Up-Dated the Critical Issues of Corneal Cross-Linking (Type-I and II): Safety Dose for Ultra-Thin Cornea, Demarcation Line Depth and the Role of Oxygen

Jui-Teng Lin
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引用次数: 4

Abstract

Purpose: To update analytic formulas for the overall efficacy of corneal collagen crosslinking (CXL) including both type-I and oxygen-mediated type-II mechanisms, the role of oxygen and the initiator regeneration. Also, to derive the formulas for the minimum corneal thickness and demarcation line depth. Study Design: Modeling the kinetics of CXL in UV light and using riboflavin as the photosensitizer. Place and Duration of Study: New Taipei City, Taiwan, between June, 2021 and July, 2021. Methodology: Coupled kinetic equations are derived under the quasi-steady state condition for the 2-pathway mechanisms of CXL. For type-I CXL, the riboflavin (RF) triplet state [T] may interact directly with the stroma collagen substrate [A] to form radical (R) and regenerate initiator. For type-II process, [T] interacts with oxygen to form a singlet oxygen [1 O2 ]. Both reactive radical (R) and [1 O2 ], can relax to their ground state, or interact with the substrate [A]) for crosslinking. Based on a safety dose, formulas for the minimum corneal thickness and demarcation line depth (DLD) are derived. Results: Our updated theory/modeling showed that oxygen plays a limited and transient role in the process, in consistent with that of Kamave. In contrary, Kling et al believed that type-II is the predominant mechanism, which however conflicting with the epi-on CXL results. For both type-I and type-II, a transient state conversion (crosslink) efficacy in an increasing function of light intensity (or dose), whereas, its steady state efficacy is a deceasing function of light intensity. RF depletion in type-I is compensated by the RF regeneration term (RGE) which is a decreasing function of oxygen. For the case of perfect regeneration case (or when oxygen=0), RF is a constant due to the catalytic cycle. Unlike the conventional Dresden rule of 400 um thickness, thin cornea CXL is still safe as far as the dose is under a threshold dose (E*), based on our minimum thickness formula (Z*). Our formula for thin cornea is also clinically shown by Hafez et al for ultra thin (214 nm) CXL. Conclusion: For both type-I and type-II, a transient state conversion (crosslink) efficacy in an increasing function of light intensity (or dose), whereas, its steady state efficacy is a deceasing function of light intensity. CXL for ultra thin corneas are still safe, as far as it is under a threshold dose (E*), based on our minimum thickness formula, which has a similar tend as that of demarcation line depth. the type-II efficacy also provides the survival rate for the treatment of corneal keratitis.
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更新角膜交联的关键问题(i型和II型):超薄角膜的安全剂量、分界线深度和氧的作用
目的:更新角膜胶原交联(CXL)整体疗效的分析公式,包括i型和氧介导的ii型机制、氧的作用和引发剂再生。并推导出最小角膜厚度和分界线深度的计算公式。研究设计:模拟CXL在紫外光下的动力学,并使用核黄素作为光敏剂。学习地点及时间:台湾新北市,2021年6月至2021年7月。方法:在准稳态条件下,推导了双通路CXL机理的耦合动力学方程。对于i型CXL,核黄素(RF)三态[T]可直接与基质胶原底物[A]相互作用形成自由基(R)和再生引发剂。对于ii型过程,[T]与氧相互作用形成单线态氧[1 O2]。活性自由基(R)和[1o2]都可以弛豫到基态,或与底物[A]相互作用进行交联。基于安全剂量,导出了最小角膜厚度和分界线深度(DLD)的公式。结果:我们更新的理论/模型表明,氧气在这一过程中起着有限和短暂的作用,与Kamave的结果一致。相反,Kling等人认为ii型是主要的机制,但这与epi-on CXL的结果相矛盾。对于i型和ii型,瞬态转换(交联)效率随光强(或剂量)的增加而增加,而其稳态效率随光强的减少而减少。i型的射频损耗由射频再生项(RGE)补偿,RGE是氧的递减函数。在完全再生情况下(或氧=0时),由于催化循环,RF为常数。与传统的400um厚度的德累斯顿规则不同,根据我们的最小厚度公式(Z*),只要剂量低于阈值剂量(E*),薄角膜CXL仍然是安全的。我们的薄角膜配方也被Hafez等人用于超薄(214 nm) CXL的临床应用。结论:无论是i型还是ii型,其瞬态转换(交联)功效都随光强(或剂量)的增加而增加,而其稳态功效则随光强的增加而减少。根据我们的最小厚度公式,对于超薄角膜,只要在阈值剂量(E*)以下,CXL仍然是安全的,其趋势与分界线深度相似。ii型疗效也为治疗角膜角膜炎提供了生存率。
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