Center for Drug Studies, Departments of Pharmacy and Neuroloy, Smith Building Room 334, Virginia Commonwealth University, School of Pharmacy, 410 North 12th Street, PO Box 980583, Richmond, VA 23298-0583, United States.
Epilepsy Res. 2011 Jan;93(1):11-6. doi: 10.1016/j.eplepsyres.2010.10.001. Epub 2010 Dec 9.
Rectal administration of diazepam (DZ) has been used effectively in patients with epilepsy who experience acute repetitive seizures, but rectal gel may be difficult to administer during a seizure and is subject to variable drug absorption. An intramuscular (IM) autoinjector DZ formulation may offer a practical alternative to rectal DZ. This single-center, open-label, 3-treatment, 3-period crossover study compared the pharmacokinetic and safety profiles of 10mg DZ administered rectally in 24 healthy, fasted and fed subjects versus IM autoinjector delivery in fasted subjects. Blood samples were collected at baseline and for up to 24h postdose and plasma DZ concentrations were determined by liquid chromatography and tandem mass spectrometry. There were no significant differences between plasma concentrations for rectal administration of DZ in fasted and fed subjects at any time point. Intramuscular DZ administration resulted in more rapid and less variable drug absorption than rectal delivery. At 30min postdose and at all subsequent evaluations, IM administration resulted in significantly higher areas under the curve versus rectal administration in fasted subjects (p<0.05). This significant difference was sustained throughout the remainder of the 24-h study period (p<0.05). All reported adverse events were considered mild, and none required treatment.
直肠给予地西泮(DZ)已被有效地用于癫痫发作患者,这些患者会经历急性重复发作,但在癫痫发作期间直肠凝胶可能难以给药,且药物吸收存在差异。肌肉内(IM)自动注射器 DZ 制剂可能是直肠 DZ 的实用替代方案。这项单中心、开放标签、3 种治疗、3 期交叉研究比较了 24 名健康、禁食和进食受试者中直肠给予 10mg DZ 的药代动力学和安全性特征,与禁食受试者中 IM 自动注射器给药进行了比较。在基线和给药后长达 24 小时采集血样,并通过液相色谱和串联质谱法测定血浆 DZ 浓度。在任何时间点,禁食和进食受试者直肠给予 DZ 的血浆浓度均无显著差异。IM 给予 DZ 的药物吸收比直肠给药更快且更具可变性。在给药后 30 分钟和所有后续评估中,IM 给药在禁食受试者中的曲线下面积均显著高于直肠给药(p<0.05)。这种显著差异在整个 24 小时研究期间的其余时间持续存在(p<0.05)。所有报告的不良事件均被认为是轻度的,且无需治疗。