Goldwater Ronald, Kramer William G, Hamilton Douglas A, Lang Eric, Wang Jianyuan, Madden Donna E, Lacouture Peter G, Ramaiya Atulkumar, Carr Daniel B
PAREXEL International, Baltimore, MD.
Kramer Consulting, LLC, North Potomac, MD.
Clin Pharmacol. 2016 Dec 15;8:203-212. doi: 10.2147/CPAA.S98437. eCollection 2016.
The analgesic and opioid-sparing effects of nonsteroidal anti-inflammatory drugs can be beneficial in postoperative populations. Hydroxypropyl-β-cyclodextrin (HPβCD)-diclofenac is an injectable formulation of diclofenac solubilized with HPβCD that is administered as a low-volume intravenous bolus. This open-label, single-dose study examined the effects of age and weight on the pharmacokinetic (PK) profile of HPβCD-diclofenac.
Eighty-eight adult volunteers were enrolled. An age-based cohort included 34 subjects 55-82 years old stratified into three groups and receiving HPβCD-diclofenac 18.75 mg. A weight-based cohort included 54 subjects stratified into five groups based on body weight and body mass index and receiving HPβCD-diclofenac 37.5 mg. PK analysis was performed on blood samples collected predosing and at predefined intervals (5, 10, 20, 30, and 45 minutes; 1, 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, and 18 hours) postdosing. Diclofenac PK parameters were examined in the individual cohorts, and regression analyses of the relationship between age, weight, and PK parameters were performed on pooled data from all enrolled subjects.
Examination of the age-based cohort revealed similar diclofenac PK parameters across age groups. PK parameters were likewise similar across weight groups in the weight-based cohort. Regression analysis on pooled data from the age- and weight-based cohorts revealed that increasing body weight was associated with a significant increase in diclofenac clearance (CL), suggesting decreased exposure in high-weight patients. Analysis of the pooled population also demonstrated an inverse relationship between age and elimination half-life (), likely due to a decrease in the volume of distribution () with increased age, not a change in CL. There were no deaths, serious adverse events, or adverse events that led to discontinuation.
This study suggests that the CL of diclofenac is not dependent on age in elderly subjects receiving HPβCD-diclofenac but indicates that diclofenac CL increases with increasing body weight.
非甾体抗炎药的镇痛和节省阿片类药物的作用对术后人群可能有益。羟丙基-β-环糊精(HPβCD)-双氯芬酸是一种用HPβCD增溶的双氯芬酸注射剂,以小容量静脉推注给药。这项开放标签的单剂量研究考察了年龄和体重对HPβCD-双氯芬酸药代动力学(PK)特征的影响。
招募了88名成年志愿者。一个基于年龄的队列包括34名55 - 82岁的受试者,分为三组,接受18.75 mg的HPβCD-双氯芬酸。一个基于体重的队列包括54名受试者,根据体重和体重指数分为五组,接受37.5 mg的HPβCD-双氯芬酸。对给药前及给药后预定时间点(5、10、20、30和45分钟;1、1.5、2、2.5、3、4、6、8、10、12和18小时)采集的血样进行PK分析。在各个队列中检查双氯芬酸的PK参数,并对所有入组受试者的汇总数据进行年龄、体重与PK参数之间关系的回归分析。
对基于年龄的队列的检查显示,各年龄组的双氯芬酸PK参数相似。基于体重的队列中,各体重组的PK参数同样相似。对基于年龄和体重的队列的汇总数据进行回归分析显示,体重增加与双氯芬酸清除率(CL)显著增加相关,提示高体重患者的暴露量降低。对汇总人群的分析还显示年龄与消除半衰期()呈负相关,这可能是由于分布容积()随年龄增加而减小,而非CL发生变化。没有死亡、严重不良事件或导致停药的不良事件。
本研究表明,接受HPβCD-双氯芬酸的老年受试者中双氯芬酸的CL不依赖于年龄,但表明双氯芬酸的CL随体重增加而增加。