“…[128] In fact, changes in the particle size and ζ potential in parallel are routinely followed to additionally support insights about the interaction of given entities, and a similar combinatorial principle could be applied with numerous other experimental techniques. Some of these methods that were used in combination with the DLS electrophoresis so as to gain more profound insights into the mechanisms of the investigated physicochemical transformations have been small angle x-ray scattering (SAXS), [129] circular dichroism (CD), [130] isothermal titration calorimetry, [131] microbalance, rheological, and conductivity analyzers, [132–137] flow fractionation technologies, [138] various infrared spectroscopies, [139,140] x-ray photoelectron spectroscopy, [141] nuclear magnetic resonance, [142] UV-vis spectroscopy, [143] electron spin resonance spectroscopy, [144] surface enhanced Raman spectroscopy, [145] a range of electron, optical, and atomic force microscopic techniques, [146–148] and many other. The main risk, however, is that the complemented methods may give contrasting and incompatible information.…”