TY - JOUR
T1 - Simultaneous determination of cromolyn sodium combined dosage forms using isocratic HPLC method
AU - Fathy, M. E.
AU - Mohamed, S. Abo El Abass
AU - Elmansi, H.
AU - Belal, F.
N1 - Publisher Copyright:
© The Author 2016.
PY - 2017/1
Y1 - 2017/1
N2 - A simple and selective reversed-phase high-performance liquid chromatography method was developed for the estimation of cromolyn sodium (CRM) with either oxymetazoline hydrochloride (OMZ) or xylometazoline hydrochloride (XMZ) in their binary mixtures. The method is based on the simultaneous separation of each drug in a reversed-phase Waters symmetry® C18 column (250mm × 4.6mm intradermally, 5-μm particle size) at 25°C. Elution was performed with a mobile phase consisting of methanol : 0.1M phosphate buffer (60:40, v/v, pH 4.0). Quantitation was achieved with ultraviolet detection at 220 nm. The method could determine the three drugs, with linearity, in the range of 2.0-100.0 μg/mL for CRM and 0.8-8.0 μg/mL for OMZ and for XMZ. Aspirin was used as internal standard. Optimization of the separation in terms of mobile phase composition is critical to the method development, which is discussed in detail. The suggested procedure was successfully applied to the analysis of the studied drugs in their nasal preparations. Statistical evaluation of the data obtained by the proposed and comparison methods revealed good accuracy of the proposed method.
AB - A simple and selective reversed-phase high-performance liquid chromatography method was developed for the estimation of cromolyn sodium (CRM) with either oxymetazoline hydrochloride (OMZ) or xylometazoline hydrochloride (XMZ) in their binary mixtures. The method is based on the simultaneous separation of each drug in a reversed-phase Waters symmetry® C18 column (250mm × 4.6mm intradermally, 5-μm particle size) at 25°C. Elution was performed with a mobile phase consisting of methanol : 0.1M phosphate buffer (60:40, v/v, pH 4.0). Quantitation was achieved with ultraviolet detection at 220 nm. The method could determine the three drugs, with linearity, in the range of 2.0-100.0 μg/mL for CRM and 0.8-8.0 μg/mL for OMZ and for XMZ. Aspirin was used as internal standard. Optimization of the separation in terms of mobile phase composition is critical to the method development, which is discussed in detail. The suggested procedure was successfully applied to the analysis of the studied drugs in their nasal preparations. Statistical evaluation of the data obtained by the proposed and comparison methods revealed good accuracy of the proposed method.
UR - http://www.scopus.com/inward/record.url?scp=85026912530&partnerID=8YFLogxK
U2 - 10.1093/chromsci/bmw142
DO - 10.1093/chromsci/bmw142
M3 - Article
C2 - 27621136
AN - SCOPUS:85026912530
SN - 0021-9665
VL - 55
SP - 14
EP - 22
JO - Journal of Chromatographic Science
JF - Journal of Chromatographic Science
IS - 1
ER -