Aie luminogens for visualization and treatment of cancer

US10935552B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10935552-B2
Application numberUS-201615737187-A
CountryUS
Kind codeB2
Filing dateJun 24, 2016
Priority dateJun 24, 2015
Publication dateMar 2, 2021
Grant dateMar 2, 2021

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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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Abstract

Official abstract text for this publication.

The present subject matter relates to ATE luminogens for visualization and treatment of cancer, particularly AIE luminogenic probes for cancer cell visualization and discrimination, lysosome-targeting AIEgens for imaging and autophagy visualization, highly fluorescent AIE-active theranostic agents for monitoring drug distribution and having anti-tumor activity to specific cancer cells, probes comprising AIE luminogens for cancer cell imaging and staining, AIE luminogens having clusteroluminogenic features and applications thereof, and methods of preparing thereof.

First claim

Opening claim text (preview).

We claim: 1. A probe for cancer cell imaging and staining comprising AIE luminogens having a chemical structure selected from the group consisting of: wherein the counteranion X− is selected from anions with single or more charges; and wherein each R is independently selected from the group consisting of alkyl, unsaturated alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, provided that R is not alkyl when R is a phenyl substituent. 2. The probe of claim 1 , wherein the AIE luminogens are selected from the group consisting of: 3. The probe of claim 1 , wherein the probe exhibits mitochondria selectivity for staining. 4. The probe of claim 1 , wherein the probe has two-photon absorption ability and can be excited by longer wavelengths. 5. The probe of claim 1 , wherein the probe is used for mitochondria imaging, as the AIE luminogens have electrostatic interaction with mitochondria. 6. The probe of claim 1 , wherein imaging is due to fluorescence emitted by probes uptaken by cells and accumulated in mitochondria. 7. The probe of claim 1 , wherein the probe is used with an imaging sample comprising any kind of cells. 8. The probe of claim 7 , wherein the imaging sample comprises any cancer cells. 9. The probe of claim 1 , wherein the probe can distinguish normal cells from cancer cells by a difference in fluorescence intensity, wherein the cancer cells and the normal cells are stained separately or in a mixture. 10. The probe of claim 9 , wherein the cancer cells have a higher fluorescence intensity and the normal cells have a lower fluorescence intensity, due to the cancer cells uptaking and accumulating more probes. 11. The probe of claim 1 , wherein the probe is subject to light irradiation, which generates ROS.

Assignees

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Classifications

  • Measuring fluorescence of biological material, e.g. DNA, RNA, cells (G01N21/6428 takes precedence) · CPC title

  • Non-condensed systems · CPC title

  • Ortho-condensed systems · CPC title

  • Condensed systems · CPC title

  • one >CH- group, e.g. cyanines, isocyanines, pseudocyanines · CPC title

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What does patent US10935552B2 cover?
The present subject matter relates to ATE luminogens for visualization and treatment of cancer, particularly AIE luminogenic probes for cancer cell visualization and discrimination, lysosome-targeting AIEgens for imaging and autophagy visualization, highly fluorescent AIE-active theranostic agents for monitoring drug distribution and having anti-tumor activity to specific cancer cells, probes c…
Who is the assignee on this patent?
Univ Hong Kong Sci & Tech
What technology area does this patent fall under?
Primary CPC classification C07D295/088. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Mar 02 2021 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).