# Sustained cysteamine delivery by nanobarrier contact lenses to replace 8xdaily drops with a daily disposable lens

> **NIH NIH R43** · DIOPTER TECHNOLOGIES, INC. · 2024 · $332,179

## Abstract

Cystinosis is a metabolic disease caused by mutations in CTNS gene and characterized by loss of the cystine efflux pathway
in lysosomes resulting in accumulation of cystine crystals in many organs including kidneys and cornea. Cystinosis patients
begin showing ocular symptoms at the age of 16 months and without appropriate treatment, the entire peripheral stroma and
endothelium can be packed with crystals. By the age of 10 years, patients develop photophobia and eventually complications
such as corneal scars can occur resulting in irreversible damage to the eye. Cysteamine (β-mercaptoethylamine) treats the
disease by reacting with intra-lysosomal cystine to produce mixed disulfide cysteine-cysteamine dimers. The oral dose of
cysteamine achieves therapeutic effects in several organs but its concentration in cornea is inadequate and thus cysteamine
eye drops (CYSTARAN® 0.44%, 8 times daily), are utilized for treating the ocular complications of cystinosis. The 8x
daily delivery of eye drops is difficult for patients and can lead to poor compliance. Additionally, the eye drops contain
preservative benzalkonium chloride which can cause toxicity due to significant exposure from 8 drops daily. The
formulations also cause side effects including burning, redness, and blurred vision due to the acidic pH which is required to
maintain stability of cysteamine. Any exposure to oxygen leads to rapid oxidation of cysteamine to the inactive cystamine,
and thus eye drop bottles are shipped frozen. The oxidation, however, begins after the bottles are thawed and opened for
use, which reduces efficacy. Our goal is to develop contact lenses that can be worn continuously for 8-hours or longer if
vision correction is also needed, to deliver the same amount of drug to the cornea as eight drops a day therapy. Contact
lenses are ideal for treating cystinosis because a higher fraction of drug loaded in the lenses reaches cornea compared to
drops. Additionally, the lenses will be single use daily disposable and thus there will be no need for preservatives. We are
formulating our lenses at neutral pH which will eliminate the discomfort from low pH of the eye drop formulation. Sustained
delivery of cysteamine is challenging from contact lenses due to the low molecular weight. The drug diffuses rapidly in a
few minutes from commercial contact lenses. We have addressed this limitation by developing a patented nanobarrier
technology which increases the release duration from a few minutes to about 2-8 hours for several drugs depending on the
loading of vitamin E nanobarriers in the lenses. Preliminary data shows 2-4 hours sustained release of cysteamine in vitro
and in vivo with 20% vitamin E lenses, and efficacy in dissolving crystals in ex vivo cadaver eyes. The pharmacokinetic
studies in rabbits show that one lens can deliver sufficient drug to match the 7 drops, so about 15% increase in dose is
required. This proposal focuses on GMP manufacturing and one-year potency testing ...

## Key facts

- **NIH application ID:** 10931847
- **Project number:** 1R43EY036347-01
- **Recipient organization:** DIOPTER TECHNOLOGIES, INC.
- **Principal Investigator:** Chris Adams
- **Activity code:** R43 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $332,179
- **Award type:** 1
- **Project period:** 2024-09-01 → 2026-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10931847

## Citation

> US National Institutes of Health, RePORTER application 10931847, Sustained cysteamine delivery by nanobarrier contact lenses to replace 8xdaily drops with a daily disposable lens (1R43EY036347-01). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/10931847. Licensed CC0.

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