Eudermal papilla cell spheres, in-vitro culture method thereof, vesicles and application
The invention belongs to the field of biological materials and regenerative medicine, and particularly relates to a dermal papilla cell sphere, an in-vitro culture method thereof, a vesicle and application. The dermal papilla cell sphere is prepared according to the following method: extracting primary dermal papilla cells from in-vitro dermal papilla tissues, and subculturing for 3-5 generations; the method comprises the following steps: inoculating the passage of the dermal papilla cells into an SLF-3D culture system, culturing, collecting semi-suspended spheres when the growth fusion degree of the dermal papilla cells is 90-100%, separating the spheres into single cells, inoculating the single cells into the original SLF-3D culture system again, culturing for 3-5 days, and collecting the formed suspended spheres, namely the dermal papilla cell spheres. The dermal papilla cell ball and the vesicle thereof provided by the invention have a better treatment effect of scar-free wound healing..
Medienart: |
Patent |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Europäisches Patentamt - (2023) vom: 25. Apr. Zur Gesamtaufnahme - year:2023 |
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Sprache: |
Englisch |
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Beteiligte Personen: |
WANG YUNWEI [VerfasserIn] |
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Links: |
Volltext [kostenfrei] |
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Anmerkungen: |
Source: www.epo.org (no modifications made), First posted: 2023-04-25, Last update posted on www.tib.eu: 2023-09-26, Last updated: 2023-09-29 |
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Patentnummer: |
CN116004529 |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
EPA002037238 |
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520 | |a The invention belongs to the field of biological materials and regenerative medicine, and particularly relates to a dermal papilla cell sphere, an in-vitro culture method thereof, a vesicle and application. The dermal papilla cell sphere is prepared according to the following method: extracting primary dermal papilla cells from in-vitro dermal papilla tissues, and subculturing for 3-5 generations; the method comprises the following steps: inoculating the passage of the dermal papilla cells into an SLF-3D culture system, culturing, collecting semi-suspended spheres when the growth fusion degree of the dermal papilla cells is 90-100%, separating the spheres into single cells, inoculating the single cells into the original SLF-3D culture system again, culturing for 3-5 days, and collecting the formed suspended spheres, namely the dermal papilla cell spheres. The dermal papilla cell ball and the vesicle thereof provided by the invention have a better treatment effect of scar-free wound healing. | ||
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