Tco conjugates and methods for delivery of therapeutic agents
US-2017095580-A1 · Apr 6, 2017 · US
US10130711B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10130711-B2 |
| Application number | US-201414899041-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 18, 2014 |
| Priority date | Jun 19, 2013 |
| Publication date | Nov 20, 2018 |
| Grant date | Nov 20, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention provides a method for selective delivery of a therapeutic or diagnostic agent to a targeted organ or tissue by implanting a biocompatible solid support in the patient being linked to a first binding agent, and administering a second binding agent to the patient linked to the therapeutic or diagnostic agent, such that the therapeutic or diagnostic agent accumulates at the targeted organ or tissue.
Opening claim text (preview).
What is claimed is: 1. A composition comprising: an implantable biocompatible solid support selected from the group consisting of polysaccharide hydrogels, alginate, cellulose, hyaluronic acid, chitosan, chitin, chondroitin sulfate, heparin, a polymer matrix, a metal, a ceramic and a plastic; at least one binding agent linked to the biocompatible solid support, wherein the at least one binding agent is capable of a bioorthogonal reaction with a corresponding binding agent and the bioorthogonal reaction is between a trans-cyclooctene and a tetrazine; and a linker covalently linking each binding agent to the implantable biocompatible solid support. 2. The composition of claim 1 , wherein the implantable biocompatible solid support comprises alginate. 3. The composition of claim 1 , wherein the composition has the structure of the formula: 4. The composition of claim 1 , wherein the implantable biocompatible solid support is selected from the group consisting of alginate, chitin, hyaluronic acid and chitosan. 5. The composition of claim 4 , wherein the implantable biocompatible solid support is hyaluronic acid. 6. The composition of claim 1 , wherein the composition is formulated in a sterile injectable preparation. 7. The composition of claim 1 , wherein the at least one binding agent comprises trans-cyclooctene or tetrazine. 8. The composition of claim 1 , wherein the at least one binding agent is trans-cyclooctene or tetrazine. 9. The composition of claim 1 , wherein the implantable biocompatible solid support comprises the polymer matrix.
Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title
Antibacterial agents · CPC title
Drugs for skeletal disorders · CPC title
for bone diseases, e.g. rachitism, Paget's disease · CPC title
Peptides containing saccharide radicals; Derivatives thereof {, e.g. bleomycin, phleomycin, muramylpeptides or vancomycin} · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.