Abstract

AbstractThe quantitative x-ray diffraction analysis offers often an exact and practical technique to determine the relative amounts of the phases of the solid in question. The sample may contain only one amorphous phase.The purpose of this paper is to estimate the suitability of this technique to quantify the phase fractions of pharmaceutical substances. Three different method were used to determine the relative amounts of phases. Methods were compared and the major sources of error were estimated. The measurements and calculations are carried out using selegilin hydrochloride, mannitol and modified starch as an example. The results show that the amount of about 2 % of selegilin hydrochloride can be observed reliably from among the mannitol (crystalline substance) or modified starch (amorphous substance). During the work it became obvious that the accuracy of these calculations can essentially be improved planning the measurements carefully.

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