Eeckhoudt S L, Desager J P, Horsmans Y, De Winne A J, Verbeeck R K
Laboratory of Pharmacokinetics (FATC 7355), School of Pharmacy, Catholic University of Louvain, Brussels, Belgium.
J Chromatogr B Biomed Sci Appl. 1998 Jun 12;710(1-2):165-71. doi: 10.1016/s0378-4347(98)00137-6.
A sensitive high-performance liquid chromatographic method is described for the quantification of midazolam and 1'-hydroxymidazolam in human plasma. Sample (1 ml plasma) preparation involved a simple solvent extraction step with a recovery of approximately 90% for both compounds. An aliquot of the dissolved residue was injected onto a 3 microm capillary C18 column (150 mm x 0.8 mm I.D.). A gradient elution was used. The initial mobile phase composition (phosphate buffer-acetonitrile, 65:35) was maintained during 16 min and was then changed linearly during a 1-min period to phosphate buffer-acetonitrile, 40:60. The flow-rate of the mobile phase was 16 microl/min and the eluate was monitored by UV detection. The limits of quantification for midazolam and 1'-hydroxymidazolam were 1 ng/ml and 0.5 ng/ml, respectively. The applicability of the method was demonstrated by studying the pharmacokinetics of midazolam, and its major metabolite 1'-hydroxymidazolam, in human volunteers following i.v. bolus administration of a subtherapeutic midazolam dose (40 microg/kg).
本文描述了一种灵敏的高效液相色谱法,用于定量测定人血浆中的咪达唑仑和1'-羟基咪达唑仑。样品(1 ml血浆)制备包括一个简单的溶剂萃取步骤,两种化合物的回收率约为90%。取一部分溶解后的残渣注入一根3微米的毛细管C18柱(150 mm×0.8 mm内径)。采用梯度洗脱。初始流动相组成(磷酸盐缓冲液-乙腈,65:35)保持16分钟,然后在1分钟内线性变化为磷酸盐缓冲液-乙腈,40:60。流动相流速为16微升/分钟,洗脱液通过紫外检测进行监测。咪达唑仑和1'-羟基咪达唑仑的定量限分别为1 ng/ml和0.5 ng/ml。通过研究咪达唑仑及其主要代谢物1'-羟基咪达唑仑在健康志愿者静脉注射低于治疗剂量的咪达唑仑(40微克/千克)后的药代动力学,证明了该方法的适用性。