School of Life Sciences, Tsinghua University, Beijing 100084, People's Republic of China; Center for Biotech and Bio-Medicine, The Shenzhen Key Lab of Gene and Antibody Therapy and Division of Life and Health Sciences, Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055, People's Republic of China.
Acta Biomater. 2013 Nov;9(11):8910-20. doi: 10.1016/j.actbio.2013.06.034. Epub 2013 Jun 28.
A star-shaped biodegradable polymer, mannitol-core poly(d,l-lactide-co-glycolide)-d-α-tocopheryl polyethylene glycol 1000 succinate (M-PLGA-TPGS), was synthesized in order to provide a novel nanoformulation for breast cancer chemotherapy. This novel copolymer was prepared by a core-first approach via three stages of chemical reaction, and was characterized by nuclear magnetic resonance, gel permeation chromatography and thermogravimetric analysis. The docetaxel-loaded M-PLGA-TPGS nanoparticles (NPs), prepared by a modified nanoprecipitation method, were observed to be near-spherical shape with narrow size distribution. Confocal laser scanning microscopy showed that the uptake level of M-PLGA-TPGS NPs was higher than that of PLGA NPs and PLGA-TPGS NPs in MCF-7 cells. A significantly higher level of cytotoxicity was achieved with docetaxel-loaded M-PLGA-TPGS NPs than with commercial Taxotere®, docetaxel-loaded PLGA-TPGS and PLGA NPs. Examination of the drug loading and encapsulation efficiency proved that star-shaped M-PLGA-TPGS could carry higher levels of drug than linear polymer. The in vivo experiment showed docetaxel-loaded M-PLGA-TPGS NPs to have the highest anti-tumor efficacy. In conclusion, the star-like M-PLGA-TPGS copolymer shows potential as a promising drug-loaded biomaterial that can be applied in developing novel nanoformulations for breast cancer therapy.
为了提供一种用于乳腺癌化疗的新型纳米制剂,合成了一种星形可生物降解聚合物,甘露醇核聚(D,L-丙交酯-共-乙交酯)-d-α-生育酚聚乙二醇 1000 琥珀酸酯(M-PLGA-TPGS)。该新型共聚物通过三步化学反应,采用核优先方法合成,并通过核磁共振、凝胶渗透色谱和热重分析进行了表征。通过改进的纳米沉淀法制备的载紫杉醇的 M-PLGA-TPGS 纳米颗粒(NPs)呈近球形,具有较窄的粒径分布。共焦激光扫描显微镜显示,M-PLGA-TPGS NPs 的摄取水平高于 PLGA NPs 和 PLGA-TPGS NPs 在 MCF-7 细胞中的摄取水平。载紫杉醇的 M-PLGA-TPGS NPs 的细胞毒性明显高于市售的 Taxotere®、载紫杉醇的 PLGA-TPGS 和 PLGA NPs。药物载药量和包封效率的检查证明,星形 M-PLGA-TPGS 可以携带更高水平的药物。体内实验表明,载紫杉醇的 M-PLGA-TPGS NPs 具有最高的抗肿瘤疗效。总之,星形 M-PLGA-TPGS 共聚物具有作为一种有前途的载药生物材料的潜力,可应用于开发用于乳腺癌治疗的新型纳米制剂。