The
present study delineates the fabrication of paper-based devices
for culturing liver cells and developing related bioassays. The devices
were prepared by conventional lab-based LaserJet printing technology
and employed for 3D cell culture. Our results demonstrated that the
devices efficiently supported the growth of multiple cell types incuding
HepG2, HUVEC, fibroblasts, and MSCs. We further showed that the device
specifications (grade of paper or design parameters) greatly impacted
the functional phenotype of the HepG2 cells. We also explored the
application of the developed devices for routine cell culture, drug
screening, coculture, and transwell migration assays. The cellular
responses observed on the paper under different culture configurations
were similar to those obtained in the case of tissue culture plate
(TCP). Moreover, we showed that the paper-based devices were compatible
with the immunocytochemistry and ELISA procedures (no indication of
nonspecific matrix-antibody interaction). Considering the simplicity,
experimental flexibility, cost-effectiveness, and multiplexibility
of the paper-based liver models, it is deemed to be ideal for developing
cell-based bioassays, especially in resource-limited settings.