School of Materials Science and Engineering, Tianjin University, Tianjin, 300072, China.
J Mater Sci Mater Med. 2010 Sep;21(9):2673-81. doi: 10.1007/s10856-010-4106-5. Epub 2010 Jun 10.
The aim of present study is to conceive a biodegradable poly(ethylene glycol)-polylactide (PEG-PLA) copolymer nanoparticle which can be surface biofunctionalized with ligands via biotin-avidin interactions and used as a potential drug delivery carrier targeting to brain glioma in vivo. For this aim, a new method was employed to synthesize biotinylated PEG-PLA copolymers, i.e., esterification of PEG with biotinyl chloride followed by copolymerization of hetero-biotinylated PEG with lactide. PEG-PLA nanoparticles bearing biotin groups on surface were prepared by nanoprecipitation technique and the functional protein transferrin (Tf) were coupled to the nanoparticles by taking advantage of the strong biotin-avidin complex formation. The flow cytometer measurement demonstrated the targeting ability of the nanoparticles to tumor cells in vitro, and the fluorescence microscopy observation of brain sections from C6 glioma tumor-bearing rat model gave the intuitive proof that Tf functionalized PEG-PLA nanoparticles could penetrate into tumor in vivo.
本研究旨在设计一种可生物降解的聚乙二醇-聚乳酸(PEG-PLA)共聚物纳米粒子,该纳米粒子可通过生物素-亲和素相互作用表面生物功能化,并用作针对体内脑胶质瘤的潜在药物递送载体。为此,采用了一种新的方法来合成生物素化的 PEG-PLA 共聚物,即 PEG 与氯化生物素的酯化反应,然后是杂生物素化的 PEG 与丙交酯的共聚反应。通过纳米沉淀技术制备了表面带有生物素基团的 PEG-PLA 纳米粒子,并利用强生物素-亲和素复合物形成将转铁蛋白(Tf)等功能蛋白偶联到纳米粒子上。流式细胞仪测量证明了纳米粒子在体外对肿瘤细胞的靶向能力,并且从 C6 脑胶质瘤荷瘤大鼠模型的脑切片的荧光显微镜观察提供了直观的证据,证明 Tf 功能化的 PEG-PLA 纳米粒子可以在体内穿透肿瘤。