Huang Miao-Chan, Macente Julia, Nauwelaerts Nina, Bonan Rodolfo Hernandes, Elmi Alberto, Ventrella Domenico, Annaert Pieter
Drug Delivery and Disposition, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
esqLABS GmbH, Saterland, Germany.
AAPS J. 2025 Jul 28;27(5):125. doi: 10.1208/s12248-025-01109-7.
Amoxicillin is frequently prescribed to peripartum women as prophylaxis and treatment for infection. Despite frequent usage of amoxicillin in lactating women, quantitative evidence regarding its transfer between systemic circulation and breastmilk remains limited. However, such data is fundamentally essential for assessing the safety risk of medicine usage during breastfeeding.
This research performed population pharmacokinetic (PopPK) modeling and simulation to characterize the pharmacokinetics of amoxicillin in plasma and breastmilk in lactating Göttingen Minipigs, a physiologically relevant animal model to humans that enables studying medication transfer during lactation.
Demographic characteristics and amoxicillin concentrations in plasma and breastmilk following daily intramuscular doses (7 mg/kg) in 9 minipigs from two studies were included in the PopPK analysis. The milk-to-plasma (M/P) ratio, daily infant dosage (DID), and relative infant dose (RID) were calculated based on the simulated steady-state exposure.
The final model consisted of a two-compartment distribution with zero-order absorption and linear elimination. The central compartment was deemed as the plasma compartment with time-varying volume of distribution, and linked to the breastmilk compartment via bidirectional first-order transfer. No covariate was included. The developed PopPK model well described amoxicillin in plasma and breastmilk in the lactating Göttingen Minipigs. The predicted M/P ratio, DID, and RID of amoxicillin following the maximal doses were approximately 0.25, 0.11 mg·kg·day, and 1.6% for Göttingen Minipigs, respectively.
The model-based simulation indicated minimal amoxicillin exposure to the breastfed piglets, suggesting a low safety risk, which was reinforced by the absence of adverse events in the piglets.
阿莫西林经常被开给围产期妇女用于感染的预防和治疗。尽管哺乳期妇女经常使用阿莫西林,但其在体循环和母乳之间转移的定量证据仍然有限。然而,这些数据对于评估母乳喂养期间用药的安全风险至关重要。
本研究进行了群体药代动力学(PopPK)建模和模拟,以表征阿莫西林在哺乳期哥廷根小型猪血浆和母乳中的药代动力学,哥廷根小型猪是一种与人类生理相关的动物模型,能够研究哺乳期药物转移情况。
两项研究中9只小型猪每日肌肉注射剂量(7mg/kg)后,其人口统计学特征以及血浆和母乳中的阿莫西林浓度被纳入PopPK分析。基于模拟的稳态暴露计算了乳-血(M/P)比值、每日婴儿剂量(DID)和相对婴儿剂量(RID)。
最终模型由具有零级吸收和线性消除的二室分布组成。中央室被视为具有时变分布容积的血浆室,并通过双向一级转移与母乳室相连。未纳入协变量。所建立的PopPK模型很好地描述了哺乳期哥廷根小型猪血浆和母乳中的阿莫西林。对于哥廷根小型猪,最大剂量后阿莫西林的预测M/P比值、DID和RID分别约为0.25、0.11mg·kg·天和1.6%。
基于模型的模拟表明,母乳喂养的仔猪接触到的阿莫西林极少,提示安全风险较低,仔猪未出现不良事件进一步证实了这一点。