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Effects of different formulations of mitoxantrone (solutions, nanospheres, liposomes) on glaucoma surgery in rabbits

P Tilleul1, P Denis, F Maignen

  • 1Department of Pharmacy, St.-Antoine Hospital, Paris, France.

Ophthalmic Research
|January 1, 1997
PubMed

Insights

Liposomes carrying mitoxantrone effectively reduced intraocular pressure after glaucoma surgery in rabbits, similar to mitomycin-C. Nanospheres were ineffective, and liposomes also reduced corneal opacity compared to mitoxantrone solutions.

Area of Science:

  • Ophthalmology
  • Pharmacology
  • Biotechnology

Background:

  • Glaucoma filtration surgery aims to reduce intraocular pressure (IOP).
  • Fibroblastic proliferation can impede surgical success.
  • Antimitotic agents are explored to prevent fibroblastic proliferation, but comparative data on formulations are limited.

Purpose of the Study:

  • To compare the efficacy of mitoxantrone (MTO) in different formulations (liposomes, nanospheres, solution) in controlling IOP after glaucoma filtration surgery.
  • To evaluate the effect of MTO formulations on post-surgical complications like corneal opacity.

Main Methods:

  • Rabbits underwent sclerectomy (a type of glaucoma filtration surgery).
  • Mitoxantrone (MTO) was administered via subconjunctival injection in solution, liposome, or nanosphere formulations before or after surgery.
  • Intraocular pressure (IOP) was monitored, and corneal opacity was assessed.

Main Results:

  • Subconjunctival MTO in solution and liposome formulations, administered post-surgery, significantly reduced IOP, comparable to mitomycin-C.
  • Pre-operative administration or subconjunctival nanosphere injections of MTO did not reduce IOP.
  • Liposome formulation of MTO reduced corneal opacity compared to MTO in solution.

Conclusions:

  • Subconjunctival liposomal mitoxantrone is a promising formulation for managing IOP after glaucoma filtration surgery.
  • Liposomal delivery of MTO offers a potential advantage by reducing corneal opacity compared to MTO solution.
  • Nanoparticle formulations require further investigation for efficacy in this context.

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