Methods and compositions for cancer treatment
US-2024424094-A1 · Dec 26, 2024 · US
US10858483B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10858483-B2 |
| Application number | US-201716314735-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 6, 2017 |
| Priority date | Jul 6, 2016 |
| Publication date | Dec 8, 2020 |
| Grant date | Dec 8, 2020 |
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Polyphosphazenes polyelectrolytes. The polyphosphazenes can be prepared by substituting pendant groups (e.g., ionic groups or pendant groups that can form ionic groups) onto a reactive macromolecular precursor for example, by reaction between the reactive chlorine atoms on the backbone of poly(dichlorophosphazene) and appropriate organic nucleophiles. In certain examples, one or more charged pendant groups of a polyphosphazene is/are further modified to introduce desired counterions, which can be hydrophobic counterions. The polyphosphazenes can activate distinct Toll-Like Receptors (TLRs) and can be used in methods of stimulating an immune response.
Opening claim text (preview).
What is claimed is: 1. A method of stimulating an immune response in an individual in need thereof, comprising administering to said individual, a polyphosphazene having the following structure: wherein R − is defined as being an anionic group independently selected from the group consisting of a carboxylate group, a sulfonate group, and a phosphonate group; wherein at least one of the Y + groups in the polyphosphazene is a cationic group independently selected from the group consisting of: N-protonated spermine group, N-protonated spermidine group, N-protonated imidazoquinoline, N-protonated substituted imidazoquinoline group, N- and/or S-protonated thiaimidazoquinoline group, and N- and/or S-protonated substituted thiaimidazoquinoline group, wherein the remaining Y + groups of the polyphosphazene are independently selected from the group consisting of: H + , Na + , K + , Ca 2+ , N-protonated spermine group, N-protonated spermidine group, N-protonated imidazoquinoline, N-protonated substituted imidazoquinoline group, N- and/or S-protonated thiaimidazoquinoline group, and N- and/or S-protonated substituted thiaimidazoquinoline group, and wherein “n” is an integer ranging from 10 to 500,000. 2. The method of claim 1 , wherein one or more Y + is: wherein R 1 is independently at each occurrence in the polyphosphazene is —H, and R 2 is independently at each occurrence in the polyphosphazene is —H, —CH 3 or CH 2 —CH 2 —CH 3 , 3. The method of claim 2 , wherein one or more Y + is: 4. The method of claim 1 , wherein the polyphosphazene is present in a composition. 5. The method of claim 1 , wherein the composition comprises a polyphosphazene and a pharmaceutically acceptable carrier. 6. The method of claim 1 , wherein the composition comprises a polyphosphazene, vaccine antigen and, optionally, a pharmaceutically acceptable carrier. 7. The method of claim 1 , wherein the composition comprises a polyphosphazene, an immunomodulating compound and/or TLR agonist, and, optionally, a pharmaceutically acceptable carrier. 8. The method of claim 1 , wherein stimulation of the immune response comprises synergistic production of tumor necrosis factor alpha (TNF-α).
Medicinal preparations containing antigens or antibodies (materials for immunoassay G01N33/53) · CPC title
Immunostimulants · CPC title
Polyphosphazenes · CPC title
characterised by the immunostimulating additives, e.g. chemical adjuvants · CPC title
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