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Ocular surface distribution and pharmacokinetics of a novel ophthalmic 1% azithromycin formulation.

Journal articles  - Journal Article
Akpek, EK; Vittitow, J; Verhoeven, RS; Brubaker, K; Amar, T; Powell, KD; Boyer, JL; Crean, C
Published in: J Ocul Pharmacol Ther
October 2009

PURPOSE: To investigate the ocular distribution of 1% azithromycin ophthalmic solution and the effect of polycarbophil-based mucoadhesive formulation on ocular tissue levels of azithromycin after single and multiple topical administrations in the rabbit eye. METHODS: Rabbits were treated with either a single administration of 1% azithromycin solution with or without polycarbophil, or with multiple administrations of 1% azithromycin solution in polycarbophil. Drug concentrations were measured using LC/MS/MS. Conjunctiva, cornea, aqueous humor, and tear samples were analyzed over a period of 144 h after a single administration of azithromycin with or without polycarbophil. Eyelid, conjunctiva, cornea, aqueous humor, and tear samples were collected over a period of 288 h during and after multiple administrations of azithromycin. RESULTS: Azithromycin was rapidly absorbed and distributed in the ocular tissues, reaching within 5 min, concentrations of 10,539 microg/mL in tear film, 108 microg/g in conjunctiva, and 40 microg/g in the cornea. The drug demonstrated tissue-specific half-lives of 15, 63, and 67 h, respectively. Following multiple administrations, the drug gradually accumulated. The polycarbophil formulation increased the bioavailability of the drug, producing peak concentrations that were between 5- and 12-fold higher than those without polycarbophil. Azithromycin also distributed rapidly in the eyelids, reaching peak concentrations of 180 mug/g at the end of the 7-day treatment, and was eliminated with a half-life of 125 h. Six days after treatment was discontinued, eyelid levels of azithromycin were above 40 microg/g. CONCLUSIONS: Sustained and high concentrations were encountered with 7-day approved administration of 1% azithromycin formulation (AzaSite, Inspire Pharmaceuticals, Inc., Durham, NC) within all ocular surface tissues, particularly the lids. Many ocular surface disorders involving the tear film, eyelids, and adnexal structures are associated with chronic, low-grade bacterial infection and may potentially lead to decreased vision secondary to corneal scarring. Various topical antibiotic and steroid combinations with or without oral tetracyclines are commonly used with variable clinical response and known potential side effects. The clinical relevance of this study is unknown; however, the long-lasting antibacterial and additional anti-inflammatory properties of topical azithromycin might offer an effective alternative treatment option and should be explored further in clinical studies.

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Published In

J Ocul Pharmacol Ther

DOI

EISSN

1557-7732

Publication Date

October 2009

Volume

25

Issue

5

Start / End Page

433 / 439

Location

United States

Related Subject Headings

  • Tissue Distribution
  • Tears
  • Rabbits
  • Ophthalmology & Optometry
  • Ophthalmic Solutions
  • Mass Spectrometry
  • Half-Life
  • Drug Carriers
  • Cornea
  • Conjunctiva
 

Citation

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Akpek, E. K., Vittitow, J., Verhoeven, R. S., Brubaker, K., Amar, T., Powell, K. D., … Crean, C. (2009). Ocular surface distribution and pharmacokinetics of a novel ophthalmic 1% azithromycin formulation. J Ocul Pharmacol Ther, 25(5), 433–439. https://doi.org/10.1089/jop.2009.0026
Akpek, Esen Karamursel, Jason Vittitow, Rozemarijn S. Verhoeven, Kurt Brubaker, Thierry Amar, Kendall D. Powell, José L. Boyer, and Christopher Crean. “Ocular surface distribution and pharmacokinetics of a novel ophthalmic 1% azithromycin formulation.J Ocul Pharmacol Ther 25, no. 5 (October 2009): 433–39. https://doi.org/10.1089/jop.2009.0026.
Akpek EK, Vittitow J, Verhoeven RS, Brubaker K, Amar T, Powell KD, et al. Ocular surface distribution and pharmacokinetics of a novel ophthalmic 1% azithromycin formulation. J Ocul Pharmacol Ther. 2009 Oct;25(5):433–9.
Akpek, Esen Karamursel, et al. “Ocular surface distribution and pharmacokinetics of a novel ophthalmic 1% azithromycin formulation.J Ocul Pharmacol Ther, vol. 25, no. 5, Oct. 2009, pp. 433–39. Pubmed, doi:10.1089/jop.2009.0026.
Akpek EK, Vittitow J, Verhoeven RS, Brubaker K, Amar T, Powell KD, Boyer JL, Crean C. Ocular surface distribution and pharmacokinetics of a novel ophthalmic 1% azithromycin formulation. J Ocul Pharmacol Ther. 2009 Oct;25(5):433–439.
Journal cover image

Published In

J Ocul Pharmacol Ther

DOI

EISSN

1557-7732

Publication Date

October 2009

Volume

25

Issue

5

Start / End Page

433 / 439

Location

United States

Related Subject Headings

  • Tissue Distribution
  • Tears
  • Rabbits
  • Ophthalmology & Optometry
  • Ophthalmic Solutions
  • Mass Spectrometry
  • Half-Life
  • Drug Carriers
  • Cornea
  • Conjunctiva