Melten J W, Wittebrood A J, Willems H J, Faber G H, Wemer J, Faber D B
J Pharm Sci. 1985 Jun;74(6):692-4. doi: 10.1002/jps.2600740625.
In this study, three techniques for measuring the free fractions of phenobarbital and phenytoin were compared: equilibrium dialysis, ultrafiltration, and the Hummel and Dreyer method for gel permeation chromatography. In their therapeutic range (15-40 and 10-20 mg/L, respectively) the free fractions of phenobarbital and phenytoin were independent of the drug concentrations. Free fractions of phenobarbital as determined by equilibrium dialysis, ultrafiltration, and gel permeation chromatography were 58.7 +/- 1.8, 58.3 +/- 1.5, and 55.1 +/- 1.7%, respectively. Free fractions of phenytoin were 18.1 +/- 1.1, 17.0 +/- 2.1, and 19.4 +/- 1.2%, respectively. On lowering the albumin concentration, a similar increase in the free fractions of both drugs was observed with all three techniques. The results of this study show that all three techniques are suitable for the determination of free fractions of phenobarbital and phenytoin. Moreover, these techniques seem to be suitable for the investigation of physiological factors that may influence albumin drug binding.
在本研究中,对三种测定苯巴比妥和苯妥英游离分数的技术进行了比较:平衡透析、超滤以及用于凝胶渗透色谱的胡默尔和德雷尔方法。在其治疗范围内(分别为15 - 40毫克/升和10 - 20毫克/升),苯巴比妥和苯妥英的游离分数与药物浓度无关。通过平衡透析、超滤和凝胶渗透色谱测定的苯巴比妥游离分数分别为58.7±1.8%、58.3±1.5%和55.1±1.7%。苯妥英的游离分数分别为18.1±1.1%、17.0±2.1%和19.4±1.2%。降低白蛋白浓度时,使用所有三种技术均观察到两种药物的游离分数有类似增加。本研究结果表明,所有这三种技术都适用于测定苯巴比妥和苯妥英的游离分数。此外,这些技术似乎适用于研究可能影响白蛋白与药物结合的生理因素。