Bosso John A, Flume Patrick A, Gray Susan L
Department of Pharmaceutical Sciences, College of Pharmacy, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
Antimicrob Agents Chemother. 2004 Jan;48(1):281-4. doi: 10.1128/AAC.48.1.281-284.2004.
The pharmacokinetics of many drugs are altered in patients with cystic fibrosis (CF), often necessitating different dosage requirements than those used in non-CF patients. The objective of this study was to determine the pharmacokinetics of linezolid, an antibiotic with good activity against gram-positive organisms such as methicillin-resistant Staphylococcus aureus, in patients with CF so that dosage requirements could be established. Twelve adult patients (6 male) ranging in age from 22 to 39 years were studied. A single 600-mg dose was administered intravenously over 0.5 h, and plasma samples were collected at 0 (predose), 0.5, 0.75, 1, 2, 4, 8, and 24 h. Linezolid concentrations were determined with a validated high-performance liquid chromatography assay. Pharmacokinetic parameters were estimated using standard noncompartmental methods. Blood chemistry and hematologic indices were determined before and after the study for safety purposes. All patients completed the study without encountering any adverse reactions. The pharmacokinetic parameters, while variable, with half-lives varying from 1.76 to 8.36 h, were similar to those previously described in other populations. Mean (+/- standard deviation) values for pharmacokinetic parameters of interest were as follows: elimination rate constant, 0.21 (0.11) h(-1); half-life, 4.41 (2.43); volume of distribution at steady state, 0.87 (0.19) liters/kg of body weight; and total body clearance, 0.12 (0.06) liters/h/kg. No patient would have achieved the pharmacodynamic target of an area under the concentration-time curve/MIC ratio of 83 h for pathogens for which the MIC was 4 micro g/ml. Patients with inadequate clinical responses to linezolid may require more frequent dosing.
许多药物的药代动力学在囊性纤维化(CF)患者中会发生改变,这常常需要与非CF患者使用不同的剂量要求。本研究的目的是确定利奈唑胺(一种对革兰氏阳性菌如耐甲氧西林金黄色葡萄球菌具有良好活性的抗生素)在CF患者中的药代动力学,以便确定剂量要求。研究了12名年龄在22至39岁之间的成年患者(6名男性)。静脉内于0.5小时内给予单次600毫克剂量,并在0(给药前)、0.5、0.75、1、2、4、8和24小时采集血浆样本。使用经过验证的高效液相色谱法测定利奈唑胺浓度。使用标准的非房室方法估计药代动力学参数。为安全起见,在研究前后测定血液化学和血液学指标。所有患者均完成研究,未出现任何不良反应。药代动力学参数虽然存在差异,半衰期从1.76至8.36小时不等,但与先前在其他人群中描述的参数相似。感兴趣的药代动力学参数的平均值(±标准差)如下:消除速率常数,0.21(0.11)h⁻¹;半衰期,4.41(2.43);稳态分布容积,0.87(0.19)升/千克体重;全身清除率,0.12(0.06)升/小时/千克。对于MIC为4微克/毫升的病原体,没有患者能够达到浓度-时间曲线下面积/MIC比值为83小时的药效学目标。对利奈唑胺临床反应不足的患者可能需要更频繁给药。