Tseng Ching-Li, Wang Tzu-Wei, Dong Guo-Chung, Yueh-Hsiu Wu Steven, Young Tai-Horng, Shieh Ming-Jium, Lou Pei-Jen, Lin Feng-Huei
Institute of Biomedical Engineering, National Taiwan University, No. 1, Sec. 1, Ren-ai Rd., Taipei City 100, Taiwan.
Biomaterials. 2007 Sep;28(27):3996-4005. doi: 10.1016/j.biomaterials.2007.05.006. Epub 2007 May 18.
Since lung cancer is the most malignant cancer today, a specific drug-delivery system has been developed for superior outcome. In this study, gelatin nanoparticles (GPs) employed as native carriers were grafted with NeutrAvidin(FITC) on the particle's surface (GP-Av). Next, the biotinylated epithelial growth factor (EGF) molecules were conjugated with NeutrAvidin(FITC), forming a core-shell-like structure (GP-Av-bEGF) to achieve the enhancement of targeting efficiency. These nanoparticles were applied as an EGF receptor (EGFR)-seeking agent to detect lung adenocarcinoma. The results showed that the modification process had no significant influence on particle size (220 nm) and zeta potential (-9.3 mV). By the in vitro cell culture test, GP-Av-bEGF resulted in higher entrance efficiency on adenocarcinoma cells (A549) than that on normal lung cells (HFL1) because A549 possessed greater amounts of EGFR. We also found that uptake of GP-Av-bEGF by A549 cells was time and dose dependent. Confocal microscopy confirmed the cellular internalization of GP-Av-bEGF, and more fluorescent spots of GP-Av-bEGF nanoparticles were obviously observed as well as lysosomal entrapment in A549. Finally, the delivery was demonstrated by in vivo aerosol administration to cancerous lung of the SCID mice model, and specific accumulation in cancerous lung was confirmed by image quantification. The targeting ability of GP-Av-bEGF was proved in vitro and in vivo, which holds promise for further anti-cancer drug applications.
由于肺癌是当今最具恶性的癌症,因此已开发出一种特定的药物递送系统以获得更好的治疗效果。在本研究中,用作天然载体的明胶纳米颗粒(GPs)在其表面接枝了中性抗生物素蛋白(FITC)(GP-Av)。接下来,将生物素化的上皮生长因子(EGF)分子与中性抗生物素蛋白(FITC)偶联,形成核壳状结构(GP-Av-bEGF)以提高靶向效率。这些纳米颗粒被用作寻找表皮生长因子受体(EGFR)的试剂来检测肺腺癌。结果表明,修饰过程对粒径(220nm)和zeta电位(-9.3mV)没有显著影响。通过体外细胞培养试验,GP-Av-bEGF对腺癌细胞(A549)的进入效率高于正常肺细胞(HFL1),因为A549具有更多的EGFR。我们还发现A549细胞对GP-Av-bEGF的摄取具有时间和剂量依赖性。共聚焦显微镜证实了GP-Av-bEGF的细胞内化,并且在A549中明显观察到更多的GP-Av-bEGF纳米颗粒的荧光斑点以及溶酶体截留。最后,通过对SCID小鼠模型的癌肺进行体内气雾剂给药证明了递送效果,并通过图像定量证实了癌肺中的特异性积累。GP-Av-bEGF的靶向能力在体外和体内均得到证实,这为进一步的抗癌药物应用带来了希望。