药物在有限时间内被吸收:生物制药和药代动力学的新时代

P. Macheras
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引用次数: 0

摘要

从早期的药代动力学(1)开始,药物吸收就被建模为一阶过程,这意味着药物吸收的时间是无限的。根据目前的科学知识和常识,药物是在有限的时间内被动吸收的。吸收“有限时间”的概念已被用于各种基于生理的药代动力学(PBPK)模型。然而,最近发表了基于生理的有限时间药代动力学(PBFTPK)模型的正式发展(2-5)。PBFTPK模型基于两个原则建立:i)药物在有限时间内被动吸收,τ和ii)时间吸收限制与药物在胃、小肠和结肠的胃肠道转运时间相关(2-5)。(PBFTPK)0和(PBFTPK)1模型分别使用零一阶输入。
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Drugs are Absorbed in Finite Time: A New Era in Biopharmaceutics and Pharmacokinetics
From the early days of Pharmacokinetics (1) drug absorption was modeled as a first-order process implying an infinite time for drug absorption. According to the current scientific knowledge and common wisdom, drugs are absorbed passively in finite time. The concept of “finite time” of absorption has been used in various Physiologically Based Pharmacokinetic (PBPK) models. However, the formal development of Physiologically Based Finite Time Pharmacokinetic (PBFTPK) models was published recently (2-5). The PBFTPK models were built on two principles: i) drugs are absorbed passively for a finite period of time, τ and ii) time absorption constrains linked with the gastrointestinal transit times of drug in the stomach, the small intestines and the colon were applied (2-5). Zeroor first-order input is used for the (PBFTPK)0 and (PBFTPK)1 models, respectively.
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