A single intravenous injection of cyclosporin A–loaded lipid nanocapsules prevents retinopathy of prematurity

Author:

Bohley Marilena1ORCID,Dillinger Andrea E.2,Schweda Frank3,Ohlmann Andreas4,Braunger Barbara M.5,Tamm Ernst R.2ORCID,Goepferich Achim1ORCID

Affiliation:

1. Department of Pharmaceutical Technology, University of Regensburg, 93053 Regensburg, Germany.

2. Department of Human Anatomy and Embryology, University of Regensburg, 93053 Regensburg, Germany.

3. Department of Physiology, University of Regensburg, 93053 Regensburg, Germany.

4. Department of Ophthalmology, Munich University Hospital, Ludwig-Maximilians-University Munich, 80336 Munich, Germany.

5. Institute of Anatomy and Cell Biology, Julius-Maximilians-University of Wuerzburg, 97070 Wuerzburg, Germany.

Abstract

Retinopathy of prematurity (ROP) is a retinal disease that threatens the vision of prematurely born infants. Severe visual impairment up to complete blindness is caused by neovascularization and inflammation, progressively destroying the immature retina. ROP primarily affects newborns in middle- and low-income countries with limited access to current standard treatments such as intraocular drug injections and laser- or cryotherapy. To overcome these limitations, we developed a nanotherapeutic that effectively prevents ROP development with one simple intravenous injection. Its lipid nanocapsules transport the antiangiogenic and anti-inflammatory cyclosporin A efficiently into disease-driving retinal pigment epithelium cells. In a mouse model of ROP, a single intravenous injection of the nanotherapeutic prevented ROP and led to normal retinal development by counteracting neovascularization and inflammation. This nanotherapeutic approach has the potential to bring about a change of paradigm in ROP therapy and prevent millions of preterm born infants from developing ROP.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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