Mebendazole crystal forms in tablet formulations. An ATR-FTIR/chemometrics approach to polymorph assignment
[Display omitted] •Polymorphs of mebendazole were differentiated by combining ATR-FTIR spectroscopy and PCA.•The mebendazole main form was assigned in differently treated commercial samples.•The procedure is simple, convenient and requires minimum sample pre-treatment.•Enabled fast, unambiguous conf...
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Published in | Journal of pharmaceutical and biomedical analysis Vol. 122; pp. 157 - 165 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier B.V
15.04.2016
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Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
•Polymorphs of mebendazole were differentiated by combining ATR-FTIR spectroscopy and PCA.•The mebendazole main form was assigned in differently treated commercial samples.•The procedure is simple, convenient and requires minimum sample pre-treatment.•Enabled fast, unambiguous confirmation of Form C as the main polymorph in tablets.•Non-destructive procedure; complies with principles of green analytical chemistry.
Structural polymorphism of active pharmaceutical ingredients (API) is a relevant concern for the modern pharmaceutical industry, since different polymorphic forms may display dissimilar properties, critically affecting the performance of the corresponding drug products. Mebendazole (MEB) is a widely used broad spectrum anthelmintic drug of the benzimidazole class, which exhibits structural polymorphism (Forms A–C). Form C, which displays the best pharmaceutical profile, is the recommended one for clinical use. The polymorphs of MEB were prepared and characterized by spectroscopic, calorimetric and microscopic means. The polymorphs were employed to develop a suitable chemometrics-assisted sample display model based on the first two principal components of their ATR-FTIR spectra in the 4000–600cm−1 region. The model was internally and externally validated employing the leave-one-out procedure and an external validation set, respectively. Its suitability for revealing the polymorphic identity of MEB in tablets was successfully assessed analyzing commercial tablets under different physical forms (whole, powdered, dried, sieved and aged). It was concluded that the ATR-FTIR/PCA (principal component analysis) association is a fast, efficient and non-destructive technique for assigning the solid-state forms of MEB in its drug products, with minimum sample pre-treatment. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0731-7085 1873-264X |
DOI: | 10.1016/j.jpba.2016.01.035 |