1988 Volume 36 Issue 7 Pages 467-472
We evaluated the gentamicin enzyme immunoassay kit (EMIT Qst GM kit) for the determination of sisomicin serum concentrations. We prepared sisomicin calibrators (0, 0.5, 1.0, 2.0, 4.0, 8.0μg/ml) instead of gentamicin calibrators and then obtained a standard curve by use of a reagent for the EMIT Qst GM assay. This standard curve was a good sigmoid curve.
The following results were obtained.
1. The within-run coefficient of variation was less than 10.4%.
2. The between-run coefficient of variation was less than 9.8%.
3. Analytical recoveries of sisomicin from serum spiked with varying concentrations of sisomicin averaged from 96.0-108.0%.
4. The relationship between the modified EMIT Qst method (Y) and high-performance liquid chromatography (X1) or bioassay (X2) was studied.
Y=0.751 X1+0.590, r=0.991; Y=0.958X2+0.268, r=0.997
We confirmed that the modified EMIT Qst method is a very reliable and useful means of monitoring for clinical sisomicin levels.