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Related Experiment Videos

Review: implants

P Ashton1, D L Blandford, P A Pearson

  • 1Department of Ophthalmology, Kentucky Clinic, University of Kentucky, Lexington.

Journal of Ocular Pharmacology
|January 1, 1994
PubMed
Summary
This summary is machine-generated.

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New implantable devices offer sustained drug delivery for chronic eye conditions like CMV retinitis and uveitis, potentially improving treatment control and reducing side effects.

Area of Science:

  • Ophthalmology
  • Biomaterials Science
  • Drug Delivery Systems

Background:

  • Chronic ocular disorders require long-term therapeutic interventions.
  • Current treatments for conditions like cytomegalovirus (CMV) retinitis and uveitis often involve frequent administration and can have significant side effects.
  • There is a need for advanced drug delivery systems to provide sustained and localized treatment within the eye.

Purpose of the Study:

  • To develop and evaluate an implantable sustained-release device for chronic eye disease treatment.
  • To assess the efficacy and duration of drug delivery for ganciclovir and cyclosporine A implants.
  • To investigate the potential of subconjunctival implants for maintaining ocular health.

Main Methods:

  • Development of a multi-layered implantable device with a drug core encased in permeable and impermeable polymers.

Related Experiment Videos

  • Subconjunctival or intravitreal implantation of devices loaded with ganciclovir for CMV retinitis and cyclosporine A for uveitis.
  • Monitoring of drug levels in the vitreous and assessment of therapeutic outcomes and intraocular pressure.
  • Main Results:

    • Ganciclovir implants maintained therapeutic vitreous drug levels for 8 months in patients with CMV retinitis, showing potential for better disease control and fewer side effects.
    • Cyclosporine A implants demonstrated sustained therapeutic vitreous levels for approximately 3 years in uveitis treatment studies.
    • Subconjunctival 5-fluorouracil (5-FU) implants maintained ocular filters in monkeys for 3 months and helped lower intraocular pressure in high-risk patients.

    Conclusions:

    • Implantable sustained-release devices offer a promising approach for managing chronic ocular diseases.
    • These devices can provide long-term, localized drug delivery, potentially improving patient outcomes and reducing systemic side effects.
    • Further research is ongoing to evaluate the full efficacy and toxicity profile of these novel ocular drug delivery systems.