Sørensen P S, Flachs H, Friis M L, Hvidberg E F, Paulson O B
Neurology. 1984 Aug;34(8):1020-4. doi: 10.1212/wnl.34.8.1020.
We measured the fluctuations in plasma pyridostigmine concentration from day to day on 3 consecutive days and hour to hour during 1 day in 11 myasthenic patients, by studying their usual dosage regime. Plasma pyridostigmine was measured by gas chromatography/mass spectrometry. The intraindividual day-to-day variation in plasma pyridostigmine levels was small. A highly significant relationship was found between the oral pyridostigmine dose and the area under the plasma concentration/time curve. The bioavailability of oral pyridostigmine was 3.6%, estimated by replacing one dose with an intravenous dose amounting to 1/30 of the oral dose. The relatively stable kinetic behavior of pyridostigmine is in contrast to the interpatient variability in dose requirement, indicating that monitoring of plasma pyridostigmine levels should be reserved for special cases.
我们通过研究11例重症肌无力患者的常规用药方案,连续3天测量了他们血浆中吡啶斯的明浓度的每日波动情况,并在1天内测量了每小时的波动情况。血浆吡啶斯的明采用气相色谱/质谱法测定。血浆吡啶斯的明水平的个体内每日变化很小。口服吡啶斯的明剂量与血浆浓度/时间曲线下面积之间存在高度显著的关系。通过用相当于口服剂量1/30的静脉剂量替代一次口服剂量来估算,口服吡啶斯的明的生物利用度为3.6%。吡啶斯的明相对稳定的动力学行为与患者间剂量需求的变异性形成对比,这表明血浆吡啶斯的明水平监测应仅用于特殊情况。