Copyright (c) 2024 Srinivasa Rao Katta
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Characterization of Degradation Products of Selpercatinib by Mass Spectrometry: Optimization of Stability-Indicating HPLC Method for Separation and Quantification of Process Related Impurities of Selpercatinib
Corresponding Author(s) : Srinivasa Rao Katta
Asian Journal of Chemistry,
Vol. 36 No. 2 (2024): Vol 36 Issue 2, 2024
Abstract
The study aimed to investigate a novel approach by utilizing liquid chromatography in coupled with mass spectrometry (LC-MS) to resolve, analyze and characterize significantly less quantity of stress degradation products (DPs) of selpercatinib along with its process related impurities. The analytes resolved on ZORBAX Eclipse (250 mm) stationary phase that was maintained employing 0.5 M sodium perchlorate at pH 5.4 methanol and acetonitrile in 50:20:30 (v/v) pumped at 0.8 mL/min isocratic flow and 241 nm wavelength. The method produces very high correlate linear curve in 30-240 μg/mL for selpercatinib and 0.03-0.24 μg/mL for its impurities with significantly low detection limit of 0.01 μg/mL for impurities. Selpercatinib pure compound was subjected to stress studies and chromatographic results confirm the formation of four DPs, which were characterized with the interpretation of their mass fragmentation pattern. The DPs were identified as 6-hydroxy-4-(6-(6-((6-methoxypyridin3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile (DP 1), 6′-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)-1,2-dihydro-[3,3′-bipyridin]-5-ol (DP 2), (6-hydroxy-4-(6-(6-(pyridin-3-ylmethyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile (DP 3), 1-amino-6′-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)-1,2-dihydro-[3,3′-bipyridin]-5-ol (DP 4), 6-(2-hydroxy-2-methyl-propoxy)-4-(6-(3-methylpiperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile (DP 5) and 6-(2-hydroxy-2-methyl-propoxy)-4-(6-(3-methylpiperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile (DP 6). Based on findings, it was concluded that this method was effectively applied for the regular quantification of impurities of selpercatinib in formulations. Additionally, it demonstrated applicability for the identification of both known and unknown impurities of selpercatinib.
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- S.R. Melo, M. Homem-de-Mello, D. Silveira and L.A. Simeoni, J. Pharm. Sci. Technol., 68, 221 (2014).
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- World Health Organization, Stability Testing of Active Pharmaceutical Ingredients and Finished Pharmaceutical Products, Geneva: Switzerland (2009).
- International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use, Stability Testing of New Drug Substances and Products Q1A(R2): Geneva, Switzerland (2000).
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- V.B. Rajesh, S.R. Battula, M.V.N.R. Kapavarapu and V.R. Mandapati, Rasayan J. Chem., 15, 2373 (2022); https://doi.org/10.31788/RJC.2022.1547008
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References
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S. Singh, M. Junwal, G. Modhe, H. Tiwari, M. Kurmi, N. Parashar and P. Sidduri, Trends Analyt. Chem., 49, 71 (2013); https://doi.org/10.1016/j.trac.2013.05.006
K. Alsante, A. Ando, R. Brown, J. Ensing, T. Hatajik, W. Kong and Y. Tsuda, Adv. Drug Deliv. Rev., 59, 29 (2007); https://doi.org/10.1016/j.addr.2006.10.006
M. Blessy, R.D. Patel, P.N. Prajapati and Y.K. Agrawal, J. Pharm. Anal., 4, 159 (2014); https://doi.org/10.1016/j.jpha.2013.09.003
World Health Organization, Stability Testing of Active Pharmaceutical Ingredients and Finished Pharmaceutical Products, Geneva: Switzerland (2009).
International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use, Stability Testing of New Drug Substances and Products Q1A(R2): Geneva, Switzerland (2000).
F. Qiu and D.L. Norwood, J. Liq. Chromatogr. Relat. Technol., 30, 877 (2007); https://doi.org/10.1080/10826070701191151
A.Y. Li, M.G. McCusker, A. Russo, K.A. Scilla, A. Gittens, R. Mehra, K. Arensmeyer, V. Adamo and C. Rolfo, Cancer Treat. Rev., 81, 101911 (2019); https://doi.org/10.1016/j.ctrv.2019.101911
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B.J. Solomon, L. Tan, J.J. Lin, S.Q. Wong, S. Hollizeck, K. Ebata, B.B. Tuch, S. Yoda, J.F. Gainor, L.V. Sequist, G.R. Oxnard, O. Gautschi, A. Drilon, V. Subbiah, C. Khoo, E.Y. Zhu, M. Nguyen, D. Henry, K.R. Condroski, G.R. Kolakowski, E. Gomez, J. Ballard, A.T. Metcalf, J.F. Blake, S.J. Dawson, W. Blosser, L.F. Stancato, B.J. Brandhuber, S. Andrews, B.G. Robinson and S.M. Rothenberg, J. Thorac. Oncol., 15, 541 (2020); https://doi.org/10.1016/j.jtho.2020.01.006
N. Singamsetty and R. Sundararajan, Int. J. Res. Pharm. Sci., 12, 931 (2021); https://doi.org/10.26452/ijrps.v12i1.4471
J.L. Gulikers, A.J. van Veelen, E.M.J. Sinkiewicz, Y.M. de Beer, M. Slikkerveer, L.M.L. Stolk, V.C.G. Tjan-Heijnen, L.E.L. Hendriks, S. Croes and R.M.J.M. van Geel, Biomed. Chromatogr., 37, e5628 (2023); https://doi.org/10.1002/bmc.5628
International Conference of Harmonisation (ICH), Q1A(R2), Stability Testing of New Drug Substances and Products. Geneva: International Conference on Harmonization (2003).
International Conference of Harmonisation (ICH), Q1B, Stability Testing: Photostability Testing of New Drug Substances and Products, Geneva: International Conference on Harmonization (1996).
International Conference of Harmonisation (ICH) Q2(R1), Validation of Analytical Procedures: Text and Methodology, Geneva: International Conference on Harmonization (1994).
R.B. Varma and B.S. Rao, Res. J. Pharm. Technol., 15, 5158 (2022); https://doi.org/10.52711/0974-360X.2022.00868
B.H.R. Varma and B.S. Rao, Res. J. Chem. Environ., 27, 54 (2023); https://doi.org/10.25303/2702rjce054061
V.B. Rajesh, S.R. Battula, M.V.N.R. Kapavarapu and V.R. Mandapati, Rasayan J. Chem., 15, 2373 (2022); https://doi.org/10.31788/RJC.2022.1547008
V.B. Rajesh, R.B. Sreenivasa, V.N.R.K. Maruthi and R.M. Varaprasad, Ann. Pharm. Fr., 81, 64 (2023); https://doi.org/10.1016/j.pharma.2022.06.012
B.K. Bikshal, R.A. Venkateswara and R.M. Useni, Indian Drugs, 55, 41 (2018); https://doi.org/10.53879/id.55.12.11185
K.S. Girija, B.B. Kasimala and V.R. Anna, Int. J. Appl. Pharm., 13, 165 (2021); https://doi.org/10.22159/ijap.2021v13i2.39895
B.K. Bikshal, R.M. Useni, R.A. Venkateswara and R.L. Maheshwara, Thai J. Pharm. Sci., 42, 27 (2018).
U.R. Mallu, V.R. Anna and B.B. Kasimala, Turk. J. Pharm. Sci., 16, 457 (2019); https://doi.org/10.4274/tjps.galenos.2018.34635