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Revista Cubana de Farmacia

ISSN 1561-2988 (Print)
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2013, Number 2

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Rev Cubana Farm 2013; 47 (2)

Simultaneous determination of Albendazol and Triclabendazol in Triclazol 22 suspension for veterinary purposes

García PCM, Gafas LM, Rosales BK, Toirac PR, Pérez CJA
Full text How to cite this article

Language: Spanish
References: 11
Page: 167-177
PDF size: 413.56 Kb.


Key words:

triclabendazol, albendazol, triclazol, validation.

ABSTRACT

Introduction: triclazol 22 suspension containing triclabendazol and albendazol is used as parasiticide for veterinary purposes.
Objective: to validate the analytical method for simultaneous determination of triclabendazol and albendazol in triclazol 22 suspension for quality control.
Methods: for quantitation of the active principle in the final product, the separation was performed through a liquid chromatographic column Lichrosorb RP-18 (5 μm) (250 × 4 mm), with ultraviolet detection range of 298 nm, by using a mobile phase of acetonitrile: ammonium acetate buffer solution of ph 6.6 (70:30); the quantitation was made against a reference sample by means of the external standard method.
Results: the results of the evaluated parameters in this validation yielded that they were within the set limits.
Conclusions: The validated analytical method was linear, precise, exact and specific in the range of studied concentrations.


REFERENCES

  1. Schistomiasis and Soil-Transmitted Parasite Infections: Preliminary Estimates of the Number of Children Treated with Albendazole or Mebendazole. WER. 2006;81(16):145-64.

  2. Incari R. Infección humana por Fasciola hepática en Venezuela: reporte de un caso geriátrico. Invest Clin. 2003;44(3):255-60.

  3. Oltean E, Nica A. Development and validation of a RP-HPLC method for quantization studies of Albendazole suspension dosage forms of Rombendazol. Medicamentul Veterinar. 2011;5(2).

  4. Waldia A. Validated Liquid Chromatographic method for simultaneous estimation of Albendazole and Virmectin in tablet dosage. Indian J Chem Technol. 2008;15:617-20.

  5. Nischal K. A Simple RP-HPLC Method for Estimation of Triclabendazole and Ivermectin in a Pharmaceutical Suspension Dosage Form. Current Pharm Res. 2011;1(4):306-10.

  6. Shurbaji M. Development and validation of a new HPLC-UV method for the simultaneous determination of triclabendazole and ivermectin B1a in a pharmaceutical formulation. Current Pharm Res. 2011;1(4).310-9.

  7. Dierksneier G. Métodos cromatograficos. La Habana: Ed. Científico-Técnica; 2005. p. 1-4, 256-412.

  8. Guidance for Industry. Analytical Procedures and Methods Validation Chemistry, Manufacturing, and Controls Documentation. Washington: FDA/Center for Drug Evaluation and Research; 2001.

  9. International Conference on Harmonization, ICH-Q2A. Validation of Analytical Procedures. Technical Requirements for the Registration of Pharmaceuticals for Human Use. Geneva: ICH; 1995.

  10. The United States Pharmacopeial Convention. USP 33. United States Pharmacopeia. 33 ed. Rovkville: Marck Printing; 2011.

  11. Regulación 41-2007. Validación de métodos analíticos. La Habana: CECMED; 2007.




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Rev Cubana Farm. 2013;47