Lin Jinyan, Li Yanxiu, Li Yang, Cui Fei, Yu Fei, Wu Hongjie, Xie Liya, Luo Fanghong, Hou Zhenqing, Lin Changjian
Department of Biomaterials and Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005, China.
J Mater Chem B. 2015 Oct 21;3(39):7707-7717. doi: 10.1039/c5tb00724k. Epub 2015 Sep 4.
Poor drug distribution and inefficient drug concentrations within the tumor intracellular environment still limit the therapeutic efficacy of drugs for cancer chemotherapy. Local drug delivery (physical targeting) combined with receptor-mediated drug delivery (chemical targeting) and assistance by a novel shape design is a promising strategy to treat the infiltrating tumor (even those that persist post surgery). In this paper, we prepared dye and methotrexate (MTX) functionalized nanobacilli (MPEG-PLA-MTX-Cy5.5 NB) by a self-assembly technique combined with extrusion through a SPG membrane for intratumoral administration, in which the bacillus-shaped MPEG-PLA-MTX-Cy5.5 NB were armed with a dual-acting MTX that can specifically and efficiently enhance their cellular uptake, while avoiding their dispersion from tumor sites. After intratumoral administration to a H xenograft mouse model, the MPEG-PLA-MTX-Cy5.5 NB delivered the drug more effectively to the tumor compared to the MPEG-PLA-Cy5.5 nanospheres (MPEG-PLA-Cy5.5 NSs) and MPEG-PLA-MTX-Cy5.5 nanospheres (MPEG-PLA-MTX-Cy5.5 NSs). Compared to the free MTX and MPEG-PLA-MTX-Cy5.5 NSs, the controlled-release MPEG-PLA-MTX-Cy5.5 NB also significantly inhibited the tumor growth and improved therapeutic efficacy. The platforms are highly convergent, flexible and simplified systems that may serve as guides in the further design of nanoparticles with a revolutionary new shape and function for clinical applications.
肿瘤细胞内环境中药物分布不佳和药物浓度低效仍然限制了癌症化疗药物的治疗效果。局部药物递送(物理靶向)与受体介导的药物递送(化学靶向)相结合,并辅以新颖的形状设计,是治疗浸润性肿瘤(甚至是术后残留的肿瘤)的一种有前景的策略。在本文中,我们通过自组装技术结合通过SPG膜挤出制备了染料和甲氨蝶呤(MTX)功能化的纳米杆菌(MPEG-PLA-MTX-Cy5.5 NB)用于瘤内给药,其中杆菌形状的MPEG-PLA-MTX-Cy5.5 NB配备了双作用MTX,可特异性且高效地增强其细胞摄取,同时避免其从肿瘤部位扩散。在对H异种移植小鼠模型进行瘤内给药后,与MPEG-PLA-Cy5.5纳米球(MPEG-PLA-Cy5.5 NSs)和MPEG-PLA-MTX-Cy5.5纳米球(MPEG-PLA-MTX-Cy5.5 NSs)相比,MPEG-PLA-MTX-Cy5.5 NB能更有效地将药物递送至肿瘤。与游离MTX和MPEG-PLA-MTX-Cy5.5 NSs相比,控释的MPEG-PLA-MTX-Cy5.5 NB也显著抑制了肿瘤生长并提高了治疗效果。这些平台是高度整合、灵活且简化的系统,可为进一步设计具有革命性新形状和功能的用于临床应用的纳米颗粒提供指导。