Vedadghavami Armin, Zhang Chenzhen, Bajpayee Ambika G
Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA.
Department of Mechanical Engineering, Northeastern University, Boston, MA, 02115, USA.
Nano Today. 2020 Oct;34. doi: 10.1016/j.nantod.2020.100898. Epub 2020 Jun 20.
Negatively charged tissues are ubiquitous in the human body and are associated with a number of common diseases yet remain an outstanding challenge for targeted drug delivery. While the anionic proteoglycans are critical for tissue structure and function, they make tissue matrix dense, conferring a high negative fixed charge density (FCD) that makes drug penetration through the tissue deep zones and drug delivery to resident cells extremely challenging. The high negative FCD of these tissues is now being utilized by taking advantage of electrostatic interactions to create positively charged multi-stage delivery methods that can sequentially penetrate through the full thickness of tissues, create a drug depot and target cells. After decades of work on attempting delivery using strong binding interactions, significant advances have recently been made using weak and reversible electrostatic interactions, a characteristic now considered essential to drug penetration and retention in negatively charged tissues. Here we discuss these advances using examples of negatively charged tissues (cartilage, meniscus, tendons and ligaments, nucleus pulposus, vitreous of eye, mucin, skin), and delve into how each of their structures, tissue matrix compositions and high negative FCDs create barriers to drug entry and explore how charge interactions are being used to overcome these barriers. We review work on tissue targeting cationic peptide and protein-based drug delivery, compare and contrast drug delivery designs, and also present examples of technologies that are entering clinical trials. We also present strategies on further enhancing drug retention within diseased tissues of lower FCD by using synergistic effects of short-range binding interactions like hydrophobic and H-bonds that stabilize long-range charge interactions. As electrostatic interactions are incorporated into design of drug delivery materials and used as a strategy to create properties that are reversible, tunable and dynamic, bio-electroceuticals are becoming an exciting new direction of research and clinical work.
带负电荷的组织在人体中普遍存在,与多种常见疾病相关,但仍然是靶向药物递送的一大挑战。虽然阴离子蛋白聚糖对组织结构和功能至关重要,但它们使组织基质致密,赋予高负固定电荷密度(FCD),这使得药物穿透组织深层区域并递送至驻留细胞极具挑战性。现在,利用静电相互作用来创建带正电荷的多级递送方法,可依次穿透组织的全层厚度、形成药物储库并靶向细胞,从而利用这些组织的高负FCD。在致力于利用强结合相互作用进行递送数十年后,最近利用弱且可逆的静电相互作用取得了重大进展,这种特性现在被认为是药物在带负电荷组织中渗透和滞留所必需的。在这里,我们以带负电荷的组织(软骨、半月板、肌腱和韧带、髓核、眼玻璃体、粘蛋白、皮肤)为例讨论这些进展,深入探讨它们各自的结构、组织基质组成和高负FCD如何对药物进入形成屏障,并探索如何利用电荷相互作用来克服这些屏障。我们回顾了基于阳离子肽和蛋白质的组织靶向药物递送的研究工作,比较和对比药物递送设计,还展示了正在进入临床试验的技术实例。我们还提出了通过利用疏水和氢键等短程结合相互作用的协同效应来进一步增强药物在较低FCD病变组织中的滞留的策略,这些短程结合相互作用可稳定长程电荷相互作用。随着静电相互作用被纳入药物递送材料的设计并用作创造可逆、可调谐和动态特性的策略,生物电药物正成为一个令人兴奋的新研究和临床工作方向。