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A reliable HPLC-DAD method for simultaneous determination of related substances in TBI-166 active pharmaceutical ingredient

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A sensitive, stability-indicating reversed-phase high-performance liquid chromatography with diode array detection (HPLC–DAD) method has been developed for the determination of TBI-166 and its 10 kinds of related impurities. Chromatographic separation was achieved on a Kromasil ODS column (250 mm × 4.6 mm, 5 μm), with a gradient elution of the mobile phase system consisting of acetonitrile and 1% ammonium formate solution (with 0.2% formic acid). The flow rate was 1.0 mL/min, and the detection wavelength was set at 251 nm. The method was validated according to the International Conference on Harmonization (ICH) guidelines with respect to selectivity, linearity, limits, accuracy, precision, and robustness. The calibration curves were linear from LOQ to 150% of the specification limit of impurity with correlation coefficients not less than 0.999. The limits of quantitation were between 0.123 and 0.257 μg/mL. Accuracy for the related substances was estimated by the recovery ranged from 94.6% to 111.2%. The method was proved to be reliable for the determination of related substances in TBI-166 bulk drug, which is essential and important in the quality control.
Rocznik
Strony
80--85
Opis fizyczny
Bibliogr. 19 poz., rys., tab.
Twórcy
  • Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
autor
  • Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
autor
  • Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
autor
  • Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
autor
  • Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
Bibliografia
  • [1.] World Health Organization Global tuberculosis report 2018 World Health Organization, Geneva, Switzerland, 2018.
  • [2.] Gandhi, N. R.; Nunn, P.; Dheda, K.; Schaaf, H.S.; Zigno, M.; Zignol, M.; Soolingen, D. V.; Jensen, P.; Bayona, J. The Lancet 2010, 375, 1830–1843.
  • [3.] Palmer, B. D.; Thompson, A. M.; Sutherland, H. S.; Thompson, A. M.; Blaser, A.; Anderson, R. F.; Shinde, S. S.; Franzblau, S. G.; Ma, Z. K.; Denny, A. W.; Palmer, B. D. J. Med. Chem. 2010, 53, 282–294.
  • [4.] Lu, Y.; Zheng, M. Q.; Wang, B.; Fu, L.; Zhao, W. J.; Li, P.; Xu, J.; Zhu, H.; Jin, H. X.; Yin, D. L.; Huang, H. H.; Upton, A. M.; Ma, Z. K. Antimicrob. Agents. Ch. 2011, 55, 5185–5193.
  • [5.] Garrelts J. C. DICP 1991, 25, 525–531.
  • [6.] Armand, V. D.; Maug, A. K. J.; Salim, M. A. H.; Das, P. K.; Sarker, M. R.; Daru, P.; Rieder, H. L. Am. J. Respir. Crit. Care Med. 2010, 182, 684–692.
  • [7.] Xu, H. B.; Jiang, R. H.; Xiao, H. P. Clin. Microbiolv. Infec. 2012, 18, 1104–1110.
  • [8.] Kasim, N. A.; Whitehouse, M.; Ramachandran, C.; Bermejo, M.; Lennernäs, H.; Hussain, A. S.; Junginger, H. E.; Stavchansky, S. A.; Midha, K. K. Mol. Pharmaceutics 2004, 1, 85–96.
  • [9.] O’Connor, R.; O’Sullivan, J. F.; O’Kennedy, R. Drug. Metab. Rev. 1995, 27, 591–614.
  • [10.] Kamal, A.; Hari, B. A.; Venkata, R. A.; Sinha, R.; Yadav, J. S.; Arora, S. K. Bioorg. Med. Chem. Lett. 2005, 15, 1923–1926.
  • [11.] Zhang, D.; Lu, Y.; Liu, K.; Liu, B.; Wang, J.; Zhang, G.; Zhang, H.; Liu, Y.; Wang, B.; Zheng, M.; Fu, L.; Hou, Y.; Gong, N.; Lv, Y.; Li, C.; Cooper, C. B.; Upton, A. M.; Yin, D.; Ma, Z.; Huang, H. J. Med. Chem. 2012, 55, 8409–8417.
  • [12.] Giovanna, P.; Martina, C.; Sara, C.; Mariangela, B. Eur. J. Med. Chem. 2014, 86, 335–351.
  • [13.] Diana, Q.; Gayathri, N.; Richard, P.; James, A.T. Int. J. Infect. Dis. 2017, 56, 212–220.
  • [14.] Li, D.; Sheng, L.; Liu, X.; Yang, S.; Liu, Z. H.; Li, Y. Chromatographia 2014, 77, 1697–1703.
  • [15.] Liu, K.; Cooper, C. B.; Huang, H. H.; Li, C.; Liu, B. N.; Liu, Y.; Ma, Z. K.; Wang, J. B.; Yin, D. L.; Zhang, D. F.; Zhang, G.; Zhang, H. (New York, NY, US). Riminophenazines with 2-(heteroaryl) amino substituents and their anti-microbial activity. US Patent 8,716,292, May 06, 2014.
  • [16.] Working Group for New TB Drugs Home Page. https://www.newtbdrugs.org/pipeline/clinical (accessed Jan 30, 2019).
  • [17.] ICH Quality Q2 (R1), Validation of Analytical Procedures: Text and Methodology. http://www.ich.org/products/guidelines/quality/article/quality-guidelines.html (accessed Dec. 2016).
  • [18.] ICH Quality Guideline Q3A (R2), Impurities in new drug substance. http://www.ich.org/products/guidelines/quality/article/quality-guidelines.html (accessed Dec. 2016).
  • [19.] ICH Quality Guideline Q1A (R2), Stability testing of new drug substances and products. http://www.ich.org/products/guidelines/quality/article/quality-guidelines.html (accessed Dec. 2016).
Uwagi
PL
Opracowanie rekordu ze środków MNiSW, umowa Nr 461252 w ramach programu "Społeczna odpowiedzialność nauki" - moduł: Popularyzacja nauki i promocja sportu (2020).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-673a556b-8f38-4d74-9cf8-a3f6555220af
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