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Setup for granulating and drying tabletted preparations

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Pharmaceutical Chemistry Journal Aims and scope

Conclusions

  1. 1.

    In the given setup the drying process is very intensive and ensures a moisture removal rate of 70 kg/m2 · h in the case of norsulfazole and 50kg/m2 · h in the case of pyramidon.

  2. 2.

    Compared with tray-type driers the duration of the process is reduced by a factor of 100 or more (2–3 min instead of 5–10 h).

  3. 3.

    The optimum process variables for the preparations studied have been found. Thus, in the case of pyramidon the air temperature should be 90° and its mass flow rate 0.7–0.5 kg/m2· h, and in the case of norsulfazone the air temperature should be 140° and the mass flow rate 0.8 kg/m2 · h. The corresponding height of the stationary layer of material should be 40–50 mm.

  4. 4.

    In the case of pyramidon drying should be continued to an equilibrium moisture content of 0.4%, and in the case of norsulfazone to a moisture content of 1.5–1.0%. If these levels are adhered to the tablets produced scarcely ever undergo compaction during storage.

    In this drying setup product carry-over is insignificant.

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Translated from Khimiko-Farmatsevticheskii Zhurnal, No. 8, pp. 51–54, August, 1968.

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Reprintseva, S.M., Chizhik, K.G. Setup for granulating and drying tabletted preparations. Pharm Chem J 2, 461–464 (1968). https://doi.org/10.1007/BF00759403

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  • DOI: https://doi.org/10.1007/BF00759403

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