结果：奥美拉唑的药时曲线符合单室模型。
RESULTS: the concentration-time curve of omeprazole complied with the single compartment model.
结论建立了单室模型药物血管外给药零级释放和一级释放的药物动力学。
Conclusion the pharmacokinetic theories of the zero-order release and the first-order release of mono-compartment drugs administered by non-parenteral route have been established.
目的建立单室模型药物血管外多剂量给药的吸收和清除药动学的残数法计算方法。
Objective To establish a feathering method for processing the pharmacokinetic parameters of mono-compartment drugs administered by non-parenteral route by repeated doses.
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