AI Article Synopsis

  • The study enhanced an on-line cloud point extraction (CPE) technique integrated with flow injection analysis (FIA), improving the detection of analytes by performing both sample preconcentration and chemiluminescence detection directly inside the collection column.
  • The new method utilized a reaction between nitrite and hydrogen peroxide for more efficient CL detection in aqueous samples, resulting in a significant increase in CL intensity, with an enhancement factor of about 1000.
  • Under optimal conditions, the method enabled precise detection of bilirubin, showing a linear calibration curve and a limit of detection of 1.8 microg L(-1), while also demonstrating strong agreement with results from established clinical methods.

Article Abstract

The on-line incorporation of cloud point extraction (CPE) to flow injection analysis (FIA) was previously based on the use of a cotton-packed column to entrap the analyte-containing surfactant aggregates after salt-induced CPE, and then the preconcentrated analyte was eluted into a separate detection cell for subsequent chemiluminescence (CL) detection (via the peroxyoxalate CL reaction). In the work, the on-line CPE/FIA technique was improved by the following: (1) sample preconcentration and CL detection were both carried out directly inside the collection column, thus avoiding the decrease in detection sensitivity due to sample dispersion and dilution, and (2) CL detection was performed through the reaction between nitrite and hydrogen peroxide, which is compatible with aqueous samples and should allow for chemical excitation to occur more efficiently inside the collection column. In addition to more effective sample preconcentration, the CL detection of the entrapped analytes directly inside the collection column, i.e., a unique heterogeneous microenvironment in which analyte-containing surfactant aggregates were embedded within the densely packed filtering material, may also contribute to the overall increase in CL intensity (e.g., a CL enhancement factor of ca. 1000). Under optimum experimental conditions, the calibration curve was found to be linear for the CL detection of bilirubin (5 to 120 microg L(-1)), the limit of detection (S/N = 3) was 1.8 microg L(-1), and the R.S.D. was ca. 2.6% (n = 30) for 20 microg L(-1) bilirubin. Good agreements were obtained for the determination of total bilirubin in certified reference human serum samples between the present approach and an established clinical method.

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http://dx.doi.org/10.1016/j.aca.2007.03.028DOI Listing

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