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Osteoarthritis In Vitro Models: Applications and Implications in Development of Intra-Articular Drug Delivery Systems

机译:骨关节炎在体外模型:在关节内药物输送系统开发中的应用和影响

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摘要

Osteoarthritis (OA) is a complex multi-target disease with an unmet medical need for the development of therapies that slow and potentially revert disease progression. Intra-articular (IA) delivery has seen a surge in osteoarthritis research in recent years. As local administration of molecules, this represents a way to circumvent systemic drug delivery struggles. When developing intra-articular formulations, the main goals are a sustained and controlled release of therapeutic drug doses, taking into account carrier choice, drug molecule, and articular joint tissue target. Therefore, the selection of models is critical when developing local administration formulation in terms of accurate outcome assessment, target and off-target effects and relevant translation to in vivo. The current review highlights the applications of OA in vitro models in the development of IA formulation by means of exploring their advantages and disadvantages. In vitro models are essential in studies of OA molecular pathways, understanding drug and target interactions, assessing cytotoxicity of carriers and drug molecules, and predicting in vivo behaviors. However, further understanding of molecular and tissue-specific intricacies of cellular models for 2D and 3D needs improvement to accurately portray in vivo conditions.
机译:骨关节炎(OA)是一种复杂的多目标疾病,具有未满足的医疗需求,对疾病的疗法进行缓慢和潜在的疾病进展的发展。近年来,关节内(IA)递送在骨关节炎的涌动中表现出浪涌。作为局部分子给药,这代表了一种旨在规避全身药物递送斗争的方法。在开发关节内配方时,主要目标是治疗药物剂量的持续和控制的释放,考虑到载体选择,药物分子和关节关节组织靶标。因此,在进行准确的结果评估,目标和偏移目标效应和体内相关翻译方面,在开发当地管理制定时,模型的选择至关重要。目前的审查突出了OA体外模型在探索其优缺点的制定中的应用。体外模型对于OA分子途径的研究至关重要,了解药物和靶相互作用,评估载体和药物分子的细胞毒性,并预测体内行为。然而,进一步了解2D和3D的细胞模型的分子和组织特异性复杂性,以便在体内条件下精确描绘。

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