Synthetic peptide, and cosmetic composition or pharmaceutical composition and application thereof
US-2024352069-A1 · Oct 24, 2024 · US
US10836795B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10836795-B2 |
| Application number | US-201716464099-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 27, 2017 |
| Priority date | Dec 27, 2016 |
| Publication date | Nov 17, 2020 |
| Grant date | Nov 17, 2020 |
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A peptide derived from the copine 7 protein and having both cell permeability and bone tissue regeneration ability, and a use of the peptide, are described. The peptide has excellent bone tissue regeneration ability and is therefore useful for treating a disease requiring bone regeneration, such as osteoporosis. Particularly, by also having cell permeability, the peptide does not require the attachment of a separate peptide or addition of another preparation for the cell permeation thereof and thus can be conveniently applied in orthopedics and the like requiring various surgical regeneration treatments.
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The invention claimed is: 1. A peptide consisting of the amino acid sequence of SEQ ID NO: 4(VNPKYKQKRR), wherein one or more amino acid is D-type amino acid. 2. The peptide according to claim 1 , wherein the peptide has dual functions of cell permeability and bone tissue regeneration ability. 3. A method for regenerating bone tissue, the method comprising administering a pharmaceutical composition comprising a peptide consisting of the amino acid sequence of SEQ ID NO: 4 or grafting a biomaterial comprising a peptide consisting of the amino acid sequence of SEQ ID NO: 4 to a subject in need of bone tissue regeneration. 4. The method according to claim 3 , wherein the composition is formulated as the one selected from the group consisting of a formulation for oral administration, a formulation for injection, and a gel formulation for topical implantation. 5. The method according to claim 4 , wherein the gel formulation for topical implantation comprises: i) a synthetic polymer selected from the group consisting of polylactic glycolic acid, a poloxamer and propylene glycol; or ii) a natural polymer selected from the group consisting of collagen, alginic acid, propylene glycol alginate, chondroitin sulfate and chitosan. 6. The method according to claim 3 , wherein the composition is administered at a dose of 1 to 60 mg per 1 kg of a body weight of a subject in need of treatment. 7. A biomaterial comprising a peptide consisting of the amino acid sequence of SEQ ID NO: 4, and a chemically synthesized bone mineral or synthetic polymer. 8. The biomaterial according to claim 7 , wherein the chemically synthesized bone mineral is hydroxyapatite. 9. The biomaterial according to claim 7 , wherein the synthetic polymer is selected from the group consisting of polylactic glycolic acid, a poloxamer and propylene glycol.
having 5 to 11 amino acids · CPC title
Ointments; Bases therefor; {Other semi-solid forms, e.g. creams, sticks, gels (composition of ointments, creams or gels A61K47/00)} · CPC title
Galenical forms characterised by the site of application · CPC title
Peptides having 5 to 11 amino acids {(A61K38/043 - A61K38/046 take precedence)} · CPC title
Phosphorus-containing materials, e.g. apatite · CPC title
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