4.6 Article

Controlling individual steps in the production process of paracetamol tablets by use of NIR spectroscopy

Journal

JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
Volume 51, Issue 4, Pages 797-804

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpba.2009.09.038

Keywords

Particle size distribution; Compaction pressure; API determination; Near infrared spectroscopy; Quality control

Funding

  1. Spain's MCyT [CrQ2006-12923]
  2. Universitat Autonoma de Barcelona

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Various physical and chemical parameters of interest to the pharmaceutical industry were determined by NIR spectroscopy with a view to assessing the potential of this technique as an effective, expeditious alternative to conventional methods for this purpose. To this end, the following two steps in the production process of tablets containing 1 g of paracetamol were studied: (1) intermediate granulation, which was characterized in terms of Active Principle Ingredient (API) content, average particle size and particle size distribution and (2) manufactured tablet, which was examined in relation to compaction pressure and API content of the tablets. The ultimate aim was to identify critical attributes of the process influencing the quality of the end-product. Based on the results, a new method for determining the API in the end-product was developed and validated for its quality control. (C) 2009 Elsevier B.V. All rights reserved.

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