Patel I H, Venkataramanan R, Levy R H, Viswanathan C T, Ojemann L M
Epilepsia. 1982 Jun;23(3):283-90. doi: 10.1111/j.1528-1157.1982.tb06193.x.
In view of the observed variation of valproic acid (VPA) free fraction (fp) during a dosing interval and the competitive binding effect of free fatty acids (FFA) in vitro, this study was designed to address the existence of diurnal variations in the fp of VPA. Six subjects were hospitalized at 7 a.m. for 25 h, and plasma samples were collected every 2 h. The protocol was repeated in 4 of the 6 subjects one week later. In vitro binding of VPA (100 micrograms/ml) was determined by equilibrium dialysis (14C-VPA), and FFAs were assayed colorimetrically. Phenytoin (PHT) binding was also determined for comparison. VPA fp ranged from 8.10 +/- 1.16 to 9.63 +/- 1.54. Intrasubject variability was also measured by the ratio of maximum to minimum fp values (fp max/fp min) over 24 h: This ratio ranged from 1.30 to 1.68 (mean +/- %SD = 1.51 +/- 7.7%, n = 10). For PHT, fp ranged from 10.88 +/- 0.50 to 12.39 +/- 1.07, and fp max/fp min from 1.09 to 1.31 (1.17 +/- 5.1%, n = 10). The fp max was observed between 2 and 6 a.m. in 7 out of 10 cases for VPA and 5 out of 10 cases for PHT. FFA levels, although in the normal range, varied two- to fourfold within 24 h. A significant correlation was observed between mean FFA levels at each sampling time and the corresponding fp values for VPA (p less than 0.001), but not for PHT.
鉴于观察到丙戊酸(VPA)游离分数(fp)在给药间隔期间的变化以及游离脂肪酸(FFA)在体外的竞争结合作用,本研究旨在探讨VPA的fp是否存在昼夜变化。6名受试者于上午7点入院25小时,每2小时采集一次血浆样本。一周后,6名受试者中的4名重复该方案。通过平衡透析法(14C-VPA)测定VPA(100微克/毫升)的体外结合情况,采用比色法测定FFA。还测定了苯妥英(PHT)的结合情况以作比较。VPA的fp范围为8.10±1.16至9.63±1.54。通过24小时内最大与最小fp值之比(fp max/fp min)来测量受试者内变异性:该比值范围为1.30至1.68(平均值±%标准差=1.51±7.7%,n = 10)。对于PHT,fp范围为10.88±0.50至12.39±1.07,fp max/fp min为1.09至1.31(1.17±5.1%,n = 10)。10例中有7例VPA和10例中有5例PHT的fp max出现在凌晨2点至6点之间。FFA水平虽在正常范围内,但在24小时内变化两到四倍。在每个采样时间点的平均FFA水平与VPA相应的fp值之间观察到显著相关性(p<0.001),但与PHT无相关性。