[1]
Joel, G.H.; Lee, E.L. Goodman and Gilman’s, The Pharmacological basis of therapeutics.10th International edition. McGraw Hill publishers; medical publishing division, New York, 2001, 829, pp. 843-995.
[2]
Parfit, M.K. The complete drug reference, 35th ed; London, UK: Pharmaceutical press, 2007, pp. 1034-1037.
[3]
Rang, H.P.; Dale, M.M.; Ritter, J.M.; Flower, R.J. Rang and Dale’s Pharmacology, 6th ed; Churchill Livingstone Elsevier, 2007, p. 307.
[4]
Page, C.; Curtis, M.; Walker, M.; Hoffman, B. Integrated pharmacology, 3rd ed; Mosby Elsevier, 2006, pp. 324-326.
[7]
Naga, P.Y.; Archana, S.; Poornima, Y.; Lalitha, S. Development and validation of spectrophotometric method for determination of trimetazidine in pharmaceutical dosage form. Int. J. Pharm. Sci. Res., 2013, 4, 1131-1134.
[8]
Khedr, A.; Sheha, M.; Darwish, I. Sensitive determination of Trimetazidine in spiked human plasma by HPLC with fluorescence detection after pre-column derivatization with 9-fluorenylmethyl chloroformate. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 2007, 856, 337-342.
[9]
Jiao, Y.; Su, M.; Chen, M.; Jia, W.; Chuo, Y. LC/ESI-MS method for determination of Trimetazidine in human plasma: Application to a bioequivalence study on chinese volunteers. J. Pharma. Biomed. Anal., 2007, 43, 1804-1807.
[10]
Zhang, T.; Meng, P.; Kou, W.; Ma, R.; Zhang, C. Rapid and sensitive UPLC-MSMS for the determination of Trimetazidine in human plasma. Chromatographia, 2010, 71, 1101-1105.
[11]
Chowdhury, M.I.; Ullah, A.; Maruf, A.A.; Mohammad, S.I.; Ahmed, M.U. Validation and optimization of a simple RP-HPLC method for determination of Trimetazidine in human serum and its application in a pharmacokinetic study with healthy Bangladeshi male volunteers. Dhaka Univ. J. Pharm. Sci., 2011, 10, 71-78.
[12]
Xiong, X.; Yang, L.; Zhai, S. Validation of a rapid and simple LC- MS/MS method to determine trimetazidine in rat plasma. J. Liquid. Chromatog. Relat. Technol., 2011, 34, 1645-1653.
[13]
Naushad, M.; Aqil, M.; Ahmad, F.; Ali, A.; Faisal, M. Development and validation of the HPLC method for the analysis of Trimetazidine hydrochloride in bulk drug pharmaceutical dosage form. J. Anal. Chem., 2008, 63, 965.
[14]
United States Pharmacopeia 38, National Formulary 33, vol. 2, The United States Pharmacopoeial Convention, Rockville. 2015, 2647.
[15]
Phale, M.D.; Hamrapurkar, P.D. A Validated and Simplified RP-HPLC of Metoprolol Succinate from bulk drugs. Asian J. Res. Chem, 2009, 2, 119-122.
[16]
Kulkarni, M.; Kshirsagar, R.; Sakarkar, D. Development and validation of spectrophotometric method for determination of Metoprolol succinate. Int. J. Chem. Tech. Res., 2009, 1, 1273-1277.
[17]
Durga, K.; Shajhan, S.; Rao, S.; Reddy, S.; Subramanyam, M. RP-HPLC method for estimation of Metoprolol in bulk drug. Int. J. Sci. Innovations Discoveries, 2011, 1, 151-157.
[18]
Padala, V.; Bommana, N.; Kalluru, S.; Vasireddy, V. Selective and sensitive method for the determination of Metoprolol in human plasma using liquid chromatography coupled with tandem mass spectrometry. Acta Pharm., 2010, 60, 177-184.
[19]
Kalisetty, S.; Reddy, T.; Reddy, A.; Palnati, J. Stability indicating reverse phase liquid chromatographic method for the determination of Metoprolol Succinate in pharmaceutical dosage forms. J. Chem. Pharmaceut. Res., 2012, 4, 4420-4425.
[20]
Motisariya, M.H.; Patel, K.G.; Shah, P.A. Validated stability indicating high performance thin layer chromatographic method for determination of ivabradine hydrochloride in bulk and marketed formulation: an application to kinetic study. Bull. Fac. Pharm. Cairo Univ., 2013, 51, 233-241.
[21]
Pikul, P.; Nowakowska, J.; Ciura, K. Chromatographic analysis of ivabradine on polar, nonpolar, and chemically modified adsorbents by HPTLC. J. Food Drug Anal., 2013, 21, 165-168.
[22]
Liliana, G.; Rodica, D.; Camelia, N.; Loredana, D. Sulfur compounds identification and quantification from Allium spp. fresh leaves. J. Food Drug Anal., 2014, 22, 425-430.
[23]
John, J.; Reghuwanshi, A.; Aravind, U.K.; Aravindakumar, C.T. Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration. J. Food Drug Anal., 2015, 23, 219-224.
[24]
Agrawal, P.; Laddha, K. Development of validated high-performance thin layer chromatography for quantification of Aristolochic acid in different species of the Aristolochiaceae family. J. Food Drug Anal., 2016, 25, 425-429.
[25]
Patel, K.G.; Shah, P.M.; Shah, P.A.; Gandhi, T.R. Validated high-performance thin-layer chromatographic (HPTLC) method for simultaneous determination of Nadifloxacin, Mometasone furoate, and Miconazole nitrate cream using fractional factorial design. J. Food Drug Anal., 2016, 24, 610-619.
[26]
Pandya, J.J.; Bhatt, N.M.; Chavadaa, V.D.; Sharmaa, P.; Sanyalb, M.; Shrivastava, P.S. Simultaneous analysis of aliskiren and hydrochlorothiazide in pharmaceutical preparations and spiked human plasma by HPTLC. J. Taibah Univ. Sci, 2017, 11(5), 667-676.
[27]
Patil, V.; Kulkarni, V.; Devdhes, J.; Kawde, R.; Kurhade, S. Simultaneous HPTLC analysis of Hydrochlorthiazide and Metoprolol Succinate in tablet and bulk dosage form. World Res. J. Organic Chem., 2012, 1, 1-5.
[28]
Kunjir, V.; Jadhav, S.; Purkar, A.; Chaudhari, P. Validated HPTLC method for simultaneous determination of Olmesartan medoximil and Metoprolol succinate in tablet dosage form. Indian Drugs, 2012, 49, 13-17.
[29]
Rath, S.; Panda, S.; Sarangi, R.; Dash, A.; Rath, S. UV-Spectrophotometric method for simultaneous estimation of Metoprolol and Amlodipine in bulk and their formulation. Int. J. Biol. Pharm. Res., 2011, 2, 50-54.
[30]
Singh, B.; Patel, D.; Ghosh, S. Development of reverse phase HPLC method for simultaneous analysis of metoprolol succinate and hydrochlorothiazide in a tablet formulation. Trop. J. Pharm. Res., 2009, 8, 539-543.
[31]
Chitlange, S.; Bhusal, R.; Nikumbh, M.; Bhole, R. Development and validation of spectrophotometric and stability indicating method RP-HPLC for the simultaneous estimation of metoprolol succinate and hydrochlorothiazide in tablet dosage form. Int. J. Pharm., 2012, 2, 591-597.
[32]
Rao, R.; Deshmukh, A.; Madhu, R. Analytical method development and validation of metoprolol succinate and hydrochlorothiazide in pharmaceutical formulation by RP-HPLC method. Int. J. Pharma. World Res., 2012, 3, 1-13.
[33]
Vora, B.; Parmar, R.; Shah, D.; Nayak, V. Absorption correction method for simultaneous estimation of metoprolol succinate and olmesartan medoxomil in combined tablet dosage form. J. Pharm. Sci. Biosci. Res., 2012, 2, 54-57.
[34]
Vachhani, K.; Patel, S. Development and validation of spectrophotometric method for simultaneous estimation of metoprolol succinate and olmesartan medoxomil in tablet. J. App. Pharm. Sci., 2011, 1, 112-115.
[35]
Jadhav, M.; Suryawanshi, S.; Tajane, S.; Tarkase, K. Development and validation of UV spectrophotometric method for determination of metoprolol succinate and telmisartan in tablet dosage form. Int. J. Pharm Sci., 2012, 4, 387-389.
[36]
Wankhede, S.; Dixit, N.; Chitlange, S. Stability indicating HPTLC method for quantitative determination of atorvastatin calcium and metoprolol succinate in capsules. Der. Pharmacia. Lettre, 2011, 3, 1-7.
[37]
ICH Harmonized Tripartite Guideline, Validation of Analytical Procedures: Text and Methodology Q2 (R1), Geneva, November 2005.
[38]
Guidance for Industry, Bioanalytical Method Validation, US Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for Veterinary Medicine (CVM), May 2001.