[In vitro corneal endothelial damage caused by intraocular lenses of PMMA, silicone and polyhema]

Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|January 1, 1989
PubMed

Insights

Polymethyl methacrylate (PMMA) intraocular lenses (IOLs) caused significantly more corneal endothelial damage than silicone or polyhema IOLs in pig eyes. Contact time did not influence damage levels between materials.

Area of Science:

  • Ophthalmology
  • Biomaterials Science
  • Corneal Research

Background:

  • Intraocular lenses (IOLs) are crucial in cataract surgery.
  • Understanding the biocompatibility of different IOL materials is essential for patient outcomes.
  • Corneal endothelial cell damage can lead to vision impairment.

Purpose of the Study:

  • To compare the endothelial damage caused by polymethyl methacrylate (PMMA), silicone, and polyhema IOLs.
  • To evaluate the effect of contact time on IOL-induced endothelial damage.
  • To assess the morphological changes in the corneal endothelium upon contact with IOLs.

Main Methods:

  • Freshly excised pig corneas (n=156) were exposed to PMMA, silicone, and polyhema IOLs.
  • Contact times included 15 seconds, 1 minute, and 30 minutes.
  • Endothelial damage was quantified using Janus green vital staining and scanning electron microscopy.

Main Results:

  • PMMA IOLs caused the most significant endothelial damage (7.6%–19.7%), followed by silicone (4.8%–10.2%) and polyhema (4.6%–8.3%).
  • Damage was statistically significant compared to control groups across all materials and contact times (P<0.01).
  • No significant difference in damage was observed between silicone and polyhema IOLs, but both were significantly less damaging than PMMA.

Conclusions:

  • PMMA IOLs pose a higher risk of corneal endothelial damage compared to silicone and polyhema IOLs.
  • The choice of IOL material is a critical factor in minimizing post-operative corneal complications.
  • Further research may explore modifications to PMMA or alternative materials to reduce endothelial toxicity.

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