,诊断前药优先聚集在肿瘤部位,提示改善和持久的肿瘤成像效果,有利于精确的癌症诊断。给药后,小鼠的肿瘤生长得到有效抑制。肿瘤几乎完全消失,直到最后治疗,肿瘤抑制率高达 96.4%。免疫组织化学分析表明,高抗肿瘤效果可能归因于前药不仅诱导肿瘤细胞凋亡,还抑制肿瘤微环境中新生血管的形成。因此,基于含糖聚合物的这种治疗诊断前药为开发用于癌症诊断和治疗的强大纳米级平台提供了潜力。