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采用柱切换结合离子对色谱法并利用短波长紫外检测对生物流体中的离子药物进行灵敏的高效液相色谱测定:应用于碱性化合物。

Sensitive high-performance liquid chromatographic determination of ionic drugs in biological fluids with short-wavelength ultraviolet detection using column switching combined with ion-pair chromatography: application to basic compounds.

作者信息

Yamashita K, Motohashi M, Yashiki T

机构信息

Analytical Laboratories, Takeda Chemical Industries, Ltd., Osaka, Japan.

出版信息

J Chromatogr. 1989 Feb 24;487(2):357-63. doi: 10.1016/s0378-4347(00)83043-1.

DOI:10.1016/s0378-4347(00)83043-1
PMID:2723002
Abstract

A highly sensitive and selective high-performance liquid chromatographic method with short-wavelength UV detection is described for the determination of ionic compounds in biological fluids, which was applied to two basic compounds, 2-(3-[4-(4-fluorophenyl)-1-piperazinyl]propyl)-6,7,8,9-tetrahydro-2H-nap htho [2,3-b][1,4]oxazin-3(4H)-one (I) and methyl 2-(4-diphenylmethyl-1-piperazinyl)ethyl (+/-)-1,4-dihydro-2,6-dimethyl-4-(m-nitrophenyl)-3,5-pyridinedicarboxyla te (II), in human serum. The method is based on the combination of the column-switching technique and ion-pair chromatography. In the first ODS column, the analyte is pre-separated from endogenous substances in serum by ion-pair chromatography. After column switching, in the second ODS column the heart-cut fraction containing the analyte is further separated by non-ion-pair chromatography from coeluted endogenous substances from the first ODS column. The proposed method offered high sensitivity and selectivity with UV detection at 215 nm for I and 230 nm for II. The detection limits were 0.2 ng/ml for both I and II using 1 ml of serum. The principle of the proposed method would be applicable to both acidic and basic compounds in biological fluids with a suitable ion-pair reagent.

摘要

本文描述了一种采用短波长紫外检测的高灵敏度、高选择性高效液相色谱法,用于测定生物流体中的离子化合物,并将其应用于测定人血清中的两种碱性化合物,即2-(3-[4-(4-氟苯基)-1-哌嗪基]丙基)-6,7,8,9-四氢-2H-萘并[2,3-b][1,4]恶嗪-3(4H)-酮(I)和2-(4-二苯甲基-1-哌嗪基)乙基(±)-1,4-二氢-2,6-二甲基-4-(间硝基苯基)-3,5-吡啶二甲酸酯(II)。该方法基于柱切换技术与离子对色谱法的结合。在第一根ODS柱上,通过离子对色谱法将分析物与血清中的内源性物质预分离。柱切换后,在第二根ODS柱上,含有分析物的中心切割馏分通过非离子对色谱法进一步与第一根ODS柱共洗脱的内源性物质分离。所提出的方法在215nm处对I进行紫外检测,在230nm处对II进行紫外检测,具有高灵敏度和选择性。使用1ml血清时,I和II的检测限均为0.2ng/ml。所提出方法的原理适用于使用合适离子对试剂的生物流体中的酸性和碱性化合物。

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