Development of an Organ-on-a-Chip-Device for Study of Placental Pathologies

Autor: E. Du, Babak Mosavati, Andrew V. Oleinikov
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0301 basic medicine
Placenta
02 engineering and technology
Placental barrier
Umbilical vein
Diffusion
lcsh:Chemistry
Pregnancy
Lab-On-A-Chip Devices
Membrane porosity
molecular concentration distribution
Maternal-Fetal Exchange
lcsh:QH301-705.5
Spectroscopy
placenta-on-a-chip
Chemistry
General Medicine
021001 nanoscience & nanotechnology
Trophoblasts
Computer Science Applications
embryonic structures
Female
Rheology
0210 nano-technology
Porosity
Microfluidics
microfluidics
Models
Biological

Organ-on-a-chip
Article
Catalysis
Inorganic Chemistry
03 medical and health sciences
Fetus
Microfluidic channel
Human Umbilical Vein Endothelial Cells
Humans
Physical and Theoretical Chemistry
Molecular Biology
Organic Chemistry
Glucose transporter
glucose transport
Biological Transport
Membranes
Artificial

Coculture Techniques
Kinetics
Glucose
030104 developmental biology
lcsh:Biology (General)
lcsh:QD1-999
Biophysics
Zdroj: International Journal of Molecular Sciences, Vol 21, Iss 8755, p 8755 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 22
ISSN: 1661-6596
1422-0067
Popis: The human placenta plays a key role in reproduction and serves as a major interface for maternofetal exchange of nutrients. Study of human placenta pathology presents a great experimental challenge because it is not easily accessible. In this paper, a 3D placenta-on-a-chip model is developed by bioengineering techniques to simulate the placental interface between maternal and fetal blood in vitro. In this model, trophoblasts cells and human umbilical vein endothelial cells are cultured on the opposite sides of a porous polycarbonate membrane, which is sandwiched between two microfluidic channels. Glucose diffusion across this barrier is analyzed under shear flow conditions. Meanwhile, a numerical model of the 3D placenta-on-a-chip model is developed. Numerical results of concentration distributions and the convection&ndash
diffusion mass transport is compared to the results obtained from the experiments for validation. Finally, effects of flow rate and membrane porosity on glucose diffusion across the placental barrier are studied using the validated numerical model. The placental model developed here provides a potentially helpful tool to study a variety of other processes at the maternal&ndash
fetal interface, for example, effects of drugs or infections like malaria on transport of various substances across the placental barrier.
Databáze: OpenAIRE