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Fibrin polymer as a

naturally derived The Spray-On


spray-on bandage.
Krissy Peterson, Abby Edward, Amanda
Moravek, Elizabeth Vargis
Bio-Bandage Conclusions
● Cell growth, and fibrinogen formation
(Figure 3), and scratching (Figure 4) was
successful
Introduction Results ● Further research is required to successfully
● Fibrin is a natural polymer that is already ● 3T3 cells were successfully grown to a confluency of 90% create a spray-on bandage
used in extreme clinical settings as an ● Clear scratches were made through the cell monolayer ● Aspects to change include cell scaffolding,
adhesive and for shallow wounds when ● Fibrin gel formation was successful spray bottle, and cell growth inhibitors
activated by the enzyme, thrombin ● The bottles’ spray exerted too much force on the cells and caused
● This study tested a spray-on bandage with additional cell death compared to the untreated cells (Figure 2, treated
thrombin and fibrinogen that enhances the and untreated cells)
body’s healing without the risks of current ● The cells migrated very quickly through the cleared area, resulting in an
formulations unclear healing progress (Figure 2, Days 1 and 3 treated cells)
A
B Day 0 Day 1 Day 3
Figure 3. Fibrin gel formation on a petri dish.

A
Scratched
Treated

Figure 1. A) Molecular mechanics of fibrinogen


formation. B) Application of the spray-on Scratched B
bio-bandage. Untreated

Methods
Inoculated cell culture plates with viable 3T3
mouse fibroblast cell Unscratched Figure 4. A) Brightfield image of scratched cells.
Treated B) Brightfield image of unscratched cells.

90% confluent cells were scratched with a References


pipette tip 1. Radhakrishnan, Arun, et al. “Spray Bandage Strategy in Topical Drug
Delivery.” Journal of Drug Delivery Science and Technology, vol. 43, 2018,
pp. 113–121.
2. Chittoria, RaviKumar, et al. “Effectiveness of Fibrin Glue in Adherence of
Cells were immediately sprayed with Unscratched Skin Graft.” Journal of Cutaneous and Aesthetic Surgery, vol. 10, no. 2,
fibrinogen and thrombin and incubated for Untreated 2017, p. 72.
3. Sigma Aldrich representative: Greg Fuchs, Technical Support Scientist II
0, 1, and 3 days 4. NIH/3T3 - CRL-1658 | ATCC. https://www.atcc.org/products/crl-1658.
5. Jonkman, James, et al. An introduction to the wound healing assay using
live-cell microscopy. Cell Adh Migr. 2014;8(5):440-51.

Cells were live/dead stain and imaged with a Figure 2. Live/Dead Stain Fluorescence Images
fluorescent microscope Utah State University
The red color is showing dead cells and green is showing live cells. Biological Engineering Department
Study conducted with funding and lab assistance
Images were analyzed in ImageJ from USU Tissue Engineering class.

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