Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Oct 22;9(10):536.
doi: 10.3390/mi9100536.

Organs-on-a-Chip Module: A Review from the Development and Applications Perspective

Affiliations
Review

Organs-on-a-Chip Module: A Review from the Development and Applications Perspective

Juan Eduardo Sosa-Hernández et al. Micromachines (Basel). .

Abstract

In recent years, ever-increasing scientific knowledge and modern high-tech advancements in micro- and nano-scales fabrication technologies have impacted significantly on various scientific fields. A micro-level approach so-called "microfluidic technology" has rapidly evolved as a powerful tool for numerous applications with special reference to bioengineering and biomedical engineering research. Therefore, a transformative effect has been felt, for instance, in biological sample handling, analyte sensing cell-based assay, tissue engineering, molecular diagnostics, and drug screening, etc. Besides such huge multi-functional potentialities, microfluidic technology also offers the opportunity to mimic different organs to address the complexity of animal-based testing models effectively. The combination of fluid physics along with three-dimensional (3-D) cell compartmentalization has sustained popularity as organ-on-a-chip. In this context, simple humanoid model systems which are important for a wide range of research fields rely on the development of a microfluidic system. The basic idea is to provide an artificial testing subject that resembles the human body in every aspect. For instance, drug testing in the pharma industry is crucial to assure proper function. Development of microfluidic-based technology bridges the gap between in vitro and in vivo models offering new approaches to research in medicine, biology, and pharmacology, among others. This is also because microfluidic-based 3-D niche has enormous potential to accommodate cells/tissues to create a physiologically relevant environment, thus, bridge/fill in the gap between extensively studied animal models and human-based clinical trials. This review highlights principles, fabrication techniques, and recent progress of organs-on-chip research. Herein, we also point out some opportunities for microfluidic technology in the future research which is still infancy to accurately design, address and mimic the in vivo niche.

Keywords: applications; biomedical; biosensors; in vivo models; microfluidics; organ-on-a-chip.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Schematic representation of flow lines in microscale and macroscale. Flow lines follow straight paths in microscale with a parabolic profile; contrary to macroscale, flow lines follow crossing paths with no defined pattern.
Figure 2
Figure 2
Overview of the advantages and challenges of both macroscopic and microfluidic cell culture. Reproduced from Halldorsson et al. [12], with permission from Elsevier.
Figure 3
Figure 3
A schematic representation of electrokinetic phenomena. (A) electro-osmosis, (B) electrophoresis, (C) dielectrophoresis, and (D) electrothermal in alternate current.
Figure 4
Figure 4
The process to produce different OoCs is in principle the same, taking into account the application. First, the design must address the properties to emulate and measure. Second, different cells must be incubated into the device. Third, cellular growth, differentiation and function are established in order for the chip to operate like an organ. Fourth, data is obtained through chemical and physical testing.
Figure 5
Figure 5
Organs-sensors-on-a-chip microfluidic representation.

References

    1. Manz A., Graber N., Widmer H.Á. Miniaturized total chemical analysis systems: A novel concept for chemical sensing. Sens. Actuators B Chem. 1990;1:244–248. doi: 10.1016/0925-4005(90)80209-I. - DOI
    1. Verpoorte E., De Rooij N.F. Microfluidics meets MEMS. Proc. IEEE. 2003;91:930–953. doi: 10.1109/JPROC.2003.813570. - DOI
    1. Whitesides G.M. The Origins and the Future of Microfluidics. Nature. 2006;442:368–373. doi: 10.1038/nature05058. - DOI - PubMed
    1. Bravard J.P., Petit F. Encyclopedia of Inland Waters. Elsevier; Amsterdam, The Netherlands: 2009. Geomorphology of Streams and Rivers; pp. 387–395.
    1. Mohammed M.I., Zainal Alam M.N.H., Kouzani A., Gibson I. Fabrication of Microfluidic Devices: Improvement of Surface Quality of CO2 Laser Machined Poly(Methylmethacrylate) Polymer. J. Micromech. Microeng. 2017;27:015021. doi: 10.1088/0960-1317/27/1/015021. - DOI

LinkOut - more resources