Melander Erik, Nielsen Elisabet I, Lindqvist Annika, Hovd Markus, Gandia Peggy, Panchaud Alice, Guidi Monia, Annaert Pieter, Baranczewski Pawel, Spigset Olav, Nordeng Hedvig
Department of Pharmacy, Uppsala Drug Optimization and Pharmaceutical Profiling (UDOPP), Uppsala University, Uppsala, Sweden.
Department of Pharmacy, Clinical Pharmacy research group, Uppsala University, Uppsala, Sweden.
Basic Clin Pharmacol Toxicol. 2025 Jan;136(1):e14100. doi: 10.1111/bcpt.14100. Epub 2024 Nov 4.
Cetirizine is an antihistamine commonly used to treat allergic rhinitis and other allergic conditions. Cetirizine is often prescribed to breastfeeding mothers although there is limited information on infant exposure via breast milk. The aim of this study was to develop a popPK model based on data from a lactation study to predict cetirizine breast milk concentrations and estimate the relative infant dose (RID) in a breastfed infant. A popPK model was developed in NONMEM on data from a human lactation study including 35 women using cetirizine or levocetirizine while breastfeeding. Serial samples of breast milk were collected (n = 205) and the cetirizine concentrations quantified using a validated LC-MS/MS method. A one-compartment model of cetirizine in breast milk was developed and employed to calculate the relative infant dose (RID). Covariates related to the maternal characteristics and breastfeeding patterns were evaluated in the model; only milk sampling pumping duration was found to be a significant covariate, with an increasing pumping duration leading to an increased apparent milk volume of distribution (V). The mean RID was 1.99% with the highest RID being 3.36% at C. PopPK modelling could be used to estimate infant exposure to cetirizine via breast milk. The low predicted exposure in infants supports that cetirizine is compatible with breastfeeding.
西替利嗪是一种常用于治疗过敏性鼻炎和其他过敏病症的抗组胺药。尽管关于婴儿通过母乳接触西替利嗪的信息有限,但西替利嗪仍经常被开给哺乳期母亲。本研究的目的是基于一项泌乳研究的数据建立一个群体药代动力学(popPK)模型,以预测西替利嗪在母乳中的浓度,并估算母乳喂养婴儿的相对婴儿剂量(RID)。利用来自一项人体泌乳研究的数据,在NONMEM中建立了一个群体药代动力学模型,该研究包括35名在哺乳期使用西替利嗪或左西替利嗪的女性。收集了系列母乳样本(n = 205),并使用经过验证的液相色谱-串联质谱(LC-MS/MS)方法对西替利嗪浓度进行定量。建立了母乳中西替利嗪的一室模型,并用于计算相对婴儿剂量(RID)。在模型中评估了与母亲特征和母乳喂养模式相关的协变量;仅发现吸乳持续时间是一个显著的协变量,吸乳持续时间增加会导致表观母乳分布容积(V)增加。平均相对婴儿剂量为1.99%,在C时最高相对婴儿剂量为3.36%。群体药代动力学建模可用于估算婴儿通过母乳接触西替利嗪的情况。预测的婴儿接触量较低,这支持西替利嗪与母乳喂养兼容。