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. 2021 Jan 4;129(1):017004. doi: 10.1289/EHP7600

Figure 3.

Figures 3A and 3C are sets of four bioactivity staining of iCell Neurons and HUVECs, namely, Control, Vehicle (0.25 percent dimethyl sulfoxide), active concentration at 50 percent uppercase h, and point-of detection uppercase h. Figure 3B is a set of four graphs titled Control, Vehicle (0.25 percent dimethyl sulfoxide), active concentration at 50 percent uppercase h, and point-of detection uppercase h, plotting iCell Cardiomyocytes Relative Light Units, ranging from 1000 to 5000 in increments of 1000 (y-axis) across Time in seconds, ranging from 0 to 100 in increments 20 (x-axis).

Representative examples of bioactivity in different cell types. (A), fluorescent (calcein) staining (objective magnification=20×) of untreated (control) iCell neurons or cell treated with vehicle, or two designed mixtures (AC50-H at lowest tested concentration, diluted by 10,000× from the highest concentration, and POD-H at an intermediate tested concentration, diluted by 100× from the highest concentration). See acronym explanations and description of the designed mixtures in Table 1. (B), characteristic kinetic imaging-derived fluorescence intensity traces indicative of the Ca2+ fluxes across cell membranes of iCell cardiomyocytes that spontaneously contract in cell culture. (C), fluorescent (calcein) staining (objective magnification=4×) of untreated (control) HUVECs or cell treated with vehicle, or two designed mixtures. See Table 1 for description of designed mixtures AC50-H and POD-H.