Optimization of HPLC-MS/MS method for determination of antimalarial adulterants in herbal products

被引:3
作者
Mwankuna, Christopher J. [1 ]
Kiros, Feven [2 ]
Mariki, Eliapenda E. [1 ]
Mabiki, Faith P. [1 ]
Malebo, Hamisi M. [3 ]
Mdegela, Robinson H. [4 ]
Styrishave, Bjarne [2 ]
机构
[1] Sokoine Univ Agr, Coll Nat & Appl Sci, Dept Chem & Phys, POB 3038, Morogoro, Tanzania
[2] Univ Copenhagen, Fac Hlth & Med Sci, Dept Pharm, Toxicol Lab, Denmark Univ Pk 2, DK-2100 Copenhagen, Denmark
[3] UNESCO Natl Commiss United Republ Tanzania, 7 Magogoni St,POB 20384, Dar Es Salaam, Tanzania
[4] Sokoine Univ Agr, Coll Vet Med & Biomed Sci, Dept Vet Med & Publ Hlth, POB 3015, Morogoro, Tanzania
关键词
Conventional drugs; Herbal products; Herbal drugs; Adulteration; LIQUID-CHROMATOGRAPHIC METHOD; ORBITRAP MASS-SPECTROMETRY; DIETARY-SUPPLEMENTS; ILLEGAL ADULTERANTS; HUMAN PLASMA; MEDICINES; DRUGS; IDENTIFICATION; CONFIRMATION; QUANTITATION;
D O I
10.1007/s44211-022-00255-8
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The use of herbal products is booming all over the world because of being believed as safer than conventional drugs and free of side effects. However, there are untrustworthy manufacturers who adulterate herbal products by adding conventional drugs which might eventually lead to microbial resistance and herb-to-drug interactions. There is a need to develop methods for detecting adulterants in herbal products. A high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method for simultaneous identification and determination of conventional antimalarials (chloroquine, quinine, sulfadoxine, pyrimethamine, mefloquine, lumefantrine, amodiaquine, artemisinin, dihydroartemisinin, artesunate and artemether) in herbal products was developed. Stable isotopically labelled compounds (artemether-d(3), quindine-d(3), and sulfadoxine-d(3)) were used as internal standards (ISs) for quantitative analysis. Extraction of analytes was performed using methanol: water: formic acid (90:10:0.1, v/v) and chromatographic separation was done in a gradient mode using mobile phase A: Ultrapure water containing 0.1% formic acid and 1 mM ammonium formate and mobile phase B: Acetonitrile/methanol (50:50) containing 0.1% formic acid and 1 mM ammonium formate. The calibration curves were linear (r(2) >= 0.991) over the range of 0.001-0.3 mu g mL(-1) for all compounds. The limit of detection (LOD) ranged from 0.002 to 0.02 mu g mL(-1) while the limit of quantification (LOQ) ranged from 0.006 to 0.08 mu g mL(-1). Accuracy, expressed as recovery of spiked herbal products ranged from 52 to 128%. The precision, expressed as percent relative standard deviation (%RSD) at two concentration levels, ranged from 1.0 to 13.8%. The matrix effect expressed as the matrix factor (MF) ranged from 0.77 to 0.97. The developed method was used to identify and quantify conventional antimalarials in herbal product samples from Tanzania. Ten out of 50 herbal products were found to contain amodiaquine, sulfadoxine, pyrimethamine, mefloquine, dihydroartemisinin, artemether and lumefantrine. The developed method is considered a valuable tool for getting a better understanding of the adulteration of conventional antimalarials in herbal products.
引用
收藏
页码:407 / 416
页数:10
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