J. M. Parekh, D. K. Shah, M. Sanyal, M. Yadav and P. S. Shrivastav, “Development of an SPE-LC-MS/MS Method for Simultaneous Quantification of Bosentan and Its Active Metabolite Hydroxybosentan in Human Plasma to Support a Bio-equivalence Study,” Journal of Pharmaceutical and Biomedical Analysis, Vol. 70, 2012, pp. 462-470.

has been cited by the following article:

• TITLE: Simple Estimation of Bosentan in Tablet Formulation by RP-HPLC

  AUTHORS: Selvadurai Muralidharan, Jaya Raja Kumar

  KEYWORDS: Estimation; Validation; RP-HPLC; Bosentan

  JOURNAL NAME: American Journal of Analytical Chemistry, Vol.3 No.11, November 16, 2012

  ABSTRACT: A simple, precise, and accurate method is developed and validated for the analysis of Bosentan tablet formulation. The method has shown adequate separation of the ingredients from Tablets. Separation was achieved on a C18 column using a mobile phase consisting of acetonitrile: 10 Mm ammonium acetate (pH 4.5) buffer (70:30, v/v) at a flow rate of 1.0 ml/min and UV detection at 265 nm. This new method is validated as per the ICH, which includes accuracy, precision, selectivity, linearity and range, robustness and ruggedness. The current method demonstrates good linearity over the range of 5 - 70 ng/ml of bosentan with r2 of 0.999. The average recovery of the method is 98.6%. The degree of reproducibility of the results obtained as an outcome of small deliberate variations in the method parameters and by changing analytical operator has proven that this method is robust and rugged.