共 10 条
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.
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页码:149 / 154
页数:6
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