American Journal of Analytical Chemistry

Volume 6, Issue 9 (August 2015)

ISSN Print: 2156-8251   ISSN Online: 2156-8278

Google-based Impact Factor: 1.49  Citations  

Analytical Stability Indicative Method Development and Validation by High Pressure Liquid Chromatography for Assay in Ciprofloxacin hydrochloride Drug Substances

HTML  XML Download Download as PDF (Size: 1047KB)  PP. 719-730  
DOI: 10.4236/ajac.2015.69069    5,937 Downloads   8,700 Views  Citations

ABSTRACT

Ciprofloxacin is an antibiotic generic drug that can treat a number of bacterial infections. It is a second generic fluoroquinolone. This work presents a simple, sensitive and stability indicative method for assay determination of drug substances ciprofloxacin hydrochloride by high pressure liquid chromatography (HPLC). Separation of impurities from the main drug substances and accurate assay quantification with a simple method is difficult by Spectrophotometry. The separation of co-eluents and impurities from the ciprofloxacin drug substances was archived by HPLC with simple mobile phase 0.15% orthophosphoric acid adjusted pH to 3.0 with triethylamine and acetonitrile using a gradient program, column inertsil C18, 250 mm × 4.0 mm, 5 μm. Flow rate was 0.7 mL/min, the column temperature and injection volume were 35°C and 10.0 μL. Chromato-graphic analysis was carried out at wavelength 278 nm. The developed method was validated according to the international conference on harmonization (ICH) guidelines regarding: Precision, specificity by degradation, linearity, accuracy, range and robustness. The proposed method showed good linearity (correlation coefficient and regression coefficient were not less than 0.999 and 0.998) in the range of 50% to 150% of working concentration. The recovery at 50%, 100% and 150% of working concentration level was within 98.0% to 102.0%. The range of the method is concluded that developed method is from 50% to 150% of target concentration for ciprofloxacin hydrochloride. The applicability of the proposed method was verified through the analysis of the samples and percentage recoveries in the range of 98% to 102% were obtained without any interference detected at the main peak in the chromatogram. The validated method is highly selective, simple, accurate, cost effective, and it is applicable for stability studies and routine quality-control analysis in the pharmaceutical industries.

Share and Cite:

Shrinivas, S. and Revanasiddappa, M. (2015) Analytical Stability Indicative Method Development and Validation by High Pressure Liquid Chromatography for Assay in Ciprofloxacin hydrochloride Drug Substances. American Journal of Analytical Chemistry, 6, 719-730. doi: 10.4236/ajac.2015.69069.

Cited by

[1] Complete abatement of the antibiotic ciprofloxacin from water using a visible-light-active nanostructured photoanode
Chemosphere, 2024
[2] ANALYTICAL METHOD DEVELOPMENT FOR SIMULTANEOUS ESTIMATION OF CIPROFLOXACIN HCL AND OLOPATADINE HCL IN BULK DRUG AND …
Indian Drugs, 2023
[3] Simultaneous spectrophotometric method for determination of both ciprofloxacin and cephalexin by using H-point standard addition method
electrophoresis, 2022
[4] Colorimetric paper test strips based on cesium lead bromide perovskite nanocrystals for rapid detection of ciprofloxacin hydrochloride
Journal of Physics: Condensed Matter, 2022
[5] Facile Fabrication of Novel NiFe2O4@Carbon Composites for Enhanced Adsorption of Emergent Antibiotics
Materials, 2021
[6] Development and validation of RP-HPLC method for simultaneous estimation of ciprofloxacin and fluocinolone acetonide in bulk and pharmaceutical …
Int J Appl Pharm, 2020
[7] Development and validation of RP-HPLC method for simultaneous estimation of ciprofloxacin and fluocinolone acetonide in bulk and pharmaceutical dosage …
2020
[8] FLUOROQUINOLONES: OFFICIAL AND REPORTED METHODS OF ANALYSIS
2020
[9] Síntese e aplicação do óxido misto de zinco e estanho (IV) na degradação fotocatalítica do cloridrato de ciprofloxacino
2020
[10] Effects of green synthesis, magnetization, and regeneration on ciprofloxacin removal by bimetallic nZVI/Cu composites and insights of degradation mechanism
2020
[11] Box–Behnken design and experimental study of ciprofloxacin degradation over Ag 2 O/CeO 2/gC 3 N 4 nanocomposites
2020
[12] Effects of ciprofloxacin on testicular tissue and sperm quality in rabbits
2020
[13] Development of a new liquid chromatographic method for the simultaneous separation of ciprofloxacin degradation products with 5-hydroxymethyl-furfural, impurity of …
2019
[14] METHOD DEVELOPMENT AND VALIDATION OF SEMAGLUTIDE BY UV SPECTROPHOTOMETRIC METHOD IN BULK AND PHARMACEUTICAL DOSAGE FORM
IJRAR- International Journal of Research and Analytical Reviews, 2019
[15] Removal of ciprofloxacin using modified advanced oxidation processes: Kinetics, pathways and process optimization
Journal of Cleaner Production, 2018
[16] Analytical methods of ciprofloxacin and its combinations review
2018
[17] METHOD DEVELOPMENT, VALIDATION AND STABILITY STUDIES FOR DETERMINATION OF BUMETANIDE IN BULK AND PHARMACEUTICAL DOSAGE …
2018
[18] Method development, validation and stability studies for determination of Bumetanide in bulk and pharmaceutical dosage form by RP-UPLC
2018
[19] Estudio comparativo de calidad biofarmacéutica de tabletas de ciprofloxacino 500mg de patente y genéricas, como evidencia para descartar desarrollo de …
2016

Copyright © 2025 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.