Comparison of different water-miscible solvents for the preparation of plasma and urine samples in metabolic profiling studies

被引:23
作者
Alzweiri, Muhammed [1 ]
Watson, David G. [1 ]
Robertson, Chris [2 ]
Sills, Graeme J. [3 ]
Parkinson, John A. [4 ]
机构
[1] Univ Strathclyde, Strathclyde Inst Pharmaceut & Biomed Sci, Glasgow G4 0NR, Lanark, Scotland
[2] Univ Strathclyde, Dept Stat & Modelling Sci, Glasgow G1 1XH, Lanark, Scotland
[3] Western Infirm & Associated Hosp, Univ Div Cardiovasc & Med Sci, Epilepsy Res Unit, Glasgow G11 6NT, Lanark, Scotland
[4] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, Glasgow G1 1XL, Lanark, Scotland
关键词
deproteination; phospholipids; capillary electrophoresis; desalting; LC-MS; profiling studies; metabonomics;
D O I
10.1016/j.talanta.2007.07.037
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The Lowry method and a capillary electrophoresis method were used to analyse protein residues in the supernatant after solvent deproteination of plasma. Acetonitrile and acetone were much more effective than methanol and ethanol at reducing the levels of proteins in plasma. The ability of different solvents to decrease levels of phospholipids in plasma samples was assessed using electrospray ionisation mass spectrometry (MS). Phospholipid signals can obscure differences between samples in general metabolite profiling (i.e. non-target compound) studies. Acetonitrile was much more effective than methanol in reducing the MS signal due to phospholipids in plasma which is a consequence of the poor solubility of phospholipids in acetonitrile. The capability of the solvents at reducing salts in urine samples was also studied by using an amperometric method. Using this approach little difference was detected between methanol, ethanol, acetonitrile and acetone in their ability to desalt urine samples. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1060 / 1065
页数:6
相关论文
共 31 条
[1]   Enhanced pharmaceutical analysis by CE using dynamic surface coating system [J].
Altria, KD .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2003, 31 (03) :447-453
[2]   Measurement of latex proteins and assessment of latex protein exposure [J].
Beezhold, DH ;
Kostyal, DA ;
Tomazic-Jezic, VJ .
METHODS, 2002, 27 (01) :46-51
[3]   Saturated phospholipids promote crystallization but slow down polymorphic transitions in triglyceride nanoparticles [J].
Bunjes, H ;
Koch, MHJ .
JOURNAL OF CONTROLLED RELEASE, 2005, 107 (02) :229-243
[4]   Determination of protein content using a solid phase spectrophotometric procedure [J].
Capitán-Vallvey, LF ;
Duque, O ;
Mirón-García, G ;
Checa-Moreno, R .
ANALYTICA CHIMICA ACTA, 2001, 433 (01) :155-163
[5]   An optimized protocol for metabolome analysis in yeast using direct infusion electrospray mass spectrometry [J].
Castrillo, JI ;
Hayes, A ;
Mohammed, S ;
Gaskell, SJ ;
Oliver, SG .
PHYTOCHEMISTRY, 2003, 62 (06) :929-937
[6]  
CATAI JR, 2005, J CHROMATOGR A, V185, P1083
[7]   Effects of liquid phase composition on salt cluster formation in positive ion mode electrospray mass spectrometry:: Implications for clustering mechanism in electrospray [J].
Charles, L ;
Pépin, D ;
Gonnet, F ;
Tabet, FC .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2001, 12 (10) :1077-1084
[8]   HIGH-MOLECULAR-WEIGHT POLYARGININE AS A CAPILLARY COATING FOR SEPARATION OF CATIONIC PROTEINS BY CAPILLARY ELECTROPHORESIS [J].
CHIU, RW ;
JIMENEZ, JC ;
MONNIG, CA .
ANALYTICA CHIMICA ACTA, 1995, 307 (2-3) :193-201
[9]   The comparison of plasma deproteinization methods for the detection of low-molecular-weight metabolites by 1H nuclear magnetic resonance spectroscopy [J].
Daykin, CA ;
Foxall, PJD ;
Connor, SC ;
Lindon, JC ;
Nicholson, JK .
ANALYTICAL BIOCHEMISTRY, 2002, 304 (02) :220-230
[10]  
ECKHARDT A, 2004, J CHROMATOGR A, V111, P1051