Validating a stability indicating HPLC method for kinetic study of cetirizine degradation in acidic and oxidative conditions

Iranian Journal of Pharmaceutical Research

Volumn 12, Issue 2, 2013, Pages 287-294

  Souri, Effat ^a   Hatami, Ali ^a   Ravari, Nazanin Shabani ^a   Alvandifar, Farhad ^a   Tehrani, Maliheh Barazandeh ^a  

^a TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Cetirizine; Degradation; High performance liquid chromatography (HPLC); Kinetics; Stability

Indexed keywords

CETIRIZINE;

ACCURACY; ARTICLE; DRUG DEGRADATION; DRUG STABILITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; KINETICS; OXIDATION; VALIDATION STUDY;

EID: 84878953208     PISSN: 17350328     EISSN: 17266890     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

1. th edition, Mc Graw-Hill Medical Publishing Division, USA (2005).
2. El Walily AFM, Korany MA, El Gindy A and Bedair MF. Spectrophotometric and high performance liquid chromatographic determination of cetirizine dihydrocholride in pharmaceutical tablets. J. Pharm. Biomed. Anal. (1998) 17: 435-442.
3. Paw B, Misztal G, Hopkata H and Drozd J. Development and validation of a HPLC method for the determination of cetirizine in pharmaceutical dosage forms. Pharmazie (2002) 57: 313-315.
4. Jaber AMY, Al Sherife HA, Al Omari MM and Badwan AA. Determination of Cetirizine dihydrochloride, related impurities and preservatives in oral solution and tablet dosage forms using HPLC. J. Pharm. Biomed. Anal. (2004) 36: 341-350.
5. Arayne MS, Sultana N and Siddiqui FA. Determination and quantification of cetirizine HCl in dosage formulations by RP-HPLC. Pak. J. Pharm. Sci. (2005) 18: 7-11.
6. Haghighi S, Shapouri MR, Amoli-Diva M, Pourghazi K, Afruzi H. HPTLC-Densitometric Determination for Cetirizine and Montelukast Analysis in Combined Tablet Dosage Forms. Iranian J. Pharm. Res. (2013) 12
7. Karakus S, Kucukguzel I and Kucukguzel 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: 295-302.
8. Hadad GM, Emara S and Mahmoud WMM. Development and validation of a stability- indicating RP-HPLC method for the determination of paracetomol with dantrolene or/and cetirizine and pseudoephedrine in two pharmaceutical dosage forms. Talanta (2009) 79: 1360-1367.
9. Likar MD, Mansour HL and Harwood JW. Development and validation of a dissolution test for a once-a-day combination tablet of immediate-release cetirizine dihydrochloride and extended-release pseudoephedrine hydrochloride J. Pharm. Biomed. Anal. (2005) 39: 543-551.
10. Azhagvuel S and Sekar R. Method development and validation for the simulthaneous determination of cetirizine dihydrocholride, paracetamol, and phenylpropanolamine hydrochloride in tablets by capillary zone electrophoresis J. Pharm. Biomed. Anal. (2007) 43: 873-878.
11. Gowekar MM, Pande VB, Kasture AV, Tekade AR and Chandorkar JG. Spectrophotometric estimation of ambroxol and cetirizine hydrochloride from tablet dosage form. Pak. J. Pharm. Sci. (2007) 20: 250-251.
12. The British Pharmacopeia, British Pharmacopoeial Commision, London, UK (2008).
13. Makhija SN and Vavia PR. Stability indicating HPTLC method for the simultaneous determination of pseudoephendrine and cetirizine in pharmaceutical formulations. J. Pharm. Biomed. Anal. (2001) 25: 663-667.
14. Zaater MF, Tahboub YR and Najib NM. RP-LC method for the determination of cetirizine in serum. J. Pharm. Biomed. Anal. (2000) 22: 739-744.