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Photochemical kinetics of corneal cross-linking with riboflavin.核黄素角膜交联的光化学动力学。
Invest Ophthalmol Vis Sci. 2012 Apr 30;53(4):2360-7. doi: 10.1167/iovs.11-9385.
2
The role of nonenzymatic glycation and carbonyls in collagen cross-linking for the treatment of keratoconus.非酶糖基化和羰基化合物在角膜交联治疗圆锥角膜中的作用。
Invest Ophthalmol Vis Sci. 2011 Aug 11;52(9):6363-9. doi: 10.1167/iovs.11-7585.
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Investigation of riboflavin sensitized degradation of purine and pyrimidine derivatives of DNA and RNA under UVA and UVB.研究 UVA 和 UVB 下核黄素敏化的嘌呤和嘧啶衍生物的 DNA 和 RNA 降解。
Biochem Biophys Res Commun. 2010 Oct 1;400(4):729-33. doi: 10.1016/j.bbrc.2010.08.138. Epub 2010 Sep 15.
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Stability of flavonoids in the presence of riboflavin-photogenerated reactive oxygen species: a kinetic and mechanistic study on quercetin, morin and rutin.类黄酮在核黄素光生反应性氧物种存在下的稳定性:槲皮素、桑色素和芦丁的动力学和机理研究。
Photochem Photobiol. 2010 Jul-Aug;86(4):827-34. doi: 10.1111/j.1751-1097.2010.00754.x. Epub 2010 Jun 7.
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Long-term biomechanical properties of rabbit sclera after collagen crosslinking using riboflavin and ultraviolet A (UVA).使用核黄素和紫外线A(UVA)对兔巩膜进行交联后其长期生物力学特性
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Photodynamic inactivation of trypsin by the aminophylline-riboflavin system: involvement of hydroxyl radical.氨茶碱-核黄素体系对胰蛋白酶的光动力失活作用:羟自由基的参与
Med Sci Monit. 2006 Aug;12(8):BR283-9. Epub 2006 Jul 12.
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Cross-linking of scleral collagen in the rabbit using riboflavin and UVA.使用核黄素和紫外线A对兔巩膜胶原进行交联。
Acta Ophthalmol Scand. 2005 Aug;83(4):477-82. doi: 10.1111/j.1600-0420.2005.00447.x.
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Visible light-induced photooxidation of glucose sensitized by riboflavin.核黄素敏化的可见光诱导葡萄糖光氧化
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Increased resistance of crosslinked cornea against enzymatic digestion.交联角膜对酶消化的抵抗力增强。
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核黄素的紫外线A照射会产生氧依赖性羟基自由基。

UVA irradiation of riboflavin generates oxygen-dependent hydroxyl radicals.

作者信息

Sel Saadettin, Nass Norbert, Pötzsch Sandy, Trau Stefanie, Simm Andreas, Kalinski Thomas, Duncker Gernot Iw, Kruse Friedrich E, Auffarth Gerd U, Brömme Hans-Jürgen

出版信息

Redox Rep. 2014 Mar;19(2):72-9. doi: 10.1179/1351000213Y.0000000076. Epub 2013 Nov 20.

DOI:10.1179/1351000213Y.0000000076
PMID:24257538
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6837670/
Abstract

OBJECTIVES/METHODS: The aim of this study was to verify the formation of hydroxyl radicals (·OH) after ultraviolet A (UVA) irradiation of riboflavin (RF) by spin trapping with 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), and electron spin resonance spectroscopy.

RESULTS

We found that ·OH were generated via hydrogen peroxide (H₂O₂) formation during UVA irradiation of RF. The ·OH radicals were trapped with DMPO yielding 2-hydroxy-5,5-dimethyl-1-pyrroline-N-oxide (·DMPO-OH). The formed radical adduct (·DMPO-OH) accumulated in the RF solution. Argon equilibration of the RF solution completely blocked the formation of the ·DMPO-OH adduct whereas subsequent aeration restored radical adduct generation. The presence of catalase inhibited ·DMPO-OH generation whereas BSA had no influence on ·DMPO-OH formation. Stopping UVA irradiation led to decay of radical adducts. UVA irradiation of H₂O₂ in the presence of DMPO but without RF also induced the formation of ·DMPO-OH adduct. When adding DMPO to an already irradiated RF solution significantly less ·DMPO-OH was formed during further irradiation. Ultraviolet-visible spectroscopy and high-performance liquid chromatography analysis of RF indicated that RF decayed during UVA irradiation.

DISCUSSION

The formation of ·OH during UVA irradiation of RF may be part of the oxygen-dependent mechanism involved in the cross-linking therapy of collagen in corneal stroma.

摘要

目的/方法:本研究的目的是通过用5,5 - 二甲基 - 1 - 吡咯啉 - N - 氧化物(DMPO)自旋捕获和电子自旋共振光谱法,验证核黄素(RF)在紫外线A(UVA)照射后羟基自由基(·OH)的形成。

结果

我们发现,在RF的UVA照射过程中,·OH是通过过氧化氢(H₂O₂)的形成而产生的。·OH自由基被DMPO捕获,生成2 - 羟基 - 5,5 - 二甲基 - 1 - 吡咯啉 - N - 氧化物(·DMPO - OH)。形成的自由基加合物(·DMPO - OH)在RF溶液中积累。RF溶液的氩气平衡完全阻止了·DMPO - OH加合物的形成,而随后的曝气恢复了自由基加合物的生成。过氧化氢酶的存在抑制了·DMPO - OH的生成,而牛血清白蛋白对·DMPO - OH的形成没有影响。停止UVA照射导致自由基加合物的衰减。在存在DMPO但没有RF的情况下,UVA照射H₂O₂也诱导了·DMPO - OH加合物的形成。当向已经照射过的RF溶液中添加DMPO时,在进一步照射期间形成的·DMPO - OH明显减少。RF的紫外可见光谱和高效液相色谱分析表明,RF在UVA照射期间发生了衰减。

讨论

RF在UVA照射过程中·OH的形成可能是角膜基质中胶原蛋白交联治疗所涉及的氧依赖性机制的一部分。