“…It can be performed using the well-elaborated hot-injection [12], heating-up (noninjection) [13], thermal decomposition of a singlesource precursor [14], tuning the relative reactivity of cationic precursors [15], or solvothermal [16,17] techniques and leads to the formation of hydrophobic I-III-VI QDs. In order to obtain water-soluble QDs, important for applications in life sciences, the ligand exchange is performed [7]. A water-based approach is the direct synthesis from aqueous solutions by the arrested precipitation with mercaptoacetic (thioglycolic) acid [10,18], mercaptopropionic acid [19], glutathione [11,20], etc.…”