Method for treating neoplasms using hollow silica spheres
US-11491110-B2 · Nov 8, 2022 · US
US11701329B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11701329-B2 |
| Application number | US-202217956887-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 30, 2022 |
| Priority date | May 3, 2019 |
| Publication date | Jul 18, 2023 |
| Grant date | Jul 18, 2023 |
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The invention pertains to a method for treating a neoplasm, such as colorectal cancer, using hollow silica spheres (“HSS”). It also is directed to a method for making uncalcined HSS, calcined HSS from which phenyl groups have been removed, and HSS incorporating particles of Fe 3 O 4 , as well as compositions containing HSS.
Opening claim text (preview).
The invention claimed is: 1. A treatment method for colon cancer, comprising: administering to a subject in need of treatment for colon cancer an aqueous composition comprising Fe 3 O 4 -hollow silica spheres (“Fe-HSS”), wherein the aqueous composition is administered in an amount sufficient to induce nuclear condensation, augmentation, and disintegration of cells of the cancer, wherein the Fe-HSS are calcined, wherein the surfaces of the Fe-HSS comprise no more than 0.05 mol. % phenyl or aryl groups, relative to an average uncalcined Fe-HSS, wherein Fe-HSS have a hollow core space containing plural individual particles of Fe 3 O 4 having an average diameter in a range of from 9.5 nm to 21.3 nm and the Fe 3 O 4 has a polycrystalline spinel structure, wherein the hollow silica spheres of the Fe 3 O 4 -hollow silica spheres have a core-shell structure with shells larger in thickness than cores, and the hollow silica spheres have an average diameter in a range of from 415 to 615 nm, wherein the Fe-HSS have an average shell thickness in a range of from 150 to 210 nm, and wherein the particles of Fe 3 O 4 are present a range of from 0.1 to 10 wt % of a combined weight of the HSS and Fe 3 O 4 in the Fe-HSS. 2. The method of claim 1 , wherein the hollow silica spheres are prepared by a process comprising hydrolysis of a mixture comprising Fe 3 O 4 and phenyl-tri-methoxysilane or another hydrolyzable aryl silane followed by condensation with a hydroxide base. 3. The method of claim 1 , wherein the surfaces of the Fe-HSS are free of phenyl or aryl groups. 4. The method of claim 1 , wherein the Fe-HSS further comprise at least one anticancer drug or agent. 5. The method of claim 1 , wherein the aqueous composition comprising the HSS is administered in situ to the site of a tumor or a tissue or organ containing cancer cells.
Agglomerates; Granulates; Microbeadlets {; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction (A61K9/20 takes precedence if the final form is a tablet; microspheres with drug-free outer coating, microcapsules A61K9/50; mixture of different granules, microcapsules, (coated) microparticles A61K9/5084; nanoparticles A61K9/51)} · CPC title
Processes · CPC title
Medicinal preparations containing inorganic active ingredients · CPC title
Iron; Compounds thereof · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
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