<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Vlasakova K</submitter><funding>Innovative Medicines Initiative</funding><pagination>769-785</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9968696</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>97(3)</volume><pubmed_abstract>Drug-induced pancreatic injury (DIPI) is an issue seen in drug development both in nonclinical and clinical contexts. DIPI is typically monitored by measurement of lipase and/or amylase, however, both enzymes lack sensitivity and specificity. Although candidate protein biomarkers specific to pancreas exist, antibody-based assay development is difficult due to their small size or the rapid cleavage by proteolytic enzymes released during pancreatic injury. Here we report the development of a novel multiplexed immunoaffinity-based liquid chromatography mass spectrometric assay (IA-LC-MS/MS) for trypsinogen activation peptide (TAP) and carboxypeptidases A1 and A2 (CPA1, CPA2). This method is based on the enzymatic digestion of the target proteins, immunoprecipitation of the peptides with speci</pubmed_abstract><journal>Archives of toxicology</journal><pubmed_title>Plasma biomarkers TAP, CPA1, and CPA2 for the detection of pancreatic injury in rat: the development of a novel multiplex IA-LC-MS/MS assay and biomarker performance evaluation.</pubmed_title><pmcid>PMC9968696</pmcid><funding_grant_id>No 821283</funding_grant_id><pubmed_authors>Ackermann BL</pubmed_authors><pubmed_authors>Haag H</pubmed_authors><pubmed_authors>Vlasakova K</pubmed_authors><pubmed_authors>Poetz O</pubmed_authors><pubmed_authors>Steinhilber A</pubmed_authors><pubmed_authors>Bailey WJ</pubmed_authors><pubmed_authors>Joos T</pubmed_authors><pubmed_authors>Erdos Z</pubmed_authors><pubmed_authors>Glaab WE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Plasma biomarkers TAP, CPA1, and CPA2 for the detection of pancreatic injury in rat: the development of a novel multiplex IA-LC-MS/MS assay and biomarker performance evaluation.</name><description>Drug-induced pancreatic injury (DIPI) is an issue seen in drug development both in nonclinical and clinical contexts. DIPI is typically monitored by measurement of lipase and/or amylase, however, both enzymes lack sensitivity and specificity. Although candidate protein biomarkers specific to pancreas exist, antibody-based assay development is difficult due to their small size or the rapid cleavage by proteolytic enzymes released during pancreatic injury. Here we report the development of a novel multiplexed immunoaffinity-based liquid chromatography mass spectrometric assay (IA-LC-MS/MS) for trypsinogen activation peptide (TAP) and carboxypeptidases A1 and A2 (CPA1, CPA2). This method is based on the enzymatic digestion of the target proteins, immunoprecipitation of the peptides with speci</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-05-29T19:42:47.397Z</modification><creation>2025-05-29T19:42:47.397Z</creation></dates><accession>S-EPMC9968696</accession><cross_references><pubmed>36481916</pubmed><doi>10.1007/s00204-022-03425-9</doi></cross_references></HashMap>