Yano I, Takayama A, Takano M, Inatani M, Tanihara H, Ogura Y, Honda Y, Inui K
Department of Pharmacy, Kyoto University Hospital, Faculty of Medicine, Kyoto University, Japan.
Eur J Clin Pharmacol. 1998 Mar;54(1):63-8. doi: 10.1007/s002280050422.
To characterize the pharmacokinetics and pharmacodynamics of acetazolamide in patients with transient intraocular pressure (IOP) elevation and to provide individual patients with the optimal dosage regimen for this drug.
We studied 17 patients with transient IOP elevation, who were given 62.5-500 mg acetazolamide orally as single or repetitive doses. Plasma acetazolamide concentration and IOP were measured at approximately 1, 3, 5, and 9 h after the last acetazolamide administration. Pharmacokinetics and pharmacodynamics were analyzed by nonlinear mixed-effect modeling using the program NONMEM.
The plasma concentration profile of acetazolamide was characterized by a one-compartment model with first-order absorption. The apparent oral clearance was related to the creatine clearance (CCR) which was estimated by the Cockcroft and Gault equation, as follows: 0.0468 x CCR1 x h(-1). The estimated apparent oral volume of distribution, first-order absorption rate constant, and absorption lag time were 0.231 l x kg(-1), 0.821 x h(-1), and 0.497 h, respectively. IOP after oral acetazolamide administration was characterized by an Emax model. The maximal effect in lowering the IOP (Emax) was 7.2 mmHg, and the concentration corresponding to 50% of the maximal effect (EC50) was 1.64 microg x ml(-1). As 70% of Emax was achieved at a plasma concentration of 4 microg x ml(-1), this concentration was considered satisfactory for lowering IOP. The recommended dosage was calculated so that the minimum plasma concentration at steady state exceeded this target concentration; 250 mg t.i.d., 125 mg t.i.d., 125 mg b.i.d., and 125 mg once daily for the patients with CCR values of 70, 50, 30, and 10 ml min(-1), respectively.
Measuring plasma concentrations of acetazolamide and subsequent pharmacokinetic and pharmacodynamic analyses are useful for estimating its concentration-dependent effectiveness in lowering the IOP in individual patients. The dosage regimen presented in this study is expected to improve the benefits of acetazolamide pharmacotherapy in most elderly patients with transient rises in IOP following intraocular surgery.
表征乙酰唑胺在短暂性眼压(IOP)升高患者中的药代动力学和药效学特征,并为个体患者提供该药物的最佳给药方案。
我们研究了17例短暂性IOP升高患者,给予他们口服62.5 - 500 mg乙酰唑胺,单次或重复给药。在最后一次给予乙酰唑胺后约1、3、5和9小时测量血浆乙酰唑胺浓度和IOP。使用NONMEM程序通过非线性混合效应模型分析药代动力学和药效学。
乙酰唑胺的血浆浓度曲线以具有一级吸收的单室模型为特征。表观口服清除率与通过Cockcroft和Gault方程估算的肌酐清除率(CCR)相关,如下:0.0468×CCR1×h⁻¹。估计的表观口服分布容积、一级吸收速率常数和吸收滞后时间分别为0.231 l×kg⁻¹、0.821×h⁻¹和0.497 h。口服乙酰唑胺后的IOP以Emax模型为特征。降低IOP的最大效应(Emax)为7.2 mmHg,对应于最大效应50%的浓度(EC50)为1.64 μg×ml⁻¹。由于在血浆浓度为4 μg×ml⁻¹时达到了Emax的70%,该浓度被认为对降低IOP是满意的。计算推荐剂量,以使稳态时的最低血浆浓度超过该目标浓度;对于CCR值分别为70、50、30和10 ml min⁻¹的患者,推荐剂量分别为250 mg每日三次、125 mg每日三次、125 mg每日两次和125 mg每日一次。
测量乙酰唑胺的血浆浓度以及随后的药代动力学和药效学分析有助于评估其在个体患者中降低IOP的浓度依赖性有效性。本研究提出的给药方案有望改善大多数老年患者在眼内手术后短暂性IOP升高时乙酰唑胺药物治疗的益处。