Pharmaceutical composition containing spirulina maxima extract as active ingredient for preventing and treating retinal diseases
A technology for retinal diseases, Spirulina maxima, applied in the field of pharmaceutical compositions for the prevention and treatment of retinal diseases containing extracts of Spirulina maxima as active ingredients, capable of solving blindness, neurons not working normally, neurasthenia And other issues
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Embodiment 1
[0080] Example 1: Preparation of Spirulina maxima extract
[0081] Spirulina maxima (Korea Marine Microalgae Cultivation Center registration number: KMMCC-1057) comes from the Korean Marine Microalgae Cultivation Center of the Ministry of Marine Biological Materials and Aquaculture, South Korea, and Pukyung University.
[0082] Specifically, the cultivated Spirulina maxima was centrifuged at 3000 rpm for 25 minutes in a multi-tube carrier refrigerated centrifuge (Vision Scientific CO. Ltd). The separated cells were briefly washed with 1.0% NaCl solution and then centrifuged again. The obtained cells were freeze-dried and used as a sample for phycocyanin extraction. The extraction was performed as follows: 10 mL of 0.1 M phosphate buffer (pH 7.0) was added to 40 mg of freeze-dried sample, and then vortexed for 15 minutes. The supernatant was obtained by centrifugation (3500 rpm, 5 minutes), which was used as an extract of Spirulina maxima.
Embodiment 2
[0083] Example 2: Preparation of allophycocyanin, R-phycoerythrin and C-phycocyanin
[0084] Allophycocyanin (A7472), R-phycoerythrin (P6161) and C-phycocyanin were purchased from Sigma-Aldrich, and they were supplied at 4mg / ml, 10mg / ml and 1mg / ml, respectively The concentration of preparation.
Embodiment 3
[0085] Example 3: Cell culture
[0086] The human adult ARPE cells (ARPE-19: catalog number CRL-2302) used in the experiments and analyses of the present invention were from the Vision Science Research Center of the Catholic University of Korea. Put the above ARPE cells in DMEM supplemented with 10% FBS, 100U / ml penicillin and 100mg / ml streptomycin, and in 5% CO 2 , Cultivate in an incubator at 37°C. Divide the cells to 5 cells or less 4 The density of cells / well was seeded in 6-well plates for further experiments.
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