Understanding the relationship between drug exposure and therapeutic response is critical in the development of effective treatments for Eosinophilic Esophagitis (EoE). Our specialized pharmacokinetic/pharmacodynamic (PK/PD) research services are designed to elucidate how candidate therapeutics are absorbed, distributed, metabolized, and eliminated, as well as their pharmacological effects in relevant biological systems. Through comprehensive PK/PD studies, we provide actionable insights that inform dosing strategies, optimize therapeutic efficacy, and support regulatory submissions for EoE therapies.
We offer a broad range of administration routes to accommodate the diverse needs of Eosinophilic Esophagitis research, including oral, intravenous, intraperitoneal, and intranasal delivery. These flexible options enable the investigation of different drug delivery strategies, facilitating the assessment of systemic versus localized exposure, and supporting the development of both traditional and novel therapeutic modalities for EoE.
Our services encompass extensive compartment analysis, allowing for precise measurement of drug concentrations and biomarkers in a wide array of biological matrices. We routinely analyze plasma, serum, blood, interstitial fluid, and key tissues such as the esophagus, lung, intestine, and associated lymphoid organs. This capability is essential for characterizing drug distribution and pharmacodynamic effects in compartments directly implicated in EoE pathophysiology.
We employ a comprehensive suite of advanced analytical techniques, including high-performance liquid chromatography (HPLC), HPLC with fluorescence (HPLC-F), HPLC with mass spectrometry (HPLC-MS), ultra-performance liquid chromatography (UPLC), UPLC-MS, liquid chromatography-mass spectrometry (LC-MS), enzyme-linked immunosorbent assay (ELISA), immunoassays, and radioactivity-based methods. These platforms support robust quantification of drugs and metabolites, as well as sensitive biomarker analysis and validation, ensuring high-quality, reproducible data.
Our facility supports studies in a diverse range of preclinical animal models, including mice, rats, rabbits, dogs, pigs, and monkeys. These models provide translational relevance for EoE research, enabling the evaluation of pharmacokinetics, tissue distribution, and pharmacodynamic responses in systems that recapitulate key aspects of human disease. Selection of appropriate models is tailored to the specific objectives of each EoE study.
Our integrated PK/PD studies deliver critical insights into drug absorption, distribution, metabolism, and excretion (ADME) properties; establish concentration-effect relationships; inform dosing optimization; and facilitate interspecies scaling to predict human pharmacokinetics and pharmacodynamics. These data are essential for advancing EoE therapeutics from preclinical development to clinical application.
With deep expertise in Eosinophilic Esophagitis and a comprehensive suite of PK/PD research services, we are committed to supporting your therapeutic development goals. Partner with us to leverage our scientific rigor, advanced technologies, and tailored study designs for impactful, translational EoE research.
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