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Diffusion of protein through the human cornea
Resmi A Charalel1, Kristin Engberg, Jaan Noolandi
1Department of Ophthalmology, Byers Eye Institute at Stanford, Stanford, Calif., USA.
Ophthalmic Research
|March 9, 2012
Summary
The human cornea allows passive diffusion of proteins up to 7.2 nm, including bovine serum albumin (BSA). This finding has implications for drug delivery and artificial cornea development.
Area of Science:
- Biomedical Engineering
- Ophthalmology
- Pharmacology
Background:
- The human cornea acts as a barrier, influencing drug delivery to the anterior eye.
- Understanding protein diffusion across the cornea is crucial for developing novel ophthalmic therapies and artificial cornea technologies.
Purpose of the Study:
- To quantify the diffusion rates of myoglobin (4.4 nm) and bovine serum albumin (BSA, 7.2 nm) through ex vivo human corneas.
- To assess the potential for passive diffusion of larger molecules across the corneal barrier.
Main Methods:
- Diffusion coefficients were measured using a diffusion chamber with ex vivo human corneas separating protein solutions from balanced salt solution.
- Protein concentrations were monitored over time, and diffusion coefficients were calculated using Fick's law and conservation of mass principles.
Main Results:
- The diffusion coefficient for myoglobin was determined to be 5.5 ± 0.9 × 10(-8) cm(2)/s.
- The diffusion coefficient for BSA was found to be 3.1 ± 1.0 × 10(-8) cm(2)/s.
Conclusions:
- The human cornea permits passive diffusion of molecules as large as 7.2 nm (BSA).
- These findings suggest potential for enhanced corneal drug delivery and inform the design of artificial corneas.
- Further research is necessary to explore the full extent of corneal diffusion and its clinical applications.
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