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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
被引:8
|作者:
Elzinga, Femke A.
[1
]
Khalili, Behrad
[1
]
Touw, Daan J.
[1
,2
]
Prins, Jelmer R.
[3
]
Olinga, Peter
[4
]
Leuvenink, Henri G. D.
[5
]
van Goor, Harry
[6
]
Gordijn, Sanne J.
[3
]
Nagelkerke, Anika
[2
]
Mian, Paola
[1
]
机构:
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Hanzepl 1, NL-9713 Groningen, Netherlands
[2] Univ Groningen, Groningen Res Inst Pharm, Dept Pharmaceut Anal, Antonius Deunsinglaan 1, NL-9713 AV Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Obstet & Gynecol, Hanzepl 1, NL-9713 GZ Groningen, Netherlands
[4] Univ Groningen, Groningen Res Inst Pharm, Dept Pharmaceut Technol & Biopharm, Antonius Deunsinglaan 1, NL-9713 AV Groningen, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Surg, Hanzepl 1, NL-9713 GZ Groningen, Netherlands
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, Pathol Sect, Hanzepl 1, NL-9713 GZ Groningen, Netherlands
关键词:
placenta-on-a-chip;
human placental barrier;
microfluidic device;
TROPHOBLAST INVASION;
MODEL;
PREGNANCY;
GROWTH;
D O I:
10.3390/jcm12134315
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
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.
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