Inhibitor for corneal epithelial cell death, inhibitor characterized by combining hyaluronic acid and flavin adenine dinucleotide
A corneal epithelial cell, flavin adenine technology, applied in the field of group, can solve the problems of undocumented corneal epithelial cell death, uninhibited death, unspecified corneal epithelial cell death, etc.
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[0088] [Pharmacological Test 1]
[0089] Before ultraviolet (UV-B) irradiation, corneal epithelial cells were treated with the agent of the present invention. In this case, it was evaluated whether the decrease in the number of viable cells caused by ultraviolet irradiation was suppressed.
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[0091] SV40 immortalized human corneal epithelial cells (HCE-T: Institute of Physics and Chemistry, BioResource Center, CellNo.: RCB2280, the same in the examples below) were seeded on a 96-well plate (1×10 4 Pcs / well), cultured in DMEM / F-12 medium containing 10% FBS for 1 day. On the second day, replace the DMEM / F-12 medium containing 10% FBS with PBS containing 0.1% (w / v) sodium hyaluronate and 0.05% (w / v) flavin adenine dinucleoside Acid disodium salt, PBS containing 0.1% (w / v) sodium hyaluronate and 0.05% (w / v) flavin adenine dinucleotide disodium salt, or PBS containing no test substance ( Hereinafter, they are also referred to as “0.1% HA group”, “0.05% FAD group”, “0.1% HA / 0.05% FAD group” or “matrix group”). After that, UV-B irradiation (80mJ / cm 2 ) About 1 minute. After replacing the medium of each group with DMEM / F-12 medium, incubate at 37°C for 24 hours, and then use CellTiter96 (registered trademark) AQueous Single Solution Cell Proliferation Assay (Promega Compa...
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