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高效液相色谱法同时定量测定唾液中的卡马西平、卡马西平-10,11-环氧化物、苯妥英和苯巴比妥。

Simultaneous quantitation of salivary carbamazepine, carbamazepine-10,11-epoxide, phenytoin and phenobarbitone by high-performance liquid chromatography.

作者信息

Herkes G K, McKinnon G E, Eadie M J

机构信息

Department of Medicine, Royal Brisbane Hospital, Queensland, Australia.

出版信息

J Chromatogr. 1989 Nov 10;496(1):147-54. doi: 10.1016/s0378-4347(00)82561-x.

Abstract

A rapid, sensitive and accurate high-performance liquid chromatographic method for the simultaneous quantitation of phenobarbitone, phenytoin, carbamazepine and carbamazepine-10,11-epoxide in saliva is described. Only small volumes of saliva (100 microliters) are required. Separation of the drugs is achieved by reversed-phase chromatography on a Nova-Pak C18 column, with a mobile phase of acetonitrile-phosphate buffer at a flow-rate of 2.0 ml/min. Detection is effected by ultra-violet absorption at 215 nm. The total run time is under 12.5 min per assay. A precipitation but no extraction step is involved, simplifying the assay method. Salivary concentrations in the range 0.25-25 micrograms/ml for carbamazepine, 0.5-20 micrograms/ml for phenytoin and phenobarbitone and 0.4-20 micrograms/ml for carbamazepine-10,11-epoxide can be measured. Recovery varies from 94 to 108%. The method has been used for routine measurements of anticonvulsants in saliva collected daily from patients with intractable epilepsy.

摘要

本文描述了一种快速、灵敏且准确的高效液相色谱法,用于同时定量测定唾液中的苯巴比妥、苯妥英、卡马西平和卡马西平-10,11-环氧化物。仅需少量唾液(100微升)。药物通过在Nova-Pak C18柱上的反相色谱法分离,流动相为乙腈-磷酸盐缓冲液,流速为2.0毫升/分钟。通过在215纳米处的紫外吸收进行检测。每次测定的总运行时间在12.5分钟以内。该方法涉及沉淀步骤但不涉及萃取步骤,简化了测定方法。卡马西平的唾液浓度测定范围为0.25 - 25微克/毫升,苯妥英和苯巴比妥为0.5 - 20微克/毫升,卡马西平-10,11-环氧化物为0.4 - 20微克/毫升。回收率在94%至108%之间。该方法已用于对难治性癫痫患者每日采集的唾液中的抗惊厥药物进行常规测定。

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