Srinivasan Srimeenakshi, Alexander Jenolyn F, Driessen Wouter H, Leonard Fransisca, Ye Hu, Liu Xuewu, Arap Wadih, Pasqualini Renata, Ferrari Mauro, Godin Biana
The Methodist Hospital Research Institute, Houston, Texas, USA.
The University of Texas MD Anderson Cancer Center, David H. Koch Center, Houston, Texas, USA.
J Mater Chem B. 2013 Oct 21;1(39). doi: 10.1039/C3TB20595A.
There has been extensive research on the use of nanovectors for cancer therapy. Targeted delivery of nanotherapeutics necessitates two important characteristics; the ability to accumulate at the disease locus after overcoming sequential biological barriers and the ability to carry a substantial therapeutic payload. Successful combination of the above two features is challenging, especially in solid porous materials where chemical conjugation of targeting entities on the particle surface will generally prevent successful loading of the therapeutic substance. In this study, we propose a novel strategy for decorating the surface of mesoporous silicon particles with targeting entities (bacteriophage) and gold nanoparticles (AuNP) while maintaining their payload carrying potential. The resulting Bacteriophage Associated Silicon Particles (BASP) demonstrates efficient encapsulation of macromolecules and therapeutic nanoparticles into the porous structures. targeting data show enhanced targeting efficiency with about four orders of magnitude lower concentration of bacteriophage. targeting data suggest that BASP maintain their integrity following intravenous administration in mice and display up to three fold higher accumulation in the tumor.
关于使用纳米载体进行癌症治疗已有广泛研究。纳米治疗剂的靶向递送需要两个重要特性:在克服一系列生物屏障后在疾病部位积累的能力以及携带大量治疗载荷的能力。成功结合上述两个特征具有挑战性,尤其是在固体多孔材料中,颗粒表面靶向实体的化学缀合通常会阻碍治疗物质的成功负载。在本研究中,我们提出了一种新颖的策略,即在保持介孔硅颗粒携带载荷潜力的同时,用靶向实体(噬菌体)和金纳米颗粒(AuNP)修饰其表面。所得的噬菌体相关硅颗粒(BASP)证明了大分子和治疗性纳米颗粒能有效包封到多孔结构中。靶向数据显示,噬菌体浓度约低四个数量级时靶向效率增强。靶向数据表明,BASP在小鼠静脉注射后保持其完整性,并在肿瘤中的积累高达三倍。