TY - JOUR
T1 - Development of a powdered activated carbon in bar adsorptive micro-extraction for the analysis of morphine and codeine in human urine
AU - Gonçalves, A. F.P.
AU - Neng, N. R.
AU - Mestre, A. S.
AU - Carvalho, A. P.
AU - Nogueira, J. M.F.
PY - 2012/8
Y1 - 2012/8
N2 - In the present work, bar adsorptive microextraction using an activated carbon (AC) adsorbent phase followed by liquid desorption and high-performance liquid chromatography with diode array detection was developed to monitor morphine (MOR) and codeine (COD) in human urine. Under optimized experimental conditions, assays performed in aqueous media spiked at the 30.0 μg/L level yielded recoveries of 41.3±1.3% for MOR and 38.4±1.7% for COD, respectively. The textural and surface chemistry properties of the AC phase were also correlated with the analytical data for a better understanding of the overall enrichment process. The analytical performance showed good precision (relative standard deviation <8.0%), suitable detection limits (0.90 and 0.06 μg/L for MOR and COD, respectively) and convenient linear dynamic ranges (r2 >0.991) from 10.0 to 330.0 μg/L. By using the standard addition methodology, the applications of this analytical approach to water and urine matrices allowed remarkable performance to monitor MOR and COD at the trace level. This new confirmatory method proved to be a suitable alternative to other sorptive micro-extraction methodologies in monitoring trace levels of opiate-related compounds, because it was easy to implement, reliable, sensitive and required a low sample volume.
AB - In the present work, bar adsorptive microextraction using an activated carbon (AC) adsorbent phase followed by liquid desorption and high-performance liquid chromatography with diode array detection was developed to monitor morphine (MOR) and codeine (COD) in human urine. Under optimized experimental conditions, assays performed in aqueous media spiked at the 30.0 μg/L level yielded recoveries of 41.3±1.3% for MOR and 38.4±1.7% for COD, respectively. The textural and surface chemistry properties of the AC phase were also correlated with the analytical data for a better understanding of the overall enrichment process. The analytical performance showed good precision (relative standard deviation <8.0%), suitable detection limits (0.90 and 0.06 μg/L for MOR and COD, respectively) and convenient linear dynamic ranges (r2 >0.991) from 10.0 to 330.0 μg/L. By using the standard addition methodology, the applications of this analytical approach to water and urine matrices allowed remarkable performance to monitor MOR and COD at the trace level. This new confirmatory method proved to be a suitable alternative to other sorptive micro-extraction methodologies in monitoring trace levels of opiate-related compounds, because it was easy to implement, reliable, sensitive and required a low sample volume.
UR - http://www.scopus.com/inward/record.url?scp=84866298008&partnerID=8YFLogxK
U2 - 10.1093/chromsci/bms051
DO - 10.1093/chromsci/bms051
M3 - Article
C2 - 22562817
AN - SCOPUS:84866298008
SN - 0021-9665
VL - 50
SP - 574
EP - 581
JO - Journal of Chromatographic Science
JF - Journal of Chromatographic Science
IS - 7
ER -