- AminosalicylatesCorticosteroids for IBDCytokine-Targeted Therapies for IBDJanus Kinase Inhibitors for IBDDrugs Targeting Leukocyte Trafficking for IBDPPAR-γ Ligands for IBDAgents Targeting the TGF-β/Smad System in IBDMatrix Metalloproteinase Inhibitors for IBDImmunotherapies for IBDDrugs Targeting Toll-like Receptors in IBDS1P Receptor Modulators for IBD
- Antibiotic Therapies for IBDProbiotic Therapies for IBDFecal Microbiota Transplantation for IBDCell-based Therapies for IBD
- Drug Target Discovery for IBDLead Discovery for IBDLead Optimization for IBD
- In Vitro ADMEIn Vivo ADME TestingPharmacokinetic EvaluationBioanalysisMetabolite Profiling and IdentificationPreclinical Toxicology Studies for IBD DrugsIn Vitro Efficacy Testing for IBD Drugs
- Disease Activity Index AssessmentColon Length and Weight AssessmentColonoscopyHistology and Immunohistochemistry EvaluationInflammatory Marker AssessmentOxidative Stress Marker AssessmentIntestinal Permeability MeasurementImaging Services
- IBD Immunopathogenesis AnalysisGut Microbiota AnalysisGenetic Studies of IBDIntestinal Barrier Dysfunction in IBD
- Serum Biomarker Discovery for IBDSerological Biomarker Discovery for IBDInquiry
Metabolite Profiling and Identification in IBD Drug Discovery
Metabolite profiling and identification are qualitative and quantitative studies of drug biotransformation in non-clinical animals and humans. These studies include metabolite search and structure elucidation, pathway characterization, and metabolite relative abundance determination. The identification of metabolic pathways of drug candidates plays a key role in drug discovery, preclinical and clinical development. Insights into the pharmacokinetics and safety of compounds can be gained through a better understanding of the metabolic profile of IBD drugs.
Fig. 1. Deletion of mucin 2 induces colitis with concomitant metabolic abnormalities in mice. (Ishida et al., 2018)
Our Metabolite Profiling and Identification Services
Ace Therapeutics provides comprehensive metabolite profiling and identification services to profile, isolate, analyze and identify metabolites in support of IBD drug discovery and safety studies.
Our ADME experts have extensive expertise in a variety of techniques, including liquid chromatography (LC)-high resolution mass spectrometry (HRMS), chemically intelligent software algorithms, mass spectrometry imaging, ultraviolet (UV), radiometric detection, and nuclear magnetic resonance (NMR). These methods allow for a more pragmatic, multidisciplinary approach to answering key questions about the biotransformation and metabolism of IBD drugs, helping you take compounds from concept to drug candidate.
Our capabilities include:
- Radio-synthesis of 3H or 14C-labelled compounds
- Isolation and purification of metabolites
- Metabolite structure elucidation
- Metabolic soft-spot determination
- Cross-species metabolite characterization using liver microsomes and hepatocytes with unlabeled and radiolabeled test compounds
- Mechanistic studies (reactive metabolites, mechanism of chiral inversion, etc.)
- In vivo metabolite profiling and identification in rodent and large animal species
- Safety testing of metabolites
Why Choose Us
- We can analyze metabolites that may be formed to support your pharmacological, pharmacokinetic and toxicological studies of IBD drugs.
- We provide advanced multi-combinatorial techniques to determine the precise quality of any metabolite at high resolution.
- We can study metabolites in different matrices, including in-vitro microsomal incubations, hepatocyte incubations, expressed enzyme incubations as well as in vivo samples (plasma, urine, and other matrices).
- Reports are project-specific, depending on the nature of the project, ranging from simple tables of proposed structures to providing extracted ion chromatograms, MS and MS/MS spectra, and interpretation of the data for each metabolite.
Ace Therapeutics has the capability to perform metabolite profiling and identification studies on early IBD drug development in vitro samples and in vivo samples from animal studies. Our team of scientists designs bespoke experiments to help our client partners overcome their unique and complex challenges when it comes to IBD drug metabolism studies. If you are interested in our services, please do not hesitate to contact us.
Reference
- Ye, J., Haskey, N., Dadlani, et al. (2021). Deletion of mucin 2 induces colitis with concomitant metabolic abnormalities in mice. American Journal of Physiology-Gastrointestinal and Liver Physiology, 320(5), G791-G803.
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