COMPARATIVE STUDY OF RP-HPLC METHOD VERSUS FOURIER TRANSFORM CONVOLUTION CHEMOMETRIC METHODS; AN APPLICATION ON PHARMACEUTICAL BINARY MIXTURES OF CANDESARTAN CILEXETIL-PITAVASTATIN CALCIUM AND CLOPIDOGREL BISULFATE-ROSUVASTATIN CALCIUM

Authors

  • Marwa K. El Jamal Department of Pharmaceutical Technology, Faculty of Pharmacy, Beirut Arab University, Beirut, Lebanon
  • Azza A. Gazy Department of Pharmaceutical Technology, Faculty of Pharmacy, Beirut Arab University, Beirut, Lebanon

DOI:

https://doi.org/10.22159/ijpps.2016v8i10.12931

Keywords:

Co-administered drugs, Rosuvastatin-clopidogrel, Pitavastatin-candesartan, Fourier function ratio spectra, RP-HPLC, Spiked plasma

Abstract

Objective: A comparative study of smart spectrophotometric chemometric assisted techniques and RP-HPLC for the determination of candesartan cilexetil (CAN)-pitavastatin calcium (PIT) and clopidogrel bisulfate (CLO)-rosuvastatin calcium (ROS), binary co-administered drugs were developed and validated.

Methods: The spectrophotometric chemometric assisted methods included two simple techniques, namely Fourier transform convolution (FF) and ratio spectra of Fourier transform convolution (FFR) methods. FFR is considered as a hybrid divisor ratio spectra method where Fourier functions are applied to divisor ratio signals. The RP-HPLC method involves a rapid separation on a C18 column using a mobile phase consisting of acetonitrile: sodium dihydrogen phosphate (adjusted to pH 2.6 using orthophosphoric acid) in the ratio of 70:30 v/v at a flow rate of 1 ml/min in isocratic mode. CLO and ROS were monitored at 220 nm however CAN and PIT were monitored at 238 nm.

Results: The spectrophotometric chemometric assisted methods proved their ability to quantify each of the studied drugs in their binary mixtures, where excellent percentage recoveries were obtained. FF and FFR method proved to be linear over the concentration range of 10-50 µg/ml for CLO, 4-20 µg/ml for ROS, 8-20 µg/ml for CAN and 2-10 µg/ml for PIT. The RP-HPLC method was able to separate the drugs in the study; retention times were found to be 3.9 min and 14.4 min for ROS-CLO, 4.2 min and 14.5 min for PIT-CAN respectively. The RP-HPLC method was found to be linear in the concentration range of 0.1-0.5 µg/ml for CLO, 0.04-0.2 µg/ml for ROS, 0.5-1 µg/ml for CAN and 0.05-0.1 µg/ml for PIT. System suitability parameters proved that peaks were well resolved from each other.

Conclusion: The spectrophotometric and chromatographic methods were validated according to ICH guidelines. Recovery was found to be in the range of 95.9 %-100.5 % in synthetic laboratory mixtures. The suggested spectrophotometric methods have the advantage over other methods that they do not require a preliminary separation. Statistical analysis between the suggested spectrophotometric chemometric assisted and RP-HPLC methods, using student's t-and F-test revealed that there is no difference between the applied methods.

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References

De Cates A, Farr M, Wright N. Fixed-dose combination therapy for the prevention of cardiovascular disease. US Natl Libr Med Natl Institutes Heal Pubmed 2014;16:15–8.

O’Neil MJ. The merck index an encyclopedia of chemicals, drugs, and biologicals senior; 2001.

Herbert JM, Frehel D, Vallee E. Cardiovascular drug reviews. Cardiovasc Drug Rev 1993;11:180–98.

Katzung BG. Basic and Clinical Pharmacology. Eighth ed; 2001.

Dermiş S, Aydoğan E. Stability indicating a spectrophotometric method for determination and validation of clopidogrel bisulfate in tablet dosage form. Commun Fac Sci Univ Ankara 2010;1:418–23.

Sahoo NK, Sahu M, Rao PS, Indira JN, Rani SN, Ghosh GK. Validation of assay for bulk clopidogrel and for some tablet forms by reverse-phase high-performance liquid chromatography. J Taibah Univ Sci 2014;8:331–6.

Derm S. Rapid and accurate determination of clopidogrel in tablets by using spectrophotometric and chromatographic techniques 2009;55:1–16.

Takahashi M, Pang H, Kawabata K, Farid AN, Kurihara A. Quantitative determination of clopidogrel active metabolite in human plasma by LC-MS/MS. J Pharm Biomed Anal 2008;48:1219–24.

Krishna Reddy Ch Sai, Tulasi BVD, Rohini A, Shanta K. Simultaneous estimation of rosuvastatin calcium and clopidogrel bisulfate by UV spectroscopy. Int J ChemTech Res 2013;5:127–30.

Rajput S, George R, Ruikar B. Chemometric simultaneous estimation of clopidogrel bisulfate and aspirin from combined dosage form. Indian J Pharm Sci 2008;70:450–4.

Mohamed SH, Issa YM, Magdy AI. H-point standard addition method for the simultaneous determination of clopidogrel bisulfate in a mixture with aspirin. Int J Res Pharm Chem 2015;5:289–94.

De Cates A, Farr M, Wright N. Bio-analytical determination of clopidogrel and pantoprazole by RP-HPLC method in rat plasma : application to drug interaction study. Asian J Pharm Clin Res 2015;7:10.

Donthula S, Kumar MK, Teja GS, Kumar YM, Krishna JY, Ramesh D. Spectrophotometric determination of rosuvastatin calcium in the marketed formulation. Sch Res Libr 2011;3:350–6.

Shekhar MC, Babu GR, Dinda SC, Sonthosh PV, Shwetha P. Estimation of rosuvastatin calcium in bulk and tablet dosage. J Appl Pharm 2014;4:335–9.

Turabi ZM, Khatatbeh OA. Stability indicating RP-HPLC method development and validation for the determination of rosuvastatin calcium in pharmaceutical dosage form. Int J Pharm Sci Drug Res 2014;6:154–9.

Trivedi HK, Patel MC. Development and validation of a stability-indicating RP-UPLC method for determination of rosuvastatin and related substances in pharmaceutical dosage form. Sci Pharm 2012;80:393–406.

El-Gizawy SM. Development and validation of HPLC method for simultaneous determination of amlodipine, valsartan, hydrochlorothiazide in the dosage form and spiked human plasma. Am J Anal Chem 2012;3:422–30.

Banerjee SK, Vasava NM. Simultaneous estimation of amlodipine and rosuvastatin in combined bulk forms by RP-HPLC using ultraviolet detection. Bull Pharm Res 2013;3:29–33.

Malakondaiah DS, Ranjeetkumar V, Naveenkumar M, Ram AS, Reddy TRM, Rao VUM. Research article development and validation of stability indicating RP-HPLC Method for simultaneous estimation of rosuvastatin and clopidogrel in pharmaceutical dosage form. Int J Pharm Res Rev 2014;3:13–21.

Badawy AM, Mostafa NM, Elaziz A, Elaleem, Abd B, Lamie NT. Stability-indicating PLS and PCR chemometric methods for the determination of rosuvastatin in the presence of its two acid degradation products. Int J Pharm Pharm Sci 2011;3:232–7.

Muralikrishna C, Rambabu C. Estimation of candesartan cilexetil in bulk and pharmaceutical formulations by using spectrophotometric methods. Asian J Pharm Chem 2014;7:929–32.

AL-Arfaj N, AL-Onazi W, Amina M. Spectrophotometric determination of candesartan cilexetil in the presence of its alkaline induced degradation product. Asian J Chem 2011;23:1696–700.

Bhadke Tejaswini K, Mohite Shrinivas K, Magdum Chandrakant S. Simultaneous estimation of candesartan cilexetil and hydrochlorothiazide in tablet dosage form by UV spectrophotometric method. Int J PharmTech Res 2012;4:786–90.

Hassan E, Jamal MK, Sayed MA. Stability indicating spectrophotometric assay of candesartan cilexetil and olmesartan medoxomil using discrete fourier transform convoluted curves. Int J Pharm Pharm Sci 2014;6:343–53.

Daharwal SJ, Singh VD. Development of a classical least square method for the determination of candesartan and hydro-chlorthiazide in tablet dosage form. Asian J Pharm Res 2015;5:90.

Patel J, Dave JB, Patel CN. Q-analysis spectrophotometric methods for estimation of candesartan cilexetil and hydrochlorothiazide in tablet dosage form. J Chem Pharm Res 2010;2:10–4.

Mukthinuthalapati MA, Sai J, Kumar P. Simultaneous derivative spectrophotometric determination of candesartan cilexetil and hydrochlorothiazide. Pharm Methods 2015;6:148–51.

Kishore Kumar H, Pankaj K, Satyanarayana V, Venkateswarlu V. LC–MS/MS method for simultaneous estimation of candesartan and hydrochlorothiazide in human plasma and its use in clinical pharmacokinetics. Bioanalysis 2012;4:95–1204.

Sujatha K, Rao JV, Polytechnic G. A new validated stability-indicating RP-HPLC method for the estimation of pitavastatin in tablet dosage forms. Int J Pharm Anal Res 2014;3:67-74.

Virupaxappa BS, Shivaprasad KH, Latha MS. Novel spectrophotometric method for the assay of pitavastatin calcium in pharmaceutical formulations. Der Chem Sin 2011;2:1–5.

Wahbi AA, Hassan E, Hamdy D, Fathy E, Barary M. Application of orthogonal functions to pharmaceutical analysis, generation of derivative curves. Saudi Pharm J 2005;13:14–33.

Wahbi AM, Abdine H, Korany MA, El yazby F. Spectrophotometric determination of chloramphenicol-sulphacetamide in eye drops. Pharmazie 1978;33:721–2.

FDA Center for drug evaluation research (CDER), Reviewer Guidance: Validation of Chromatographic Methods, Washington, USA; 1994.

Validation of Analytical Procedures: Text and Methodology. International Conference on HarmonisationICH Harmonised Tripartite Guideline. Q2(R1). Geneva; 1995.

ICH, Validation of Analytical Procedures: Text and Methodologyâ€, Q2(R1); 2005.

P and Berry G. Statistical Methods in Medical research. 4th ed.; 2002.

Published

01-10-2016

How to Cite

El Jamal, M. K., and A. A. Gazy. “COMPARATIVE STUDY OF RP-HPLC METHOD VERSUS FOURIER TRANSFORM CONVOLUTION CHEMOMETRIC METHODS; AN APPLICATION ON PHARMACEUTICAL BINARY MIXTURES OF CANDESARTAN CILEXETIL-PITAVASTATIN CALCIUM AND CLOPIDOGREL BISULFATE-ROSUVASTATIN CALCIUM”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 10, Oct. 2016, pp. 125-33, doi:10.22159/ijpps.2016v8i10.12931.

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