McKnight R P, Willis J E
Clin Chem. 1981 Jul;27(7):1256-61.
This enzymic radiochemical procedure for measuring tobramycin and amikacin in serum is based on the transfer of the 14C-acetyl group from [14C]acetyl-coenzyme A to the 6' nitrogen atom of the drug by the enzyme kanamycin 6'-acetyltransferase (EC 2.3.1.55). The transfer, stoichiometric and quantitative, is complete after 10-min incubation at 37 degrees C. The labeled acetylaminoglycoside is adsorbed onto phosphocellulose paper discs, which are washed to removed any unreacted [14C]acetyl-coenzyme A. The radioactivity is then eluted into liquid scintillation counting vials and counted for 1 min each. The assay detects as little as 2 ng of either drug and the standard curve is linear into the toxic range of concentrations. Most of the commonly administered aminoglycosides act as substrates in the assay, except for the C1 component of gentamicin C complex. Neither hemolysis, lipemia, nor icterus interfere with the assay. Results compare favorably with those determined by radioimmunoassay and a microbiological method.
这种用于测定血清中妥布霉素和阿米卡星的酶促放射化学方法基于卡那霉素6'-乙酰基转移酶(EC 2.3.1.55)将[14C]乙酰辅酶A中的14C-乙酰基转移至药物的6'氮原子上。这种转移是化学计量且定量的,在37℃孵育10分钟后完成。标记的乙酰氨基糖苷吸附在磷酸纤维素纸盘上,经洗涤以去除任何未反应的[14C]乙酰辅酶A。然后将放射性洗脱到液体闪烁计数瓶中,每个计数1分钟。该测定法可检测低至2 ng的任何一种药物,并且标准曲线在浓度的毒性范围内呈线性。除庆大霉素C复合物的C1组分外,大多数常用的氨基糖苷类药物在该测定中可作为底物。溶血、脂血和黄疸均不干扰该测定。结果与放射免疫测定法和微生物学方法所测定的结果相比具有优势。