TY - JOUR
T1 - Continuous-flow/stopped-flow system for determination of ascorbic acid using an enzymatic rotating bioreactor
AU - Messina, German A
AU - Torriero, Angel Alberto Jesus
AU - De Vito, Irma E
AU - Raba, Julio
PY - 2004
Y1 - 2004
N2 - The high sensitivity that can be attained using an enzymic system and mediated by hydroquinone, has been verified by online interfacing of a rotating bioreactor and continuous flow/stopped-flow/continuous-flow processing. Horseradish peroxidase, HRP, [EC 1.11.1.7], immobilized on a rotating disk, in presence of hydrogen peroxide catalyzes the oxidn. of hydroquinone to p-benzoquinone, whose electrochem. redn. back to hydroquinone is detected on glassy carbon electrode (GCE) surface at -0.15 V. Thus, when L-ascorbic acid is added to the soln., this acid is reduced chem. (p-benzoquinone to hydroquinone) and acts as mediator of HRP, decreasing the peak current obtained proportionally to the increase of its concn. The recovery of l-ascorbic acid from four samples ranged from 99.09 to 101.10 . This method could be used to det. l-ascorbic acid concn. in the range 12 nM-3.5 micro M (r = 0.998). The detn. of l-ascorbic acid was possible with a limit of detection of 6 nM in the processing of as many as 25 samples h-1. The method was successfully applied for the anal. of l-ascorbic acid in pharmaceutical formulations. [on SciFinder (R)]
AB - The high sensitivity that can be attained using an enzymic system and mediated by hydroquinone, has been verified by online interfacing of a rotating bioreactor and continuous flow/stopped-flow/continuous-flow processing. Horseradish peroxidase, HRP, [EC 1.11.1.7], immobilized on a rotating disk, in presence of hydrogen peroxide catalyzes the oxidn. of hydroquinone to p-benzoquinone, whose electrochem. redn. back to hydroquinone is detected on glassy carbon electrode (GCE) surface at -0.15 V. Thus, when L-ascorbic acid is added to the soln., this acid is reduced chem. (p-benzoquinone to hydroquinone) and acts as mediator of HRP, decreasing the peak current obtained proportionally to the increase of its concn. The recovery of l-ascorbic acid from four samples ranged from 99.09 to 101.10 . This method could be used to det. l-ascorbic acid concn. in the range 12 nM-3.5 micro M (r = 0.998). The detn. of l-ascorbic acid was possible with a limit of detection of 6 nM in the processing of as many as 25 samples h-1. The method was successfully applied for the anal. of l-ascorbic acid in pharmaceutical formulations. [on SciFinder (R)]
UR - http://www.sciencedirect.com.ezproxy.lib.monash.edu.au/science?_ob=MImg&_imagekey=B6THP-4CS4RPV-7-N&_cdi=5288&_user=542840&_pii=S0039914004002267&_ori
M3 - Article
VL - 64
SP - 1009
EP - 1017
JO - Talanta
JF - Talanta
SN - 0039-9140
IS - 4
ER -