Institute of Pharmaceutics, College of Pharmaceutical Sciences, Zhejiang University, PR China.
J Control Release. 2010 Oct 15;147(2):154-62. doi: 10.1016/j.jconrel.2010.05.015. Epub 2010 May 19.
The targeting drug delivery systems (TDDS) have attracted extensive attention of researchers in recent years. More and more drug/gene targeted delivery carriers, such as liposome, magnetic nanoparticles, ligand-conjugated nanoparticles, microbubbles, etc., have been developed and under investigation for their application. However, the currently investigated drug/gene carriers have several disadvantages, which limit their future use in clinical practice. Therefore, design and development of novel drug/gene delivery vehicles has been a hot area of research. Recent studies have shown the ability of mesenchymal stem cells (MSCs) to migrate towards and engraft into the tumor sites, which make them a great hope for efficient targeted-delivery vehicles in cancer gene therapy. In this review article, we examine the promising of using mesenchymal stem cells as a targeted-delivery vehicle for cancer gene therapy, and summarize various challenges and concerns regarding these therapies.
近年来,靶向药物传递系统(TDDS)引起了研究人员的广泛关注。越来越多的药物/基因靶向递送载体,如脂质体、磁性纳米颗粒、配体偶联的纳米颗粒、微泡等,已经被开发出来并正在进行研究,以探索其在临床上的应用。然而,目前研究的药物/基因载体存在一些缺点,限制了它们在临床实践中的未来应用。因此,设计和开发新型药物/基因递送载体一直是一个热门的研究领域。最近的研究表明,间充质干细胞(MSCs)具有向肿瘤部位迁移并植入的能力,这使它们成为癌症基因治疗中高效靶向递送载体的一大希望。在这篇综述文章中,我们探讨了使用间充质干细胞作为癌症基因治疗的靶向递送载体的前景,并总结了这些疗法存在的各种挑战和关注点。
J Control Release. 2010-5-19
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