Franke Ryan M, Morton Terri, Devarakonda Krishna
Department of Clinical Pharmacology, Mallinckrodt Pharmaceuticals, Hazelwood, MO, USA.
Drug Des Devel Ther. 2015 Aug 11;9:4587-97. doi: 10.2147/DDDT.S79499. eCollection 2015.
This analysis evaluated the single-dose population pharmacokinetics (PK) of biphasic immediate-release (IR)/extended-release (ER) oxycodone (OC)/acetaminophen (APAP) 7.5/325 mg tablets administered under fasted conditions and the effects of a meal on their single-dose population PK. Data were pooled from four randomized, single-dose crossover trials enrolling healthy adult (18-55 years old) participants (three trials) and nondependent recreational users of prescription opioids (one trial) with a body weight of ≥59 kg. Participants received IR/ER OC/APAP 7.5/325 mg tablets in single doses of 7.5/325 mg (one tablet), 15/650 mg (two tablets), or 30/1,300 mg (four tablets) under fasted or fed conditions. Six variables were examined: sex, race, age, weight, height, and body mass index. Single-dose population PK was analyzed using first-order conditional estimation methods. A total of 151 participants were included in the analysis under fasted conditions, and 31 participants were included in the fed analysis. Under fasted conditions, a 10% change in body weight was accompanied by ~7.5% change in total body clearance (CL/F) and volume of distribution (V/F) of OC and APAP. Black participants had 17.3% lower CL/F and a 16.9% lower V/F of OC compared with white participants. Under fed conditions, the absorption rate constant of OC and APAP decreased significantly, although there was no effect on CL/F and V/F. Considering that the recommended dose for IR/ER OC/APAP 7.5/325 mg tablets is two tablets every 12 hours, adjustments of <50% are not clinically relevant. Dose adjustment may be necessary for large deviations from average body weight, but the small PK effects associated with race and consumption of a meal are not clinically relevant.
本分析评估了在禁食条件下给予的双相速释(IR)/缓释(ER)羟考酮(OC)/对乙酰氨基酚(APAP)7.5/325毫克片剂的单剂量群体药代动力学(PK),以及进餐对其单剂量群体PK的影响。数据来自四项随机、单剂量交叉试验,纳入了健康成年(18至55岁)参与者(三项试验)和非依赖性处方阿片类药物娱乐使用者(一项试验),体重≥59千克。参与者在禁食或进食条件下接受单剂量为7.5/325毫克(一片)、15/650毫克(两片)或30/1300毫克(四片)的IR/ER OC/APAP 7.5/325毫克片剂。检查了六个变量:性别、种族、年龄、体重、身高和体重指数。使用一阶条件估计方法分析单剂量群体PK。共有151名参与者纳入禁食条件下的分析,31名参与者纳入进食分析。在禁食条件下,体重10%的变化伴随着OC和APAP的总体清除率(CL/F)和分布容积(V/F)约7.5%的变化。与白人参与者相比,黑人参与者的OC的CL/F低17.3%,V/F低16.9%。在进食条件下,OC和APAP的吸收速率常数显著降低,尽管对CL/F和V/F没有影响。考虑到IR/ER OC/APAP 7.5/325毫克片剂的推荐剂量是每12小时两片,小于50%的调整在临床上不相关。对于与平均体重有较大偏差的情况可能需要调整剂量,但与种族和进餐相关的小PK效应在临床上不相关。