QUALITY BY DESIGN-BASED OPTIMIZATION AND VALIDATION OF NEW REVERSE PHASE-HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY METHOD FOR SIMULTANEOUS ESTIMATION OF LEVOFLOXACIN HEMIHYDRATE AND AMBROXOL HYDROCHLORIDE IN BULK AND ITS PHARMACEUTICAL DOSAGE FORM

Authors

  • Sumithra m Vels University
  • Shanmugasundaram P
  • Ravichandiran V

DOI:

https://doi.org/10.22159/ajpcr.2016.v9s3.14040

Abstract

ABSTRACT
Objective: Innovative application of quality by design (QbD) technique for simultaneous estimation of levofloxacin and ambroxol hydrochloride (HCL)
in bulk and its pharmaceutical dosage form using reverse phase-high-performance liquid chromatography (RP-HPLC) method.
Method: A method has been developed for the separation of levofloxacin and ambroxol HCL using RP-HPLC on C18 column (250 4.6 mm, 5 ml) with
ultraviolet detection at 306 nm. Experimental designs were applied for multivariate optimization of the experimental conditions of RP-HPLC method.
Three independent factors: Acetonitrile content in the mobile phase composition, buffer pH, and flow rate were used to design mathematical models.
Here, central composite design (CCD) experimental design was used to study the response surface technique and to study in depth the effects of
these independent factors. Derringer's desirability function was applied to simultaneously optimize the retention time of last eluting peak (ambroxol
hydrochloride) and resolution between levofloxacin and ambroxol hydrochloride.
Result and Discussion: The predicted optimum assay condition consisted of acetonitrile, potassium dihydrogen phosphate buffer (pH 5.00;
potassium dihydrogen phosphate), and methanol in a proportion of 20:70:10% v/v, respectively, as the mobile phase at a flow rate of 1.2 ml/minute.
Using this optimum condition, baseline separation of both drugs with good resolution and a run time of <5 minutes were achieved. The optimized
assay condition was validated according to the ICH guidelines to confirm specificity, linearity, accuracy, and precision.
Keywords: Levofloxacin, Ambroxol hydrochloride, Experimental design, Response surface methodology, Derringer's desirability, Quality by design
approach.

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References

Available from: http://www.drugbank.com. [Last accessed on 2016 Jan 10].

Available from: http://www.wikipedia.org/wiki/Levofloxacin. [Last accessed on 2016 Jan 10].

Available from: http://www.wikipedia.org/wiki/ambroxol. [Last accessed on 2016 Jan 10].

Indian Pharmacopoeia. Ministry of Health and Family Welfare. Ghaziabad: Indian Pharmacopoeial Commission; 2014.

Nguyen HA, Grellet J, Ba BB, Quentin C, Saux MC. Simultaneous determination of levofloxacin, gatifloxacin and moxifloxacin in serum by liquid chromatography with column switching. J Chromatogr B Analyt Technol Biomed Life Sci 2004;810(1):77-83.

Srinivas N, Narasu L, Shankar BP, Mullangi R. Development and validation of a HPLC method for simultaneous quantitation of gatifloxacin, sparfloxacin and moxifloxacin using levofloxacin as internal standard in human plasma: Application to a clinical pharmacokinetic study. Biomed Chromatogr 2008;22(11):1288-95.

Heinanen M, Barbas C. Validation of an HPLC method for the quantification of ambroxol hydrochloride and benzoic acid in a syrup as pharmaceutical form stress test for stability evaluation. J Pharm Biomed Anal 2001;24(5-6):1005-10.

Indrayanto G, Handayani R. Quantitative determination of ambroxol hydrochloride in tablets. J Pharm Biomed Anal 1993;11(8):781-4.

Pérez-Ruiz T, Martínez-Lozano C, Sanz A, Teresa San Miguel M. Automatic extraction-spectrophotometric method for the determination of ambroxol in pharmaceutical preparations. Talanta 1996;43(7):1029-34.

Ulu ST. Rapid and sensitive spectrofluorimetric determination of enrofloxacin, levofloxacin and ofloxacin with 2, 3, 5, 6-tetrachloro-p-benzoquinone. Spectrochim Acta A Mol Biomol Spectrosc 2009;72(5):1038-42.

Chepurwar SB, Shirkhedkar AA, Bari SB, Fursule RA, Surana SJ. Validated HPTLC method for simultaneous estimation of levofloxacin hemihydrate and ornidazole in pharmaceutical dosage form. J Chromatogr Sci 2007;45(8):531-6.

Agrawal OD, Shirkhedkar AA, Surana SJ. Simultaneous determination of levofloxacin hemihydrate and ambroxol hydrochloride in tablets by thin layer chromatography combined with densitometry. J Anal Chem 2010;65(4):418-22.

Liu YM, Cao JT, Tian W, Zheng YL. Determination of levofloxacin and norfloxacin by capillary electrophoresis with electro chemiluminescence detection and applications in human urine. Electrophoresis 2008;29(15):3207-12.

Krupa M, Kothekara B, Balasundaramjayakar N. Quantitative determination of levofloxacin and ambroxol hydrochloride in pharmaceutical dosage form by reversed-phase high performance liquid chromatography. Eurasian J Anal Chem 2007;2(1):21-2.

Zar JH. Biostatical Analysis. 5th ed. New Jersey: Pearson Education Inc.; 2010.

US Food and Drug Administration (FDA), Department of Health and Human Services. Pharmaceutical Quality for the 21st Century, A Risk-Based Approach Progress Report, May 2007.

ICH Q8 (R2). Pharmaceutical Development; 2009. Available from: http://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q1A_R2/Step 4/Q1A_R2__Guideline.pdf> (ICH online).

ICH Q2 (R1). Validation of Analytical Procedures; 1994. Available from: http://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q1A_R1/Step 4/Q1A_R1__Guideline.pdf> (ICH online).

ICH Q9 (R2). Quality Risk Management; 2005. Available from: http://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q1A_R2/Step 4/Q1A_R2__Guideline.pdf> (ICH online).

Kleinschmidt In: Ermer J, Miller JH, editors. Method Validation in Pharmaceutical Analysis: A Guide to Best Practice. Weinheim: Wiley-VCH Verlag GmbH & Co. KGaA; 2005.

Schmidt AH, Molnár I. Using an innovative quality-by-design approach for development of a stability indicating UHPLC method for ebastine in the API and pharmaceutical formulations. J Pharm Biomed Anal 2013;78-79:65-74.

Sivakumar T, Manavalan R, Muralidharan C, Valliappan K. Multi-criteria decision making approach and experimental design as chemometric tools to optimize HPLC separation of domperidone and pantoprazole. J Pharm Biomed Anal 2007;43(5):1842-8.

Krishna MV, Dash RN, Reddy BJ, Venugopal P, Sandeep P, Madhav G. Quality by design (QbD) approach to develop HPLC method for eberconazole nitrate: Application to hydrolytic, thermal, oxidative and photolytic degradation kinetics. J Saudi Chem Soc 2013;2:1-9.

Molnár I, Rieger HJ, Monks KE. Aspects of the ‘‘Design Space’’ in high pressure liquid chromatography method development. J Chromatogr A 2010;1217(19):3193-200.

Ebrahimzadeh H, Asgharinezhad AA, Abedi H, Kamarei F. Optimization of carrier-mediated three-phase hollow fiber microextraction combined with HPLC–UV for determination of propylthiouracil in biological samples. Talanta 2011;85(2):1043-9.

Ebrahimzadeh H, Shekari N, Saharkhiz Z, Asgharinezhad AA. Simultaneous determination of chloropheniramine maleate and dextromethorphan hydrobromide in plasma sample by hollow fiber liquid phase microextraction and high performance liquid chromatography with the aid of chemometrics. Talanta 2012;94:77-83.

Deming SN. Multiple-criteria optimization. J Chromatogr A 1991;550:15-25.

Bezerra MA, Santelli RE, Oliveira EP, Villar LS, Escaleira LA. Response surface methodology (RSM) as a tool for optimization in analytical chemistry. Talanta 2008;76(5):965-77.

Published

01-12-2016

How to Cite

m, S., S. P, and R. V. “QUALITY BY DESIGN-BASED OPTIMIZATION AND VALIDATION OF NEW REVERSE PHASE-HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY METHOD FOR SIMULTANEOUS ESTIMATION OF LEVOFLOXACIN HEMIHYDRATE AND AMBROXOL HYDROCHLORIDE IN BULK AND ITS PHARMACEUTICAL DOSAGE FORM”. Asian Journal of Pharmaceutical and Clinical Research, vol. 9, no. 9, Dec. 2016, pp. 190-6, doi:10.22159/ajpcr.2016.v9s3.14040.

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