Univ. Lille, CNRS, Univ. Polytechnique Hauts-de-France, UMR 8520 - IEMN, F-59000 Lille, France.
Taipei Medical University, Graduate Institute of Biomedical Materials and Tissue Engineering (GIBMTE), New Taipei City 235603, Taiwan.
Nanoscale Horiz. 2023 Dec 18;9(1):14-43. doi: 10.1039/d3nh00306j.
Paracellular permeability across epithelial and endothelial cells is, in large part, regulated by apical intercellular junctions also referred to as tight junctions (TJs). These junctions contribute to the spatial definition of different tissue compartments within organisms, separating them from the outside world as well as from inner compartments, with their primary physiological role of maintaining tissue homeostasis. TJs restrict the free, passive diffusion of ions and hydrophilic small molecules through paracellular clefts and are important for appropriate cell polarization and transporter protein localisation, supporting the controlled transcellular diffusion of smaller and larger hydrophilic as well as hydrophobic substances. This traditional diffusion barrier concept of TJs has been challenged lately, owing to a better understanding of the components that are associated with TJs. It is now well-established that mutations in TJ proteins are associated with a range of human diseases and that a change in the membrane fluidity of neighbouring cells can open possibilities for therapeutics to cross intercellular junctions. Nanotechnological approaches, exploiting ultrasound or hyperosmotic agents and permeation enhancers, are the paradigm for achieving enhanced paracellular diffusion. The other widely used transport route of drugs is transcellular transport, allowing the passage of a variety of pro-drugs and nanoparticle-encapsulated drugs different mechanisms based on receptors and others. For a long time, there was an expectation that lipidic nanocarriers and polymeric nanostructures could revolutionize the field for the delivery of RNA and protein-based therapeutics across different biological barriers equipped with TJs (., blood-brain barrier (BBB), retina-blood barrier (RBB), corneal TJs, ). However, only a limited increase in therapeutic efficiency has been reported for most systems until now. The purpose of this review is to explore the reasons behind the current failures and to examine the emergence of synthetic and cell-derived nanomaterials and nanotechnological approaches as potential game-changers in enhancing drug delivery to target locations both at and across TJs using innovative concepts. Specifically, we will focus on recent advancements in various nanotechnological strategies enabling the bypassing or temporally opening of TJs to the brain and to the retina, and discuss their advantages and limitations.
细胞旁通透性穿过上皮细胞和内皮细胞,在很大程度上受细胞顶端连接(也称为紧密连接(TJ))调节。这些连接有助于在生物体中为不同组织隔室提供空间定义,将它们与外界以及内部隔室分开,其主要生理作用是维持组织内环境稳定。TJ 限制离子和亲水分子通过细胞旁间隙的自由被动扩散,对于适当的细胞极化和转运蛋白定位很重要,支持较小和较大亲水以及疏水分子的受控跨细胞扩散。最近,由于对与 TJ 相关的成分有了更好的理解,TJ 的这种传统扩散屏障概念受到了挑战。现在已经确定,TJ 蛋白的突变与一系列人类疾病有关,并且相邻细胞的膜流动性变化可以为穿过细胞连接的治疗方法提供可能性。利用超声或高渗剂和渗透增强剂的纳米技术方法是实现增强细胞旁扩散的范例。药物的另一种广泛使用的转运途径是跨细胞转运,允许各种前药和纳米颗粒包封药物通过,其基于受体和其他机制。长期以来,人们一直期望脂质纳米载体和聚合物纳米结构可以彻底改变 TJ (例如血脑屏障(BBB)、视网膜血屏障(RBB)、角膜 TJ、) 跨越不同生物屏障输送 RNA 和基于蛋白质的治疗药物的领域。然而,直到现在,大多数系统的治疗效率仅略有提高。本综述的目的是探讨当前失败的原因,并研究合成和细胞衍生的纳米材料和纳米技术方法的出现,这些方法作为增强药物递送到 TJ 处和 TJ 处的目标位置的潜在变革者,使用创新概念。具体而言,我们将重点介绍最近在各种纳米技术策略方面的进展,这些策略可以绕过或暂时打开 TJ 以到达大脑和视网膜,并讨论它们的优点和局限性。