Abstract

Retinopathy leads to irreparable vision loss via capillary closure and areas of nonperfusion. However, the current instillation systems do not allow a sufficient amount of drug required to treat retinopathy to reach the posterior segment (retina); therefore, a new formulation targeting the posterior segment is expected as therapy for retinopathy. We prepared ophthalmic formulations containing nilvadipine nanoparticles (NILnano), and demonstrated whether the instillation of NILnano can prevent retinal dysfunction in rats injected with excessive streptozotocin (STZ rats) in this study. NILnano (mean particle size, 77 nm) was prepared by wet bead mill treatment, with the inclusion of various additives (2-hydroxypropyl-β-cyclodextrin, benzalkonium chloride, d-mannitol, and methylcellulose). Retinal dysfunction was observable two weeks after rats received intraperitoneal injections of streptozotocin (100 mg/kg × 2, consecutive days, STZ rat). Changes in retinal function were evaluated by electroretinogram (ERG) and immunological methods. The retinal thickness, measured as the distance between the ganglion cell layer and the distal border of the outer nuclear layer, increased two weeks after the injection of streptozotocin, resulting in decreases in the levels of a-waves, b-waves, and oscillatory potential amplitudes in ERG of rats. The instillation of NILnano allowed the topical supplement of nilvadipine into the retina, and repeated instillation of NILnano (2 times/day) attenuated the retinal disorders led by the excessive streptozotocin. In conclusion, we found that retinal dysfunction in rats injected with streptozotocin can be prevented by the NILnano instillation. These results are useful in further studies aimed at the therapeutic treatment of retinopathy.

Highlights

  • Retinopathy comprises diseases in the posterior segment, such as glaucoma, diabetic macular edema, diabetic retinopathy, age-related macular degeneration, and proliferative vitreoretinopathy, and leads to irreparable vision loss

  • No aggregation or precipitation of NIL nanoparticles was observed for nilvadipine nanoparticles (NILnano)

  • The NIL content in the right retina of STZ rats instilled with NILnano was approximately 3.4-fold higher than that in the left retina

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Summary

Introduction

Retinopathy comprises diseases in the posterior segment, such as glaucoma, diabetic macular edema, diabetic retinopathy, age-related macular degeneration, and proliferative vitreoretinopathy, and leads to irreparable vision loss. The corneal epithelium acts as a barrier, and metabolism of drugs by anterior segment enzymes is related to the bioavailability of topically administered agents. The amount of drug reaching the aqueous humor is only about 1% of the drug administered [1,2]. In the case of systemic administration, the blood–retinal barrier, inhibits the movement of systemically administered drugs to the retina. It is necessary to administer high doses for delivery into the retina, which results in potentially serious toxicity and unwanted side effects. Within this context, the development of a drug delivery system to the posterior segment is greatly anticipated

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