1997
DOI: 10.1016/s0731-7085(96)01915-2
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Determination of captopril in human serum by high performance liquid chromatography using solid-phase extraction

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Cited by 46 publications
(26 citation statements)
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“…[1][2][3] Different analytical methods have been applied to the determination of the remaining drugs analyzed by us, and also by HPLC techniques. Many of the HPLC analytical methods exist for the assay of ENA, [4][5][6][7] SOT, [8][9][10][11][12][13][14][15] CAP, [16][17][18][19][20][21][22][23][24] MET, [25][26][27][28][29][30][31] 62,63 and SPI [64][65][66][67][68] in different biological fluids and tissues. HPLC methods were applied to the simultaneous quantification of selected β-blockers (also: SOT, MET and PRO) in human fluids (plasma, serum, urine).…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3] Different analytical methods have been applied to the determination of the remaining drugs analyzed by us, and also by HPLC techniques. Many of the HPLC analytical methods exist for the assay of ENA, [4][5][6][7] SOT, [8][9][10][11][12][13][14][15] CAP, [16][17][18][19][20][21][22][23][24] MET, [25][26][27][28][29][30][31] 62,63 and SPI [64][65][66][67][68] in different biological fluids and tissues. HPLC methods were applied to the simultaneous quantification of selected β-blockers (also: SOT, MET and PRO) in human fluids (plasma, serum, urine).…”
Section: Introductionmentioning
confidence: 99%
“…5 Therefore, determination of this compound is very important. Various instrumental methods have been developed for the determination of captopril including high-performance liquid chromatography, [6][7][8][9][10] Highly Selective and Sensitive Voltammetric Sensor for Captopril Determination [30][31][32][33][34] The comparisons of the proposed method for captopril determination with the other electrochemical published papers are given in Table 1. Carbon nanotubes (CNTs) continue to receive considerable attention in electrochemistry.…”
Section: Introductionmentioning
confidence: 99%
“…In our case the UV active agent was p-bromophenacyl bromide (p-BPB), which prevents captopril binding to plasma constituents and is also a chemical stabilizer. [5][6][7][8] The resulted product can be determined at a more specific wavelength (λ = 260 nm). The possible reaction between the derivatizing agent and captopril involves the -SH group of the latter and the carbocation of the alkylhalide, 9 resulting a derivative with greater molecular mass and less polarity ( Figure 1).…”
Section: Introductionmentioning
confidence: 99%