2008
DOI: 10.1016/j.jchromb.2008.06.015
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Determination of plasma aminothiols by high performance liquid chromatography after precolumn derivatization with N-(2-acridonyl)maleimide

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Cited by 37 publications
(29 citation statements)
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References 32 publications
(28 reference statements)
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“…4. MIAC [68], MMPB [69] and 3-MB [70] are new maleimide-type reagents for the derivatization of sulfhydryl-containing compounds. Because the reactivity to the SH group is based on the coupling with the maleimide structure, the derivatization conditions are almost comparable for each maleimide reagent.…”
Section: Maleimidesmentioning
confidence: 99%
“…4. MIAC [68], MMPB [69] and 3-MB [70] are new maleimide-type reagents for the derivatization of sulfhydryl-containing compounds. Because the reactivity to the SH group is based on the coupling with the maleimide structure, the derivatization conditions are almost comparable for each maleimide reagent.…”
Section: Maleimidesmentioning
confidence: 99%
“…The simultaneous determination of the plasma low molecularmass weight thiols concentrations, such as homocysteine (Hcy), cysteine (Cys), cysteinyl-glycine (Cys-Gly), and glutathione (GSH), is of potential interest for the understanding the dynamic relationship among them, as well as for clinical diagnosis and screening of various human disorders [1], including diabetes, cancer, neurodegenerative and cardiovascular diseases (CVD) [2,3]. These aminothiols ( Fig.…”
Section: Introductionmentioning
confidence: 99%
“…Different types of labeling reagents have been used, including monobromobimane [30,37], ortho-phthaldialdehyde [38,39], N-(1-pyrenil)maleimide [40,41], 9-acetoxy-2-(4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)phenyl)-3-oxo-3H-naphtho[2,1-b]pyran (ThioGlo 3) [42], N-(2-acridonyl)maleimide [1], ammonium 7-fluorobenzo-2-oxa-1,3-diazole-4-sulphonate (SBD-F) [20,[43][44][45], and 7-fluoro-2,1,3-benzoxadiazole-4-sulfonamide (ABD-F) [46,47]. The halogenobenzofurazans reagents (SBD-F and ABD-F) are the most often used, since they react selectively with thiol compounds (Fig.…”
Section: Introductionmentioning
confidence: 99%
“…Biogenic amines are usually determined by separation techniques like thin layer chromatography (TLC) [22][23][24], capillary electrophoresis (CE) [17,[25][26][27][28][29], gas chromatography (GC) [30][31][32][33][34] and High performance liquid chromatography (HPLC) [21,[35][36][37][38][39][40][41][42][43][44][45][46][47][48][49]. HPLC is the technique most extensively used due to its high resolution, sensitivity, great versatility, and simple sample treatment.…”
Section: Introductionmentioning
confidence: 99%
“…Biogenic amines do not exhibit satisfactory absorption at the visible or ultraviolet wavelengths, nor do they exhibit fluorescence. Therefore, many derivatization agents is usually applied for their analysis such as 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate (AQC) [40], N-(2-acridonyl)-maleimide (MIAC) [48], benzoyl chloride [38], bis [2-ethylhexyl] sulphosuccinate (AOT) [41], dabsyl chloride (Dbs-Cl) [21,36,37], dansyl chloride (Dns-Cl) [43,44,46], 3,5-dinitrobenzoyl chloride (DNBZ-Cl) [35], 9-fluorenylmethyl chloroformate (FMOC) [51], 9-fluorenylmethyloxy carbonyl chloride (Fmoc-Cl) [45], N-(9-fluorenylmethoxycarbonyloxy) succinimide (Fmoc-Osu) [39], N-hydroxysuccinimidyl fluorescein-o-acetate (SIFA) [49], 8-phenyl-(4-oxy-acetic acid N-hydroxysuccinimideester)-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene (TMPAB-OSu) [42], and o-phthalaldehyde (OPA) [47]. 4-Chloro-3,5-dinitrobenzotrifluoride (CNBF) is an important fine chemical, which has been known to react with primary or secondary amines in presence of base to produce stable N-substituted-2,6-dinitro-4-(trifluoromethyl)-benzamine derivatives which are satisfactory ultraviolet absorption [50][51][52][53][54].…”
Section: Introductionmentioning
confidence: 99%