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Investigating the Influence of Temperature and Supplementation Timing on Antifungal Efficacy in Storage Medium for Corneal Transplantation.
Liu, Hsin-Yu; Chen, Pao-Yu; Chu, Hsiao-Sang; Chiu, Ya-Ting; Chen, Yee-Chun; Hu, Fung-Rong.
Affiliation
  • Liu HY; Department of Ophthalmology, National Taiwan University Hospital, College of Medicine, National Taiwan University, No. 7, Zhongshan S. Rd, Zhongzheng Dist., Taipei, 10002, Taiwan.
  • Chen PY; National Eye Bank of Taiwan, Ministry of Health and Welfare, Taipei, Taiwan.
  • Chu HS; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Chiu YT; Department of Internal Medicine, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Chen YC; Department of Ophthalmology, National Taiwan University Hospital, College of Medicine, National Taiwan University, No. 7, Zhongshan S. Rd, Zhongzheng Dist., Taipei, 10002, Taiwan.
  • Hu FR; National Eye Bank of Taiwan, Ministry of Health and Welfare, Taipei, Taiwan.
Ophthalmol Ther ; 13(8): 2151-2161, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38831126
ABSTRACT

INTRODUCTION:

Although antifungal supplementation reduces the fungal load in the corneal storage medium, consensus is lacking on the influence of dosing and temperature. The study aims to evaluate the impact of eye bank warming protocol and timing of antifungal supplements on efficacy in Optisol-GS and tissue.

METHODS:

Corneoscleral rims contaminated with Candida albicans (C. albicans) were incubated in Optisol-GS, either without antifungal agents or with the addition of amphotericin B or voriconazole at various concentrations (2 ×, 5 ×, 10 ×, and 20 × MIC), at different time points, and under various preservation temperatures (2-8 °C versus 2 h-room temperature exposure). Antifungal efficacy was evaluated by counting viable yeast colonies cultured from Optisol-GS samples. Tissue sterility was determined through direct tissue culture and histological examination of the contaminated rims after a 14-day incubation period.

RESULTS:

Room temperature exposure did not increase colony growth at the same multiple MIC of antifungal agents. Although antifungal addition reduced C. albicans growth in a concentration-dependent manner, yeast growth was still observed in all Optisol-GS samples with a single supplementation after a 14-day incubation. Only groups with additional antifungal supplementation on either day 2 or day 6 showed a 99% or greater reduction of C. albicans growth in Optisol-GS samples and yielded negative results in direct tissue culture.

CONCLUSIONS:

The eye bank warming protocol did not compromise antifungal efficacy. To sustain the required concentration and effectively reduce C. albicans growth in Optisol-GS and contaminated tissue, additional antifungal supplementation on either day 2 or day 6 was necessary during a 2-week preservation period.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ophthalmol Ther Year: 2024 Document type: Article Affiliation country: Taiwán

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ophthalmol Ther Year: 2024 Document type: Article Affiliation country: Taiwán
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