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V. Kumar, S. Malik and S. Singh, “Polypill for the Treatment of Cardiovascular Diseases Part 2. LC-MS/ TOF Characterization of Interaction/Degradation Pro- ducts of Atenolol/Lisinopril and Aspirin, and Mechanisms of Formation Thereof,” Journal of Pharmaceutical and Biomedical Analysis, Vol. 48, No. 3, 2008, pp. 619-628. doi:10.1016/j.jpba.2008.06.003

has been cited by the following article:

• TITLE: RP-HPLC Method for the Simultaneous Determination of Lisinopril and NSAIDs in API, Pharmaceutical Formulations and Human Serum

  AUTHORS: Najma Sultana, M. Saeed Arayne, Rubina Siddiqui, Safila Naveed

  KEYWORDS: Lisinopril; NSAIDs; Method Validation; HPLC Determination

  JOURNAL NAME: American Journal of Analytical Chemistry, Vol.3 No.2, February 22, 2012

  ABSTRACT: High performance liquid chromatographic method was developed valdated and applied for the simultaneous determi- nation of lisinopril and NSAIDs in bulk, pharmaceuticals formulations and human serum. A Purospher star C18 (5 μm, 25 × 0.46 cm) column was used with mobile phase consisting of methanol: water: acetonitrile (80:17.5:2.5 v/v, pH 3.0) and quantitative evaluation was performed at 225 nm with a flow rate of 1.0 mL?min–1. The retention time of lisinopril was 2.2 min while naproxen, flurbiprofen, diclofenac sodium and mefenamic acid were found to be 4.0, 4.5, 5.0 and 6.7 min respectively. Suitability of this method for the quantitative determination of the drugs was proved by validation in accordance with the requirements laid down by International Conference on Harmonization (ICH) guidelines. The method is selective, precise, accurate and can be used for analysis of pharmaceutical preparations in quality control and clinical laboratories.