Sustained release of brimonidine from BRI@SR@TPU implant for treatment of glaucoma

Drug Deliv. 2022 Dec;29(1):613-623. doi: 10.1080/10717544.2022.2039806.

Abstract

Glaucoma is the leading cause of irreversible vision loss worldwide, and reduction of intraocular pressure (IOP) is the only factor that can be interfered to delay disease progression. As the first line and preferred method to treat glaucoma, eye drops have many shortcomings, such as low bioavailability, poor patient compliance, and unsustainable therapeutic effect. In this study, a highly efficient brimonidine (BRI) silicone rubber implant (BRI@SR@TPU implant) has been designed, prepared, characterized, and administrated for sustained relief of IOP to treat glaucoma. The in vitro BRI release from BRI@SR@TPU implants shows a sustainable release profile for up to 35 d, with decreased burst release and increased immediate drug concentration. The carrier materials are not cytotoxic to human corneal epithelial cells and conjunctival epithelial cells, and show good biocompatibility, which can be safely administrated into rabbit's conjunctival sac. The BRI@SR@TPU implant sustainably released BRI and effectively reduced IOP for 18 d (72 times) compared to the commercial BRI eye drops (6 h). The BRI@SR@TPU implant is thus a promising noninvasive platform product for long-term IOP-reducing in patients with glaucoma and ocular hypertension.

Keywords: Sustained release; brimonidine; conjunctival sac implant; glaucoma; intraocular pressure (IOP).

MeSH terms

  • Animals
  • Antihypertensive Agents / administration & dosage
  • Antihypertensive Agents / adverse effects
  • Antihypertensive Agents / pharmacology*
  • Brimonidine Tartrate / administration & dosage
  • Brimonidine Tartrate / adverse effects
  • Brimonidine Tartrate / pharmacology*
  • Cell Line
  • Delayed-Action Preparations
  • Dose-Response Relationship, Drug
  • Drug Delivery Systems / methods*
  • Drug Implants
  • Drug Liberation
  • Glaucoma / pathology*
  • Humans
  • Intraocular Pressure / drug effects
  • Ophthalmic Solutions
  • Rabbits
  • Random Allocation
  • Silicones / chemistry

Substances

  • Antihypertensive Agents
  • Delayed-Action Preparations
  • Drug Implants
  • Ophthalmic Solutions
  • Silicones
  • Brimonidine Tartrate

Grants and funding

The authors acknowledge the support from the National Key Research and Development Program of China (2020YFA0112700), the State Key Program of National Natural Science Foundation of China (82030027), the Subject of Major Projects of National Natural Science Foundation of China (81790641), National Natural Science Foundation of China (81870630), the Scientific and Innovative Action Plan of Shanghai (19441900600), and the Natural Science Foundation of Shanghai (15ZR1405900, 19ZR1408300).