Belletti Daniela, Pederzoli Francesca, Forni Flavio, Vandelli Maria Angela, Tosi Giovanni, Ruozi Barbara
a Laboratory of Nanomedicine, Te.Far.T.I., Department of Life Sciences , University of Modena and Reggio Emilia , Modena , Italy.
Expert Opin Drug Deliv. 2017 Jul;14(7):825-840. doi: 10.1080/17425247.2017.1243528. Epub 2016 Oct 21.
New frontiers in nanomedicine are moving towards the research of new biomaterials. Apoferritin (APO), is a uniform regular self-assemblies nano-sized protein with excellent biocompatibility and a unique structure that affords it the ability to stabilize small active molecules in its inner core. Areas covered: APO can be loaded by applying a passive process (mainly used for ions and metals) or by a unique formulative approach based on disassemby/reassembly process. In this article, we aim to organize the experimental evidence provided by a number of studies on the loading, release and targeting. Attention is initially focused on the most investigated antineoplastic drug and contrast agents up to the most recent application in gene therapy. Expert opinion: Various preclinical studies have demonstrated that APO improved the potency and selectivity of some chemotherapeutics. However, in order to translate the use of APO into therapy, some issues must be solved, especially regarding the reproducibility of the loading protocol used, the optimization of nanocarrier characterization, detailed understanding of the final structure of loaded APO, and the real mechanism and timing of drug release.
纳米医学的新前沿正朝着新型生物材料的研究发展。脱铁铁蛋白(APO)是一种均匀规则的自组装纳米级蛋白质,具有出色的生物相容性和独特的结构,使其能够在其内核中稳定小的活性分子。涵盖领域:APO可以通过被动过程(主要用于离子和金属)或基于拆卸/重新组装过程的独特配方方法进行负载。在本文中,我们旨在整理多项关于负载、释放和靶向研究提供的实验证据。最初关注的是研究最多的抗肿瘤药物和造影剂,直至基因治疗中的最新应用。专家意见:各种临床前研究表明,APO提高了某些化疗药物的效力和选择性。然而,为了将APO的应用转化为治疗,必须解决一些问题,特别是关于所用负载方案的可重复性、纳米载体表征的优化、对负载APO最终结构的详细了解以及药物释放的真正机制和时间。