光热损伤和光化学损伤的统一建模。

Frontiers in ophthalmology Pub Date : 2024-08-19 eCollection Date: 2024-01-01 DOI:10.3389/fopht.2024.1408869
Michael L Denton, Clifton D Clark, Gary D Noojin, Haleigh West, Allison Stadick, Taufiquar Khan
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引用次数: 0

摘要

将损伤结果与视网膜激光照射联系起来,对于诊断和选择适当的治疗方法至关重要。因此,了解激光参数(如波长、功率密度和照射时间)与任何损伤之间的因果关系非常重要。在体外视网膜模型中利用培养的视网膜色素上皮细胞区分光热和光化学过程将是实现这一目标的第一步。几十年来,阿伦尼乌斯的一阶速率常数一直被用于近似细胞热损伤。该方程的一个修正称为损伤积分(Ω),已被广泛用于预测关键细胞蛋白光热失活产生的激光损伤累积。光化学过程造成的损伤研究较少,大多数模型尚未得到验证,因为它们需要量化一种或多种未定性的化学物质。此外,很少有关于光化学损伤的报告会报告测量或模拟的温度历史。我们使用之前体外研究中的模拟阈值温度来区分光热和光化学过程。假定纯粹的光化学过程也会使关键的细胞蛋白质失活,我们报告了光热Ω和光化学Ω的使用情况,它们协同作用以显示总体损伤累积。综合损伤积分(ΩCDI)应用了一种数学开关,旨在描述相对于波长和光子传输速率的光化学损伤。虽然只在体外模型中进行了测试,但这种方法可以过渡到预测哺乳动物视网膜的损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unified modeling of photothermal and photochemical damage.

Correlating damage outcomes to a retinal laser exposure is critical for diagnosis and choosing appropriate treatment modalities. Therefore, it is important to understand the causal relationships between laser parameters, such as wavelength, power density, and length of exposure, and any resulting injury. Differentiating photothermal from photochemical processes in an in vitro retinal model using cultured retinal pigment epithelial cells would be a first step in achieving this goal. The first-order rate constant of Arrhenius has been used for decades to approximate cellular thermal damage. A modification of this equation, called the damage integral (Ω), has been used extensively to predict the accumulation of laser damage from photothermal inactivation of critical cellular proteins. Damage from photochemical processes is less well studied and most models have not been verified because they require quantification of one or more uncharacterized chemical species. Additionally, few reports on photochemical damage report temperature history, measured or simulated. We used simulated threshold temperatures from a previous in vitro study to distinguish between photothermal and photochemical processes. Assuming purely photochemical processes also inactivate critical cellular proteins, we report the use of a photothermal Ω and a photochemical Ω that work in tandem to indicate overall damage accumulation. The combined damage integral (ΩCDI) applies a mathematical switch designed to describe photochemical damage relative to wavelength and rate of photon delivery. Although only tested in an in vitro model, this approach may transition to predict damage at the mammalian retina.

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