CPC C12N 5/0665 (2013.01) [A61K 9/50 (2013.01); A61K 9/5068 (2013.01); A61K 31/713 (2013.01); A61K 35/28 (2013.01); A61K 38/179 (2013.01); A61K 41/10 (2020.01); A61K 41/17 (2020.01); C12N 5/0605 (2013.01); C12N 15/111 (2013.01); C12N 15/113 (2013.01); A61P 9/00 (2018.01); A61P 29/00 (2018.01); A61P 35/00 (2018.01); C12N 2310/141 (2013.01); C12N 2320/32 (2013.01); C12N 2500/02 (2013.01); C12N 2500/30 (2013.01); C12N 2501/65 (2013.01)] | 4 Claims |
1. A method of treating a degenerative disease in a subject, comprising administering to the subject an effective amount of a formulation including an extracellular vesicle (EV) derived from a mesenchymal stem cell and curcumin encapsulated in the EV, wherein the mesenchymal stem cell is isolated from Wharton jelly of umbilical cord, and is CD29+, CD34−, CD44+ and CD73+, and wherein the formulation is prepared by:
(a-2) culturing the mesenchymal stem cell in the presence of aspirin;
(b-2) culturing the mesenchymal stem cell obtained in step (a-2) under 1% to 5% O2 and in serum free medium;
(c-2) isolating the EV from the cultured mesenchymal stem cell obtained in step (b-2); and
(d-2) encapsulating the curcumin in the isolated EV obtained in step (c-2).
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