Ueshima Satoshi, Nagahara Serina, Nakaya Kenta, Kawamura Mayu, Hira Daiki, Matsuura Yu, Toyama Hiroaki, Kawamae Kaneyuki, Kakumoto Mikio
Laboratory of Clinical Pharmacy, College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Noji-higashi, Kusatsu, 525-8577, Shiga, Japan.
Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606- 8507, Japan.
Sci Rep. 2025 Jul 10;15(1):24979. doi: 10.1038/s41598-025-10015-z.
The pharmacokinetic and pharmacodynamic characteristics of remimazolam (RMZ), a novel ultrashort-acting anesthetic, administration alone in clinical practice remain poorly understood. Therefore, we aimed to evaluate the relationship between patient characteristics and the pharmacokinetics and pharmacodynamics of RMZ in older Japanese adults who underwent general anesthesia at the early stage of infusion. Plasma samples were collected from 20 patients (median age: 71.7 years; range: 42.2-88.6 years) who were intravenously administered RMZ without other anesthetics such as remifentanil or fentanyl. The pharmacokinetic profiles of RMZ and its metabolite (CNS7054) were described using three- and two-compartment models with a transit compartment, respectively. The bispectral index was selected as a clinical measure of sedation. The pharmacokinetic-pharmacodynamic profile of RMZ was described using a maximum inhibitory model with an effect compartment. The population pharmacokinetic and pharmacodynamic parameters of RMZ were obtained using the nonlinear mixed-effects modeling program. RMZ clearance (CL) was increased nonlinearly with increasing body weight (BW), and the population mean CL for a typical patient (BW, 60.4 kg) was 1.38 L/min. No patient characteristics affected CNS7054 pharmacokinetics. The population mean of the half-maximal inhibitory RMZ concentration decreased nonlinearly with increasing age or BW. However, these characteristics did not meet the criteria for pharmacokinetic and pharmacodynamic covariates. Our results suggest that BW is an intrinsic factor affecting RMZ pharmacokinetics in Japanese patients under general anesthesia in the early stages of infusion; however, no patient characteristics affected RMZ pharmacodynamics.
新型超短效麻醉药瑞米唑仑(RMZ)在临床实践中单独给药时的药代动力学和药效学特征仍知之甚少。因此,我们旨在评估在输注早期接受全身麻醉的老年日本成年人中,患者特征与RMZ药代动力学和药效学之间的关系。从20例患者(年龄中位数:71.7岁;范围:42.2 - 88.6岁)中采集血浆样本,并静脉注射RMZ,未使用其他麻醉药如瑞芬太尼或芬太尼。分别使用带有转运室的三室和二室模型描述RMZ及其代谢物(CNS7054)的药代动力学特征。选择脑电双频指数作为镇静的临床指标。使用带有效应室的最大抑制模型描述RMZ的药代动力学-药效学特征。使用非线性混合效应建模程序获得RMZ的群体药代动力学和药效学参数。RMZ清除率(CL)随体重(BW)增加呈非线性增加,典型患者(BW,60.4 kg)的群体平均CL为1.38 L/min。没有患者特征影响CNS7054的药代动力学。半数最大抑制RMZ浓度的群体平均值随年龄或BW增加呈非线性下降。然而,这些特征不符合药代动力学和药效学协变量的标准。我们的结果表明,BW是影响输注早期全身麻醉下日本患者RMZ药代动力学的内在因素;然而,没有患者特征影响RMZ的药效学。