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In vitro and in vivo studies with sodium hyaluronate as a carrier for intraocular gentamicin

C A Moreira1, A T Moreira, D K Armstrong

  • 1Department of Ophthalmology, Doheny Eye Institute, Los Angeles, CA.

Acta Ophthalmologica
|February 11, 1991
PubMed

Insights

Sodium hyaluronate (SH) combined with gentamicin shows promise as an intraocular drug delivery system. This combination significantly reduced endophthalmitis incidence and prolonged drug half-life compared to aqueous gentamicin alone.

Area of Science:

  • Ophthalmology
  • Microbiology
  • Pharmacology

Background:

  • Endophthalmitis remains a significant risk following intraocular surgery.
  • Effective intraocular antibiotic delivery is crucial for preventing and treating post-operative infections.

Purpose of the Study:

  • To evaluate sodium hyaluronate (SH) as a carrier for gentamicin in treating intraocular infections.
  • To compare the efficacy of gentamicin/SH with aqueous gentamicin in a rabbit model of Pseudomonas aeruginosa endophthalmitis.

Main Methods:

  • In vitro determination of minimal inhibitory concentrations (MICs) of gentamicin/SH against Staphylococcus aureus, S. epidermidis, and P. aeruginosa.
  • Induction of endophthalmitis in rabbit eyes via P. aeruginosa inoculation after posterior capsulotomy.
  • Comparison of untreated eyes, eyes treated with aqueous gentamicin, and eyes treated with SH/gentamicin combination.

Main Results:

  • Gentamicin/SH demonstrated effective in vitro inhibition of pathogens.
  • SH/gentamicin significantly reduced endophthalmitis incidence (4/15 eyes) compared to aqueous gentamicin (10/15 eyes) and untreated controls (15/15 eyes).
  • The half-life of gentamicin was extended when formulated with SH (2.2 h) compared to aqueous administration (0.9 h).

Conclusions:

  • Sodium hyaluronate serves as an effective carrier for intraocular gentamicin delivery.
  • The SH/gentamicin combination offers improved therapeutic potential for managing intraocular infections.
  • Further investigation into SH as a drug delivery vehicle for ophthalmic applications is warranted.

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