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Development of a highly sensitive chemiluminescent assay for hydrogen peroxide under neutral conditions using acridinium ester and its application to an enzyme immunoassay

https://doi.org/10.1002/bio.2555
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/bio.1170040116openalex-snapshot
1,2‐Dioxetanes: Novel chemiluminescent enzyme substrates. Applications to immunoassays
inferredcites →https://doi.org/10.1002/bio.1170040121openalex-snapshot
Chemiluminescent assay of various enzyme activites and its application to enzyme immunoassays
inferredcites →https://doi.org/10.1002/bio.1170080302openalex-snapshot
Chemiluminescent enzyme immunoassay for alpha‐fetoprotein using β‐ D ‐galactosidase as label and 5‐bromo‐4‐chloro‐3‐indolyl‐β‐ D ‐galactopyranoside as substrate
inferredcites →https://doi.org/10.1002/bio.958openalex-snapshot
Chemiluminescence assay for tetrahydrobiopterin based on the generation of hydrogen peroxide using isoluminol‐microperoxidase in the presence of 1‐methoxy PMS
inferredcites →https://doi.org/10.1016/0003-2697(79)90352-xopenalex-snapshot
Chemiluminescence enzyme immunoassay of cortisol using peroxidase as label
inferredcites →https://doi.org/10.1016/0003-2697(80)90017-2openalex-snapshot
New fluorogenic substrates for horseradish peroxidase: Rapid and sensitive assays for hydrogen peroxide and the peroxidase
inferredcites →https://doi.org/10.1016/0003-2697(91)90096-copenalex-snapshot
Chemiluminescent assay of various enzymes using indoxyl derivatives as substrate and its applications to enzyme immunoassay and DNA probe assay
inferredcites →https://doi.org/10.1016/s0003-2670(03)00809-2openalex-snapshot
Clinical applications of chemiluminescence
inferredcites →https://doi.org/10.1021/ar50102a001openalex-snapshot
Chemical mechanisms in bioluminescence
inferredcites →https://doi.org/10.1021/jp104060xopenalex-snapshot
Chemiluminescence Arising from the Decomposition of Peroxymonocarbonate and Enhanced by CdTe Quantum Dots
inferredcites →https://doi.org/10.2116/analsci.15.1269openalex-snapshot
Chemiluminescent Assay for Catecholamines by the Generation of Hydrogen Peroxide in Basic Solution and the Use of Isoluminol-Microperoxidase
inferredcites →https://doi.org/10.2116/analsci.6.645openalex-snapshot
Micelle-Enhanced Lucigenin Chemiluminescence for the Determination of Catecholamines

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4751208openalex-extracted
Aromatic Acridinium Thioesters as New Chemiluminescence Indicators In The Analysis of Biological Antioxidants
inferred← citeshttps://doi.org/10.1002/ange.202007649openalex-snapshot
NIR‐II Chemiluminescence Molecular Sensor for In Vivo High‐Contrast Inflammation Imaging
inferred← citeshttps://doi.org/10.1002/anie.202007649openalex-snapshot
NIR‐II Chemiluminescence Molecular Sensor for In Vivo High‐Contrast Inflammation Imaging
inferred← citeshttps://doi.org/10.1002/anse.202000033openalex-snapshot
Activatable Chemiluminescent Molecular Probes for Bioimaging and Biosensing
inferred← citeshttps://doi.org/10.1002/cphc.202200166openalex-snapshot
Solvent Effect on the Chemiluminescence of Acridinium Thioester: A Computational Study
inferred← citeshttps://doi.org/10.1007/978-3-319-63953-6_10openalex-snapshot
Acridines Used for Staining
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.107628openalex-snapshot
Synthesis, chemiluminescence, and application of 2,4-disubstituted phenyl 10-methyl-10λ4-acridine-9-carboxylates
inferred← citeshttps://doi.org/10.1016/j.dyepig.2023.111175openalex-snapshot
Strong chemiluminescence intensities of bis-acridinium esters under neutral and alkaline conditions
inferred← citeshttps://doi.org/10.1016/j.jlumin.2024.120745openalex-snapshot
Aromatic acridinium thioesters–a new class of chemiluminogenic compounds and their interactions with some biological antioxidants
inferred← citeshttps://doi.org/10.1016/j.microc.2018.12.056openalex-snapshot
Recent advances in chemiluminescence for reactive oxygen species sensing and imaging analysis
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02748openalex-snapshot
Strongly Chemiluminescent Acridinium Esters under Neutral Conditions: Synthesis, Properties, Determination, and Theoretical Study
inferred← citeshttps://doi.org/10.1039/c9tb02310kopenalex-snapshot
Aggregation-induced emission luminogens for RONS sensing
inferred← citeshttps://doi.org/10.3390/ijms21124417openalex-snapshot
Computational Insights on the Mechanism of the Chemiluminescence Reaction of New Group of Chemiluminogens—10-Methyl-9-thiophenoxycarbonylacridinium Cations
inferred← citeshttps://doi.org/10.3390/ijms24119468openalex-snapshot
What Other Than Acridinium Esters? Computational Search for New Acridinium-Based Chemiluminogens
inferred← citeshttps://doi.org/10.3390/medicines13020012openalex-snapshot
Quantification of In Vitro Replicative Lifespan Elongation Activity of Hormones, Antioxidants, Plant Extract and Bacterial Exudate by Updated “Overlay Method”
inferred← citeshttps://doi.org/10.3390/molecules29163736openalex-snapshot
Why Do Ionic Surfactants Significantly Alter the Chemiluminogenic Properties of Acridinium Salt?
inferred← citeshttps://doi.org/10.3390/molecules31061041openalex-snapshot
Acridinium Chemiluminogenic Labels—Synthesis, Analytical Performance, and Mechanism of Light Generation—A Comparison in View of Biomedical Diagnostics
inferred← citeshttps://doi.org/10.3390/nano13111726openalex-snapshot
Recent Advances in Nanomaterial-Based Chemiluminescence Probes for Biosensing and Imaging of Reactive Oxygen Species
inferred← citeshttps://doi.org/10.5650/jos.ess21186openalex-snapshot
Acridinium Ester Chemiluminescence: Methyl Substitution on the Acridine Moiety
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