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Development and validation of a GC-FID method for quantitation of impurities in kemantane drug substance

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Pharmaceutical Chemistry Journal Aims and scope

The objective of the study was to develop and validate a new GC-FID method for determination of impurities in kemantane (5-hydroxyadamantan-2-one) drug substance. The chromatographic mobilities of potential impurities in kemantane such as adamantan-2-one, adamantan-1-ol, adamantan-2-ol, adamantane-1,4-diol, adamantane-1,4-diol (syn-isomer), adamantane-2,6-diol, and adamantane-2,6-dione were studied. The chromatographic separation was performed on a quartz capillary column (VF-624ms, 60 m × 0.32 mm, 1.80 μm film thickness). The chromatographic system suitability parameters and method robustness factor were determined. The method had acceptable specificity, accuracy, linearity, and precision and high sensitivity. The developed method detected an impurity of adamantane-2,6-dione from 1.01 to 2.97% in four batches of kemantane drug substance.

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Authors and Affiliations

  1. Zakusov State Foundation Institute of Pharmacology, RAMS (SF IPh RAMS), Moscow, Russia

    A. V. Tolkacheva, L. N. Grushevskaya, N. I. Avdyunina, B. M. Pyatin & L. M. Gaevaya

  2. I. M. Sechenov First Moscow State Medical University, Moscow, Russia

    A. V. Tolkacheva & V. I. Prokofeva

Authors
  1. A. V. Tolkacheva
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  2. L. N. Grushevskaya
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  3. N. I. Avdyunina
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  4. B. M. Pyatin
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  5. V. I. Prokofeva
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  6. L. M. Gaevaya
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Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 47, No. 6, pp. 44 – 50, June, 2013.

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Tolkacheva, A.V., Grushevskaya, L.N., Avdyunina, N.I. et al. Development and validation of a GC-FID method for quantitation of impurities in kemantane drug substance. Pharm Chem J 47, 330–336 (2013). https://doi.org/10.1007/s11094-013-0955-9

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  • DOI: https://doi.org/10.1007/s11094-013-0955-9

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