Development of a topical tissue cross-linking solution using sodium hydroxymethylglycinate (SMG): viscosity effect

• Published in: Bioscience reports Vol. 40; no. 1
• Main Authors: Mehta, Jaya, Takaoka, Anna, Zyablitskaya, Mariya, Nagasaki, Takayuki, Paik, David C
• Format: Journal Article
• Language: English
• Published: England Portland Press Ltd 31-01-2020
• Subjects: Biochemical Techniques & Resources; Pharmacology & Toxicology; Therapeutics & Molecular Medicine; sodium hydroxymethylglycinate; Cornea; formaldehyde releaser; Tissue cross-linking; Sclera
• ISSN: 0144-8463; 1573-4935
• DOI: 10.1042/BSR20191941

Hyperviscosity agents are commonly used in ophthalmic formulations for improving corneal drug penetration by increasing tissue contact time. One such viscosity agent is hydroxypropyl methylcellulose (HPMC). HPMC has been used in riboflavin solutions for photochemical UVA cross-linking (CXL). Sodium hydroxymethylglycinate (SMG) is a small molecule formaldehyde releaser that can function as a therapeutic tissue cross-linker for corneal and scleral applications. The present study was undertaken in order to study formulation factors using HPMC and SMG that could positively influence the cross-linking effect in these ocular tissues. Formulations containing 10 mM SMG and 100 mM sodium bicarbonate were prepared with varying HPMC concentrations from 0 to 4.4%. Their cross-linking effects on porcine and rabbit eyes were measured using differential scanning calorimetry (DSC), expressed as the change/difference in melting temperature (ΔTm) compared with the control. SMG in 4.4% HPMC solution resulted in ΔTm of 6.3 ± 1.21, while other concentration showed no differences in Tm shift on porcine cornea. In ex vivo rabbit cornea, there was a trend toward an increasing cross-linking effect with higher viscosity albeit mild differences. While a significant Tm shift was observed in porcine and rabbit sclera, there was no difference in effect of cross-linking between four HPMC concentrations. Increasing the HPMC concentration does not negatively affect the cross-linking efficacy attributed by SMG and could still be a positive cross-linking enhancer by virtue of increasing tissue contact time in a dynamic biological system. This information will be useful for planning further animal and human studies.