Simultaneous Determination of Epinephrine, Noradrenaline and Dopamine in Human Serum Samples by High Performance Liquid Chromatography with Chemiluminescence Detection
Abstract:A simple, rapid and accurate high performance liquid chromatographic (HPLC) technique coupled with chemiluminescence (CL) detection was developed for the simultaneous determination of epinephrine (E), noradrenaline (NA) and dopamine (DA). It was based on the analyte enhancement effect on the CL reaction between luminol and potassium ferricyanide. The effects of various parameters, such as potassium ferricyanide concentration, luminol concentration, pH value and component of the mobile phase on chromatographic … Show more
“…[16][17][18][19] The advantages of CL technique include superb sensitivity, wide dynamic range, simple instrumentation and easy automation. Some of the reported CL methods utilized the enhancing effect of catetcolamines on the CL emission of luminol-periodate, [8,[12][13][14]19] while others took advantage of their inhibiting effect on the CL emission from the oxidation of luminol with hypochlorite, [7] ferricyanide, [9,10,17,18] chlorate, [11] iodine, [15] or hydrogen peroxide. [16] The detection limits of catecholamines for these methods varied from subnmol/L [12,13] to μmol/L.…”
Section: Introductionmentioning
confidence: 99%
“…However, some of these methods lack sensitivity and selectivity or require derivation steps or sophisticated instruments. Another attractive method for sensitive detection of catechoamines is based on chemiluminescence (CL), which is usually coupled with flow injection (FI), [7][8][9][10][11][12][13] high-performance liquid chromatography (HPLC) [14,15] or capillary electrophoresis (CE). [16][17][18][19] The advantages of CL technique include superb sensitivity, wide dynamic range, simple instrumentation and easy automation.…”
Chemiluminescence (CL) from the oxidation of luminol with potassium periodate in strong alkaline solutions was greatly enhanced by the combined effect of gallic acid, acetaldehyde and Mn(2+). The CL spectra exhibited only one emission band at 425 nm, indicating 3-aminophthalate as the emitting species. Various scavengers for superoxide anion, hydroxyl radical and singlet oxygen quenched the CL emission very efficiently (74-100%), suggesting the possible involvement of these reactive oxygen species (ROS) in the CL reactions. It is postulated that oxidation of gallic acid and acetaldehyde by periodate catalyzed by Mn(2+) generates these ROS, which then react with luminol to enhance the CL emission. We also found that the enhanced CL emission was strongly inhibited by catecholamines, probably because of their effective scavenging of ROS. Based on this observation, a simple, rapid and sensitive new CL method was developed for the determination of catecholamines. The detection limits (3sigma) for dopamine, l-dopa, norepinephrine and epinephrine were 0.63, 1.37, 0.56 and 14.3 nmol/L, respectively. The linear range was 1-10 nmol/L; relative standard deviations were 0.71-1.34% for 0.1 micromol/mL catecholamines. This CL method was applied to the determination of catecholamines in pharmaceutical injections with satisfactory results.
“…[16][17][18][19] The advantages of CL technique include superb sensitivity, wide dynamic range, simple instrumentation and easy automation. Some of the reported CL methods utilized the enhancing effect of catetcolamines on the CL emission of luminol-periodate, [8,[12][13][14]19] while others took advantage of their inhibiting effect on the CL emission from the oxidation of luminol with hypochlorite, [7] ferricyanide, [9,10,17,18] chlorate, [11] iodine, [15] or hydrogen peroxide. [16] The detection limits of catecholamines for these methods varied from subnmol/L [12,13] to μmol/L.…”
Section: Introductionmentioning
confidence: 99%
“…However, some of these methods lack sensitivity and selectivity or require derivation steps or sophisticated instruments. Another attractive method for sensitive detection of catechoamines is based on chemiluminescence (CL), which is usually coupled with flow injection (FI), [7][8][9][10][11][12][13] high-performance liquid chromatography (HPLC) [14,15] or capillary electrophoresis (CE). [16][17][18][19] The advantages of CL technique include superb sensitivity, wide dynamic range, simple instrumentation and easy automation.…”
Chemiluminescence (CL) from the oxidation of luminol with potassium periodate in strong alkaline solutions was greatly enhanced by the combined effect of gallic acid, acetaldehyde and Mn(2+). The CL spectra exhibited only one emission band at 425 nm, indicating 3-aminophthalate as the emitting species. Various scavengers for superoxide anion, hydroxyl radical and singlet oxygen quenched the CL emission very efficiently (74-100%), suggesting the possible involvement of these reactive oxygen species (ROS) in the CL reactions. It is postulated that oxidation of gallic acid and acetaldehyde by periodate catalyzed by Mn(2+) generates these ROS, which then react with luminol to enhance the CL emission. We also found that the enhanced CL emission was strongly inhibited by catecholamines, probably because of their effective scavenging of ROS. Based on this observation, a simple, rapid and sensitive new CL method was developed for the determination of catecholamines. The detection limits (3sigma) for dopamine, l-dopa, norepinephrine and epinephrine were 0.63, 1.37, 0.56 and 14.3 nmol/L, respectively. The linear range was 1-10 nmol/L; relative standard deviations were 0.71-1.34% for 0.1 micromol/mL catecholamines. This CL method was applied to the determination of catecholamines in pharmaceutical injections with satisfactory results.
“…However, some of these methods lack sensitivity and selectivity or require derivation steps or sophisticated instruments. Another attractive method for sensitive detection of CAs is based on chemiluminescence (CL), which is usually coupled with flow injection (FI), [12][13][14][15][16][17][18][19] high-performance liquid chromatography (HPLC) 20,21 or capillary electrophoresis (CE). [22][23][24][25] The advantages of the CL technique include superb sensitivity, wide dynamic range, simple instrumentation and easy automation.…”
A novel, simple, cheap, and high sensitivity batch chemiluminescent method for the determination of catecholamine drugs, epinephrine (E), dopamine (DA) and methyldopa (MD) at microgram levels in pharmaceutical formulations is described. The method is based on a chemiluminescence (CL) system arising from the reaction of bis(2,4,6-trichlorophenyl) oxalate (TCPO) with H2O2 in the presence of a novel fluorescer, furandicarboxylate, and is proposed as a new analytical method for the determination of catecholamines. The method is based on the inhibition of CL emission by DA and its enhancement by E and MD. Under optimal conditions, good linear ranges were obtained, 0.5 -12.7, 0.06 -1.83 and 0.069 -3.52 μg/mL with detection limits of 0.30, 0.03 and 0.04 μg/mL (S/N = 3) for DA, E and MD, respectively. Moreover, a pooled-intermediate model was used to determine the kinetic parameters of CL with and without catecholamines and a possible CL mechanism was discussed.
“…A number of methods were reported for the determination of catecholamines by spectrophotometry (Salem, 1987), capillary electrophoresis (Peterson et al, 2002) and chromatography equipped with an electrochemical detection (Patel and Chau, 2008), chemiluminescence (Chen et al, 2007) and fluorescence (Fotopoulou and Ioannou, 2002). Among them high-performance liquid chromatography (HPLC) coupled to electrochemical detection offered advantages of high resolution with low detection limits (Holmes et al, 1994).…”
a b s t r a c tOxidized Single-Wall Carbon Nanohorns (o-SWCNHs) were used, for the first time, to assemble chemically modified Screen Printed Electrodes (SPEs) selective towards the electrochemical detection of Epinephrine (Ep), in the presence of Serotonine-5-HT (S-5HT), Dopamine (DA), Nor-Epineprhine (NorEp), Ascorbic Acid (AA), Acetaminophen (Ac) and Uric Acid (UA). The Ep neurotransmitter was detected by using Differential Pulse Voltammetry (DPV), in a wide linear range of concentration (2-2500 μM) with high sensitivity (55.77 A M À 1 cm À 2 ), very good reproducibility (RSD% ranging from 2 to 10 for different SPEs), short response time for each measurement (only 2 s) and low detection of limit (LOD ¼0.1 μM). o-SWCNHs resulted in higher analytical performances when compared with other nanomaterials used in literature for electrochemical sensors assembly.
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