To achieve the mass ALK inhibitor cancer balance, the total amount of vanillin was determined

using one or both the calibration curves depending on the vanillin structures present in the media. After the validation of the methods used for the quantification of the biomolecules, their partition coefficients were addressed. The partition analysis of these ATPS was assessed making use of the logarithmic function of the partition coefficient (log K). According to Fig. 2, it is observed that vanillin and l-ascorbic acid preferentially migrate to opposite phases, the top and bottom phases, respectively. While vanillin preferentially migrates to the alcohol-rich phase (log K > 0), l-ascorbic acid has a higher affinity for the salt-rich phase (log K < 0). Aiming at explaining the preference of the acid for the salt-rich phase, some assumptions can be taken into account. The first is related to the l-ascorbic acid chemical structure (depicted in Fig. 2). This biomolecule is highly polar and has the capacity to establish a vast number of hydrogen bonds with water, having more affinity to the

more hydrophilic (salt-rich) phase. In an opposite way, vanillin is less Selleck Enzalutamide polar since it presents a lower number of hydrogen-bond acceptors, and has a consequently higher aptitude for the hydrophobic (alcohol-rich) phase. This trend is also in close agreement with the 1-octanol–water partition coefficients reported in literature for each biomolecule. Reported experimental Orotidine 5′-phosphate decarboxylase values of this parameter, log Kow = 1.19 ( Noubigh et al., 2010) for vanillin and log Kow = −1.85 ( Takács-Novak & Avdeef, 1996) for l-ascorbic acid, show that these molecules have a different hydrophilic/lipophilic aptitude. l-ascorbic acid is more hydrophilic (log Kow < 0), while vanillin is more hydrophobic (log Kow > 0). The partition results obtained here are indeed in good agreement with the log

Kow values ( Noubigh et al., 2010 and Takács-Novak and Avdeef, 1996), suggesting that the molecules’ hydrophobicity control the partition nature of these ATPS. Moreover, in order to evaluate the alcohol and salt influence in the partitioning of both biomolecules, the recovery percentages of vanillin in the top phase (Rvan−T) and l-ascorbic acid in the bottom phase (RAA−B), were also evaluated and are presented in Fig. 3. For all the aqueous systems studied, the recovery of vanillin for the alcohol-rich phase is between (98.37 ± 0.08)% and (99.94 ± 0.01)%, while the recovery of l-ascorbic acid for the salt-rich phase is between (85.15 ± 1.27)% and (95.50 ± 0.19)%. Finally, the recovery results obtained also show that the effect of the alcohol molecular structure on the extraction of both antioxidants is marginal; yet, stronger salting-out inducing inorganic salts, namely K3PO4 and K2HPO4, largely enhance the recovery achieved at each phase.