Fourier transform infrared spectroscopy has been used for the quantita
tive determination of caffeine in several pharmaceutical products: ace
tyl salicylic acid, paracetamol and propyphenazone. The method is simp
le, rapid and selective, and allows the determination of caffeine with
out sample pretreatment and without separation from the matrix. Two te
chniques for measuring the infrared spectra of caffeine are described:
transmission through pellets and diffuse reflectance from powder (DRI
FT). In both methods, samples were diluted (1%) with KBr. Caffeine in
pharmaceutical matrices was recovered within 5% error in pellets and 1
0% by DRIFT. Relative standard deviations were generally less-than-or-
equal-to 1.5% for repeated measurements on a single pellet and less-th
an-or-equal-to 5% for measurements on different pellets. DRIFT in the
vacuum mode gave rather large RSDs. The limit of detection of the pell
et technique was about 0.5% caffeine in the original sample.