4.7 Article

Polyoxometalate incorporated polymer monolith microextraction for highly selective extraction of antidepressants in undiluted urine

Journal

TALANTA
Volume 170, Issue -, Pages 252-259

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2017.04.020

Keywords

Polyoxometalates; Strong cation-exchange interaction; Polymer monolith microextraction; Urine sample; Antidepressants

Funding

  1. National Basic Research Program of China (973 Program) [2013CB910702]
  2. National Natural Science Foundation of China [21475098, 31670373]

Ask authors/readers for more resources

In this work, a polyoxometalate (POM) incorporated polymer monolith microextraction (PMME) was successfully proposed and employed in the selective extraction of basic antidepressants in undiluted urine sample. This hybrid monolith exhibited strong cation-exchange interaction (SCX) with positively charged antidepressants when pH was 3.0, because of the multiple ionizable moieties on polyanionic POM. As such, antidepressants in complex sample matrices were efficiently extracted by the monolith, and the matrix effect was significantly reduced. In addition, due to the high amount of anionic POM, the monolith exhibited remarkable extraction capacities for target antidepressants ranging from 4.7 to 5.8 mg/g. Further, the POM incorporated PMME was coupled with high-performance liquid chromatography-ultraviolet (HPLC-UV). Thus, antidepressants in undiluted urine sample was efficiently extracted under optimized extraction conditions online. The limits of detection (LODs) for the target antidepressants ranged from 0.7 to 1.4 ng/mL, and the linear range was 5-1000 ng/mL with determination coefficients (R-2) higher than 0.9960. The recoveries ranged from 86.8% to 104.0% with relative standard deviations (RSDs) of 0.4-10.1%. The proposed procedure was successfully applied to determine antidepressant in human urine. Taken together, the developed method presented a new strategy for the analysis of basic drugs in undiluted urine sample, which could be used for monitoring medicines in pharmacokinetic analysis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available