Cite

[1]. R. de Barros Silva, Hypertension and renin – angiotensin system, in: H. Babaei Antihypertensive drugs, InTech, 2012, pp. 85-94. Doi: 10.5772/36723.10.5772/36723 Search in Google Scholar

[2]. B. Stanisz, Evaluation of stability of enalapril maleate in solid phase, J. Pharm. Biomed. Anal. 21 (2003) 375-380. Doi: 10.1016/S0731-7085(02)00325-4.10.1016/S0731-7085(02)00325-4 Search in Google Scholar

[3]. A. Zoppi, C. Garnero, Y. Garro Linck, A.K. Chattab, G.A. Monti, M.R. Longhi, Enalapril: β-CD complex: stability enhancement in solid state, Carboh. Polym. 86 (2011) 716-721. Doi: 10.1016/j.carbpol.2011.05.008.10.1016/j.carbpol.2011.05.008 Search in Google Scholar

[4]. M.M. Ayad, A.A. Shalaby, H.E. Abdellatef, M.M. Hosny, Spectrophotometric and AAS determination of ramipril and enalapril through ternary complex formation, J. Pharm. Biomed. Anal. 28 (2002) 311-321. Doi: 10.1016/S0731-7085(01)00595-7.10.1016/S0731-7085(01)00595-7 Search in Google Scholar

[5]. S. Gherman, D. Zavastin, A. Spac, V. Dorneanu, Spectrophotometric determination of enalapril using tropeolin 00, Rev. Chim. (Bucharest) 64 (2013) 1224-1228. Search in Google Scholar

[6]. M. Manoranjani, K. Kamala Karuna, UV-visible spectroscopic estimation and validation of enalapril maleate in bulk and pharmaceutical dosage forms, Int. J. Res. Pharm. Biomed. Sci. 2 (2011) 1651-1656. Search in Google Scholar

[7]. N. Rahman, Sk. M. Haque, Optimized and validated spectrophotometric methods for the determination of enalapril maleate in commercial dosage forms, Anal. Chem. Insights. 3 (2008) 31-43. Doi: 10.4137/aci.s643.10.4137/ACI.S643 Search in Google Scholar

[8]. P.S. Patil, H.N. More, Difference spectrophotometric estimation of enalapril maleate from tablet dosage form, Int. J. Res. Pharm. Biomed. Sci. 2 (2011) 629-633. Search in Google Scholar

[9]. S.A. Shama, A.S. Amin, H. Omara, Spectrophotometric microdetermination of some antihypertensive drugs in pure form and in pharmaceutical formulations, J. Chil. Chem. Soc. 56 (2011) 566-570. Doi: 10.4067/S0717-97072011000100009.10.4067/S0717-97072011000100009 Search in Google Scholar

[10]. M. Mohan, S.Z. Haider, A.K. Anand, A.K. Srivastva, Validation of stability indicating HPLC method for the determination of enalapril maleate in tablet formulation, Int. J. Pharm. Pharm. Sci. 3 (2011) 180-183. Search in Google Scholar

[11]. M.Ž. Milenković, P.S. Sibinović, V.D. Marinković, R.M. Palić, G.S. Stojanović, D.M. Milenović, Optimization and validation of an HPLC method for determination of related compounds in enalapril maleate tablets, Anal. Chem. Ind. J. 13 (2013) 135-145. Search in Google Scholar

[12]. L. Logoyda, A.M. Abdel-Megied, Y. Kondratova, O. Trofimenko, D. Korobko, I. Dakhym, Development and validation of HPLC method for the simultaneous determination of enalapril maleate in present of their impurities: application to tablet analysis, Int. J. App. Pharm. 10 (2018) 98-102. Doi: 10.22159/ijap.2018v10i1.22805.10.22159/ijap.2018v10i1.22805 Search in Google Scholar

[13]. ICH, Validation of Analytical Procedures: Text and Methodology Q2(R1), 2005 Search in Google Scholar

[14]. European Pharmacopoeia, Ed. 10, Strasbourg: Council of Europe, 2020. Search in Google Scholar

[15]. A.D. Panainte, M. Vieriu, G. Tantaru, M. Apostu, N. Bibire, L. Avasilcai, I.D. Morariu, RP-HPLC analysis method of bisoprolol fumarate in a new tablet formulation, Med. Surg. J. 122 (2018) 634-639. Search in Google Scholar

[16]. G. Tantaru, N. Bibire, A.D. Panainte, M. Vieriu, M. Apostu, Aniline derived bis-Schiff Base - analytical reagent for the assay of Fe (III), Rev. Chim. (Bucharest) 69 (2018) 3097-3099.10.37358/RC.18.11.6690 Search in Google Scholar

[17]. T.J. Purohit, Z. Wu, S.M. Hanning, Simple and reliable extraction and a validated high performance liquid chromatographic assay for quantification of amoxicillin from plasma, J. Chromatogr. A. 22 (2019). Doi 10.1016/j.chroma.2019.460611. Search in Google Scholar

[18]. A.D. Panainte, L. Agoroaei, N. Bibire, G. Tantaru, M. Apostu, M. Vieriu, A.F. Spac, A HPLC method for the determination of bisoprolol in tablets and its application to a bioequivalence study, Rev. Chim. (Bucharest) 66 (2015) 1791-1795. Search in Google Scholar

[19]. K. Konam, J. Soujanya, M. Sasikala, A. Kiran Kumar, Development and validation of RP-HPLC method for the determination of bisoprolol fumarate tablets. Int. J. Res. Pharm. Nano. Sci. 2 (2013) 57-67. Search in Google Scholar

[20]. FDA, Reviewer Guidance, Validation of chromatographic methods, Center for Drug Evaluation and Research (CDER), (1994). Search in Google Scholar

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