Loonen A J, Toll P J, Nijdam J R
Psychiatrische Instituten van de Godshuizen, GB Vught, The Netherlands.
Pharm Weekbl Sci. 1989 Feb 24;11(1):23-6. doi: 10.1007/BF01972911.
In an open, randomized, two-centre, cross-over study 20 patients formerly adjusted to a stable oral twice daily 200-600 mg carbamazepine dose, used ordinary tablets and divitabs (a new sustained-release formulation) for periods of three weeks, whereafter the serum level courses of carbamazepine and its metabolite carbamazepine-10,11-epoxide were measured. The mean peak/mean trough carbamazepine-serum concentration ratio was slightly lower after the intake of divitabs in comparison to normal formulation: 1.14 +/- 0.447 versus 1.23 +/- 0.545 (mean +/- SD). The mean trough levels of carbamazepine and its metabolite were 9% and 16% lower in the case of divitabs. In patients with peak/trough carbamazepine-serum level ratios of at least 1.30 after the intake of normal formulation, divitabs had a significant advantage.
在一项开放、随机、双中心、交叉研究中,20名之前已调整至每日两次口服200 - 600毫克卡马西平稳定剂量的患者,使用普通片剂和Divitabs(一种新的缓释制剂)各为期三周,之后测量卡马西平及其代谢物卡马西平 - 10,11 - 环氧化物的血清浓度变化过程。与普通制剂相比,服用Divitabs后卡马西平的平均峰浓度/平均谷浓度比值略低:分别为1.14±0.447和1.23±0.545(平均值±标准差)。Divitabs组中卡马西平及其代谢物的平均谷浓度分别低9%和16%。在服用普通制剂后卡马西平血清峰谷浓度比至少为1.30的患者中,Divitabs具有显著优势。