“…However, our model lacks the complexity of the GI tract, and therefore extrapolation of our results can only be performed with great caution. In vivo, many factors induce variability in phosphate binding capacity, like distribution of phosphate binders, presence of bile salts, passage time through the stomach and intestines, the use of food additives, a variable phosphate absorption even when using the same binder, and a less acidic environment when proton pump inhibitors are used …”