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Abstrakty
We developed and validated a sensitive, heart-cutting, two-dimensional liquid chromatography–tandem mass spectrometry (2D-LC‒MS/MS) method to determine the concentration of mometasone furoate in human plasma after nasal spray administration. Isotopically labeled mometasone furoate-13¹³C,d₆ was used as an internal standard (IS). Plasma samples were prepared using a solid-phase extraction (SPE) method. With this 2D-LC strategy, the analytes were trapped in the first dimension (1D) column, and only judiciously selected portions of the 1D effluent were transferred to the second dimension (2D) column for further separation to obtain high-resolution information. MS/MS quantification was performed in positive ionization mode via multiple-reaction monitoring (MRM). This analytical method was fully validated according to related regulatory guidance, and the results showed that the method is robust and sensitive enough for pharmacokinetic investigation of mometasone furoate with satisfactory linearity from 0.25 to 30 pg mL⁻¹. This method was successfully applied to a bioequivalence (BE) study of mometasone furoate aqueous nasal sprays in healthy volunteers.
Czasopismo
Rocznik
Tom
Strony
14--22
Opis fizyczny
Bibliogr. 15 poz., rys., tab., wykr.
Twórcy
autor
- Chengdu Finelyse Pharmaceutical Technology Co., Ltd., Chengdu, China
autor
- Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, Department of Clinical Pharmacy and Pharmacy Administration, West China School of Pharmacy, Sichuan University, Chengdu, China
autor
- Chengdu Finelyse Pharmaceutical Technology Co., Ltd., Chengdu, China
autor
- Chengdu Finelyse Pharmaceutical Technology Co., Ltd., Chengdu, China
autor
- Sichuan Purity Pharmaceutical Co., Ltd., Chengdu, China
autor
- Sichuan Purity Pharmaceutical Co., Ltd., Chengdu, China
autor
- Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, Department of Clinical Pharmacy and Pharmacy Administration, West China School of Pharmacy, Sichuan University, Chengdu, China
Bibliografia
- 1. Kasemsuk, N.; Ngaotepprutaram, P.; Kanjanawasee, D.; Suwanwech, T.; Durham, S. R.; Canonica, G. W.; Tantilipikorn, P. Local nasal immunotherapy for allergic rhinitis: a systematic review and meta-analysis. Int. Forum Allergy Rhinol 2022.
- 2. Nur Husna, S. M.; Tan, H. T.; Md Shukri, N.; Mohd Ashari, N. S.; Wong, K. K. Allergic rhinitis: a clinical and pathophysiological overview. Front. Med. (Lausanne) 2022, 9, 874114.
- 3. Schenkel, E. Features of mometasone furoate nasal spray and its utility in the management of allergic rhinitis. Expert Opin. Pharmacother. 2003, 4(9), 1579–91.
- 4. Byrro, R. M.; César, I. C.; de Santana e Silva Cardoso, F. F.; Mundim, I. M.; Teixeira Lde, S.; Bonfim, R. R.; Gomes, S. A.; Pianetti, G. A. A rapid and sensitive HPLC-APCI-MS/MS method determination of fluticasone in human plasma: application for a bioequivalency study in nasal spray formulations. J. Pharm. Biomed. Anal. 2012, 61, 38–43.
- 5. Zitt, M.; Kosoglou, T.; Hubbell, J. Mometasone furoate nasal spray: a review of safety and systemic effects. Drug Saf. 2007, 30(4), 317–26.
- 6. Fattinger, K.; Benowitz, N. L.; Jones, R. T.; Verotta, D. Nasal mucosal versus gastrointestinal absorption of nasally administered cocaine. Eur. J. Clin. Pharmacol. 2000, 56(4), 305–10.
- 7. Berkhout, M. C.; van Velzen, A. J.; Touw, D. J.; de Kok, B. M.; Fokkens, W. J.; Heijerman, H. G. Systemic absorption of nasally administered tobramycin and colistin in patients with cystic fibrosis. J. Antimicrob. Chemother. 2014, 69(11), 3112–5.
- 8. Brannan, M. D.; Herron, J. M.; Affrime, M. B. Safety and tolerability of once-daily mometasone furoate aqueous nasal spray in children. Clin. Ther. 1997, 19(6), 1330–9.
- 9. GorellaT.; Rajesh, PMN; Wagh, Dr. P. Development of a High Sensitivity, Sub-Picogram SPE LC-MS Method for Quantification of Mometasone from Human Plasma; Waters Corporation, 2018. https://www.waters.com/content/dam/waters/en/app-notes/2018/720006399/720006399-en.pdf.
- 10. Fernández, A. S.; Rodríguez-González, P.; Álvarez, L.; García, M.; Iglesias, H. G.; García Alonso, J. I. Multiple heart-cutting two dimensional liquid chromatography and isotope dilution tandem mass spectrometry for the absolute quantification of proteins in human serum. Anal. Chim. Acta 2021, 1184, 339022.
- 11. Pugajeva, I.; Ikkere, L. E.; Jansons, M.; Perkons, I.; Sukajeva, V.; Bartkevics, V. Two-dimensional liquid chromatography - mass spectrometry as an effective tool for assessing a wide range of pharmaceuticals and biomarkers in wastewater-based epidemiology studies. J. Pharm. Biomed. Anal. 2021, 205, 114295.
- 12. Carr, P. W.; Stoll, D. R. Two-dimensional Liquid Chromatography. Principles, Practical Implementation and Applications: Primer; Agilent Technologies, 2015. https://www.agilent.com/cs/library/primers/public/5991-2359EN.pdf.
- 13. Food and Drug Administration Bioanalytical Method Validation Guidance for Industry; Food and Drug Administration, Center for Drug Evaluation and Research, 2018. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/bioanalytical-method-validation-guidance-industry.
- 14. National Medical Products Administration Technical Guidelines for Clinical Pharmacokinetics of Chemical Drugs; National Medical Products Administration, Center for Drug Evaluation, 2005. https://www.cde.org.cn/zdyz/domesticinfopage?zdyzIdCODE54247ffceca57f2b47aa0f67a3fdc7c43.
- 15. Fast, D. M.; Kelley, M.; Viswanathan, C. T.; O’Shaughnessy, J.; King, S. P.; Chaudhary, A.; Weiner, R.; DeStefano, A. J.; Tang, D. Workshop report and follow-up–AAPS Workshop on current topics in GLP bioanalysis: assay reproducibility for incurred samples–implications of Crystal City recommendations. AAPS J 2009, 11(2), 238–41.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-b65dbcc5-b0e4-4a16-9389-d27c697dcde9