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丙泊酚与美索比妥1:1混合物的化学和物理稳定性。

The chemical and physical stability of a 1:1 mixture of propofol and methohexital.

作者信息

Bennett J, Gross J, Nichols F, Chidambaram N, Burgess D

机构信息

Department of Oral and Maxillofacial Surgery, University of Connecticut School of Dental Medicine, Farmington 06030-1720, USA.

出版信息

Anesth Prog. 2001 Spring;48(2):61-5.

Abstract

Anesthetic drugs are frequently mixed or coadministered to optimize anesthetic effects while minimizing adverse effects. Methohexital advantages include its low cost and rapid onset, while propofol provides improved airway anesthesia and extremely rapid clearance from the plasma. Therefore, a mixture of these agents might well be superior to either drug given alone. We wished to determine whether a mixture of methohexital and propofol is chemically and physically stable. A 1:1 mixture of propofol 10 mg/ml and methohexital was prepared. At times varying from 0 to 48 hours, mixtures with an internal standard of thymol kept at room temperature were thrice extracted with a 2:1 v/v mixture of diethyl ether:pentane, dried under nitrogen, and treated overnight with bis-trimethylsilyl-trifluoroacetamide. The resultant derivatives were transferred to microsample vials and analyzed by GC-MS. Drug stability was quantified by electronic integration of peak areas representing characteristic ions for each drug. For each sample, the peak area of the methohexital ion (m/z 239) or propofol ion (m/z 235) relative to the corresponding thymol ion (m/z 207) served as an index of the concentration of the drug in the sample. At times varying from 0 to 48 hours, mixtures without thymol were used to determine mean droplet size of the particles. This was accomplished using both an Accusizer and a Nicomp 370 Particle Sizer. One way ANOVA tested for significant changes in drug concentrations and mean particle size as a function of time. There was no significant breakdown of propofol or methohexital when combined in a 1:1 mixture and allowed to stand for 48 hours, nor was there an increase in particle size suggestive of emulsion instability. We concluded that a 1:1 mixture of propofol and methohexital was stable up to 48 hours after mixing.

摘要

麻醉药物经常混合使用或联合给药,以优化麻醉效果并将不良反应降至最低。美索比妥的优点包括成本低和起效快,而丙泊酚能改善气道麻醉且从血浆中清除极快。因此,这两种药物的混合物可能比单独使用任何一种药物都更具优势。我们希望确定美索比妥和丙泊酚的混合物在化学和物理性质上是否稳定。制备了10mg/ml丙泊酚与美索比妥的1:1混合物。在0至48小时的不同时间点,将含有内标百里酚并保存在室温下的混合物用乙醚:戊烷2:1 v/v混合物萃取三次,在氮气下干燥,并用双三甲基硅基三氟乙酰胺处理过夜。所得衍生物转移至微量样品瓶中,通过气相色谱-质谱联用仪(GC-MS)进行分析。通过对代表每种药物特征离子的峰面积进行电子积分来量化药物稳定性。对于每个样品,美索比妥离子(m/z 239)或丙泊酚离子(m/z 235)的峰面积相对于相应百里酚离子(m/z 207)的峰面积用作样品中药物浓度的指标。在0至48小时的不同时间点,使用不含百里酚的混合物来测定颗粒的平均液滴大小。这通过使用Accusizer和Nicomp 370颗粒大小分析仪来完成。单因素方差分析用于测试药物浓度和平均颗粒大小随时间的显著变化。当以1:1混合物混合并静置48小时时,丙泊酚或美索比妥没有明显分解,也没有出现表明乳液不稳定的颗粒大小增加。我们得出结论,丙泊酚和美索比妥的1:1混合物在混合后长达48小时是稳定的。

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