A subconjunctival degradable implant for cyclosporine delivery in corneal transplant therapy

Curr Eye Res. 1995 Aug;14(8):659-67. doi: 10.3109/02713689508998493.

Abstract

The effect of local cyclosporine therapy upon corneal transplant survival was investigated. A high risk rabbit model with vascularized corneas was used to assess the efficacy of subconjunctivally implanted degradable devices for cyclosporine therapy. Animals were divided into four groups, receiving either no therapy, a placebo PLGA device, or drug containing devices implanted either at the time of transplantation or two weeks previous. The mean survival times of animals in the control and placebo groups were statistically equivalent (21 +/- 4 days vs 18 +/- 4 days). Devices containing CsA improved the survival time of grafts. Predosing the animals with CsA improved the survival time to 28 +/- 7 days, and CsA devices implanted at the time of transplantation increased the survival time to 35 +/- 7 days. The improvement in survival times was consistent with the in vitro drug release profiles. No systemic CsA was detected, suggesting that the effect may have been local. Histological assessment indicated that devices were well tolerated.

MeSH terms

  • Animals
  • Anterior Eye Segment / pathology
  • Biocompatible Materials
  • Biodegradation, Environmental
  • Conjunctiva
  • Cornea / drug effects
  • Cornea / pathology
  • Corneal Transplantation* / pathology
  • Cyclosporine / administration & dosage*
  • Drug Delivery Systems*
  • Drug Implants
  • Graft Rejection / pathology
  • Graft Rejection / prevention & control
  • Graft Survival / drug effects*
  • Lactic Acid*
  • Polyglycolic Acid*
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Polymers*
  • Rabbits

Substances

  • Biocompatible Materials
  • Drug Implants
  • Polymers
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Polyglycolic Acid
  • Lactic Acid
  • Cyclosporine