“…in vitro and in vivo (x-axis timei, ~i,-o and y-axis tim% vitro)' A continuous, piecewise linear function was adjusted to the time points by a least squares method. The different slopes of this function describe different phases of absorption [6], Since the first slope of the polyphasic correlation came close to unity, the in vitro dissolution could be used as an input function to the body system, and the individual concentration/time-profiles could be predicted by convolution of this input function with the individual weighting functions [6], Pharmacokinetic calculations, adjustment of exponential functions and the deconvolution and convolution were carried out using the HOEREP-PC program [9] (Brockmeier D, unpublished data).…”