I. Introduction
The potential of fluorescence spectroscopy as a tool for minimally invasive detection of precancers and determination of exogenous drug concentration is well established [1], [2]. Medical fluorescence devices frequently incorporate fiberoptic probes for instrument-tissue interfacing, as these components are relatively inexpensive, highly versatile and enable the acquisition of optical data in a wide variety of clinical and laboratory situations. However, the range of designs capable with fiberoptic probes adds complexity to the problem of system optimization.