Wallace S M, Shah V P, Riegelman S
J Pharm Sci. 1977 Apr;66(4):527-30. doi: 10.1002/jps.2600660416.
An electron-capture GLC assay for acetazolamide in biological fluids was developed. Extraction efficiency was 69-104%. The minimum detectable amount of acetazolamide was 10 ng/sample. Concentrations of acetazolamide were determined by GLC in blood, plasma, plasma water, and saliva after oral administration of a single 250-mg dose to five volunteers. Erythrocyte levels were calculated from whole blood and plasma data. Concentration of free drug in the plasma was measured in samples of plasma water obtained by microultrafiltration. Peak plasma levels of 10-18 microng/ml were reached 1-3 hr after the dose. At least 1 hr later, erythrocyte levels reached peak concentrations of 13-29 microng/ml. Over 31 hr, plasma levels declined more rapidly than erythrocyte levels. Saliva concentrations averaged 1% of those in plasma and decreased at a rate equal to that of plasma. Saliva levels were proportional to, but not equal to, water concentration. Saliva to plasma ratios were consistent for any given individual and, therefore, offer a means of monitoring drug dosage without resorting to frequent blood sampling.
开发了一种用于生物流体中乙酰唑胺的电子捕获气相色谱分析方法。提取效率为69 - 104%。乙酰唑胺的最低检测量为10 ng/样本。对五名志愿者单次口服250 mg剂量后,通过气相色谱法测定血液、血浆、血浆水和唾液中乙酰唑胺的浓度。根据全血和血浆数据计算红细胞水平。通过微超滤获得的血浆水样本中测量血浆中游离药物的浓度。给药后1 - 3小时达到血浆峰值水平10 - 18 μg/ml。至少1小时后,红细胞水平达到峰值浓度13 - 29 μg/ml。在31小时内,血浆水平下降速度比红细胞水平快。唾液浓度平均为血浆浓度的1%,且下降速率与血浆相同。唾液水平与水浓度成正比,但不相等。对于任何给定个体,唾液与血浆的比率是一致的,因此提供了一种无需频繁采血即可监测药物剂量的方法。