Shelton Mark J, Cloen Denise, DiFrancesco Robin, Berenson Charles S, Esch Andrew, de Caprariis Pascal J, Palic Branka, Schur Jane L, Buggé Christopher J L, Ljungqvist Anders, Espinosa Orlando, Hewitt Ross G
GlaxoSmithKline, Five Moore Drive, P.O. Box 13398, Research Triangle Park, NC 27709, USA.
J Clin Pharmacol. 2004 Mar;44(3):293-304. doi: 10.1177/0091270003262956.
Twelve methadone-maintained HIV-negative subjects were given saquinavir/ritonavir (SQV/rtv) 1600 mg/100 mg once daily for 14 days. Pharmacokinetic evaluations of total and unbound methadone enantiomers (R and S) were conducted before and after SQV/rtv. SQV/rtv was well tolerated, with no ACTG Grade 3-4 adverse events, no evidence of sedation, and no changes in methadone dose. For R-methadone (active isomer), C(max), AUC(0-24 h), and C(min) were unchanged, but percent unbound 4 hours after dosing was reduced by 12%. For S-methadone, no differences in pharmacokinetic parameters of total drug were seen, but unbound concentrations were reduced by 15% and 21% at 4 and 24 hours after dosing, respectively. SQV trough concentrations exceeded the anticipated EC(50) (50 ng/mL) in 10/12 subjects, persisting for at least 6 hours after the final dose in 4/6 subjects. Once-daily SQV/rtv in methadone-maintained subjects is safe and not associated with any clinically significant interaction with methadone during 14 days of concomitant administration.
12名接受美沙酮维持治疗的HIV阴性受试者每天一次服用1600毫克/100毫克的沙奎那韦/利托那韦(SQV/rtv),持续14天。在服用SQV/rtv前后对美沙酮对映体(R和S)的总药代动力学和游离药代动力学进行了评估。SQV/rtv耐受性良好,无美国国立过敏与传染病研究所(ACTG)3 - 4级不良事件,无镇静迹象,美沙酮剂量无变化。对于R - 美沙酮(活性异构体),C(max)、AUC(0 - 24小时)和C(min)未改变,但给药后4小时的游离百分比降低了12%。对于S - 美沙酮,总药物的药代动力学参数未见差异,但给药后4小时和24小时的游离浓度分别降低了15%和21%。12名受试者中有10名的SQV谷浓度超过预期的EC(50)(50纳克/毫升),4/6的受试者在最后一剂后至少持续6小时。美沙酮维持治疗的受试者每日一次服用SQV/rtv是安全的,在14天的联合给药期间与美沙酮无任何临床显著相互作用。