Inhibitor of corneal epithelial cell death characterized by a combination of hyaluronic acid and flavin adenine dinucleotide
A corneal epithelial cell and flavin adenine technology is applied in the field of an inhibitor of corneal epithelial cell death which is characterized by a combination of hyaluronic acid and flavin adenine dinucleotide, and can solve the problem of undocumented corneal epithelial cells. 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, and in this case, whether the decrease in the number of living cells caused by ultraviolet irradiation was suppressed was evaluated.
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[0091] SV40 immortalized human corneal epithelial cells (HCE-T: RIKEN, BioResourceCenter, CellNo.: RCB2280, the same as in Examples) were seeded in 96-well plates (1×10 4 cells / well), cultured in DMEM / F-12 medium containing 10% FBS for 1 day. The next day, replace the DMEM / F-12 medium containing 10% FBS with PBS containing 0.1% (w / v) sodium hyaluronate, 0.05% (w / v) flavin adenine dinucleoside PBS containing 0.1% (w / v) sodium hyaluronate and 0.05% (w / v) flavin adenine dinucleotide disodium salt, or PBS without the 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", respectively). Afterwards, the corneal epithelial cells were irradiated with UV-B (80mJ / cm 2 ) for about 1 minute. After the culture medium of each group was replaced with DMEM / F-12 medium, cultured at 37°C for 24 hours, thereafter, CellTiter96 (registered trademark) AQueous One Solution Cell Proliferation Assay (Aqueous One So...
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