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Analysing the Crystal Purity of Mebendazole Raw Material and Its Stability in a Suspension Formulation by S. Agatonovic-Kustrin; B.D. Glass; M. Mangan; J. Smithson is a Pharmacology, Toxicology and Pharmaceutics article available to read on EtoBox.

What is Analysing the Crystal Purity of Mebendazole Raw Material and Its Stability in a Suspension Formulation about?

The objective of this study was to develop a simple, direct and non-destructive method to assess crystal purity of mebendazole raw material and to establish its stability in a suspension formulation using diffuse reflectance ultraviolet (DRA-UV) spectroscopy and attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy. Quantitation of mebendazole, found to exhibit polymorphism with three polymorphic forms A, B and C identified, was carried out with ATR-FTIR spectroscopy. Artificial neural network (ANN) was employed as a data-modelling tool. The developed ANN models confirmed that the characteristic absorptions in the infrared (IR) spectral region are directly proportional to the measured amounts of mebendazole crystal forms present in the samples (r 2 > 0.94), which was confirmed with X-ray diffraction (XRD) at r 2 > 0.97. These models also predicted that the mebendazole raw material contained 7.21 ± 1.25% (ATR-FTIR data) and 10.38 ± 0.18% (XRD data) of form A as an impurity. ATR-FTIR data for the suspension formulation showed some dissolution of form C and recrystalisation as the more stable form A. These quantitative results obtained for the binary crystal

Who reads Analysing the Crystal Purity of Mebendazole Raw Material and Its Stability in a Suspension Formulation?

It is typically read by researchers, students, and practitioners in Pharmacology, Toxicology and Pharmaceutics.

Author
S. Agatonovic-Kustrin; B.D. Glass; M. Mangan; J. Smithson
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 0378-5173)
Published
2008
Language
EN
Field
Pharmacology, Toxicology and Pharmaceutics (Life Sciences)

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