Page 462 - IJB-10-5
P. 462

International Journal of Bioprinting                            3D-printed plasma devices for decontamination















































            Figure 7. Virus infectivity reduction after cold atmospheric plasma (CAP) treatment for (A) SARS-CoV-2; (B) influenza A H1N1; (C) adenovirus; and
            (D) rhinovirus. The viral inoculum was spotted on parafilm, air-dried, and subsequently exposed to CAP for specific durations. The residual infectivity of
            the viruses was determined in cell culture, and the results are plotted as relative percentages to untreated control samples. The average of three biological
            replicates with the standard error of the mean are displayed for all the measurements. Increasing the duration of CAP exposure resulted in a progressive
            reduction in viral infectivity, and optimized devices 2 and 3 were superior to original device 1. If complete elimination of infectivity was achieved, residual
            infectivity was not analyzed at longer exposure times (n.a.).


            (Figure 8A; Table S1 in Supplementary File). Hence, the   complete  elimination after  30  min  of exposure,
            virucidal effect of the optimized devices occurred more   whereas  the  original  device  was  unable  to  completely
            rapidly, with device 3 exhibiting slightly higher efficiency   inactivate HRV even after 120 min (Figure 7D;  Table
            than device 2.                                     S4 in Supplementary File). The number of viral genome

               All the tested 3D-printed devices completely    copies decreased by approximately 75% after 30 min of
            abrogated the infectivity of IAV. The original device   treatment with devices 2 or 3, whereas device 1 produced
            required 90 min to completely eliminate the infectious   similar results after only 120 min (Figure 8D; Table S4 in
            capacity of IAV, whereas the optimized devices required   Supplementary File).
            only 30 min (Figure 7B; Table S2 in Supplementary File).   As expected, the HAdV samples were more resistant
            Device 3 demonstrated significantly better performance   to treatment with CAP than the tested RNA viruses
            in terms of particle destruction than did device 2   were and required longer exposures to decrease  their
            (Figure 8B; Table S2 in Supplementary File). The inferior   infectivity. The optimized devices facilitated the
            performance of the original device was also documented   complete elimination of the HAdV infectious capacity
            by qPCR analysis.                                  after 120 min, whereas the original device only reduced

               Following CAP treatment using the optimized     the infectivity by approximately 80% after the same
            devices, HRV infectivity decreased over time, reaching   exposure time (Figure 7C;  Table S3). Viral genome


            Volume 10 Issue 5 (2024)                       454                                doi: 10.36922/ijb.3679
   457   458   459   460   461   462   463   464   465   466   467