Elzinga Femke A, Khalili Behrad, Touw Daan J, Prins Jelmer R, Olinga Peter, Leuvenink Henri G D, van Goor Harry, Gordijn Sanne J, Nagelkerke Anika, Mian Paola
Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands.
Department of Pharmaceutical Analysis, Groningen Research Institute of Pharmacy, University of Groningen, Antonius Deunsinglaan 1, 9713 AV Groningen, The Netherlands.
J Clin Med. 2023 Jun 27;12(13):4315. doi: 10.3390/jcm12134315.
Quantification of fetal drug exposure remains challenging since sampling from the placenta or fetus during pregnancy is too invasive. Currently existing in vivo (e.g., cord blood sampling) and ex vivo (e.g., placenta perfusion) models have inherent limitations. A placenta-on-a-chip model is a promising alternative. A systematic search was performed in PubMed on 2 February 2023, and Embase on 14 March 2023. Studies were included where placenta-on-a-chip was used to investigate placental physiology, placenta in different obstetric conditions, and/or fetal exposure to maternally administered drugs. Seventeen articles were included that used comparable approaches but different microfluidic devices and/or different cultured maternal and fetal cell lines. Of these studies, four quantified glucose transfer, four studies evaluated drug transport, three studies investigated nanoparticles, one study analyzed bacterial infection and five studies investigated preeclampsia. It was demonstrated that placenta-on-a-chip has the capacity to recapitulate the key characteristics of the human placental barrier. We aimed to identify knowledge gaps and provide the first steps towards an overview of current protocols for developing a placenta-on-a-chip, that facilitates comparison of results from different studies. Although models differ, they offer a promising approach for in vitro human placental and fetal drug studies under healthy and pathological conditions.
由于孕期从胎盘或胎儿取样具有高度侵入性,胎儿药物暴露的定量分析仍然具有挑战性。目前现有的体内模型(如脐血取样)和体外模型(如胎盘灌注)都有其固有的局限性。芯片上胎盘模型是一种很有前景的替代方案。于2023年2月2日在PubMed以及2023年3月14日在Embase上进行了系统检索。纳入的研究中,芯片上胎盘模型用于研究胎盘生理学、不同产科情况下的胎盘以及/或胎儿对母体给药的暴露情况。共纳入17篇文章,这些文章采用了类似的方法,但使用了不同的微流控装置和/或不同的母体和胎儿细胞系进行培养。在这些研究中,4项对葡萄糖转运进行了定量分析,4项研究评估了药物转运,3项研究探讨了纳米颗粒,1项研究分析了细菌感染,5项研究调查了先兆子痫。结果表明,芯片上胎盘模型有能力再现人胎盘屏障的关键特征。我们旨在找出知识空白,并为概述当前开发芯片上胎盘模型的方案提供初步步骤,以便于比较不同研究的结果。尽管模型各有不同,但它们为在健康和病理条件下进行体外人胎盘和胎儿药物研究提供了一种很有前景的方法。