Colorimetric hydrogel based nanosensor for detection of therapeutic levels of ionizing radiation
US-10428160-B2 · Oct 1, 2019 · US
US9944722B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9944722-B2 |
| Application number | US-201113701074-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 30, 2011 |
| Priority date | Jun 1, 2010 |
| Publication date | Apr 17, 2018 |
| Grant date | Apr 17, 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 relates to dimeric pentadentate chelators with exceptionally strong binding of metal ions, for detection, immobilization and purification of biomolecules. Dimeric chelators offer a cooperativity of binding of two adjacent immobilized metal ions simultaneously to a histidine-tagged biomolecule, which gives advantageous properties regarding strength of binding compared to a corresponding monomer chelator. In addition, a dimer increases the selectivity (ease of separation) against non-tagged biomolecules with low metal-ion affinity. The dimeric pentadentate chelator according to the invention has the following general formula: wherein Sc is a scaffold or a connecting structure that contains at least two functional groups enabling coupling of two pentadentate chelators (PD), and PD is a pentadentate chelator having the formula:
Opening claim text (preview).
The invention claimed is: 1. A dimeric pentadentate chelator having the following general formula: wherein PD is a pentadentate chelator having the formula: wherein S p1 is 6-amino hexanoic acid; wherein Sc is diethylenetriamine; wherein an amine of S p1 is coupled to PD to form an amide bond; and wherein a carboxyl of S p1 is coupled to a primary amine of Sc to form an amide bond. 2. The dimeric pentadentate chelator of claim 1 , further comprising a group Q and having the following general formula: wherein Q is selected from a solid phase, a detection label, and a biomarker. 3. The dimeric pentadentate chelator of claim 2 , wherein Q is a solid phase comprising a natural or synthetic polymer. 4. The dimeric pentadentate chelator of claim 2 , wherein the solid phase is a porous chromatographic support. 5. The dimeric pentadentate chelator of claim 3 , wherein Q is made of a cross-linked carbohydrate material selected from the group consisting of agarose, agar, cellulose, dextran, chitosan, konjac, carrageenan, gellan and alginate. 6. The dimeric pentadentate chelator of claim 3 , wherein Q is made of synthetic polymers selected from the group consisting of styrene derivatives, divinylbenzene, acryl amides, acrylate esters, methacrylate esters, vinyl esters and vinyl amides. 7. The dimeric pentadentate chelator of claim 2 , wherein Q comprises magnetic particles. 8. The dimeric pentadentate chelator of claim 2 , wherein Q is a solid phase comprising a sensor surface. 9. The dimeric pentadentate chelator of claim 5 , wherein Q is made of agarose.
Agar; Agarose, i.e. D-galactose, 3,6-anhydro-D-galactose, methylated, sulfated, e.g. from the red algae Gelidium and Gracilaria; Agaropectin; Derivatives thereof, e.g. Sepharose, i.e. crosslinked agarose · CPC title
with an organic functional group containing a metal, e.g. a metal affinity ligand · CPC title
comprising at least two different types of heteroatoms selected from nitrogen, oxygen or sulphur · CPC title
Sorbents specially adapted for preparative, analytical or investigative chromatography · CPC title
having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms not being part of nitro or nitroso groups · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.