The present invention relates to an exosome for stimulating T cells and the pharmaceutical use thereof. Immune exosomes secreted from artificial antigen-presenting cells which express HLA, CD32, and co-stimulatory molecules CD32, CD80, CD83, and 4-1BBL are used to stimulate naive CD8+ T cells whereby preventive and therapeutic effects on tumors, pathogen infections, or autoimmune diseases can be provided.

The present application is related to a pharmaceutical composition a biphasic lipid vesicle comprising a lipid bilayer comprising vesicle forming lipids; an oil-in-water emulsion stabilized by one or more surfactants; one or more compounds; and one or more penetration enhancing agents. The one or more penetration enhancing agents include one or more non-ionic surfactants having a hydrophilic-lipophilic balance (HLB) of about 10 or less, alone or combination with one or more penetration enhancing agents selected from one or more of terpenes, alkaloids, salicylate derivatives, and polycationic surfactants and combinations thereof. The present application is also related to a pharmaceutical composition comprising a biphasic lipid vesicle comprising a lipid bilayer comprising vesicle forming lipids; an oil-in-water emulsion stabilized by one or more polycationic surfactants; and one or more compounds.

The present application is related to a pharmaceutical composition a biphasic lipid vesicle comprising a lipid bilayer comprising vesicle forming lipids; an oil-in-water emulsion stabilized by one or more surfactants; one or more compounds; and one or more penetration enhancing agents. The one or more penetration enhancing agents include one or more non-ionic surfactants having a hydrophilic-lipophilic balance (HLB) of about 10 or less, alone or combination with one or more penetration enhancing agents selected from one or more of terpenes, alkaloids, salicylate derivatives, and polycationic surfactants and combinations thereof. The present application is also related to a pharmaceutical composition comprising a biphasic lipid vesicle comprising a lipid bilayer comprising vesicle forming lipids; an oil-in-water emulsion stabilized by one or more polycationic surfactants; and one or more compounds.

The invention relates to novel nature-derived and synthetic active peptide- or peptide-derived agents designed for the cosmetic treatment of the human skin, as well to cosmetic formulations and compositions containing them. The active agents are effective in restoring, promoting and maintaining a healthy skin. In particular, the invention discloses combinations or sets of said skin effective agents including stem-cell factors that modulate the skin micromilieu and modulate skin stem cell behaviour, thereby effectively healing, regenerating and improving the state of aged or damaged skin.

The invention relates to novel nature-derived and synthetic active peptide- or peptide-derived agents designed for the cosmetic treatment of the human skin, as well to cosmetic formulations and compositions containing them. The active agents are effective in restoring, promoting and maintaining a healthy skin. In particular, the invention discloses combinations or sets of said skin effective agents including stem-cell factors that modulate the skin micromilieu and modulate skin stem cell behaviour, thereby effectively healing, regenerating and improving the state of aged or damaged skin.

The present invention provides a method for producing lipid particles that have a desired particle diameter, the method comprising: (A) a step for preparing, in a first mixing region, a primary dilution by mixing a first solution containing a lipid and an alcohol with a second solution containing water; (B) a step for feeding the primary dilution from the first mixing region to a second mixing region through a liquid feed pipe within a prescribed time; and (C) a step for preparing a secondary dilution by mixing the primary dilution with a third solution containing water in the second mixing region, wherein the steps (A)-(C) are continuously carried out, and the particle diameter of the lipid particles is controlled by adjusting at least one condition selected from the group consisting of the concentration of the alcohol and the concentration of the lipid in the primary dilution, the prescribed time, and the temperature during mixing.

A method for obtaining a collagen peptide from a starfish, an elastic liposome containing a starfish-derived collagen peptide, and a cosmetic composition containing the same are disclosed. Methods of using the collagen peptide or the elastic liposome are disclosed. The collagen peptide obtained from a starfish has excellent skin absorption rate and having anti-oxidation and wrinkle-improving activity. Thus, the collagen peptide may replace existing animal collagen to provide collagen with high extraction efficiency.

A method for obtaining a collagen peptide from a starfish, an elastic liposome containing a starfish-derived collagen peptide, and a cosmetic composition containing the same are disclosed. Methods of using the collagen peptide or the elastic liposome are disclosed. The collagen peptide obtained from a starfish has excellent skin absorption rate and having anti-oxidation and wrinkle-improving activity. Thus, the collagen peptide may replace existing animal collagen to provide collagen with high extraction efficiency.

The present disclosure provides compositions suitable for delivering lipophilic bioactive agents. The compositions may be utilized to treat numerous diseases and conditions that would benefit from the application of a lipophilic bioactive agent.

The present disclosure provides compositions suitable for delivering lipophilic bioactive agents. The compositions may be utilized to treat numerous diseases and conditions that would benefit from the application of a lipophilic bioactive agent.