Hi
@br2pi5 -
For the table (in passage 1), the fact that they describe it as a ratio suggests that it is a unitless number. This is not true for
all ratios, but it is true for ratios where you divide two values with the same units, which is a common way of coming up with analytically useful ratios. The fact that it's described as a "solubility enhancement" ratio suggests that it's an indication of how much the solubility shown in each row of the table is increased compared to some baseline. In Q3, which asks about this directly, we can eliminate A and B immediately because we're given no information about what the "hydrophobic solubility" of A would even mean, and then we can eliminate D because a ratio must involve dividing something -- so we can get away with only having a very general sense of how it's defined. However, we could also do some math to confirm that it's defined as the observed solubility of A in some MH solution divided by the baseline solubility of A in water, which gives us a measure of how much a certain MH solution increases the solubility of A.
For Q25, each cell in Table 1 contains an IC50 value in units of uM. Each of those values is specific for a certain compound (4a, 4b, 4c, 5a, or 5b) and a certain cell line (H1975, A549, or HCT116). Therefore, we can read down the table to determine how cytotoxic the compounds were for a given cell line, or read across to see how cytotoxic a certain compound was across various cell lines. That serves as the basis of comparison for Q25.
Hope this helps clarify these questions!