Optimisation of magnification levels for near infrared chemical imaging of blending of pharmaceutical powders

摘要

A critical parameter in the evaluation of pharmaceutical dosage forms by hyperspectral imaging is the level of magnification. If the magnification (as set by the optical objective) is inadequate to resolve the relevant features, then the value of the imaging is diminished; if the magnification level is greater than is required, then the field of view is unnecessarily reduced. The purpose of this study was to determine an optimum magnification level for the study of powder mixing. Relevant features in this system include distribution of individual components within samples and the overall content of a given sample. In the present study, three magnification levels of near infrared (NIR) chemical imaging objectives were evaluated for their effects on imaging a blend of pharmaceutical materials (powders). High, medium and low objective magnification levels were investigated by comparing the resulting blend surface images of a two-component (salicylic acid and lactose) pharmaceutical powder mixture. Multiple images from high and medium magnification were concatenated so that an equivalent field of view was obtained for all magnification levels. Univariate images, principal component analysis score images, partial least squares predicted images and spectra extracted from different intensity regions in the area images were analysed qualitatively and quantitatively for comparison. A series of images spanning a strip across the centre of the circular field were collected at each magnification level and compared with respect to surface features elucidated and area of blend surface imaged. Analyses of images indicate that the three magnification levels delineate the component distribution for this particular powder system similarly. Images obtained at the low magnification level demonstrated adequate resolution and provided the broadest view of the blend surface. It is concluded that the low optical magnification level was adequate for the system being studied and is the preferred mode for pharmaceutical powder blend image data collection for this system.