surface of an appropriate substrate with the support of special polymers which are
sensitive only to the well-defined wavelengths of light which would finally create
desired geometric patterns on a substrate. These microfluidic systems are employed
(Ma et al. 2017) to create lab-on-a-chip devices which are illustrated in Figs. 16.26
and 16.27. The next section deals with a specific application known as heart-on-a-
chip which would help and go a long way to find solutions for CAD.
16.7.1 Heart-on-a-Chip
The standard static cell culture approach lacks in fully capturing the intricate in vivo
environment. In addition, the current drug discovery process is currently a very
difficult and costly process. Moreover, majority of the drug candidates fail to enter
even clinical trials. In such a scenario, microfluidics play a vital role in biological
research domains which include diagnostic sector, disease modeling, and therapeutic
approaches. These include cardiac research area also. Microfluidic technology along
with stem cell technology has been playing a revolutionary role in the cardiac tissue
engineering which has resulted in fabrication of cardiac lab-on-a-chip which is also
known as heart-on-a-chip device (Kitsara et al. 2019). It has been made possible to
recreate cardiac tissues using cell culturing techniques in a highly spatiotemporally
controlled microenvironment (Chan et al. 2015) from patient-specific models to
mimic the natural habitat of the heart cells. This has resulted in heart-on-a-chip
devices consisting of numerous imprinted microchambers as well as microchannels
on a polymer which is bonded on another material (normally a glass). Transparency
and biocompatibility (which is defined as the extent of its permeability to oxygen
and carbon dioxide) (Crone 1963) are two required properties of the polymeric
material to be used for this application. Such characteristic properties are easily
met by the material polydimethylsiloxane (PDMS).
Cells are housed in microchannels and microchambers to which reagents like
growth factors, cytokines, and nutrients are delivered. ECM-derived hydrogels
(biological reagents) and enzyme/protein stick the cells to the surface and monitor
the dynamics of cell culture. Microchambers are usually lined with primary heart
cells and controlled with the help of microchannels, microvalves, and actuators.
Monitoring is done with the help of digital and biological sensors in addition to the
imaging devices (Zhang et al. 2020; Lammertsma 2002).
Flow in the main and side microchannels usually control transportation of
nutrition (Renkin 1959) as well as waste discharge. Real-time monitoring of the
cells in these microfluidic devices can be carried out by engaging pressure and flow
sensors. Electrophysiology and mechanobiology of the experiment could be con-
trolled by tailoring the chip (Liu et al. 2020) by adding electrical and mechanical
components. This could also help in mimicking the in vivo conditions. These are
known as electrical and mechanical actuators. This can help in actually placing
different electrodes in the chip for stimulating the cell as well as using it as a readout
system. This device is very helpful in probing the cellular behavior against a number
of stimuli.
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