STABILITY-INDICATING CHROMATOGRAPHIC METHOD FOR THE DETERMINATION OF BENZONATATE, DIPHENHYDRAMINE, GUAIFENESIN, AND PHENYLEPHRINE

被引:6
作者
Kishk, Safaa M. [1 ]
Salama, Ismail [1 ]
Mostafa, Samia [1 ]
El-Sadek, Mohamed [2 ]
机构
[1] Suez Canal Univ, Fac Pharm, Dept Pharmaceut Chem, Ismailia 41552, Egypt
[2] Zagazig Univ, Fac Pharm, Dept Med Chem, Zagazig, Egypt
关键词
benzonatate; diphenhydramine; guaifenesin; phenylephrine; RP-HPLC; stability-indicating; LIQUID-CHROMATOGRAPHY; SPECTROPHOTOMETRIC DETERMINATION; PHARMACEUTICAL FORMULATIONS; CAPILLARY-ELECTROPHORESIS; QUANTITATIVE-ANALYSIS; NASAL SOLUTIONS; COLD MEDICINES; HUMAN PLASMA; CHLORPHENIRAMINE; HYDROCHLORIDE;
D O I
10.1080/10826076.2012.758140
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A high-performance liquid chromatographic method has been developed for the simultaneous analysis of benzonatate (BNZ), diphenhydramine hydrochloride (DPH), guaifenesin (GFN), and phenylephrine hydrochloride (PEP). The separation was achieved using a Thermo C18 reversed-phase column (250mmx4.6mm ID, particle size 5 mu). Dual mode gradient elution was used for the separation and UV detection was carried out at 222nm. The method was specific and stability indicating as chromatographic conditions provided adequate separation of degradation products. The method showed good linearity in the range of 5-400, 1-120, 3-300, and 2-100 mu g/mL for BNZ, DPH, GFN, and PEP, respectively. All the square of the correlation coefficients are 0.999. The degradation products were isolated and identified by NMR, IR, and mass spectroscopy. The proposed method proved to be accurate, precise, selective, and robust. The applicability of the method was evaluated in commercial dosage form analysis as well as in stability studies.
引用
收藏
页码:726 / 747
页数:22
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