Rapid quantification of miglustat in human plasma and cerebrospinal fluid by liquid chromatography coupled with tandem mass spectrometry

被引:18
作者
Guitton, Jerome [1 ,2 ,3 ]
Coste, Sylvie [4 ]
Guffon-Fouilhoux, Nathalie [3 ,5 ]
Cohen, Sabine [4 ]
Manchond, Monique [4 ]
Guillaumont, Marc [4 ]
机构
[1] Ctr Hosp Lyon Sud, Hosp Civils Lyon, Lab Ciblage Therapeut Cancerol, F-69495 Pierre Benite, France
[2] Univ Lyon 1, Fac Pharm, Toxicol Lab, ISPB, F-69008 Lyon, France
[3] Univ Lyon, Fac Med A Carrel, Lab Inserm Metab & Malad Metab U820, F-69372 Lyon, France
[4] Ctr Hosp Lyon Sud, Hosp Civils Lyon, Toxicol & Biochem Lab, F-69495 Pierre Benite, France
[5] Hop Edouard Herriot, Hosp Civils Lyon, Serv Malad Metab, F-69437 Lyon, France
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2009年 / 877卷 / 03期
关键词
Miglustat; OGT; 918; Deoxynojirimycin; Mass spectrometry; Liquid chromatography; SEPARATION;
D O I
10.1016/j.jchromb.2008.11.040
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Miglustat (OGT 918) is an iminosugar recently introduced in therapeutic as potential alternative therapy in disorders found in several diseases such as Tay-Sachs, Gaucher or Niemann-Pick diseases. A highly sensitive liquid-chromatography-electrospray tandem mass spectrometry (LC-MS/MS) assay was developed for the quantification of miglustat in human plasma and cerebrospinal fluid (CSF). The sample preparation consists in a simple protein precipitation with a mixture of acetonitrile/methanol (75/25) which yields 100% recovery. The isocratic separation utilizes an Atlantis Hilic (3 mu m, 150 mm x 2.1 mm) column, with a mobile phase of acetonitrile/water/ammonium acetate buffer (75/10/15, v/v/v) delivered at 230 mu l/min. Selected reaction monitoring (SRM) mode was used with the transitions m/z 220 -> 158 for the miglustat and m/z 208 -> m/z 146 for the miglitol (internal standard). Good linearity was observed in a range from 125 to 2500ng/ml and from 50 to 1000ng/ml, for plasma and CSF, respectively. The within-run precision of the assay was less than 6%, and the between-run run precision was less than 6.5%, for six replicates at each of three concentrations and evaluated on three separated days for both plasma and CSF mediums. Assay accuracy was in the range of 98-106.5%. Stability of miglustat was reported under a variety of storage conditions. The miglustat concentrations in two children are presented to demonstrate the clinical interest of this new method. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 154
页数:6
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