Liposome composition for treating acne, containing conjugate of lysophosphatidylcholine and chlorin e6
A liposome composition, a technology for lysolecithin, which is applied in the field of liposome compositions for treating acne containing a conjugate of lysolecithin and chlorin e6, and can solve unsuccessful use cases, etc. problem, to achieve the effect of treating acne
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preparation example
[0037] Preparation Example: Preparation of LPC-Ce6
[0038] 10 mg of lysophosphatidylcholine (L-α-lysophosphatidylcholine) was dissolved in 10 ml of anhydrous dichloromethane (anhydrous dichloromethane), and 10 mg of chlorin e6 (Ce6), 5.35 mg of N,N '-Dicyclohexylcarbodiimide (N,N'-dicyclohexylcarbodiimide, DCC) and 5.35 mg of 4-dimethylaminopyridine (4-dimethylaminopyridine: DMAP) were added to 10 ml of anhydrous dichloromethane, and stirred 4 hours. Then, the chlorin e6 solution dissolved in anhydrous dichloromethane was mixed with the lysolecithin solution dissolved in anhydrous dichloromethane, and reacted at normal temperature for 48 hours. After the reaction, after evaporation of anhydrous dichloromethane under evapration at 40°C for 30 minutes, the prepared conjugate was refrigerated at 4°C until use.
[0039] [Reaction 2]
[0040]
Embodiment 1
[0041] Embodiment 1: the preparation of the liposome composition containing LPC-Ce6
[0042] At 80°C, dissolve sucrose laurate, polyethylene glycol-5 brassicasterol, sunflower oil and medium chain triglycerides. Then, glycerin, purified water, sodium deoxycholate, and sodium stearyl glutamate were heated to 80° C. or higher, and added to the oil phase, followed by wetting at 100° C. for 1 hour. After cooling the mixture to 40°C, put LPC-Ce6 into it, emulsify it, and pass it through a high-pressure microemulsifier continuously at 1,000 bar 3 times, and then cooled and degassed to obtain a liposome composition.
[0043] Table 1
[0044]
Embodiment 2
[0049] Embodiment 2: Preparation of lotion containing liposomes
[0050] According to the composition in Table 3 below, a lotion containing the liposome of the present invention was prepared.
[0051] table 3
[0052]
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