1998
DOI: 10.1016/s0378-4347(97)00667-1
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Simple high-performance liquid chromatographic method with electrochemical detection for the simultaneous determination of artesunate and dihydroartemisinin in biological fluids

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Cited by 61 publications
(30 citation statements)
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“…25 • C) using Reacti-Vap TM 18780 drying system (Pierce, Rockford, IL, USA). The dried extracts containing AS, DHA and QHS were reconstituted with 100 l of ethanol-water (1:1, v/v) and kept at 4 • C for at least 18 h before analysis to ensure that the tautomerization of ␣ and ␤ isomers of DHA reaches equilibrium [4,12,13,16]. Dried extracts of AQ, DeAQ and IB-DeAQ were reconstituted with 100 l of 0.01 M HCl.…”
Section: Solid Phase Extraction (Spe)mentioning
confidence: 99%
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“…25 • C) using Reacti-Vap TM 18780 drying system (Pierce, Rockford, IL, USA). The dried extracts containing AS, DHA and QHS were reconstituted with 100 l of ethanol-water (1:1, v/v) and kept at 4 • C for at least 18 h before analysis to ensure that the tautomerization of ␣ and ␤ isomers of DHA reaches equilibrium [4,12,13,16]. Dried extracts of AQ, DeAQ and IB-DeAQ were reconstituted with 100 l of 0.01 M HCl.…”
Section: Solid Phase Extraction (Spe)mentioning
confidence: 99%
“…HPLC with electrochemical detection (EC) remains the standard as it is affordable and sensitive enough for pharmacokinetic studies. However, the existing HPLC-EC methods for the quantification of AS [12,13] and AQ [14,15] ing AS, AQ and their metabolites simultaneously. Hence, this article reports a validated analytical method which allows simultaneous extraction of AS, AQ and their metabolites from human plasma, followed by the determination of these analytes using HPLC-EC systems.…”
Section: Introductionmentioning
confidence: 99%
“…Several publications on the determination of artemisinin and its derivatives using ECD have been published [12][13][14]. The limit of detection for these methods is around 5-20 ng/ml using 0.5-1 ml plasma.…”
Section: Introductionmentioning
confidence: 99%
“…Due to the absence of appropriate UV absorption of the DHA structure, high performance liquid chromatography (HPLC) with postcolumn alkaline or acidic derivatization for UV detection are popular techniques [7][8][9][10]. The presence of a peroxide bridge in the structure of DHA offers the advantage of using HPLC with reductive electrochemical detection [11][12][13]. HPLC with mass spectrometry (LC-MS) for the assay of DHA [14][15][16][17][18] was recently reported.…”
Section: Introductionmentioning
confidence: 99%