首页> 外文期刊>IDrugs: the investigational drugs journal >Remimazolam, a short-acting GABAA receptor agonist for intravenous sedation and/or anesthesia in day-case surgical and non-surgical procedures.
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Remimazolam, a short-acting GABAA receptor agonist for intravenous sedation and/or anesthesia in day-case surgical and non-surgical procedures.

机译:Remimazolam是一种短效GABA A 受体激动剂,可在日间手术和非手术过程中用于静脉镇静和/或麻醉。

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摘要

Remimazolam (CNS-7056) is a short-acting GABAA receptor agonist, under development by PAION, in collaboration with Japanese licensee Ono Pharmaceutical, as an intravenous sedative agent for potential use in day-case procedures, and the induction and maintenance of anesthesia. A member of the benzodiazapene class of drugs, the structure of remimazolam was modified to produce a drug that displays organ-independent metabolism. The incorporation of a carboxylic ester moiety into the benzodiazapene core of remimazolam renders it susceptible to non-specific tissue esterases and it is rapidly metabolized into its pharmacologically inactive metabolite CNS-7054. Preclinical studies in sheep demonstrated that remimazolam produced a more rapid onset of action, and a shorter duration of action, compared with midazolam. In a phase IIa clinical trial evaluating remimazolam as a procedural sedative for upper gastrointestinal endoscopy in patients, the time to recovery from sedation was shorter and more consistent with remimazolam, relative to midazolam. Because of its organ-independent metabolism and rapid and predictable onset and recovery, remimazolam appears to have potential advantages over other currently available short-acting sedatives.
机译:Remimazolam(CNS-7056)是一种短效GABAA受体激动剂,由PAION与日本被许可方Ono Pharmaceutical合作开发,可作为静脉镇静剂,可用于日间手术以及诱导和维持麻醉。 remimazolam是苯二氮杂p类药物的成员,其结构被修饰以产生显示器官非依赖性代谢的药物。在remimazolam的苯并二氮杂烯核中掺入羧酸酯部分使其易受非特异性组织酯酶的影响,并迅速代谢成其无药理活性的代谢产物CNS-7054。在绵羊中进行的临床前研究表明,与咪达唑仑相比,雷马咪唑仑起效更快,作用时间更短。在一项IIa期临床试验中,评价了雷马咪唑仑作为患者上消化道内窥镜检查的手术镇静剂,与咪达唑仑相比,从镇静中恢复的时间更短,并且与雷马咪唑仑更加一致。由于其不依赖器官的新陈代谢以及快速和可预测的起效和恢复,与其他目前可用的短效镇静剂相比,雷马马唑仑似乎具有潜在的优势。

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