摘要:
The present invention relates to a composition containing cells, cultured by adding 15-PGDH inhibitor to PGE2-expressing cells, or a culture thereof and a use thereof. More specifically, the present invention relates to: a pharmaceutical composition, containing cells, cultured by adding 15-PGDH inhibitor to PGE2-expressing cells, or a culture thereof, for the prevention or treatment of immunological diseases, inflammatory diseases, or wounds; a method for inhibiting an immune response, an inflammatory response, or wounds in a subject, the method comprising a step for administering the pharmaceutical composition, or the cells or the culture thereof, to the subject; a method for preparing an immunosuppressive agent, an antiinflammatory agent, or a wound healing agent, using the cells or the culture thereof; a method for preparing PGE2, the method comprising a step for adding a 15-PGDH inhibitor to PGE2-expressing cells, followed by culturing; an implant comprising PGE2-expressing cells and a 15-PGDH inhibitor; a method for preparing the implant; a complex comprising PGE2-expressing cells and a 15-PGDH inhibitor; and a culture obtained by adding a 15-PGDH inhibitor to PGE2-expressing cells.
摘要:
The present invention relates to a novel polyene compound similar to nystatin, a method for preparing the same, and an antifungal drug comprising the novel polyene compound as an active ingredient. Compared to nystatin comprising one sugar, NNP, which is the polyene compound similar to nystatin, displays 300 times higher solubility and ten times lower cytotoxicity while maintaining antifungal activity, and thus can be useful in developing a novel polyene antifungal agent having improved solubility and less toxicity in terms of pharmacokinetics.
摘要:
The present invention relates to a novel polyene compound similar to nystatin, a method for preparing the same, and an antifungal drug comprising the novel polyene compound as an active ingredient. Compared to nystatin comprising one sugar, NNP, which is the polyene compound similar to nystatin, displays 300 times higher solubility and ten times lower cytotoxicity while maintaining antifungal activity, and thus can be useful in developing a novel polyene antifungal agent having improved solubility and less toxicity in terms of pharmacokinetics.
摘要:
The present invention relates to a method of producing recombinant modified Staphylococcal toxin having improved stability, comprising the steps of preparing a modified toxin in which a specific amino acid sequence is substituted and a vector for expressing the modified toxin, and culturing E. coli transformed with the vector, and a use thereof for the vaccine.