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Determining Adulterated Drugs by Modern Analytical Techniques

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REFERENCES

  1. Counterfeit Drugs: Guidelines for the Development of Measures to Combat Counterfeit Drugs, WHO, Geneva (1999).

  2. Counterfeit Drugs: Threat to Public Health, 55 World Health Assembly, Geneva (2002).

  3. Basic Tests for Drugs, WHO, Geneva (1998).

  4. Basic Tests for Pharmaceutical Dosage Forms, WHO, Geneva (1991).

  5. Basic Tests for Pharmaceutical Substances, WHO, Geneva (1986).

  6. A. S. Kenyon and T. P. Layoff, A Compendium of Unofficial Methods for Rapid Screening of Pharmaceuticals by Thin-Layer Chromatography, FDA, St. Louis, MO (1999).

    Google Scholar 

  7. A. S. Kenyon, Rapid Screening of TB Pharmaceuticals by Thin-Layer Chromatography, FDA, St. Louis, MO (1999).

    Google Scholar 

  8. State Industrial Standard 91500.05.001-00. Drug Quality Standards. Main Stipulations.

  9. General Pharmacopoeial Article 42-0003-00. Dissolution.

  10. British Pharmacopoeia (2001).

  11. European Pharmacopoeia, 4th ed. (2002).

  12. The United States Pharmacopeia, 26th revision (2003).

  13. H. H. Blume and K. K. Midha (eds.), Bio-International 2: Bioavailability, Bioequivalence and Pharmacokinetic Studies, Medpharm Scientific Publ., Stuttgart (1995).

    Google Scholar 

  14. A. I. Tentsova and I. S. Azhgikhin, Medicinal; Form and Therapeutic Efficacy of Drugs [in Russian], Meditsina, Moscow (1974).

    Google Scholar 

  15. L. E. Kholodov and V. P. Yakovlev, Clinical Pharmacokinetics [in Russian], Meditsina, Moscow (1985).

    Google Scholar 

  16. Dissolution Discussion Group, Vol. 1, A User's Perspective on Dissolution, VanKel Technology Group (1999).

  17. Dissolution Testing of Immediate Release Solid Oral Dosage Forms: Guidance for Industry, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (1997).

  18. Lewis J. Leeson, J. Thuro Carstensen, Dissolution Technology, Whitlock Press Inc. (1974).

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Authors and Affiliations

  1. Sechenov Medical Academy, Moscow, Russia

    A. P. Arzamastsev, V. L. Dorofeev, A. A. Konovalov, V. Yu. Kochin, N. N. Lebedeva & I. V. Titov

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  1. A. P. Arzamastsev
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  2. V. L. Dorofeev
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  3. A. A. Konovalov
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  4. V. Yu. Kochin
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  5. N. N. Lebedeva
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  6. I. V. Titov
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Arzamastsev, A.P., Dorofeev, V.L., Konovalov, A.A. et al. Determining Adulterated Drugs by Modern Analytical Techniques. Pharmaceutical Chemistry Journal 38, 166–169 (2004). https://doi.org/10.1023/B:PHAC.0000034308.08754.33

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  • DOI: https://doi.org/10.1023/B:PHAC.0000034308.08754.33

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