Department of Pharmaceutics, School of Pharmacy, Jilin Medical College, Jilin 132013, PR China; Department of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing 100191, PR China.
Department of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing 100191, PR China.
J Control Release. 2014 Nov 28;194:53-70. doi: 10.1016/j.jconrel.2014.08.014. Epub 2014 Aug 23.
Cell-penetrating peptides (CPPs), often vividly termed as the "Trojan Horse" peptides, have attracted considerable interest for the intracellular delivery of a wide range of cargoes, such as small molecules, peptides, proteins, nucleic acids, contrast agents, nanocarriers and so on. Some preclinical and clinical developments of CPP conjugates demonstrate their promise as therapeutic agents for drug discovery. There is increasing evidence to suggest that CPPs have the potential to cross several bio-barriers (e.g., blood-brain barriers, intestinal mucosa, nasal mucosa and skin barriers). Despite revolutionary process in many aspects, there are a lot of basic issues unclear for these entities, such as internalization mechanisms, translocation efficiency, translocation kinetics, metabolic degradation, toxicity, side effect, distribution and non-specificity. Among them, non-specificity remains a major drawback for the in vivo application of CPPs in the targeted delivery of cargoes. So far, diverse organelle-specific CPPs or controlled delivery strategies have emerged and improved their specificity. In this review, we will look at the opportunities of CPPs in clinical development, bio-barriers penetration and nanocarriers delivery. Then, a series of basic problems of CPPs will be discussed. Finally, this paper will highlight the use of various controlled strategies in the organelle-specific delivery and targeted delivery of CPPs. The purpose of this review will be to emphasize most influential advance in this field and present a fundamental understanding for challenges and utilizations of CPPs. This will accelerate their translation as efficient vectors from the in vitro setting into the clinic arena, and retrieve the entry art to "Troy".
细胞穿透肽(CPPs),通常被生动地称为“特洛伊木马”肽,因其能够将各种载物(如小分子、肽、蛋白质、核酸、造影剂、纳米载体等)递送至细胞内而受到广泛关注。一些 CPP 缀合物的临床前和临床发展表明它们有望成为药物发现的治疗剂。越来越多的证据表明,CPP 具有穿过多种生物屏障(如血脑屏障、肠黏膜、鼻黏膜和皮肤屏障)的潜力。尽管在许多方面具有革命性的进展,但这些实体仍存在许多基本问题尚未阐明,例如内化机制、转位效率、转位动力学、代谢降解、毒性、副作用、分布和非特异性。其中,非特异性仍然是 CPP 用于靶向递送载物的体内应用的主要缺点。到目前为止,已经出现了多种细胞器特异性 CPP 或控制递药策略,从而提高了它们的特异性。在这篇综述中,我们将探讨 CPP 在临床开发、生物屏障穿透和纳米载体递送上的机会。然后,我们将讨论 CPP 面临的一系列基本问题。最后,本文将重点介绍各种控制策略在 CPP 的细胞器特异性递药和靶向递药中的应用。本文的目的是强调该领域最具影响力的进展,并为 CPP 的挑战和应用提供基本的理解。这将加速它们从体外环境转化为临床应用的有效载体,并恢复“特洛伊”的进入艺术。