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Pharmacokinetic study

Investigate in depth the dynamic processes of drug absorption, distribution, metabolism, and excretion (ADME) within living organisms.
In vivo PK studies: Support multiple administration routes, including intravenous (IV), oral (PO), subcutaneous (SC), and intraperitoneal (IP), enabling high‑precision plasma concentration monitoring and pharmacokinetic analysis in both rodent (large and small mice) and non‑rodent species.
Tissue Distribution and Barrier Penetration: Clarify the drug’s organ‑specific distribution in vivo, with a particular focus on assessing its ability to cross the blood–brain barrier (BBB), thereby providing critical data for the development of central nervous system therapeutics.
Excretion Studies and Metabolite Profiling: Urine, feces, and bile are collected to conduct precise analyses of drug excretion ratios and metabolite profiles.
In vitro early-stage ADME screening: Provides plasma protein binding, metabolic stability, CYP450 enzyme inhibition and induction assays, Caco-2 permeability studies, and more.