复方咪达唑仑胶囊一年内的物理化学稳定性

P. Boivin, P. Legendre, Anne-Claire Bonnaure, M. Lester
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引用次数: 1

摘要

摘要目的慢性肝病患者肝脏药物代谢紊乱,代谢能力难以评估。咪达唑仑可以作为表型探针来预测CYP3A的代谢能力,以调节这种细胞色素的药物底物的剂量。在此背景下,我单位即将开展前瞻性临床试验,并研制出适合临床试验的咪达唑仑胶囊医院制剂。本研究的目的是评估该制剂在12个月内的物理化学稳定性,以确定保质期。方法以盐酸咪达唑仑和微晶纤维素为稀释液,制备3批1 mg胶囊。这些胶囊在室温下储存,并遮光。为了测定胶囊含量的演变,建立了254 nm紫外检测的高效液相色谱法(HPLC)。采用液相色谱-串联质谱(LC-MS/MS)分析方法对数据进行验证。结果1年后,胶囊中盐酸咪达唑仑的含量仍高于初始浓度的95%。结论:1 mg咪达唑仑胶囊在室温和黑暗条件下稳定性为12个月。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physicochemical stability of compounded midazolam capsules over a one-year storage period
Abstract Objectives In patients suffering from chronic liver disease, the hepatic metabolism of drugs is perturbed and the metabolic capacity is difficult to assess. Midazolam could be used as a phenotypical probe to predict the metabolic capacity of CYP3A to adjust dosages of drug substrates of this cytochrome. In this context, a prospective clinical trial is going to be conducted in our institution and a hospital preparation of midazolam capsules suitable for the clinical trial was developed. The objective of the present work was to assess the physicochemical stability of the formulation over 12 months to set shelf life. Methods Three batches of 1 mg capsules were prepared using midazolam hydrochloride and microcrystalline cellulose as a diluent. The capsules were stored at ambient temperature and protected from light. To measure the evolution of the capsules content, a stability-indicating high-performance liquid chromatography (HPLC) method was developed with ultraviolet (UV) detection at 254 nm. Data were confirmed using a liquid chromatography-tandem mass spectrometry (LC-MS/MS) analytical method. Results After one year, midazolam hydrochloride content remained higher than 95% of the initial concentration in capsules. Conclusions The results show that 1 mg midazolam capsules are stable for 12 months at room temperature and under dark conditions.
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