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a author for correspondence: fax (409) 772-9231, e-mail aamohamm@utmb.edu
Measurement of 24-h urinary free cortisol (UFC) provides the most sensitive and specific diagnostic information for adrenal malfunctions, especially for Cushing syndrome (1)(2). The existing methodologies include immunoassays (3)(4)(5) and HPLC, with and without solid-phase extraction and derivatization (6)(7). Immunoassays for UFC are precise but overestimate the concentration because of antibodies' cross-reactivity with various metabolites and with synthetic corticoids having a chemical configuration similar to that of cortisol (8). HPLCs, on the other hand, although very specific, require large volumes of mobile phase, as well as sample pretreatment. Capillary electrophoresis (CE) overcomes many of these problems through the use of an open-tubular format, thus avoiding interaction of analytes with the solid-phase resin. Earlier, we reported the feasibility of rapid UFC detection in solid-phase extraction CE with a neutral capillary (9). Using a neutral capillary, we could demonstrate a detection limit of 552 nmol/L for UFC in human urine.
However, neutral capillaries have several disadvantages: Not only are
they expensive, they also are unstable and lack a uniform capillary
coating. This makes the neutral capillary unattractive for the
development of a routine clinical laboratory assay. In the present
study, we developed a solid-phase microparticle extraction (SPME)
coupled micellar electrokinetic capillary chromatography (MEKC) with
Footnotes
References
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