Prucalopride succinate tablet composition
A technology of prucalopride and succinic acid, which is applied in the directions of drug combination, pill delivery, medical preparations of inactive ingredients, etc., can solve the problems of accelerated reaction, toxic substances, and laxatives are not completely satisfied, and achieves drug use. High safety, reasonable prescription and uniform content
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Embodiment 1~6
[0037] Embodiment 1~6 prucalopride succinate tablet
[0038] Prescription (unit: g):
[0039]
[0040] Note: in embodiment 1-3, the weight ratio of mannitol and crospovidone is 5:1.
[0041] Preparation Process:
[0042] According to the prescription of Example 1-6 respectively, prucalopride succinate, mannitol, crospovidone, and binder were mixed evenly, added pure water to make soft material, passed through a 14-20 mesh sieve for granulation, and 50 Dry at -80°C, granulate, add lubricant (or lubricant and glidant), mix well, and compress into tablets.
Embodiment 7
[0043] Embodiment 7 prucalopride succinate tablet stability experiment
[0044] Utilize the prucalopride succinate tablet of the present invention prepared in Examples 1-6 and the commercially available product "Lilo", carry out long-term stability experiment (25 ℃, 60%RH), press the following inspection method, measure related substances .
[0045] Chromatographic conditions and system suitability test use octadecyl bonded silica gel as filler; use 25mmol / L ammonium acetate aqueous solution containing 0.2% diethylamine as mobile phase A; use acetonitrile-isopropanol (80:20) It is mobile phase B; carry out linear gradient elution according to the table below; the detection wavelength is 275nm, the flow rate is 1.0ml / min; the column temperature is 35°C. The number of theoretical plates should not be less than 5000 based on the prucalopride succinate peak.
[0046]
[0047]Determination method gets the sample prepared by embodiment 1-6 appropriate amount, grinds finely, acc...
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