Particles for the treatment of cancer in combination with radiotherapy

US10137149B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10137149-B2
Application numberUS-201013514487-A
CountryUS
Kind codeB2
Filing dateDec 8, 2010
Priority dateDec 9, 2009
Publication dateNov 27, 2018
Grant dateNov 27, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The invention provides a particle comprising a metal oxide which is doped with at least one rare earth element, wherein the metal oxide is selected from titanium dioxide, zinc oxide, cerium oxide and mixtures of two or more thereof. The invention also provides a pharmaceutical composition comprising the particles, and to uses of the particles and composition in the treatment and diagnosis of cancer.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method of treating cancer in a subject comprising: administering a particle to a locus or site of the cancer or to tumour tissue in the subject, which particle comprises a metal oxide, which metal oxide is titanium dioxide doped with from 0.1 to 25 mol % of at least one rare earth element, wherein the titanium dioxide is a host lattice and the at least one rare earth element is present as a dopant within said host lattice; and applying X-ray radiation suitable for radiotherapy to the locus or site of the cancer or tumour tissue and thereby exciting the metal oxide in the particle at the locus or site of the cancer or tumour tissue and generating reactive oxygen species at the locus or site of the cancer or tumour tissue. 2. The method according to claim 1 , wherein the particle comprises a core consisting of titanium dioxide doped with from 0.1 to 25 mol % of at least one rare earth element. 3. The method according to claim 1 , wherein the metal oxide is doped with at least two different rare earth elements. 4. The method according to claim 1 , wherein the metal oxide is doped with gadolinium. 5. The method according to claim 1 wherein the metal oxide is doped with europium. 6. The method according to claim 1 wherein the metal oxide is doped with erbium. 7. The method according to claim 1 wherein the metal oxide is doped with neodymium. 8. The method according to claim 1 , wherein the particle has a size of less than 400 nm. 9. The method according to claim 1 , wherein the particle has a coating comprising silica, alumina, polyethylene glycol, polystyrene, a saccharide, an oligosaccharide, a polysaccharide or a mixture of two or more thereof. 10. The method according to claim 9 wherein a targeting moiety is attached to the coating. 11. The method according to claim 9 , wherein an optical contrast agent, a radioisotope, a paramagnetic contrast agent or a superparamagnetic contrast agent is attached to the coating. 12. The method according to claim 1 wherein the cancer is a cancer of the lung, liver, kidney, bladder, breast, head, neck, brain, ovaries, prostate, intestine, colon, rectum, uterus, pancreas, eye, bone marrow, lymphatic system or thyroid gland. 13. The method according to claim 1 comprising: (a) administering the particle by intra-tumoral injection into the tumour tissue or at the cancer site or locus; or (b) parenterally administering to the subject the particle and allowing the particle to localize at the locus or site of the cancer or tumour tissue. 14. The method according to claim 1 further comprising the step of detecting the presence of the particle at the locus or site of the cancer or tumour tissue before directing X-ray radiation to the locus or site of the cancer or tumour tissue. 15. An in vitro method of destroying cancer cells comprising adding a particle to a cell culture, medium or solution comprising cancer cells, then directing X-ray radiation at the cancer cells, wherein the particle comprises a metal oxide, which metal oxide is titanium dioxide and is doped with from 0.1 to 25 mol % of at least one rare earth element, and wherein the titanium dioxide is a host lattice and the at least one rare earth element is present as a dopant within said host lattice. 16. A method according to claim 1 , wherein the host lattice is substitution doped or interstitial doped with the at least one rare earth element. 17. A method according to claim 1 , wherein the host lattice is substitution doped with the at least one rare earth element.

Assignees

Inventors

Classifications

  • Radiosensitizing, i.e. administration of pharmaceutical agents that enhance the effect of radiotherapy (radiotherapy per se A61N5/10) · CPC title

  • Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title

  • with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface (with further drug-free outer coating A61K9/5073) · CPC title

  • Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery · CPC title

  • Antineoplastic agents · CPC title

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What does patent US10137149B2 cover?
The invention provides a particle comprising a metal oxide which is doped with at least one rare earth element, wherein the metal oxide is selected from titanium dioxide, zinc oxide, cerium oxide and mixtures of two or more thereof. The invention also provides a pharmaceutical composition comprising the particles, and to uses of the particles and composition in the treatment and diagnosis of ca…
Who is the assignee on this patent?
Dobson Peter James, Wakefield Gareth, Townley Helen Elizabeth, and 1 more
What technology area does this patent fall under?
Primary CPC classification A61K41/0038. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Nov 27 2018 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).