CE-LIF method for the separation of anthracyclines: Application to protein binding analysis in plasma using ultrafiltration

✍ Scribed by Gillian Whitaker; Amy Lillquist; Stephanie A. Pasas; Robert O'Connor; Fiona Regan; Craig E. Lunte; Malcolm R. Smyth

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 399 KB
• Volume: 31
• Category: Article
• ISSN: 1615-9306
• DOI: 10.1002/jssc.200700629

✦ Synopsis

Abstract

Anthracyclines are chemotherapeutic drugs that are widely used in the treatment of cancers such as lung and ovarian cancers. The simultaneous determination of the anthracyclines, daunorubicin, doxorubicin and epirubicin, was achieved using CE coupled to LIF, with an excitation and emission wavelength of 488 and 560 nm, respectively. Using a borate buffer (105 mM, pH 9.0) and 30% MeOH, a stable and reproducible separation of the three anthracyclines was obtained. The method developed was shown to be capable of monitoring the therapeutic concentrations (50–50 000 ng/mL) of anthracyclines. LODs of 10 ng/mL, calculated at an S/N = 3, were achieved. Using the CE method developed, the in vitro protein binding to plasma was measured by ultrafiltration, and from this investigation the estimated protein binding was determined to be in the range of 77–94%.