M. Manduru et al., STABILITY OF CEFTAZIDIME SODIUM AND TEICOPLANIN SODIUM IN A PERITONEAL-DIALYSIS SOLUTION, American journal of health-system pharmacy, 53(22), 1996, pp. 2731-2734
The stability of ceftazidime sodium and teicoplanin sodium separately
and in combination in a peritoneal dialysis (PD) solution was studied.
PD solutions containing ceftazidime 100 mu g/mL (as the sodium salt),
teicoplanin 25 mu g/mL (as the sodium salt), or ceftazidime 100 mu g/
mL plus teicoplanin 24 mu g/mL mt were prepared in triplicate for each
of two conditions: condition A, storage at 25 degrees C (room tempera
ture) for 24 hours, then at 37 degrees C for eight hours; and conditio
n B, storage for seven days at 4 degrees C, followed by 16 hours at 25
degrees C and 8 hours at 37 degrees C. The dialysis solution used was
Dianeal PD-2 with 1.5% dextrose. Samples were removed at intervals an
d analyzed by stability-indicating high-performance liquid chromatogra
phy. Under condition A, ceftazidime sodium alone was stable for 24 hou
rs at 25 degrees C but only 2 hours when then heated to 37 degrees C.
Under condition B, ceftazidime sodium alone was stable throughout the
observation period. Teicoplanin sodium alone was stable throughout the
observation periods under both conditions. In combination, the drugs
were stable if initially refrigerated and then brought to room tempera
ture one week later, but were unstable when initially stored at 25 deg
rees C. No visual changes were noted, and pH did not vary substantiall
y. Ceftazidime 100 mu g/mL (as the sodium salt) and teicoplanin 25 mu
g/mL (as the sodium salt) combined in a PD solution were unstable when
first kept at 25 degrees C before storage at 37 degrees C. The drugs
in the combination remained stable when the solution was kept at 4 deg
rees C before storage at 37 degrees C.