Scholarlink

<p>The performance of ophthalmic surgeries, particularly penetrating keratoplasty, is associated with an increased risk of ocular infections, especially fungal keratitis. In addition to infections such as post-surgical occlusions, microbial contamination of the donor’s tissue, predominantly fungal in nature, can also lead to the disposal of said tissue. The genus <i>Fusarium</i>, along with several species from the <i>Candida</i> genus, emerge as the primary fungal agents, displaying notable biofilm-forming abilities on surfaces. To address these issues, the addition of antifungals to preservation media vials has been explored, although conventional antifungal agents exhibit limitations. In light of this, compounds such derived from 8-hydroxyquinoline, clioquinol (CLQ) and PH151, emerge as promising alternatives. Hence, this study aimed to assess the efficacy of two derivatives of 8-hydroxyquinoline, both individually and in combination with antifungal agents, as additives in preservation media for human corneas intended for transplantation. Given the antifungal potential of CLQ and the combination voriconazole-amphotericin B-clioquinol, the ability to inhibit fungal growth and biofilm formation in human corneas preserved in Optisol-GS medium was investigated, as well as the endothelial viability of this tissue in the presence of these compounds. Among the tested antifungal agents, the combination of voriconazole, amphotericin B, and clioquinol stood out for its excellent antibiofilm action and potential to reduce the fungal load on the surface of the corneas, did not present endothelial toxicity. Thus, the results underscore the promising nature of this combination as a potential additive in hypothermic corneal preservation media, outlining a viable pathway to enhance corneal transplant efficacy.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Optimization of corneal preservation media with novel antifungal agents

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年3月28日

查看全文
  • Paula Reginatto,
  • Giovanna de Jesus Agostinetto,
  • Claudete Inês Locatelli,
  • Felipe Silva Guareze,
  • Angélica Rocha Joaquim,
  • Maria Eduarda Krummenauer,
  • Rúbia do Nascimento Fuentefria,
  • Marilene Henning Vainstein,
  • Diane Ruschel Marinho,
  • Saulo Fernandes de Andrade,
  • Alexandre Meneghello Fuentefria

摘要

The performance of ophthalmic surgeries, particularly penetrating keratoplasty, is associated with an increased risk of ocular infections, especially fungal keratitis. In addition to infections such as post-surgical occlusions, microbial contamination of the donor’s tissue, predominantly fungal in nature, can also lead to the disposal of said tissue. The genus Fusarium, along with several species from the Candida genus, emerge as the primary fungal agents, displaying notable biofilm-forming abilities on surfaces. To address these issues, the addition of antifungals to preservation media vials has been explored, although conventional antifungal agents exhibit limitations. In light of this, compounds such derived from 8-hydroxyquinoline, clioquinol (CLQ) and PH151, emerge as promising alternatives. Hence, this study aimed to assess the efficacy of two derivatives of 8-hydroxyquinoline, both individually and in combination with antifungal agents, as additives in preservation media for human corneas intended for transplantation. Given the antifungal potential of CLQ and the combination voriconazole-amphotericin B-clioquinol, the ability to inhibit fungal growth and biofilm formation in human corneas preserved in Optisol-GS medium was investigated, as well as the endothelial viability of this tissue in the presence of these compounds. Among the tested antifungal agents, the combination of voriconazole, amphotericin B, and clioquinol stood out for its excellent antibiofilm action and potential to reduce the fungal load on the surface of the corneas, did not present endothelial toxicity. Thus, the results underscore the promising nature of this combination as a potential additive in hypothermic corneal preservation media, outlining a viable pathway to enhance corneal transplant efficacy.