Safety of Intracameral Injection of Minimal Bactericidal Concentration of Povidone Iodine on the Corneal Endothelium

Rania S ElKitkat1, Weam M Ebeid, Eman K Habib

  • 1Departments of *Ophthalmology; and †Anatomy and Embryology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

Cornea
|November 12, 2015
PubMed
Abstract

Insights

Intracameral injection of minimum bactericidal concentration (MBC) of povidone iodine (PI) showed toxicity to rabbit corneal endothelium. However, complete healing occurred within two weeks, suggesting potential for future research in endophthalmitis prophylaxis.

Area of Science:

  • Ophthalmology
  • Microbiology
  • Toxicology

Background:

  • Postoperative endophthalmitis is a severe complication following intraocular surgery.
  • Povidone-iodine (PI) is commonly used for surface antisepsis, but its intracameral safety is not well-established.
  • Minimum bactericidal concentration (MBC) of PI is proposed for endophthalmitis prophylaxis.

Purpose of the Study:

  • To evaluate the safety of intracameral injection of MBC of PI on corneal endothelium.
  • To assess the regenerative capacity of the corneal endothelium after PI exposure.
  • To investigate PI's potential as an endophthalmitis prophylactic agent.

Main Methods:

  • 32 New Zealand white rabbits were used.
  • Intracameral injections of 0.25% PI or saline were administered.
  • Corneal endothelium was examined via slit-lamp, pachymetry, and histopathology at intervals.

Main Results:

  • 0.25% PI caused corneal edema, increased thickness, and histopathological damage on day 1.
  • Signs of healing were observed by day 7.
  • Corneal edema subsided and thickness normalized by day 14, indicating significant regeneration.

Conclusions:

  • MBC (0.25%) of PI is toxic to rabbit corneal endothelium but demonstrates progressive regeneration and complete healing within 2 weeks.
  • This is the first study to use MBC of PI in intracameral injection trials.
  • Further primate studies are recommended to assess endothelial healing in a more human-comparable model.

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