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Development and validation of a rapid RP-HPLC method for the determination of cetirizine or fexofenadine with pseudoephedrine in binary pharmaceutical dosage forms.
J Pharm Biomed Anal. 2008 Jan 22; 46(2):295-302.JP

Abstract

The objective of the current study was to develop a simple, accurate, precise and rapid reversed-phase HPLC method and subsequent validation using ICH suggested approach for the determination of antihistaminic-decongestant pharmaceutical dosage forms containing binary mixtures of pseudoephedrine hydrochloride (PSE) with fexofenadine hydrochloride (FEX) or cetirizine dihydrochloride (CET). The chromatographic separation of PSE, FEX and CET was achieved on a Zorbax C8 (150 mm x 4.6mm; 5 microm particle size) column using UV detection at 218 and 222 nm. The optimized mobile phase was consisted of TEA solution (0.5%, pH 4.5)-methanol-acetonitrile (50:20:30, v/v/v). The retention times were 1.099, 2.714 and 3.808 min for PSE, FEX and CET, respectively. The proposed method provided linear responses within the concentration ranges 30-240 and 1.25-10 microg ml(-1) with LOD values of 1.75 and 0.10 microg ml(-1) for PSE and CET, respectively. Linearity range for PSE-FEX binary mixtures were 10-80 and 5-40 microg ml(-1) with LOD values of 0.75 and 0.27 microg ml(-1) for PSE and FEX, respectively. Correlation coefficients (r) of the regression equations were greater than 0.999 in all cases. The precision of the method was demonstrated using intra- and inter-day assay R.S.D. values which were less than 1% in all instances. No interference from any components of pharmaceutical dosage forms or degradation products was observed. According to the validation results, the proposed method was found to be specific, accurate, precise and could be applied to the quantitative analysis of these drugs in capsules containing PSE-CET or extended-release tablets containing PSE-FEX binary mixtures.

Authors+Show Affiliations

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Marmara University, Haydarpaşa, 34668 Istanbul, Turkey.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Validation Study

Language

eng

PubMed ID

18054459

Citation

Karakuş, Sevgi, et al. "Development and Validation of a Rapid RP-HPLC Method for the Determination of Cetirizine or Fexofenadine With Pseudoephedrine in Binary Pharmaceutical Dosage Forms." Journal of Pharmaceutical and Biomedical Analysis, vol. 46, no. 2, 2008, pp. 295-302.
Karakuş S, Küçükgüzel I, Küçükgüzel SG. Development and validation of a rapid RP-HPLC method for the determination of cetirizine or fexofenadine with pseudoephedrine in binary pharmaceutical dosage forms. J Pharm Biomed Anal. 2008;46(2):295-302.
Karakuş, S., Küçükgüzel, I., & Küçükgüzel, S. G. (2008). Development and validation of a rapid RP-HPLC method for the determination of cetirizine or fexofenadine with pseudoephedrine in binary pharmaceutical dosage forms. Journal of Pharmaceutical and Biomedical Analysis, 46(2), 295-302.
Karakuş S, Küçükgüzel I, Küçükgüzel SG. Development and Validation of a Rapid RP-HPLC Method for the Determination of Cetirizine or Fexofenadine With Pseudoephedrine in Binary Pharmaceutical Dosage Forms. J Pharm Biomed Anal. 2008 Jan 22;46(2):295-302. PubMed PMID: 18054459.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Development and validation of a rapid RP-HPLC method for the determination of cetirizine or fexofenadine with pseudoephedrine in binary pharmaceutical dosage forms. AU - Karakuş,Sevgi, AU - Küçükgüzel,Ilkay, AU - Küçükgüzel,S Güniz, Y1 - 2007/10/22/ PY - 2007/04/10/received PY - 2007/10/07/revised PY - 2007/10/08/accepted PY - 2007/12/7/pubmed PY - 2008/5/6/medline PY - 2007/12/7/entrez SP - 295 EP - 302 JF - Journal of pharmaceutical and biomedical analysis JO - J Pharm Biomed Anal VL - 46 IS - 2 N2 - The objective of the current study was to develop a simple, accurate, precise and rapid reversed-phase HPLC method and subsequent validation using ICH suggested approach for the determination of antihistaminic-decongestant pharmaceutical dosage forms containing binary mixtures of pseudoephedrine hydrochloride (PSE) with fexofenadine hydrochloride (FEX) or cetirizine dihydrochloride (CET). The chromatographic separation of PSE, FEX and CET was achieved on a Zorbax C8 (150 mm x 4.6mm; 5 microm particle size) column using UV detection at 218 and 222 nm. The optimized mobile phase was consisted of TEA solution (0.5%, pH 4.5)-methanol-acetonitrile (50:20:30, v/v/v). The retention times were 1.099, 2.714 and 3.808 min for PSE, FEX and CET, respectively. The proposed method provided linear responses within the concentration ranges 30-240 and 1.25-10 microg ml(-1) with LOD values of 1.75 and 0.10 microg ml(-1) for PSE and CET, respectively. Linearity range for PSE-FEX binary mixtures were 10-80 and 5-40 microg ml(-1) with LOD values of 0.75 and 0.27 microg ml(-1) for PSE and FEX, respectively. Correlation coefficients (r) of the regression equations were greater than 0.999 in all cases. The precision of the method was demonstrated using intra- and inter-day assay R.S.D. values which were less than 1% in all instances. No interference from any components of pharmaceutical dosage forms or degradation products was observed. According to the validation results, the proposed method was found to be specific, accurate, precise and could be applied to the quantitative analysis of these drugs in capsules containing PSE-CET or extended-release tablets containing PSE-FEX binary mixtures. SN - 0731-7085 UR - https://www.unboundmedicine.com/medline/citation/18054459/Development_and_validation_of_a_rapid_RP_HPLC_method_for_the_determination_of_cetirizine_or_fexofenadine_with_pseudoephedrine_in_binary_pharmaceutical_dosage_forms_ DB - PRIME DP - Unbound Medicine ER -