College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, FL, USA.
College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, FL 32307, USA.
Crit Rev Ther Drug Carrier Syst. 2021;38(3):1-31. doi: 10.1615/CritRevTherDrugCarrierSyst.2021035222.
There is emergent need for in vitro models which are physiologically correct, easy to reproduce, and mimic characteristic functionalities of desired tissue, organ, or diseases state for ophthalmic drug screening, as well as disease modeling. To date, a variety of in vitro models have been developed for the applications ranging from 2D cell culture-based monolayers, multilayer, or co-culture models, to 3-dimensional (3D) organoids, 3D printed and organ on chip systems. Each model has its own pros and cons. While simple models are easier to create, and faster to reproduce, they lack recapitulation of the complex framework, functionalities, and properties of tissues or their subunits. Recent advancements in technologies and integration with tissue engineering and involvement of microfluidic systems have offered novel platforms which can better mimic the in vivo microenvironment, thus possessing potential in transformation of ophthalmic drug development. In this review we summarize existing in vitro ocular models while discussing applicability, drawbacks associated with them, and possible future applications.
目前非常需要体外模型,这些模型在生理上要正确,易于复制,并能模拟所需组织、器官或疾病状态的特征功能,以用于眼科药物筛选和疾病建模。迄今为止,已经开发出了多种用于各种应用的体外模型,包括基于 2D 细胞培养的单层、多层或共培养模型,到 3 维(3D)类器官、3D 打印和器官芯片系统。每种模型都有其自身的优缺点。虽然简单的模型更容易创建,并且更容易复制,但它们缺乏对组织或其亚单位的复杂结构、功能和特性的再现。最近在技术上的进步以及与组织工程的结合和微流控系统的参与提供了新的平台,这些平台可以更好地模拟体内微环境,因此在眼科药物开发方面具有潜在的转化能力。在这篇综述中,我们总结了现有的眼表体外模型,同时讨论了它们的适用性、相关缺点以及可能的未来应用。