AI Article Synopsis

  • Riboflavin, when exposed to UVA radiation, generates reactive oxygen species (ROS), which can alter biological systems and be utilized in treating ocular and dermal diseases.
  • In corneal cross-linking (CXL) for keratoconus, riboflavin and UVA work together to promote collagen fibril formation, but polysaccharides like dextran are added to mitigate the harmful effects of ROS.
  • The study investigates how riboflavin affects collagen fibril formation using methods such as microcalorimetry, rheology, and STEM imaging, with evidence of ROS production in collagen, hyaluronic acid, and riboflavin solutions from spin trapping experiments.

Article Abstract

Riboflavin under UVA radiation generates reactive oxygen species (ROS) that can induce various changes in biological systems. Under controlled conditions, these processes can be used in some treatments for ocular or dermal diseases. For instance, corneal cross-linking (CXL) treatment of keratoconus involves UVA irradiation combined with riboflavin aiming to induce the formation of new collagen fibrils in cornea. To reduce the damaging effect of ROS formed in the presence of riboflavin and UVA, the CXL treatment is performed with the addition of polysaccharides (dextran). Hyaluronic acid is a polysaccharide that can be found in the aqueous layer of the tear film. In many cases, keratoconus patients also present dry eye syndrome that can be reduced by the application of topical solutions containing hyaluronic acid. This study presents physico-chemical evidence on the effect of riboflavin on collagen fibril formation revealed by the following methods: differential scanning microcalorimetry, rheology, and STEM images. The collagen used was extracted from calf skin that contains type I collagen similar to that found in the eye. Spin trapping experiments on collagen/hyaluronic acid/riboflavin solutions evidenced the formation of ROS species by electron paramagnetic resonance measurements.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746477PMC
http://dx.doi.org/10.3390/molecules27010190DOI Listing

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