Abstract
The separation of a long peptide chain without derivatization, without amide columns and by using routine reversed-phase HPLC columns is itself a big task. Increase in the basic nature of the mobile phase as well as in column temperature and low flow rate of the mobile phase were demonstrated to permit the separation of polar compounds containing long peptide chains. The aim of this study was to develop a procedure for the determination of an antithrombing agent Bivalirudin containing a long peptide chain. This method was developed on a Princeton SPHER-C18 100 Å (4.6 × 250 mm, 5 µm) column and a mobile phase consisting of water-acetonitrile (pH 7, adjusted with triethylamine) in the ratio of 95 : 5. The flow rate was 0.7 mL/min at the thermostat temperature of 45°C. Validation of the method was performed as per the International Conference on Harmonization. The method was applied to the analysis of a pharmaceutical formulation. The developed method was accurate, fast, easy for implementation and economy as it did not require sophisticated equipment or tedious derivatization process.
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REFERENCES
Goodman and Gilman’s The Pharmacological Basis of Therapeutics, Brunton, L., Chabner, B., and Knollman, B., Eds., New York: McGraw-Hill, 2011, 12th ed.
Warkentin, T.E., Greinacher, A., and Koster, A., J. Thromb. Haemostasis, 2008, vol. 99, no. 5, p. 830.
Shammas, N.W., J. Cardiovasc. Pharmacol. Ther., 2005, vol. 23, no. 4, p. 345.
Issaq, H.J., Chan, K.C., Janini, G.M., Conrads, T.P., and Veenstra, T.D., J. Chromatogr. B: Anal. Technol. Biomed. Life Sci., 2005, vol. 817, no. 7, p. 35.
Farthing, D., Larus, T., Fakhry, I., Gehr, T., Prats, J., and Sica, D., J. Chromatogr. B: Anal. Technol. Biomed. Life Sci., 2004, vol. 802, no. 2, p. 355.
Van den Broek, I., Sparidans, R.W., Schellens, J.H., and Beijnen, J.H., J. Chromatogr. B: Anal. Technol. Biomed. Life Sci., 2008, vol. 872, no. 1, p. 1.
Pan, G., Wang, X., Huang, Y., Gao, X., and Wang, Y., J. Pharm. Biomed. Anal., 2010, vol. 52, no. 1, p. 105.
Li, X.J., Sun, Y.T., Yin, L., Zhang, X.J., Yang, Y., and Fawcett, J.P., J. Pharm. Anal., 2013, vol. 3, no. 1, p. 1.
Chai, D., Wang, R., Bai, N., Cai, Y., and Liang, B., Biomed. Chromatogr., 2013, vol. 27, no. 12, p. 1788.
Sadekar, S.D., Chilkawar, R.N., Patil, S.M., Saboji, J.K., and Nanjwade, B.K., Austin J. Anal. Pharm. Chem., 2014, vol. 1, no. 5, p. 1024.
ICH Validation of Analytical Procedure Methodology (Q2B), ICH Harmonised Tripartite Guidelines, Geneva, 1997.
ACKNOWLEDGMENTS
The authors are thankful to Cipla Pvt. for providing Bivalirudin as a gift sample. Thankful to R.C. Patel, Institute of Pharmaceutical Education and Research, Shirpur, Dist: Dhule (MS) 425 405 India, for giving all types of facilities and supports required for completion of this work.
Funding
The authors are thankful to University Grant Commission New Delhi for giving funding for the work under Minor Research Project scheme.
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Khan Mohammad Mojeeb Gulzar, Atul, S. & Surana, S. Development of a Novel Separation Technique by High Performance Liquid Chromatography for the Determination of Bivalirudin. J Anal Chem 74, 1035–1038 (2019). https://doi.org/10.1134/S1061934819100071
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DOI: https://doi.org/10.1134/S1061934819100071