Department of Pharmaceutics, National Institute of Pharmaceutical Education & Research, Hyderabad, Telangana, India.
Department of Pharmaceutical Sciences & Drug Research, Punjabi University, Patiala, Punjab, India.
Ther Deliv. 2024;15(12):977-995. doi: 10.1080/20415990.2024.2405456. Epub 2024 Sep 30.
Osteoarthritis (OSA) is a prevalent joint disorder characterized by losing articular cartilage, primarily affecting the hip, knee and spine joints. The impact of OSA offers a major challenge to health systems globally. Therapeutic approaches encompass surgical interventions, non-pharmacological therapies (exercise, rehabilitation, behavioral interventions) and pharmacological treatments. Inflammatory processes within OSA joints are regulated by pro-inflammatory and anti-inflammatory cytokines. Etodolac, a COX-2-selective inhibitor, is the gold standard for OSA management and uniquely does not inhibit gastric prostaglandins. This comprehensive review offers insights into OSA's pathophysiology, genetic factors and biological determinants influencing disease progression. Emphasis is placed on the pivotal role of etodolac in OSA management, supported by both preclinical and clinical evidences in topical drug delivery. Notably, - docking studies suggested potential synergies between etodolac and baicalein, considering ADAMTS-4, COX-2, MMP-3 and MMP-13 as essential therapeutic targets. Integration of artificial neural network (ANN) techniques with nanotechnology approaches emerges as a promising strategy for optimizing and personalizing topical etodolac delivery. Furthermore, the synergistic potential of etodolac and baicalein warrants in-depth exploration. Hence, by embracing cutting-edge technologies like ANN and nanomedicine, the optimization of topical etodolac delivery could guide a new era of OSA treatment.
骨关节炎(OSA)是一种常见的关节疾病,其特征是关节软骨丧失,主要影响髋关节、膝关节和脊柱关节。OSA 的影响对全球卫生系统构成了重大挑战。治疗方法包括手术干预、非药物疗法(运动、康复、行为干预)和药物治疗。OSA 关节内的炎症过程受促炎和抗炎细胞因子的调节。依托度酸是 COX-2 选择性抑制剂,是 OSA 管理的金标准,它独特地不抑制胃前列腺素。本综述深入探讨了 OSA 的病理生理学、遗传因素和生物决定因素对疾病进展的影响。强调了依托度酸在 OSA 管理中的关键作用,这得到了局部药物递送的临床前和临床证据的支持。值得注意的是,对接研究表明依托度酸和黄芩素之间可能存在协同作用,因为 ADAMTS-4、COX-2、MMP-3 和 MMP-13 是重要的治疗靶点。将人工神经网络 (ANN) 技术与纳米技术方法相结合,成为优化和个性化局部依托度酸递送的有前途的策略。此外,依托度酸和黄芩素的协同作用值得深入研究。因此,通过采用 ANN 和纳米医学等前沿技术,优化局部依托度酸递送可能引领 OSA 治疗的新时代。