In Vitro and Ex Vivo Models for Screening Topical Anti-Inflammatory Drugs

IF 2.3 Q3 PHARMACOLOGY & PHARMACY
Juan Luis Pérez-Salas, M. Moreno‐Jiménez, N. Rocha‐Guzmán, R. González-Laredo, L. Medina‐Torres, J. Gallegos‐Infante
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Abstract

Skin inflammation occurs as an immune response to various stimuli such as ultraviolet light, irritants, or any type of skin barrier injury. Finding safe and effective drugs to combat skin inflammation remains a research challenge. Ethical and legal considerations in animal testing encourage the development of in vitro and ex vivo models for the detection of skin inflammation. This report presents an updated review of non-animal study models available for screening drugs with anti-inflammatory potential. It includes a description of the basic methods used to inhibit protein denaturation and red blood cell membrane stability. Three in vitro inhibition assay methods for enzymes relevant to the skin inflammatory process are then described. The development of cell culture models is described: relatively simple and easy-to-produce two-dimensional (2D) skin cell cultures that allow assessment of response to a given stimulus, three-dimensional (3D) cell cultures that better mimic human skin physiology by more accurately replicating mechanical and chemical signals, and vascularized 3D skin models with dynamic perfusion and microfluidic devices known as skin on a chip. Finally, ex vivo skin models are presented that could more accurately represent human skin in terms of structure, cell signaling mechanisms, and absorption effects. Although the current development of models without the use of animals is promising, improvements and refinements are needed to make the models more suitable as screening platforms for topical anti-inflammatory drugs.
筛选局部抗炎药的体外和离体模型
皮肤炎症是对各种刺激的免疫反应,如紫外线、刺激物或任何类型的皮肤屏障损伤。寻找安全有效的药物来对抗皮肤炎症仍然是一项研究挑战。动物试验中的伦理和法律考虑鼓励开发用于检测皮肤炎症的体外和离体模型。本报告对可用于筛选具有抗炎潜力的药物的非动物研究模型进行了最新综述。它包括用于抑制蛋白质变性和红细胞膜稳定性的基本方法的描述。然后描述了与皮肤炎症过程相关的酶的三种体外抑制测定方法。描述了细胞培养模型的发展:相对简单和容易产生允许评估对给定刺激的反应的二维(2D)皮肤细胞培养物、通过更准确地复制机械和化学信号更好地模拟人类皮肤生理学的三维(3D)细胞培养物,以及具有动态灌注和被称为芯片上皮肤的微流体设备的血管化3D皮肤模型。最后,提出了离体皮肤模型,该模型可以在结构、细胞信号机制和吸收效应方面更准确地代表人类皮肤。尽管目前在不使用动物的情况下开发模型是有希望的,但仍需要改进和完善,使模型更适合作为局部抗炎药的筛选平台。
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
Scientia Pharmaceutica
Scientia Pharmaceutica Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.60
自引率
4.00%
发文量
67
审稿时长
10 weeks
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