Intravitreal chlorhexidine for sterilizing the vitreous cavity in an animal model of bacterial endophthalmitis


HONDUR A. M., Zeng Q., Ucgul Y., Arioz I., ŞAHİN E. A., Erayman G. G., ...Daha Fazla

CUTANEOUS AND OCULAR TOXICOLOGY, cilt.43, sa.4, ss.299-304, 2024 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 43 Sayı: 4
  • Basım Tarihi: 2024
  • Doi Numarası: 10.1080/15569527.2024.2402410
  • Dergi Adı: CUTANEOUS AND OCULAR TOXICOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, CAB Abstracts, EMBASE, Environment Index, MEDLINE, Veterinary Science Database
  • Sayfa Sayıları: ss.299-304
  • Anahtar Kelimeler: Bacterial endophthalmitis, bacterial resistance, chlorhexidine, intravitreal injection, Staphylococcus epidermidis
  • Gazi Üniversitesi Adresli: Evet

Özet

Purpose: To evaluate the efficacy and safety of intravitreal chlorhexidine (CHX) for sterilising the vitreous cavity in bacterial endophthalmitis. Methods: For in-vitro experiments, full-thickness retina explants were harvested from freshly enucleated pig eyes. Six-millimeter circular sensory retina patches were then incubated in varying concentrations of CHX (0.625-800 mu g/mL) for 24 hours. Retinal cell viability was determined at the end of the incubation period with a live-dead assay. The bactericidal effects of the tested CHX concentrations were determined using a quantitative suspension test on Staphylococcus epidermidis. The safety of CHX was also tested by injecting varying doses of CHX (50-400 mu g/mL) into the vitreous cavity of albino rabbits followed by flash electroretinography (ERG) and light microscopy. The bactericidal effect of the non-toxic CHX doses was determined using the rabbit model of endophthalmitis created by injecting 3000 CFU/0.1 mL of Staphylococcus epidermidis. Results: In vitro concentrations of CHX greater than 6.25 mu gr/mL exerted a bactericidal effect, while concentrations of CHX less than 200 mu g/mL did not impair retinal cell viability. Intravitreal concentrations of CHX between 20-100 mu g/mL were adequate to sterilise the infected rabbit vitreous cavity in the animal model. No significant functional or anatomical deleterious effect was observed with ERG or light microscopy. Conclusion: CHX can sterilise the vitreous cavity in an animal model of bacterial endophthalmitis without impairing retinal cell viability. Our results encourage further research for clinical use of chlorhexidine in treatment of bacterial endophthalmitis.