Author(s): Saleh Trefi, Yaser Bitar, Véronique Gilard

Email(s): salehtrefi@yahoo.com

DOI: 10.5958/0974-360X.2019.00168.9   

Address: Saleh Trefi1*, Yaser Bitar1, Véronique Gilard2
1Pharmaceutical Quality and Pharmaceutical Chemistry Department-University of Aleppo-Syria
2Laboratoire SPCMIB (UMR CNRS 5068), Université Paul Sabatier, Université de Toulouse, 118 route de Narbonne, 31062 Toulouse cedex, France
*Corresponding Author

Published In:   Volume - 12,      Issue - 3,     Year - 2019


ABSTRACT:
The objective of this study was to develop and validate a new ion-pair reversed phase high performance liquid chromatographic method on a standard C18-type stationary phase with UV detection for the analysis of the recent two-drugs combination sacubitril/valsartan in tablets. The mobile phase consisted of a mixture of 45% of 10-3 M of cetyltrimethylammonium bromide (cetrimide) as the ion-pairing agent and 55% acetonitrile. The method validation was based on linearity, accuracy, precision, robustness and specificity. This method exhibits good linearity and accuracy with mean recovery values between 95.0-105.0%, precision with relative standard deviations of the calculated concentrations less than 5.0% and specificity in the presence of degradation products. These results indicates that the proposed method is simple and applicable for the separation and determination of sacubitril, valsartan combination in tablets and could be a relevant method to implement in quality control laboratories.


Cite this article:
Saleh Trefi, Yaser Bitar, Véronique Gilard. Separation and Quantification of Sacubitril-Valsartan Combination in Tablets by a New Ion-pair HPLC. Research J. Pharm. and Tech. 2019; 12(3): 1017-1022. doi: 10.5958/0974-360X.2019.00168.9

Cite(Electronic):
Saleh Trefi, Yaser Bitar, Véronique Gilard. Separation and Quantification of Sacubitril-Valsartan Combination in Tablets by a New Ion-pair HPLC. Research J. Pharm. and Tech. 2019; 12(3): 1017-1022. doi: 10.5958/0974-360X.2019.00168.9   Available on: https://rjptonline.org/AbstractView.aspx?PID=2019-12-3-7


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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

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