Prato Maurizio, Kostarelos Kostas, Bianco Alberto
Dipartimento di Scienze Farmaceutiche, Università di Trieste, 34127 Trieste, Italy.
Acc Chem Res. 2008 Jan;41(1):60-8. doi: 10.1021/ar700089b. Epub 2007 Sep 15.
Carbon nanotubes (CNTs) have been proposed and actively explored as multipurpose innovative carriers for drug delivery and diagnostic applications. Their versatile physicochemical features enable the covalent and noncovalent introduction of several pharmaceutically relevant entities and allow for rational design of novel candidate nanoscale constructs for drug development. CNTs can be functionalized with different functional groups to carry simultaneously several moieties for targeting, imaging, and therapy. Among the most interesting examples of such multimodal CNT constructs described in this Account is one carrying a fluorescein probe together with the antifungal drug amphotericin B or fluorescein and the antitumor agent methotrexate. The biological action of the drug in these cases is retained or, as in the case of amphotericin B constructs, enhanced, while CNTs are able to reduce the unwanted toxicity of the drug administered alone. Ammonium-functionalized CNTs can also be considered very promising vectors for gene-encoding nucleic acids. Indeed, we have formed stable complexes between cationic CNTs and plasmid DNA and demonstrated the enhancement of the gene therapeutic capacity in comparison to DNA alone. On the other hand, CNTs conjugated with antigenic peptides can be developed as a new and effective system for synthetic vaccine applications. What makes CNTs quite unique is their ability, first shown by our groups in 2004, to passively cross membranes of many different types of cells following a translocation mechanism that has been termed the nanoneedle mechanism. In that way, CNTs open innumerable possibilities for future drug discovery based on intracellular targets that have been hard to reach until today. Moreover, adequately functionalized CNTs as those shown in this Account can be rapidly eliminated from the body following systemic administration offering further encouragment for their development. CNT excretion rates and accumulation in organs and any reactivity with the immune system will determine the CNT safety profile and, consequently, any further pharmaceutical development. Caution is advised about the need for systematic data on the long-term fate of these very interesting and versatile nano-objects in correlation with the type of CNT material used. CNTs are gradually plyaing a bigger and more important role in the emerging field of nanomedicine; however, we need to guarantee that the great opportunities they offer will be translated into feasible and safe constructs to be included in drug discovery and development pipelines.
碳纳米管(CNTs)已被提出并积极探索作为用于药物递送和诊断应用的多功能创新载体。它们多样的物理化学特性使得能够通过共价和非共价方式引入多种与药学相关的实体,并允许合理设计用于药物开发的新型候选纳米级构建体。碳纳米管可以用不同的官能团进行功能化,以同时携带多个用于靶向、成像和治疗的部分。本综述中描述的此类多模态碳纳米管构建体中最有趣的例子之一是一种同时携带荧光素探针和抗真菌药物两性霉素B,或者荧光素和抗肿瘤药物甲氨蝶呤的构建体。在这些情况下,药物的生物活性得以保留,或者如两性霉素B构建体的情况那样得到增强,同时碳纳米管能够降低单独给药时药物的不良毒性。铵功能化的碳纳米管也可被认为是用于基因编码核酸的非常有前景的载体。事实上,我们已经在阳离子碳纳米管和质粒DNA之间形成了稳定的复合物,并证明与单独的DNA相比,基因治疗能力有所增强。另一方面,与抗原肽缀合的碳纳米管可被开发为用于合成疫苗应用的新型有效系统。碳纳米管非常独特的一点是它们具有一种能力,这在2004年由我们的团队首次展示,即通过一种被称为纳米针机制的转运机制被动穿过许多不同类型细胞的膜。通过这种方式,碳纳米管为基于迄今难以触及的细胞内靶点的未来药物发现开辟了无数可能性。此外,如本综述中所示的充分功能化的碳纳米管在全身给药后可以迅速从体内清除,这为它们的开发提供了进一步的鼓励。碳纳米管的排泄率、在器官中的积累以及与免疫系统的任何反应性将决定碳纳米管的安全性概况,进而决定任何进一步的药物开发。建议谨慎对待关于这些非常有趣且多功能的纳米物体的长期命运与所用碳纳米管材料类型相关的系统数据的需求。碳纳米管在新兴的纳米医学领域正逐渐发挥越来越大且更重要的作用;然而,我们需要确保它们所提供的巨大机会能够转化为可行且安全的构建体,以纳入药物发现和开发流程。