Polymerizable absorbers of uv and high energy visible light
US-2019271798-A1 · Sep 5, 2019 · US
US12275708B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12275708-B2 |
| Application number | US-202418442393-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 15, 2024 |
| Priority date | Jul 8, 2013 |
| Publication date | Apr 15, 2025 |
| Grant date | Apr 15, 2025 |
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.
Hydrophilic, high quantum yield, chemiluminescent acridinium compounds with increased light output, improved stability, fast light emission and decreased non specific binding are disclosed. The chemiluminescent acridinium esters possess hydrophilic, branched, electron-donating functional groups at the C2 and/or C7 positions of the acridinium nucleus.
Opening claim text (preview).
The invention claimed is: 1. An acridinium compound having the structure: wherein, R 1 is a methyl or sulfopropyl group; R 2a is alkylene or arylene, R 3a is alkyl or aryl, G is, at both occurrences, a branched group selected from: and R 12 is selected from the group consisting of (1) —OH; (2) —O—N-succinimidyl; (3) —NH—(CH 2 ) 5 —C(O)—O—N-succinimidyl; (4) —NH—(CH 2 ) 5 —COOH; (5) —NH—(C 2 H 4 O) p —C 2 H 4 NH—C(O)—(CH 2 ) 3 —C(O)—O—N—R″ wherein p=1 to 5; and where R″ is hydrogen or —N-succinimidyl; and (6) —NH—(C 2 H 4 O) q —C 2 H 4 NH 2 , wherein q=1 to 5. 2. The acridinium compound according to claim 1 , wherein G is a group: at both occurrences. 3. The acridinium compound according to claim 1 , wherein G is a group: at both occurrences. 4. The acridinium compound according to claim 1 , wherein G is a group: at both occurrences. 5. The acridinium compound according to claim 1 , wherein G is a group: at both occurrences. 6. The acridinium compound according to claim 1 , wherein said acridinium compound is characterized in that ≥89% of the chemiluminescence of said acridinium compound is emitted within one second of said adding chemiluminescence triggering reagents. 7. The acridinium compound according to claim 1 , wherein said acridinium compound is characterized in that said acridinium compound retains more than 60% of its chemiluminescent activity after 33 days at 37° C. 8. A method for the detection or quantification of an analyte in a sample suspected of containing the analyte comprising the steps of: (a) providing a conjugate comprising (i) an antibody specific for the analyte; and (ii) an acridinium compound having the structure: wherein, R 1 is a methyl or sulfopropyl group; R 2a is alkylene or arylene, R 3a is alkyl or aryl, G is, at both occurrences, a branched group selected from: and R 12 is conjugated to the antibody specific for the analyte; (b) providing a solid support having immobilized thereon a second antibody specific for the analyte; (c) mixing the conjugate, the solid phase and the sample suspected of containing the analyte to form a binding complex; (d) separating the binding complex captured on the solid support; (e) triggering chemiluminescence of the binding complex from step (d) by adding chemiluminescence triggering reagents; (f) detecting the presence or calculating the concentration of the analyte by comparing the amount of light emitted from the reaction mixture with a standard dose response curve which relates the amount of light emitted to a known concentration of the analyte. 9. The method according to claim 8 , wherein R 12 is formed from the antibody reacting with one of: (1) —OH; (2) —O—N-succinimidyl; (3) —NH—(CH 2 ) 5 —C(O)—O—N-succinimidyl; (4) —NH—(CH 2 ) 5 —COOH; (5) —NH—(C 2 H 4 O) p —C 2 H 4 NH—C(O)—(CH 2 ) 3 —C(O)—O—N—R″ wherein p=1 to 5; and where R″ is hydrogen or —N-succinimidyl; and (6) —NH—(C 2 H 4 O) q —C 2 H 4 NH 2 , wherein q=1 to 5.
having chemically-interreactive components, e.g. reactive chemiluminescent compositions · CPC title
with an insoluble carrier for immobilising immunochemicals · CPC title
with fluorescent label · CPC title
using chemiluminescence · CPC title
Chemiluminescence; Bioluminescence · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.