Cortina Villar J C, Costa García A, Tuñón Blanco P
Department of Physical and Analytical Chemistry, University of Oviedo, Principality of Asturias, Spain.
J Pharm Biomed Anal. 1992 Apr;10(4):263-7. doi: 10.1016/0731-7085(92)80038-o.
Mitoxantrone was determined by flow injection analysis using a flow cell modified in the laboratory and fitted with carbon paste as an amperometric detector. The sample solution (100 microliters, 5 x 10(-8)-1 x 10(-5) M) was injected into the carrier stream of 0.1 M perchloric acid (pH 1.12). Mitoxantrone was determined by oxidation at the carbon paste electrode (CPE) at +0.90 V. A 60-cm delay coil (0.5 mm i.d.) was incorporated just before the detector (a canal thin layer) and a flow rate of about 4 ml min-1 was used. The system was successfully applied to the determination of mitoxantrone in a pharmaceutical preparation; the method was fast and reproducible.