1992
DOI: 10.1016/0378-4347(92)80044-q
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Simultaneous determination of chloroquine and its three metabolites in human plasma, whole blood and urine by ion-pair high-performance liquid chromatography

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Cited by 19 publications
(5 citation statements)
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“…Linearity is likewise excellent across the relevant range of therapeutic concentrations. In comparison to previously published assays for CQ and other AQs [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28]30], the advantages of this method include its ability to measure the concentrations of AQ-13, CQ and their metabolites simultaneously (in the same blood specimen), solid-phase extraction using commercially available extraction cartridges, the choice of an appropriate IS, and the 60% borate plus 40% acetonitrile mobile phase. The IS used for these studies (AQ-18) was chosen because of its structural similarity to AQ-13 and CQ, its elution time, and its lack of antiparasite activity.…”
Section: Discussionmentioning
confidence: 98%
See 1 more Smart Citation
“…Linearity is likewise excellent across the relevant range of therapeutic concentrations. In comparison to previously published assays for CQ and other AQs [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28]30], the advantages of this method include its ability to measure the concentrations of AQ-13, CQ and their metabolites simultaneously (in the same blood specimen), solid-phase extraction using commercially available extraction cartridges, the choice of an appropriate IS, and the 60% borate plus 40% acetonitrile mobile phase. The IS used for these studies (AQ-18) was chosen because of its structural similarity to AQ-13 and CQ, its elution time, and its lack of antiparasite activity.…”
Section: Discussionmentioning
confidence: 98%
“…Mobile phases used have included methanol-phosphate buffer-perchloric acid (0.1 M, pH 3; 250:747.5:2.5, v/v/v) [12], acetonitrile-phosphate buffer (10 mM, pH 3.5; 69:31, v/v) [13], acetonitrile-phosphate buffer (pH 6.5; 20:80, v/v) [14], and methanol-water (70:30, v/v) with 0.1% triethylamine (0.1%, v/v) [15]. These HPLC methods have been used to estimate the concentrations of CQ and other AQs in plasma [16][17][18][19][20][21][22], serum [23], blood cells [16][17][18]24], human biological fluids [18,25], urine [18,19,21,24,[26][27][28], saliva [21] and whole blood [23,27].…”
Section: Introductionmentioning
confidence: 99%
“…Several HPLC methods have been published for the measurement of chloroquine and its metabolites [3,[14][15][16][17], proguanil and cycloguanil [6,[18][19][20] or all these compounds in a single run of biological samples [21,22] or pharmaceutical preparations [23]. The aim of this study was to develop an HPLC procedure for the combined analysis of chloroquine, proguanil (and their main metabolites) in a small volume (80 L) of blood dried on a filter paper.…”
Section: Introductionmentioning
confidence: 99%
“…Esta investigación muestra evidencias del efecto clastogénico de la CQ en linfocitos humanos de sangre periférica in vitro expuestos a diferentes concentraciones de CQ. Estos daños genéticos pueden presentarse en los diferentes tejidos y fluidos de pacientes tratados con CQ, desde concentraciones que fluctúan entre 0,05 µg/ml hasta 334,4 µg/ml (15,16) .…”
Section: Discussionunclassified