Challenges and Advances in Magnetic Nanoparticle-Guided Delivery of Cultured Human Corneal Endothelial Cells—A Review

Author:

Vilkelyte Virginija1,Thompson Polly2ORCID,Coelho Maria1,Woronkowicz Małgorzata34ORCID,Skopinski Piotr56,Roberts Harry12

Affiliation:

1. University of Exeter Medical School, St Luke’s Campus, University of Exeter, Exeter EX1 2HZ, UK

2. West of England Eye Unit, Royal Devon University Healthcare NHS Foundation Trust, Exeter EX2 5DW, UK

3. NDDH, Royal Devon University Healthcare NHS Foundation Trust, Barnstaple EX31 4JB, UK

4. Moorfields Eye Hospital NHS Foundation Trust, 162 City Road, London EC1V 2PD, UK

5. Department of Ophthalmology, SPKSO Ophthalmic University Hospital, Medical University of Warsaw, 00-576 Warsaw, Poland

6. Department of Histology and Embryology, Medical University of Warsaw, 02-004 Warsaw, Poland

Abstract

The cornea relies on a healthy endothelium to maintain transparency, and damage to endothelial cells can result in corneal oedema and vision loss. Current treatments, which often involve the use of donor corneas, face significant limitations due to a shortage of donor tissue. Although human corneal endothelial cells (HCECs) can be cultured and transplanted, their low attachment rates limit the effectiveness of these treatments. In this review, we examined studies that explore the use of magnetic nanoparticles (MNPs) to enhance the attachment of HCECs to the cornea. We evaluated the effectiveness, cell viability, and safety of this approach. Findings indicate that MNPs facilitate the targeted delivery of HCECs under a magnetic field, resulting in improved corneal clarity and reduced oedema in animal models. Cell viability remained high, and no significant safety concerns were identified. MNPs present a promising strategy to enhance HCEC transplantation. However, further research, including ongoing clinical trials, is necessary to confirm the safety and efficacy of this approach before it can be adopted for widespread clinical use.

Publisher

MDPI AG

Reference106 articles.

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