Vitreous concentration of triamcinolone acetonide after a single transseptal depot injection

Ocul Immunol Inflamm. 2009 May-Jun;17(3):216-20. doi: 10.1080/09273940802687838.

Abstract

Purpose: To determine vitreous concentrations of triamcinolone acetonide(TA) following transseptal injection.

Methods: TA (40 mg/l ml) was administered at varying intervals prior to vitrectomy. Vitreous samples from 18 patients were obtained. TA concentrations were quantified using HPLC-MS.

Results: Vitreous levels of TA were detected in all samples (range 0.64-168.0 ng/ml). The interval from injection to sampling ranged from 0.5-20 days. Tmax was attained at 0.5 days. TA concentrations were negatively correlated with scleral thickness (P = 0.0184) and depot location (P = 0.0230) but not with PVD status (P = 0.9633).

Conclusion: Significant vitreous concentrations of TA are achieved after a single transseptal injection. Scleral thickness, depot location and time influence vitreous TA levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Biological Availability
  • Chromatography, High Pressure Liquid
  • Female
  • Glucocorticoids / pharmacokinetics*
  • Humans
  • Injections
  • Male
  • Middle Aged
  • Orbit
  • Triamcinolone Acetonide / pharmacokinetics*
  • Vitreous Body / metabolism*

Substances

  • Glucocorticoids
  • Triamcinolone Acetonide