Placenta-on-a-Chip as an In Vitro Approach to Evaluate the Physiological and Structural Characteristics of the Human Placental Barrier upon Drug Exposure: A Systematic Review

Author:

Elzinga Femke A.1ORCID,Khalili Behrad1ORCID,Touw Daan J.12ORCID,Prins Jelmer R.3ORCID,Olinga Peter4ORCID,Leuvenink Henri G. D.5,van Goor Harry6ORCID,Gordijn Sanne J.3,Nagelkerke Anika2ORCID,Mian Paola1ORCID

Affiliation:

1. Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands

2. Department of Pharmaceutical Analysis, Groningen Research Institute of Pharmacy, University of Groningen, Antonius Deunsinglaan 1, 9713 AV Groningen, The Netherlands

3. Department of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands

4. Department of Pharmaceutical Technology and Biopharmacy, Groningen Research Institute of Pharmacy, University of Groningen, Antonius Deunsinglaan 1, 9713 AV Groningen, The Netherlands

5. Department of Surgery, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands

6. Department of Pathology and Medical Biology, Pathology Section, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands

Abstract

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.

Publisher

MDPI AG

Subject

General Medicine

Reference53 articles.

1. (2023, February 28). Eurocat—Use of Teratogenic Medication during Pregnancy. Available online: https://umcgresearch.org/w/eurocat-use-of-teratogenic-medication-during-pregnancy.

2. Placental Drug Transport-on-a-Chip: A Microengineered In Vitro Model of Transporter-Mediated Drug Efflux in the Human Placental Barrier;Blundell;Adv. Healthc. Mater.,2018

3. Drug transport across the human placenta: Review of placenta-on-a-chip and previous approaches;Pemathilaka;Interface Focus,2019

4. 3D microfluidics-assisted modeling of glucose transport in placental malaria;Mosavati;Sci. Rep.,2022

5. Growth and function of the normal human placenta;Gude;Thromb. Res.,2004

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