TY - JOUR
T1 - Rapid determination of gallamine triethiodide (Flaxedil®) and pancuronium bromide (Pavulon®) in pharmaceutical and urine matrices by means of modified-carbon-paste ion-selective electrodes
AU - Salem, Alaa A.
AU - Barsoum, Barsoum N.
AU - El Said, Dalia M.
PY - 2005
Y1 - 2005
N2 - A new analytical method for the determination of gallamine triethiodide (Flaxedil®; 1) and pancuronium bromide (Pavulon®; 2), two muscle relaxants used in surgical operations and in pain relief, has been developed. Our approach relies on rapid, precise, and sensitive potentiometric sensors based on modified-carbon-paste ion-selective electrodes (CP-ISEs). Linear calibration graphs in the working ranges of ca. 4.5-892 and 7.3-733 μg/ ml (in H2O, pH 7.0, T = 25°) were established for 1 and 2, respectively; and Nernst slopes corresponding to three- or two-electrons transfers, respectively, were obtained. The method works best in a pH range of 7-9. Average relative errors of 2.12 and 2.14%, with average standard deviations of 1.98-2.47 and 2.64-3.45, respectively, were obtained for urine samples of 1 and 2. The corresponding relative errors for the pharmaceutical samples were 1.59 and 1.64%, with standard deviations of 0.54 -1.34 and 0.52 -1.67, respectively. Statistical Student and F tests were applied to the data, and satisfactory results were obtained.
AB - A new analytical method for the determination of gallamine triethiodide (Flaxedil®; 1) and pancuronium bromide (Pavulon®; 2), two muscle relaxants used in surgical operations and in pain relief, has been developed. Our approach relies on rapid, precise, and sensitive potentiometric sensors based on modified-carbon-paste ion-selective electrodes (CP-ISEs). Linear calibration graphs in the working ranges of ca. 4.5-892 and 7.3-733 μg/ ml (in H2O, pH 7.0, T = 25°) were established for 1 and 2, respectively; and Nernst slopes corresponding to three- or two-electrons transfers, respectively, were obtained. The method works best in a pH range of 7-9. Average relative errors of 2.12 and 2.14%, with average standard deviations of 1.98-2.47 and 2.64-3.45, respectively, were obtained for urine samples of 1 and 2. The corresponding relative errors for the pharmaceutical samples were 1.59 and 1.64%, with standard deviations of 0.54 -1.34 and 0.52 -1.67, respectively. Statistical Student and F tests were applied to the data, and satisfactory results were obtained.
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U2 - 10.1002/hlca.200590064
DO - 10.1002/hlca.200590064
M3 - Article
AN - SCOPUS:18744408120
SN - 0018-019X
VL - 88
SP - 861
EP - 872
JO - Helvetica Chimica Acta
JF - Helvetica Chimica Acta
IS - 4
ER -