Nitsche V, Mascher H
J Pharm Sci. 1984 Nov;73(11):1556-8. doi: 10.1002/jps.2600731117.
A high-performance liquid chromatographic (HPLC) method for the determination of codeine in human plasma is described. The specific, precise, and sensitive method can be used to determine plasma codeine levels after administration of therapeutic doses of codeine. After purification on a C18 extraction column, codeine in the form of hydrochloride is eluted. After addition of the internal standard, the codeine is separated on a reverse-phase C18 column using a slightly alkaline mobile phase and is then determined by UV detection. The analysis takes 3.5 min per run; the limit of detection is approximately 3 micrograms/L for a 50-microL loop and 800 microL of plasma. The absolute recovery is 98.4 +/- 6.7% (n = 14) in the 10-300-micrograms/L range. Within the range, the calibration curve is linear.
本文描述了一种用于测定人血浆中可待因的高效液相色谱(HPLC)方法。该方法特异性强、精密度高且灵敏度高,可用于测定治疗剂量可待因给药后的血浆可待因水平。在C18萃取柱上进行纯化后,以盐酸盐形式存在的可待因被洗脱。加入内标后,可待因在反相C18柱上使用微碱性流动相进行分离,然后通过紫外检测进行测定。每次分析运行时间为3.5分钟;对于50微升定量环和800微升血浆,检测限约为3微克/升。在10 - 300微克/升范围内,绝对回收率为98.4±6.7%(n = 14)。在此范围内,校准曲线呈线性。