A sensitive microbore HPLC method was developed for the simultaneous determ
ination of unbound cefoperazone in rat blood and brain using microdialysis.
Two microdialysis probes were inserted into the jugular vein/right atrium a
nd brain striatum of Sprague-Dawley rats, Cefoperazone (50 mg kg(-1), i.v.)
was then administered via the femoral vein. Blood and brain dialysates wer
e collected and eluted with a mobile phase containing methanol-100 mM monos
odium phosphoric acid (30:70, v/v, pH 5.5). The wavelength of the UV detect
or was set at 254 nm. The detection limit of cefoperazone was 20 ngmL(-1) I
socratic separation of cefoperazone was achieved within 10 min. The intra-
and inter-assay accuracy and precision of the analyses were less than or eq
ual to 10% in the range of 0.05-10 mu g mL(-1).
The ratio of the area under the concentration curve of cefoperazone in rat
brain and blood was estimated to be about 7.8%. It is concluded that cefope
razone is capable of penetrating the blood-brain barrier.