Endosseous implant

US9730795B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9730795-B2
Application numberUS-201414319223-A
CountryUS
Kind codeB2
Filing dateJun 30, 2014
Priority dateNov 20, 2000
Publication dateAug 15, 2017
Grant dateAug 15, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Endosseous implant to be applied to a human or animal bone, wherein the surface of the implant is made from titanium or a titanium alloy, said implant having a smooth or rough surface texture, which is characterized in that said surface has been treated with at least one selected organic phosphonate compound or a pharmaceutically acceptable salt or ester or an amide thereof; process for producing said implants.

First claim

Opening claim text (preview).

The invention claimed is: 1. A pharmaceutically acceptable amide of a compound corresponding to the formula (I): A-[P(O)(OH) 2 ] p   (I), wherein: A is A 1 , wherein A l is a residue of a linear, branched or cyclic, saturated or unsaturated, hydrocarbon with n carbon atoms, carrying p phosphonic acid groups, wherein said residue is substituted by hydroxyl and/or carboxyl or said residue is unsubstituted, and wherein said residue is interrupted by one or more oxygen and/or sulphur and/or nitrogen atoms or said residue is not interrupted, and wherein n is a number from 4 to 70, and p is 3 to 6; or A is A 2 , wherein A 2 is a residue of an amino acid or of a sequence of amino acids respectively of a protein or of a polypeptide or a residue of a specific drug molecule, wherein each residue A 2 carries p phosphonic acid groups, and p is 3 to 6. 2. The amide of claim 1 , wherein A is A 1 , and A 1 is a saturated hydrocarbon residue of the formula —(C n H 2n+2−p )—, wherein n is 4 to 70. 3. The amide of claim 1 , wherein n is 4 to 40. 4. The amide of claim 1 , wherein n is 4 to 22. 5. The amide of claim 1 , wherein p is 3 or 4. 6. The amide of claim 1 , wherein the compound of formula (I) is selected from the group consisting of butane-1,1,4-triphosphonic acid, pentane-1,1,5-triphosphonic acid, pentane-2,2,5-triphosphonic acid, hexane-2,2,6-triphosphonic acid, pentane -1,1,5,5-tetraphosphonic acid, heptane-1,4,4,7-tetraphosphonic acid, and nonane-1,5,5,9-tetraphosphonic acid. 7. The amide of claim 1 , wherein the compound of formula (I) is a Transforming Growth Factor beta (TGF-β) as defined by the members of the superfamily of growth factors, wherein a peptide chain has been modified to contain p alkylphosphonic acid amide groups. 8. The amide of claim 7 , wherein the compound of formula (I) is a Transforming Growth Factor beta (TGF-β) selected from the group consisting of TGF-β1, TGF -β2, TGF-β3, TGF-β4, and TGF-β5, wherein the peptide chain has been modified to contain p alkylphosphonic acid amide groups. 9. The amide of claim 1 , wherein the compound of formula (I) is a Bone Morphogenic Protein (BMP), wherein a peptide chain has been modified to contain p alkylphosphonic acid amide groups. 10. The amide of claim 9 , wherein the compound of formula (I) is a Bone Morphogenic Protein (BMP) selected from the group consisting of BMP-2, BMP-3, BMP -4, BMP-5, BMP-6, BMP-7, BMP-8, BMP-9, BMP-10, BMP-11, BMP-12, and BMP-13, wherein the peptide chain has been modified to contain p alkylphosphonic acid amide groups. 11. The amide of claim 1 , wherein the compound of formula (I) is one of the principal twenty amino acids, wherein the amino acid has been modified to contain p alkylphosphonic acid amide groups. 12. The amide of claim 11 , wherein the compound of formula (I) is an amino acid selected from the group consisting of arginine, glycine, aspartic acid, alanine, valine, proline, serine, threonine, cysteine, and lysine, wherein the amino acid has been modified to contain p alkylphosphonic acid amide groups. 13. The amide of claim 1 , wherein the compound of formula (I) is an RGD-containing peptide, which has been modified to contain p alkylphosphonic acid amide groups. 14. The amide of claim 13 , wherein the compound of formula (I) is an RGD-containing peptide selected from the group consisting of an RGDS-peptide, a GRGDS-peptide, an RGDV-peptide, an RGDE-peptide, and an RGDT-peptide, wherein the RGD-containing peptide has been modified to contain p alkylphosphonic acid amide groups. 15. A pharmaceutically acceptable amide of a compound corresponding to the formula (I): A-[P(O)(OH) 2 ] p   (I), wherein A is a residue of a linear, branched or cyclic, saturated or unsaturated, hydrocarbon with n carbon atoms, carrying p phosphonic acid groups, wherein said residue is substituted by hydroxyl and/or carboxyl or said residue is unsubstituted, and wherein said residue is interrupted by one or more oxygen and/or sulphur and/or nitrogen atoms or said residue is not interrupted, and wherein n is a number from 1 to 70, and p is 2. 16. The amide of claim 15 , wherein A is a saturated hydrocarbon residue of the formula —(C n H 2n+2−p )—, wherein n is 1 to 70. 17. The amide of claim 15 , wherein n is 11 to 70. 18. The amide of claim 15 , wherein n is 11 to 40. 19. The amide of claim 15 , wherein n is 11 to 22.

Assignees

Inventors

Classifications

  • Drugs for skeletal disorders · CPC title

  • Coating made of chromium or Cr-based alloys · CPC title

  • Titanium or titanium-based alloys, e.g. Ti-Ni alloys · CPC title

  • containing sulfur substituents · CPC title

  • Coating or prosthesis-covering structure made of proteins or of polypeptides, e.g. of bone morphogenic proteins BMP or of transforming growth factors TGF · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9730795B2 cover?
Endosseous implant to be applied to a human or animal bone, wherein the surface of the implant is made from titanium or a titanium alloy, said implant having a smooth or rough surface texture, which is characterized in that said surface has been treated with at least one selected organic phosphonate compound or a pharmaceutically acceptable salt or ester or an amide thereof; process for produci…
Who is the assignee on this patent?
Univ Geneve, Ecole Polytechnique Fed Lausanne Epfl
What technology area does this patent fall under?
Primary CPC classification A61C8/0012. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Aug 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).