Lubricant Strategies in Osteoarthritis Treatment: Transitioning from Natural Lubricants to Drug Delivery Particles with Lubricant Properties.

IF 6.8 Q1 TOXICOLOGY Journal of Xenobiotics Pub Date : 2024-09-19 DOI:10.3390/jox14030072
Agnese Fragassi, Antonietta Greco, Roberto Palomba
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引用次数: 0

Abstract

Osteoarthritis (OA) is a debilitating joint disease characterized by cartilage degradation, leading to pain and functional impairment. A key contributor to OA progression is the decline in cartilage lubrication. In physiological conditions, synovial fluid (SF) macromolecules like hyaluronic acid (HA), phospholipids, and lubricin play a crucial role in the boundary lubrication of articular cartilage. In early OA, cartilage damage triggers inflammation, altering SF composition and compromising the lubrication layer. This increases friction between mating interfaces, worsening cartilage degradation and local inflammation. Therefore, early-stage restoration of lubrication (by injecting in the joint different classes of compounds and formulations) could alleviate, and potentially reverse, OA progression. In the light of this, a broad variety of lubricants have been investigated for their ability to reduce friction in OA joints and promote cartilage repair in clinical and preclinical studies. This review examines recent advancements in lubricant-based therapy for OA, focusing on natural, bioinspired, and alternative products. Starting from the currently applied therapy, mainly based on natural lubricants as HA, we will present their modified versions, either in hydrogel form or with specific biomimetic moieties with the aim of reducing their clearance from the joint and of enhancing their lubricating properties. Finally, the most advanced and recent formulation, represented by alternative strategies, will be proposed. Particular emphasis will be placed on those ones involving new types of hydrogels, microparticles, nanoparticles, and liposomes, which are currently under investigation in preclinical studies. The potential application of particles and liposomes could foster the transition from natural lubricants to Drug Delivery Systems (DDSs) with lubricant features; transition which could provide more complete OA treatments, by simultaneously providing lubrication replacement and sustained release of different payloads and active agents directly at the joint level. Within each category, we will examine relevant preclinical studies, highlighting challenges and future prospects.

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骨关节炎治疗中的润滑剂策略:从天然润滑剂过渡到具有润滑特性的给药颗粒。
骨关节炎(OA)是一种使人衰弱的关节疾病,其特点是软骨退化,导致疼痛和功能障碍。导致 OA 恶化的一个关键因素是软骨润滑功能下降。在生理条件下,滑液(SF)中的透明质酸(HA)、磷脂和润滑素等大分子在关节软骨的边界润滑中起着至关重要的作用。在早期 OA 中,软骨损伤会引发炎症,改变 SF 的成分并破坏润滑层。这增加了配合界面之间的摩擦,加剧了软骨退化和局部炎症。因此,早期恢复润滑(通过在关节中注射不同种类的化合物和配方)可以缓解并有可能逆转 OA 的发展。有鉴于此,在临床和临床前研究中,对各种润滑剂进行了研究,以确定它们是否能够减少 OA 关节中的摩擦并促进软骨修复。本综述探讨了基于润滑剂的治疗 OA 的最新进展,重点关注天然、生物启发和替代产品。从目前应用的主要基于天然润滑剂(如 HA)的疗法开始,我们将介绍它们的改良版本,或为水凝胶形式,或含有特定的生物仿生分子,目的是减少它们从关节中的清除并增强其润滑特性。最后,我们将提出以替代策略为代表的最先进的最新配方。重点将放在涉及新型水凝胶、微颗粒、纳米颗粒和脂质体的配方上,这些配方目前正在进行临床前研究。微粒和脂质体的潜在应用可促进从天然润滑剂向具有润滑功能的给药系统(DDSs)过渡;这种过渡可同时提供润滑替代,并直接在关节水平持续释放不同的有效载荷和活性剂,从而提供更全面的 OA 治疗。在每个类别中,我们都将考察相关的临床前研究,强调挑战和未来前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.30
自引率
1.70%
发文量
21
审稿时长
10 weeks
期刊介绍: The Journal of Xenobiotics publishes original studies concerning the beneficial (pharmacology) and detrimental effects (toxicology) of xenobiotics in all organisms. A xenobiotic (“stranger to life”) is defined as a chemical that is not usually found at significant concentrations or expected to reside for long periods in organisms. In addition to man-made chemicals, natural products could also be of interest if they have potent biological properties, special medicinal properties or that a given organism is at risk of exposure in the environment. Topics dealing with abiotic- and biotic-based transformations in various media (xenobiochemistry) and environmental toxicology are also of interest. Areas of interests include the identification of key physical and chemical properties of molecules that predict biological effects and persistence in the environment; the molecular mode of action of xenobiotics; biochemical and physiological interactions leading to change in organism health; pathophysiological interactions of natural and synthetic chemicals; development of biochemical indicators including new “-omics” approaches to identify biomarkers of exposure or effects for xenobiotics.
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