Stability indicating RP-HPLC method for simultaneous determination of guaifenesin and pseudoephedrine hydrochloride in the presence of syrup excepients

Arabian Journal of Chemistry - Tập 10 - Trang S2896-S2901 - 2017
Nada S. Abdelwahab1, Eglal A. Abdelaleem1
1Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Bani-Suef University, Alshaheed Shehata Ahmad Hegazy St., 62514 Beni-Suef, Egypt

Tài liệu tham khảo

Hassib, 2011, Development and validation of RP-HPLC stability-indicating methods for the determination of butamirate citrate and sodium cromoglycate, J. Chem. Pharmaceut. Res., 3, 243 Histochi, 2005, Simultaneous determination of ingredients in a cold medicine by cyclodextrin modified microemulsion electrokinetic chromatography, J. Pharm. Biomed. Anal., 37, 517, 10.1016/j.jpba.2004.11.011 ICH, 2005. Q2 (R1) Validation of Analytical Procedures, Proceedings of the International Conference on Harmonization, Geneva. Lei, 2004, Determination of four main ingredients in photifed-m children cough syrup, Yaowu Fenxi Zazhi, 24, 44 Leroy, 1998, Stability indicating methods for the quantitative determination of Pseudoephedrine HCl, Guaifenesin and dextromethorphan hydrobromide in cough syrup using HPLC, Saudi Pharmaceut. J., 6, 53 Louhaichi, 2009, Simultaneous determination of Pseudoephedrine HCl, Pheniramine, Guaifenesin, pyrilamine, chlorpheniramine and dextromethorphan in cough and cold medicines by high performance liquid chromatography, Talanta, 78, 991, 10.1016/j.talanta.2009.01.019 Martindale-Extra Pharmacopoeia, 2005 Moussa, 2011, Development and validation of a stability-indicating HPLC method for the analysis of desvenlafaxine succinate in the presence of its acidic induced degradation product in bulk and pharmaceutical preparation, J. Chem. Pharmaceut. Res., 3, 425 Patel, 2011, Development and validation of a stability indicating RP-HPLC method for simultaneous determination of Lamivudine and Stavudine in combined dosage forms, J. Chem. Pharmaceut. Res., 3, 200 Rahul, 2011, Spectrophotometric determination of Guaifenesin and Pseudoephedrine Hydrochloride in tablet dosage form, Int. J. Res. Pharm. Sci., 1, 42 Rao, 2010, Development and validation of UV-Spectroscopic method for estimation of Voglibose in bulk and tablets, J. Chem. Pharmaceut. Res., 2, 350 Shervington, 1997, A quantitative simultaneous HPLC determination of Pseudoephedrine HCl. Guaifenesin and dextromethorphan hydrobromide, Anal. Lett., 30, 927, 10.1080/00032719708002307 Shuhan, 2005, Simultaneous determination of the contents of the three components in Guaifenesin, Pseudoephedrine HCl and dextromethorphan hydrobromide capsules by HPLC, Shenyang Yoake Daxue Xuebao, 22, 119 Siavash, 2011, A new technique for spectrophotometric determination of Guaifenesin and Pseudoephedrine HCl in syrup and synthetic mixture, Drug Test. Anal., 3, 319, 10.1002/dta.235 The British Pharmacopoeia, 2007. Her Majesty’s, The Stationary Office, London. The United States Pharmacopeia, 2009. 32 Ed., National Formulary 27, United States Pharmacopeial convention INC, USA. Thresiana, 2005, Simultaneous determination of some active ingredients in cough and cold preparations by gas chromatography and method validation, JAOAC Int., 88, 1093, 10.1093/jaoac/88.4.1093 US FDA Guidance, 2000 Vaidya, 2001, Simultaneous HPLC assay of a four- component anti-multisymptomatic dosage using ion pair and flow rate programming, Indian Drugs, 38, 16 Wilcox, 2000, HPLC determination of Guaifenesin with selected medications on underivatized silica with an aqueous organic mobile phase, J. Pharm. Biomed. Anal., 23, 909, 10.1016/S0731-7085(00)00359-9 Xiaohui, 2000, MEKC determination of Guaifenesin, Pseudoephedrine HCl and dextromethorphan hydrobromide in capsule dosage form, J. Liq. Chromatogr. Relat. Technol., 23, 1, 10.1081/JLC-100101431 Yongqing, 2000, Determination of Guaifenesin, Pseudoephedrine HCl and dextromethorphan hydrobromide in Redentai oral solution by HPLC, Yaowu Fenxizaahi, 20, 97