期刊
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS
卷 64, 期 3, 页码 351-359出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejpb.2006.06.008
关键词
expert system; preformulation; formulation; bulk density (Da); tapped density (Dc); inter-particle porosity (Ie); angle of repose (alpha); flowability (t); particle size (%Pf); direct compression (DC)
The new SeDeM Method is proposed for testing the batch-to-batch reproducibility of the same active pharmaceutical ingredient (API) in powder form. The procedure describes the study of the galenic properties of substances in powder form in terms of the applicability of direct compression technology. Through experimental determination of the SeDeM Method parameters, and their subsequent mathematical treatment and graphical expression (SeDeM Diagram), three batches of the same API were analysed to determine whether it was suitable for direct compression. Batch-to-batch reproducibility of the results was verified. It was concluded that the SeDeM Method is suitable for testing batch-to-batch reproducibility of characteristics in powdered APIs substances. The results obtained confirm that the SeDeM Method is a useful, effective tool for drug-preformulation studies providing the pharmaco technical data required when formulating a drug in tablet form. In addition, the results were effective for defining the most appropriate manufacturing technology. (c) 2006 Elsevier B.V. All rights reserved.
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