2014, Number 2
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Rev Cubana Farm 2014; 48 (2)
Validation of the ultraviolet spectrophotometry method for the quality control of ciprofloxacin chlorhydrate in Ciprecu tablets
Pérez NM, Rodríguez HY, Suárez PY
Language: Spanish
References: 10
Page: 199-212
PDF size: 225.23 Kb.
ABSTRACT
Introduction: quinolones are a group of antimicrobials of high clinical significance.
Ciprofloxacin hydrochloride monohydrate is a second-generation antibacterial
fluoroquinolone for treatment of several infections and is marketed as eye drops,
injections, capsule and tablets.
Objective: to develop and to validate an ultraviolet spectrophotometric analytical
method to be used in the quality control of ciprofloxacin hydrochloride monohydrate
in newly manufactured Ciprecu tablets.
Methods: this method was devised at the laboratory and thoroughly validated pursuant to the category I parameters. The method was selected on account of the
existence of chromophore groups in the structure of the analyzed compound. The maximum absorption wavelength was set at 273 nm of 5 µg/mL in 0.1 mol/L hydrochloric acid.
Results: based on the validation process, it was demonstrated that this method
has adequate specificity against the study matrix components, as well as its
linearity, accuracy and precision in the range of 2.5 to 7.5 µg/mL. The results of the
application of this method were similar to those of the official procedure suggested
for the same purposes in USP 33, 2010.
Conclusions: The analytical method was valid for the suggested purposes, so it is
a new simple, rapid and economic alternative for the quality control of Ciprofloxacin
hydrochloride in Ciprecu tablets.
REFERENCES
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British Pharmacopoeia. Medicinal and Pharmaceutical Substances. London: The Stationery Office; 2009.
The United Stated Pharmacopoeia 33 and National Formulary 28 (USP33-NF28). Washington: The United States Pharmacopeial Convention, Inc; 2010.
De Witte B, Dewulf J, Demeestere K, De Ruyck M, Van Langenhove H. Critical points in the analysis of ciprofloxacin by high-performance liquid chromatography. J Chromatogr A. 2007;1140:126-30.
Adhoum N, Monser L, Toumi M, Boujlel K, Pascual MI, Pérez G, et al. Solid-phase UV spectrophotometric method for determination of ciprofloxacin. Microchem J. 2004;77:79-84.
Suna J, Sakaia S, Tauchia Y, Deguchia Y, Chenb J, Zhangb R, et al. Determination of lipophilicity of two quinolone antibacterials, ciprofloxacin and grepafloxacin, in the protonation equilibrium. Eur J Pharmaceut Biopharmaceut. 2002;54:51-8.
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Regulación 41. Validación de métodos analíticos. Centro para el Control Estatal de la Calidad de los Medicamentos (CECMED). Ministerio de Salud Pública. La Habana, Cuba. 2007.