Kinetic and structural features of a dyestuff coaggregation studied by time-resolved static light scattering

J Phys Chem B. 2013 Dec 5;117(48):15165-75. doi: 10.1021/jp405206p. Epub 2013 Nov 20.

Abstract

A binary dyestuff aggregate with a distinct stoichiometry is formed in dilute aqueous solution upon addition of Mg(2+) ions. The aggregation process was investigated with time-resolved multiangle static light scattering resulting in a sequence of static scattering curves. The scattering curves were analyzed with respect to the aggregation kinetics as well as the structure of the growing aggregates. The aggregation kinetics was based on the time evolution of the weight-averaged molar mass values extracted from the intercepts of the static scattering curves. A kinetic model that considers solely a nucleation step and monomer addition in its most simple form was developed in order to describe the evolution of time-dependent mass data. In addition, a kinetic model introduced by Lomakin et al. (Proc. Natl. Acad. Sci. U.S.A. 1996, 93, 1125) for the description of β-amyloid aggregation was adapted to the same experimental data. Application of the two kinetic models offered significant information on the role of magnesium ions within the aggregation process and provided a deeper understanding of the aggregation mechanism. Correlation of the size parameters extracted from the initial slopes of the scattering curves with the respective mass data as well as direct fitting of the scattering curves with the wormlike chain model yield a consistent set of model parameters.