Variability in perfusion conditions and set-up parameters used in ex vivo human placenta models: A literature review

IF 3 2区 医学 Q2 DEVELOPMENTAL BIOLOGY
S.C. Glättli , F.A. Elzinga , W. van der Bijl , H.G.D. Leuvenink , J.R. Prins , H. van Goor , S.J. Gordijn , P. Olinga , D.J. Touw , P. Mian
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Abstract

The ex vivo human placenta perfusion model has proven to be clinically relevant to study transfer- and fetal exposure of various drugs. Although the method has existed for a long period, the setup of the perfusion model has not been generalized yet. This review aims to summarize the setups of ex vivo placental perfusion models used to examine drug transfer across the placenta to identify generalized properties and differences across setups. A literature search was carried out in PubMed September 26, 2022. Studies were labeled as relevant when information was reported, between 2000 and 2022, on the setups of ex vivo placental perfusion models used to study drug transfer across the placenta. The placenta perfusion process, and the data extraction, was divided into phases of preparation, control, drug, and experimental reflecting the chronological timeline of the different phases during the entire placental perfusion process. 135 studies describing an ex vivo human placental perfusion experiment were included. Among included studies, the majority (78.5%) analyzed drug perfusion in maternal to fetal direction, 18% evaluated bi-directional drug perfusion, 3% under equilibrium conditions, and one study investigated drug perfusion in fetal to maternal direction. This literature review facilitates the comparison of studies that employ similar placenta perfusion protocols for drug transfer studies and reveals significant disparities in the setup of these ex vivo placental perfusion models. Due to interlaboratory variability, perfusion studies are not readily comparable or interchangeable. Therefore, a stepwise protocol with multiple checkpoints for validating placental perfusion is needed.
体外人类胎盘模型所用灌注条件和设置参数的变异性:文献综述
体外人类胎盘灌注模型已被证明与临床相关,可用于研究各种药物的转移和胎儿暴露。虽然这种方法存在已久,但灌注模型的设置尚未普及。本综述旨在总结用于研究药物通过胎盘转移的体外胎盘灌注模型的设置,以确定不同设置的通用特性和差异。2022 年 9 月 26 日在 PubMed 上进行了文献检索。2000年至2022年期间,用于研究药物跨胎盘转移的体外胎盘灌注模型设置的相关研究均被标记为相关研究。胎盘灌注过程和数据提取分为准备阶段、对照阶段、药物阶段和实验阶段,反映了整个胎盘灌注过程中不同阶段的时间顺序。共纳入 135 项描述体外人类胎盘灌注实验的研究。在纳入的研究中,大多数(78.5%)分析了从母体到胎儿方向的药物灌注,18%评估了双向药物灌注,3%在平衡条件下进行,还有一项研究调查了从胎儿到母体方向的药物灌注。本文献综述有助于对采用类似胎盘灌注方案进行药物转移研究的研究进行比较,并揭示了这些体外胎盘灌注模型的设置存在显著差异。由于实验室间的差异,灌注研究不具有可比性或互换性。因此,需要一个包含多个检查点的分步方案来验证胎盘灌注。
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来源期刊
Placenta
Placenta 医学-发育生物学
CiteScore
6.30
自引率
10.50%
发文量
391
审稿时长
78 days
期刊介绍: Placenta publishes high-quality original articles and invited topical reviews on all aspects of human and animal placentation, and the interactions between the mother, the placenta and fetal development. Topics covered include evolution, development, genetics and epigenetics, stem cells, metabolism, transport, immunology, pathology, pharmacology, cell and molecular biology, and developmental programming. The Editors welcome studies on implantation and the endometrium, comparative placentation, the uterine and umbilical circulations, the relationship between fetal and placental development, clinical aspects of altered placental development or function, the placental membranes, the influence of paternal factors on placental development or function, and the assessment of biomarkers of placental disorders.
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