Abstract

Barded-Biedl syndrome (BBS) is a rare genetic disorder with an unmet medical need for retinal degeneration. Small-molecule drugs were previously identified to slow down the apoptosis of photoreceptors in BBS mouse models. Clinical translation was not practical due to the necessity of repetitive invasive intravitreal injections for pediatric populations. Non-invasive methods of retinal drug targeting are a prerequisite for acceptable adaptation to the targeted pediatric patient population. Here, we present the development and functional testing of a non-invasive, topical, magnetically assisted delivery system, harnessing the ability of magnetic nanoparticles (MNPs) to cargo two drugs (guanabenz and valproic acid) with anti-unfolded protein response (UPR) properties towards the retina. Using magnetic resonance imaging (MRI), we showed the MNPs’ presence in the retina of Bbs wild-type mice, and their photoreceptor localization was validated using transmission electron microscopy (TEM). Subsequent electroretinogram recordings (ERGs) demonstrated that we achieved beneficial biological effects with the magnetically assisted treatment translating the maintained light detection in Bbs−/− mice (KO). To our knowledge, this is the first demonstration of efficient magnetic drug targeting in the photoreceptors in vivo after topical administration. This non-invasive, needle-free technology expands the application of SMDs for the treatment of a vast spectrum of retinal degenerations and other ocular diseases.

Highlights

  • The non-invasive, targeted delivery of therapeutic agents to the retina is utterly challenging

  • We studied the eyes of three different mice per group

  • We investigated the impact of various magnetic nanoparticles (MNPs) parameters: the type of coating, electrostatic charge, hydrodynamic size, and polydispersity index (PDI) (Table 1)

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Summary

Introduction

The non-invasive, targeted delivery of therapeutic agents to the retina is utterly challenging. Millions of patients are treated with this invasive and unpleasant method every year, intraocular injection involves rare but serious risks for the patient’s sight [3,4,5], such as retinal detachment, vitreal haemorrhage, endophthalmitis, cataracts and others. Owing to these reasons, the treatment of pediatric retinopathy patients with repeated intraocular injections is considered ethically unacceptable

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