Fig. 2. FT-Raman spectra of the four analysed commercial diclofenac sodium injection solutions DTo construct the calibration models spectra of 28 samples, prepared as described above were used. Six mixtures were chosen for the validation procedure and six other were treated as “unknown” samples. The concentration varied in the range 1–4% for diclofenac sodium, 10–28% for propylenediol, 1–5% for benzyl alcohol and 64–83% for the aqueous solution of NaOH, d-mannitol and sodium pyrosulfite.The second analysed system consists of three substances only. Aminophylline, which is a complex of theophylline with ethylenediamine (2:1) is dissolved in water. As mentioned before, it may contain an excess of ethylenediamine. In the spectra of diluted aminophylline solutions there are only two peaks at 564 and 683 cm−1, clearly visible for the active compound (Fig. 3).1–D4; the spectra are offset for clarity by 0.5.
Fig. 2. FT-Raman spectra of the four analysed commercial diclofenac sodium injection solutions DTo construct the calibration models spectra of 28 samples, prepared as described above were used. Six mixtures were chosen for the validation procedure and six other were treated as “unknown” samples. The concentration varied in the range 1–4% for diclofenac sodium, 10–28% for propylenediol, 1–5% for benzyl alcohol and 64–83% for the aqueous solution of NaOH, d-mannitol and sodium pyrosulfite.<br><br>The second analysed system consists of three substances only. Aminophylline, which is a complex of theophylline with ethylenediamine (2:1) is dissolved in water. As mentioned before, it may contain an excess of ethylenediamine. In the spectra of diluted aminophylline solutions there are only two peaks at 564 and 683 cm−1, clearly visible for the active compound (Fig. 3).1–D4; the spectra are offset for clarity by 0.5.
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