A Novel Plated Hepatocyte Relay Assay (PHRA) for In Vitro Evaluation of Hepatic Metabolic Clearance of Slowly Metabolized Compounds

孵化 体外 肝细胞 低温保存 体内 化学 新陈代谢 药理学 生物 生物化学 胚胎 细胞生物学 生物技术
作者
Chi‐Chi Peng,Utkarsh Doshi,Chandra Prakash,Albert P. Li
出处
期刊:Drug Metabolism Letters [Bentham Science Publishers]
卷期号:10 (1): 3-15 被引量:9
标识
DOI:10.2174/1872312809666150818111500
摘要

Objective: Development and validation of a novel assay, the Plated Hepatocyte Relay Assay (PHRA), for the determination of the metabolic fates of slowly metabolized compounds. Method: Cryopreserved human hepatocytes were cultured for 4 h followed by incubation with slowly metabolized compounds for 24 h (initial incubation). On the next day, the incubated media were collected and added to hepatocytes was similarly prepared on the day of incubation (48 h incubation; 1st relay). The procedures were repeated on the next days (72 h (2nd relay), 96 h (3rd relay), and 120 h (4th relay) incubations). Results: A proof-of-concept study with two low clearance compounds, diazepam and tolbutamide, and a validation study with 15 ultra-low clearance compounds (CLnon-renal < 1 mL/min/kg) and low clearance compounds (CLnon-renal 1- 5.1 mL/min/kg) were performed. Linear time-dependent disappearance of the parent compounds was observed for all compounds. Application of published free fraction values in combination with a correction factor with in vitro hepatic clearance results obtained with the PHRA accurately predicted in vivo hepatic clearance. Conclusion: PHRA represents a useful experimental system for the evaluation of the metabolic fates of low clearance compounds in drug development.. Keywords: Cryopreserved hepatocytes, hepatic clearance, human hepatocytes, low clearance compounds, metabolic clearance, relay assay, slowly metabolized compounds.
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