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Current Pharmaceutical Analysis

Editor-in-Chief

ISSN (Print): 1573-4129
ISSN (Online): 1875-676X

Research Article

Development of a Fast and Highly Sensitive UPLC–MS/MS Technique for Simultaneous Estimation of Artemether and Dihydroartemisinin with its Application to Pharmacokinetic and Biodistribution Studies

Author(s): Mohammad Akhlaquer Rahman*

Volume 18, Issue 8, 2022

Published on: 18 August, 2022

Page: [815 - 823] Pages: 9

DOI: 10.2174/1573412918666220610111532

Price: $65

Abstract

Background: Artemether (ART) has been recognized as a potent and rapidly acting antimalarial agent metabolized by cytochrome P450 isoenzyme 3A4 into a more active form dihydroartemisinin (DHA). Hence, it was required to study the pharmacokinetics and biodistribution of ART and DHA for the optimization of dose.

Objective: The current research aims to develop an ultra-performance liquid chromatographytandem mass spectrometry (UPLC-MS/MS) technique with high sensitivity for quantification of ART and DHA simultaneous in the biological fluid.

Methods: An isocratic elution mode was applied for delivery of mobile phase (A) ammonium acetate (2mM) in UPLC grade water and (B) acetonitrile (20:80, v/v) comprising 0.1% v/v formic acid in each solvent system with the rate of flow maintained at 400 μL/min. For analyte detection and parent to daughter ion transition tracking, multiple reaction monitoring system was adopted. Artemisinin was selected as the internal standard (IS) for its structural similarity with the analytes.

Results: The linearity range of the calibration curve was between 0.5-200 ng/mL. The regression equation indicated r2 = 0.996 for ART and r2 = 0.997 for DHA. Precision and accuracy set in terms of relative error (RE%: ±15) and relative standard deviation (RSD%: ±15) expressed in percentage were within the acceptability range. The % recoveries were within the acceptable limit (90–110%). The detection and quantification limits of the analyte were 0.2 ng/mL and 0.5 ng/mL, respectively.

Conclusion: The method demonstrated a useful technique for quantification of ART and DHA for evaluating the pharmacokinetics and biodistribution studies in rat plasma following orally administered nanoformulation.

Keywords: UPLC-MS/MS, artemether, dihydroartemisinin, validation, matrix effect, stability.

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[1]
Carballeira, N.M. New advances in fatty acids as antimalarial, antimycobacterial and antifungal agents. Prog. Lipid Res., 2008, 47(1), 50-61.
[http://dx.doi.org/10.1016/j.plipres.2007.10.002] [PMID: 18023422]
[2]
Greenwood, B.; Mutabingwa, T. Malaria in 2002. Nature. 415, 670-672.
[3]
Djimdé, A.; Lefèvre, G.; Malar, J. Understanding the pharmacokinetics of Coartem. Malar. J., 2009, 8(S1)(Suppl. 1), S4.
[http://dx.doi.org/10.1186/1475-2875-8-S1-S4] [PMID: 19818171]
[4]
Navaratnam, V.; Mansor, S.M.; Chin, L.K.; Mordi, M.N.; Asokan, M.; Nair, N.K. Determination of artemether and dihydroartemisinin in blood plasma by high-performance liquid chromatography for application in clinical pharmacological studies. J. Chromatogr. B Biomed. Appl., 1995, 669(2), 289-294.
[http://dx.doi.org/10.1016/0378-4347(94)00109-I] [PMID: 7581905]
[5]
Sandrenan, N.; Sioufi, A.; Godbillon, J.; Netter, C.; Donker, M.; van Valkenburg, C. Determination of artemether and its metabolite, dihydroartemisinin, in plasma by high-performance liquid chromatography and electrochemical detection in the reductive mode. J. Chromatogr. B Biomed. Sci. Appl., 1997, 691(1), 145-153.
[http://dx.doi.org/10.1016/S0378-4347(96)00431-8] [PMID: 9140768]
[6]
Huang, Y.X.; Xie, G.H.; Zhou, Z.M.; Sun, X.M.; Wang, Y.L. Determination of artemether in plasma and whole blood using HPLC with flow-through polarographic detection. Biomed. Chromatogr., 1987, 2(2), 53-56.
[http://dx.doi.org/10.1002/bmc.1130020203] [PMID: 3506834]
[7]
Laxmi, M.; Ghosh, S.; Ravikumar, B.V.V. Analytical method development and validation of artemether in bulk drug by RP-HPLC method as per ICH guidelines. Int. J. Pharm. Pharm. Sci., 2015, 7(2), 498-501.
[8]
Ali, S.; Jafery, N.; Farhat, K.; Waheed, A. Mini Review - Analysis of Artemether and Dihydroartemisinin by high performance high liquid chromatography in biological fluids-issues and solutions. Pak. J. Pharm. Sci., 2017, 30(4), 1395-1401.
[PMID: 29039344]
[9]
Tayade, N.G.; Nagarsenker, M.S. Validated HPTLC method of analysis for artemether and its formulations. J. Pharm. Biomed. Anal., 2007, 43(3), 839-844.
[http://dx.doi.org/10.1016/j.jpba.2006.08.029] [PMID: 17045768]
[10]
Mohamed, S.S.; Khalid, S.A.; Ward, S.A.; Wan, T.S.M.; Tang, H.P.O.; Zheng, M.; Haynes, R.K.; Edwards, G. Simultaneous determination of artemether and its major metabolite dihydroartemisinin in plasma by gas chromatography-mass spectrometry-selected ion monitoring. J. Chromatogr. B Biomed. Sci. Appl., 1999, 731(2), 251-260.
[http://dx.doi.org/10.1016/S0378-4347(99)00232-7] [PMID: 10510778]
[11]
Blum, W.; Pfaar, U.; Kuhnol, J. Rapid characterization of artemether and its in-vitro metabolites on incubation with bovine hemoglobin, rat blood and dog blood by capillary gas chromatography-chemical ionization mass spectrometry. J. Chromatogr. A, 1998, 710(1-2), 101-113.
[http://dx.doi.org/10.1016/S0378-4347(98)00113-3]
[12]
Xing, J.; Yan, H.; Zhang, S.; Ren, G.; Gao, Y. A high-performance liquid chromatography/tandem mass spectrometry method for the determination of artemisinin in rat plasma. Rapid Commun. Mass Spectrom., 2006, 20(9), 1463-1468.
[http://dx.doi.org/10.1002/rcm.2467] [PMID: 16586460]
[13]
Ortelli, D.; Rudaz, S.; Cognard, E.; Veuthey, J.L. Analysis of dihydroartemisinin in plasma by liquid chromatography-mass spectrometry. Chromatographia, 2000, 52(7-8), 445-450.
[http://dx.doi.org/10.1007/BF02535717]
[14]
Naik, H.; Murry, D.J.; Kirsch, L.E.; Fleckenstein, L. Development and validation of a high-performance liquid chromatography-mass spectroscopy assay for determination of artesunate and dihydroartemisinin in human plasma. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 2005, 816(1-2), 233-242.
[http://dx.doi.org/10.1016/j.jchromb.2004.11.042] [PMID: 15664355]
[15]
Peys, E.; Vandenkerckhove, J.; Hemel, J.V.; Sas, B. Simultaneous determination of β-artemether and its metabolite dihydroartemisinin in human plasma and urine by a high-performance liquid chromatography-mass spectrometry assay using electrospray ionization. Chromatographia, 2005, 61(11-12), 637-641.
[http://dx.doi.org/10.1365/s10337-005-0556-1]
[16]
Shi, B.; Yu, Y.; Li, Z.; Zhang, L.; Zhong, Y.; Su, S.; Liang, S. Quantitative analysis of artemether and its metabolite dihydroartemisinin in human plasma by LC with tandem mass spectrometry. Chromatographia, 2006, 64(9-10), 523-530.
[http://dx.doi.org/10.1365/s10337-006-0064-y]
[17]
Souppart, C.; Gauducheau, N.; Sandrenan, N.; Richard, F. Development and validation of an HPLC-mass spectrometry assay for determination of artemether and its metabolite, dihydroartemisinin in human. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 2002, 774, 195-203.
[http://dx.doi.org/10.1016/S1570-0232(02)00207-6] [PMID: 12076689]
[18]
Huang, L.; Jayewardene, A.L.; Li, X.; Marzan, F.; Lizak, P.S.; Aweeka, F.T. Development and validation of a high-performance liquid chromatography/tandem mass spectrometry method for the determination of artemether and its active metabolite dihydroartemisinin in human plasma. J. Pharm. Biomed. Anal., 2009, 50(5), 959-965.
[http://dx.doi.org/10.1016/j.jpba.2009.06.051] [PMID: 19646837]

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