首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Direct determination of pindolol enantiomers in human serum by column-switching LC-MS/MS using a phenylcarbamate-beta-cyclodextrin chiral column.
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Direct determination of pindolol enantiomers in human serum by column-switching LC-MS/MS using a phenylcarbamate-beta-cyclodextrin chiral column.

机译:通过使用苯基氨基甲酸酯-β-环糊精手性色谱柱切换LC-MS / MS,可直接测定人血清中的Pindolol对映体。

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摘要

A direct analytical method of pindolol enantiomers in body fluids was developed by means of column-switching semi-microcolumn liquid chromatography/tandem mass spectrometry (LC-MS/MS). A pre-column packed with a silica-based cation-exchanger was used for on-line sample cleanup. Subsequent enantioseparation was conducted with a phenylcarbamate-beta-cyclodextrin (ph-beta-CD) bonded semi-micro chiral column (2.0 mm inner diameter (i.d.)). A 25-microl aliquot of serum/urine samples was directly injected into the system after simple filtration with a membrane filter. Separated enantiomers were monitored with positive electrospray ionization (ESI) and selected reaction monitoring (SRM). R(+)- and S(-)-pindolol in serum and urine were determined separately within 16 min at a resolution factor of 1.9. The detection limits at a signal-to-noise (S/N) ratio of 5 were 0.13 ng ml(-1) for both enantiomers. The linearity of the method was in the range of 0.25-100 ng ml(-1) with regression coefficient greater than 0.997. Recoveries from spiked serum and urine samples, estimated by the external standard method, were between 94.8 and 117.6% with a relative standard deviation (RSD) ranging from 2.1 to 18%.
机译:通过柱切换半微柱液相色谱/串联质谱法(LC-MS / MS)建立了体液中潘多洛尔对映体的直接分析方法。使用装有硅胶基阳离子交换剂的预柱进行在线样品净化。随后用对氨基甲酸酯-β-环糊精(ph-β-CD)键合的半微手性色谱柱(内径2.0毫米)进行对映体分离。用膜滤器简单过滤后,将25微升血清/尿液样品等分试样直接注入系统中。分离的对映异构体用正电喷雾电离(ESI)进行监测,并选择反应监测(SRM)。在16分钟内分别以1.9的分离度测定血清和尿液中的R(+)-和S(-)-哌多洛尔。两种对映异构体的信噪比(S / N)为5时的检测限为0.13 ng ml(-1)。该方法的线性范围为0.25-100 ng ml(-1),回归系数大于0.997。通过外标方法估计的加标血清和尿液样品的回收率在94.8%至117.6%之间,相对标准偏差(RSD)为2.1%至18%。

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