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眼前节器官培养模型用于开放性眼球损伤的特性研究。

Characterization of an anterior segment organ culture model for open globe injuries.

机构信息

Department of Sensory Trauma, United States Army Institute of Surgical Research, Fort Sam Houston, TX, 78234, USA.

出版信息

Sci Rep. 2021 Apr 20;11(1):8546. doi: 10.1038/s41598-021-87910-8.

Abstract

Open-globe injuries have poor visual outcomes and have increased in frequency. The current standard of care is inadequate, and a therapeutic is needed to stabilize the injury until an ophthalmic specialist is reached. Unfortunately, current models or test platforms for open-globe injuries are insufficient. Here, we develop and characterize an open-globe injury model using an anterior segment organ-culture platform that allows therapeutic assessment for up to 72 h post-injury. Anterior segments maintained in organ culture were kept at physiological intraocular pressure throughout, and puncture injuries were created using a novel pneumatic-powered system. This system can create high-speed, military-relevant injuries up to 4.5 mm in diameter through the cornea. From intraocular pressure readings, we confirmed a loss of pressure across the 72 h after open-globe injury. Proof-of-concept studies with a Dermabond tissue adhesive were performed to show how this model system could track therapeutic performance for 72 h. Overall, the organ-culture platform was found to be a suitable next step towards modeling open-globe injuries and assessing wound closure over the critical 72 h post-injury. With improved models such as this, novel biomaterial therapeutics development can be accelerated, improving care, and, thus, improving the prognosis for the patients.

摘要

开放性眼外伤的预后较差,且其发病率呈上升趋势。目前的治疗标准并不完善,需要一种治疗方法来稳定损伤,直到眼科专家介入。不幸的是,目前的开放性眼外伤模型或测试平台还不够完善。在这里,我们使用眼前节器官培养平台开发并描述了一种开放性眼外伤模型,该模型允许在损伤后长达 72 小时进行治疗评估。整个器官培养过程中,眼前节始终保持生理眼压,使用新型气动动力系统进行穿刺损伤。该系统可通过角膜产生高达 4.5 毫米直径的高速、与军事相关的损伤。通过眼压读数,我们证实了开放性眼外伤后 72 小时内眼压的丧失。使用 Dermabond 组织粘合剂进行了概念验证研究,以展示该模型系统如何在 72 小时内跟踪治疗效果。总的来说,该器官培养平台是朝着模拟开放性眼外伤和评估损伤后关键 72 小时内伤口闭合的方向迈出的合适的下一步。通过此类改进后的模型,可以加速新型生物材料治疗药物的开发,改善患者的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be15/8058041/fc4efff78ae0/41598_2021_87910_Fig1_HTML.jpg

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