Kilpatrick Gavin J
GJK Pharma Ltd., Eltisley, United Kingdom.
Front Pharmacol. 2021 Jul 20;12:690875. doi: 10.3389/fphar.2021.690875. eCollection 2021.
A program to identify novel intravenous sedatives with a short and predictable duration of action was initiated in the late 1990's by Glaxo Wellcome. The program focussed on the identification of ester-based benzodiazepine derivatives that are rapidly broken down by esterases. Remimazolam was identified as one of the lead compounds. The project at Glaxo was shelved for strategic reasons at the late lead optimization stage. Via the GSK ventures initiative, the program was acquired by the small biotechnology company, TheraSci, and, through successive acquisitions, developed as the besylate salt at CeNeS and PAION. The development of remimazolam besylate has been slow by industry standards, primarily because of the resource limitations of these small companies. It has, however, recently been approved for anesthesia in Japan and South Korea, procedural sedation in the United States, China, and Europe, and for compassionate use in intensive care unit sedation in Belgium. A second development program of remimazolam was later initiated in China, using a slightly different salt form, remimazolam tosylate. This salt form of the compound has also recently been approved for procedural sedation in China. Remimazolam has the pharmacological profile of a classical benzodiazepine, such as midazolam, but is differentiated from other intravenous benzodiazepines by its rapid conversion to an inactive metabolite resulting in a short onset/offset profile. It is differentiated from other intravenous hypnotic agents, such as propofol, by its low liability for cardiovascular depression, respiratory depression, and injection pain. The benzodiazepine antagonist flumazenil can reverse the effects of remimazolam in case of adverse events and further shorten recovery times. The aim of this review is to provide an analysis of, and perspective on, published non-clinical and clinical information on 1) the pharmacology, metabolism, pharmacokinetics, and pharmacodynamic profile of remimazolam, 2) the profile of remimazolam compared with established agents, 3) gaps in the current understanding of remimazolam, 4) the compound's discovery and development process and 5) likely future developments in the clinical use of remimazolam.
20世纪90年代末,葛兰素威康公司启动了一项旨在识别作用时间短且可预测的新型静脉镇静剂的计划。该计划聚焦于鉴定可被酯酶快速分解的酯基苯二氮䓬衍生物。瑞马唑仑被确定为主要化合物之一。葛兰素威康的该项目在后期先导优化阶段因战略原因被搁置。通过葛兰素史克风险投资计划,该项目被小型生物技术公司TheraSci收购,并通过一系列收购,在CeNeS和PAION公司开发成苯磺酸盐形式。按照行业标准,瑞马唑仑苯磺酸盐的开发进展缓慢,主要是因为这些小公司资源有限。然而,它最近已在日本和韩国获批用于麻醉,在美国、中国和欧洲获批用于程序性镇静,在比利时获批用于重症监护病房的同情性镇静。后来在中国启动了瑞马唑仑的第二个开发项目,使用了略有不同的盐形式——瑞马唑仑甲苯磺酸盐。该化合物的这种盐形式最近也在中国获批用于程序性镇静。瑞马唑仑具有经典苯二氮䓬类药物(如咪达唑仑)的药理学特征,但与其他静脉苯二氮䓬类药物的区别在于它能迅速转化为无活性代谢物,从而具有起效/消退迅速的特点。它与其他静脉催眠药(如丙泊酚)的区别在于其导致心血管抑制、呼吸抑制和注射疼痛的可能性较低。在发生不良事件时,苯二氮䓬拮抗剂氟马西尼可逆转瑞马唑仑的作用,并进一步缩短恢复时间。本综述的目的是对已发表的关于瑞马唑仑的非临床和临床信息进行分析并提供观点,内容包括:1)瑞马唑仑的药理学、代谢、药代动力学和药效学特征;2)瑞马唑仑与现有药物相比的特征;3)目前对瑞马唑仑认识上的差距;4)该化合物的发现和开发过程;5)瑞马唑仑临床应用未来可能的发展。