Smith R B, Smith R V, Yakatan G J
J Pharm Sci. 1976 Aug;65(8):1208-11. doi: 10.1002/jps.2600650819.
A rapid, accurate, sensitive, and reproducible assay for hydroflumethiazide in plasma and urine was developed after studies of its UV and fluorescence spectral properties and partitioning behavior. The assay is based on initial extraction from acidified plasma or urine into ether, back-extraction into basic solution followed by acidification to about pH 1, and measurement of the fluorescence derived from the unionized molecule. Analysis of variance indicated no significant differences in assays performed on the same day. The mean recovery was 98.8 +/- 7.4% for plasma over a concentration range of 0.2-2.0 mug/ml. The method is convenient for routine clinical use and has sufficient sensitivity to quantify hydroflumethiazide levels after administration of therapeutic doses.
在研究了氢氟噻嗪的紫外光谱和荧光光谱特性以及分配行为后,开发了一种快速、准确、灵敏且可重复的血浆和尿液中氢氟噻嗪检测方法。该检测方法基于以下步骤:首先将酸化的血浆或尿液用乙醚萃取,再反萃取至碱性溶液中,然后酸化至pH约为1,最后测量非离子化分子产生的荧光。方差分析表明同一天进行的检测无显著差异。血浆中氢氟噻嗪浓度在0.2 - 2.0μg/ml范围内时,平均回收率为98.8±7.4%。该方法便于临床常规使用,且具有足够的灵敏度来定量治疗剂量给药后氢氟噻嗪的水平。