TY - JOUR
T1 - Application of continual injection liquid-phase microextraction method coupled with liquid chromatography to the analysis of organophosphorus pesticids
AU - Raharjo, Yanuardi
AU - Sanagi, Mohd Marsin
AU - Ibrahim, Wan Aini Wan
AU - Naim, Ahmedy Abu
AU - Aboul-Enein, Hassan Y.
PY - 2009
Y1 - 2009
N2 - A liquid-phase microextraction coupled with LC method has been developed for the determination of organophosphorus pesticides (methidation, quinalphos and profenofos) in drinking water samples. In this method, a small amount (3 μL) of isooctane as the acceptor phase was introduced continually to fill-up the channel of a 1.5 cm polypropylene hollow fiber using a microsyringe while the hollow fiber was immersed in an aqueous donor solution. A portion of the acceptor phase (ca. 0.4 μL) was first introduced into the hollow fiber and additional amounts (ca. 0.2 μL) of the acceptor phase were introduced to replenish at intervals of 3 min until set end of extraction (40 min). After extraction, the acceptor phase was withdrawn and transferred into a 2 mL vial for a drying step prior to injection into a LC system. Parameters that affect the extraction efficiency were studied including the organic solvent, length of fiber, volume of acceptor and donor phase, stirring rate, extraction time, and effect of salting out. The proposed method provided good enrichment factors of up to 189.50, with RSD ranging from 0.10 to 0.29%, analyte recoveries of over 79.80% and good linearity ranging from 10.0 to 1.25 mg/L. The LOD ranged from 2.86 to 82.66 μg/ L. This method was applied successfully to the determination of organophosphorus pesticides in selected drinking water samples.
AB - A liquid-phase microextraction coupled with LC method has been developed for the determination of organophosphorus pesticides (methidation, quinalphos and profenofos) in drinking water samples. In this method, a small amount (3 μL) of isooctane as the acceptor phase was introduced continually to fill-up the channel of a 1.5 cm polypropylene hollow fiber using a microsyringe while the hollow fiber was immersed in an aqueous donor solution. A portion of the acceptor phase (ca. 0.4 μL) was first introduced into the hollow fiber and additional amounts (ca. 0.2 μL) of the acceptor phase were introduced to replenish at intervals of 3 min until set end of extraction (40 min). After extraction, the acceptor phase was withdrawn and transferred into a 2 mL vial for a drying step prior to injection into a LC system. Parameters that affect the extraction efficiency were studied including the organic solvent, length of fiber, volume of acceptor and donor phase, stirring rate, extraction time, and effect of salting out. The proposed method provided good enrichment factors of up to 189.50, with RSD ranging from 0.10 to 0.29%, analyte recoveries of over 79.80% and good linearity ranging from 10.0 to 1.25 mg/L. The LOD ranged from 2.86 to 82.66 μg/ L. This method was applied successfully to the determination of organophosphorus pesticides in selected drinking water samples.
KW - Liquid-phase microextraction
KW - Organophosphorus pesticides
KW - Sample preparation
KW - Water analysis
UR - http://www.scopus.com/inward/record.url?scp=64149116144&partnerID=8YFLogxK
U2 - 10.1002/jssc.200800566
DO - 10.1002/jssc.200800566
M3 - Article
C2 - 19165835
AN - SCOPUS:64149116144
SN - 1615-9306
VL - 32
SP - 623
EP - 629
JO - Journal of Separation Science
JF - Journal of Separation Science
IS - 4
ER -