The solubility of GLZ in all studied solvents was determined using an experimental approach such as the “isothermal saturation shake flask method” at T = 298.2–318.2 K and p = 0.1 MPa.46 The operational conditions and experimental procedures were same as mentioned in our previous work.40,45 Therefore, the experimental details are not included in the present study. Experiments were carried out in triplicate manner (n = 3). The content of GLZ in the solubility samples of 12 different neat solvents was analyzed by the UPLC-UV technique described above at λmax = 230 nm. The content of GLZ (μg g–1) was estimated using a calibration curve of GLZ. The xe values of GLZ were calculated by applying eq 1(26,27)
where m1 = mass of GLZ; m2 = mass of neat solvent; M1 = molar mass of GLZ; and M2 = molar mass of neat solvent.
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