SBIR/STTR Research Award

Non-Linear Optical femtosecond laser device to alter corneal curvature and stiffness.

Award identifier 4afdceb2ea24bc6e8eb2b72d3652e83eb092f8154c5ea8c33d2b0ca06c9d3762Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$255,671

Program and phase

SBIR · Phase I

Award year

2022

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
M2-COR, Inc.
Proposal award date
2022-03-01
Contract end date
2023-02-28
UEI
EEJ9JEJLM9V7
Solicitation number
PA20-260
Topic code
NEI

Research abstract

We have recently shown that photo-activation of riboflavin and mechanical stiffening of the cornea can be achieved using 760 nm infrared Femtosecond laser light through a two photon, nonlinear optical (NLO) process. The primary advantage of NLO over the existing technology is that cross linking occurs only within the two-photon focal volume of the FS laser light, providing precise control over the area, depth and geometry of the mechanically stiffened cornea that can be easily tailored to the patient's corneal topography. We have further patented an FS laser delivery system and shown that can vary the two-photon focal volume by changing the numerical aperture (NA) of the focusing lens to greatly expand the lateral and axial dimensions of the CXL region up to 150 μm of the corneal thickness. This greatly speeds up the NLO process, providing a more rapid procedure compared to that of standard treatments. We have also established that using regeneratively amplified FS laser pulses, mechanical stiffening of rabbit corneas can be achieved with an overall power of lt46.1 mW, below the ANSI thermal limits for laser exposure to the eye. Additionally, we have shown in a live rabbit model that our NLO CXL device can crosslink a 4 mm diameter central corneal region in 5 minutes and produce 1-2 diopters of corneal flattening. We have further developed an FS corneal epithelial micromachining method to enhance penetration of chemicals through the epithelium without producing epithelial damage before or after the procedure, thus avoiding the major adverse effects of standard protocols. With this novel technology now in hand, we are ready to develop a clinical prototype that will allow for the testing of this device to treat keratoconus and low degrees of myopia, hyperopia, presbyopia and astigmatism.

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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