Design strategy of fluorescent probes for live drug-induced acute liver injury imaging

D Cheng, W Xu, X Gong, L Yuan… - Accounts of Chemical …, 2020 - ACS Publications
Conspectus Drug-induced acute liver injury (DIALI) is increasingly recognized as a
significant cause of acute liver injury (ALI), which is characterized by a rapid loss of …

The current state of serum biomarkers of hepatotoxicity

J Ozer, M Ratner, M Shaw, W Bailey, S Schomaker - Toxicology, 2008 - Elsevier
The level of serum alanine aminotransferase (ALT) activity reflects damage to hepatocytes
and is considered to be a highly sensitive and fairly specific preclinical and clinical …

Characterization of primary human hepatocytes, HepG2 cells, and HepaRG cells at the mRNA level and CYP activity in response to inducers and their predictivity for …

HHJ Gerets, K Tilmant, B Gerin, H Chanteux… - Cell biology and …, 2012 - Springer
In the pharmaceutical industry, improving the early detection of drug-induced hepatotoxicity
is essential as it is one of the most important reasons for attrition of candidate drugs during …

Dichloro-dihydro-fluorescein diacetate (DCFH-DA) assay: a quantitative method for oxidative stress assessment of nanoparticle-treated cells

A Aranda, L Sequedo, L Tolosa, G Quintas, E Burello… - Toxicology in vitro, 2013 - Elsevier
No consensus exists on how to address possible toxicity of nanomaterials as they interfere
with most in vitro screening tests based on colorimetric and fluorimetric probes such as the …

A critical evaluation of in vitro cell culture models for high-throughput drug screening and toxicity

A Astashkina, B Mann, DW Grainger - Pharmacology & therapeutics, 2012 - Elsevier
Drug candidate and toxicity screening processes currently rely on results from early-stage in
vitro cell-based assays expected to faithfully represent essential aspects of in vivo …

A critical perspective on 3D liver models for drug metabolism and toxicology studies

AS Serras, JS Rodrigues, M Cipriano… - Frontiers in cell and …, 2021 - frontiersin.org
The poor predictability of human liver toxicity is still causing high attrition rates of drug
candidates in the pharmaceutical industry at the non-clinical, clinical, and post-marketing …

[PDF][PDF] Clinical biochemistry of hepatotoxicity

A Singh, TK Bhat, OP Sharma - J Clinic Toxicol S, 2011 - academia.edu
Liver plays a central role in the metabolism and excretion of xenobiotics which makes it
highly susceptible to their adverse and toxic effects. Liver injury caused by various toxic …

The human hepatoma HepaRG cells: a highly differentiated model for studies of liver metabolism and toxicity of xenobiotics

A Guillouzo, A Corlu, C Aninat, D Glaise, F Morel… - Chemico-biological …, 2007 - Elsevier
Although they have several important limitations primary human hepatocytes still represent
the in vitro gold standard model for xenobiotic metabolism and toxicity studies. The large use …

High concordance of drug-induced human hepatotoxicity with in vitro cytotoxicity measured in a novel cell-based model using high content screening

PJ O'Brien, W Irwin, D Diaz, E Howard-Cofield… - Archives of …, 2006 - Springer
To develop and validate a practical, in vitro, cell-based model to assess human
hepatotoxicity potential of drugs, we used the new technology of high content screening …

Cellular imaging predictions of clinical drug-induced liver injury

JJ Xu, PV Henstock, MC Dunn, AR Smith… - Toxicological …, 2008 - academic.oup.com
Drug-induced liver injury (DILI) is the most common adverse event causing drug
nonapprovals and drug withdrawals. Using drugs as test agents and measuring a panel of …