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A. A. El-Emam, S. H. Hansen, M. A. Moustafa, S. M. El-Ashry and D.T. El-Sherbiny, “Determination of Lisi- nopril in Dosage Forms and Spiked Human Plasma through Derivatization with 7-Chloro-4-nitrobenzo-2- oxa-1,3-diazole (NBD-Cl) Followed by Spectrophotome- try or HPLC with Fluorimetric Detection,” Journal of Pharmaceutical and Bio-medical Analysis, Vol. 34, No. 1, 2004, pp. 35-44. doi:10.1016/j.japna.2003.08.021

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.