Factors influencing the determination of analyte ion surface partitioning coefficients in electrosprayed droplets

被引:18
作者
Sjöberg, PJR [1 ]
Bökman, CF [1 ]
Bylund, D [1 ]
Markides, KE [1 ]
机构
[1] Univ Uppsala, Dept Analyt Chem, SE-75121 Uppsala, Sweden
关键词
D O I
10.1016/S1044-0305(01)00281-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The observed response in mass spectrometry utilizing electrospray as a sample introduction technique can be affected by a number of factors. In this study a series of two-electrolyte systems was investigated and the mass spectrometric responses were modeled by the use of droplet surface partitioning coefficients and instrumental response factors according to a recently reported method (Sjoberg et al., Anal. Churn. 2001, 73, 23-28). The partitioning coefficient and the instrumental response factor were found to be affected by the chosen experimental conditions. Experimental parameters that were investigated include spray position relative to the orifice, spray potential, nebulizer and curtain gas flow rates, ionic strength, and organic content of the sprayed solution. The time history of the generated droplets turned out to be of importance to both the partitioning coefficients and the instrumental response factor. For example, a general increase in the surface partitioning coefficients for the tetrapentylammonium ion was initially observed when the spray was aiming closer to the sampling orifice. Furthermore, it was shown with a small amount of deuterium labeled electrolyte that the total ionic strength and not just the electrolyte concentration influence the instrumental response factor. (C) 2001 American Society for Mass Spectrometry.
引用
收藏
页码:1002 / 1010
页数:9
相关论文
共 44 条
[1]   MECHANISM OF ELECTROSPRAY MASS-SPECTROMETRY - ELECTROSPRAY AS AN ELECTROLYSIS CELL [J].
BLADES, AT ;
IKONOMOU, MG ;
KEBARLE, P .
ANALYTICAL CHEMISTRY, 1991, 63 (19) :2109-2114
[2]   ION SPRAY INTERFACE FOR COMBINED LIQUID CHROMATOGRAPHY/ATMOSPHERIC PRESSURE IONIZATION MASS-SPECTROMETRY [J].
BRUINS, AP ;
COVEY, TR ;
HENION, JD .
ANALYTICAL CHEMISTRY, 1987, 59 (22) :2642-2646
[3]   SPACE-CHARGE-DOMINATED MASS-SPECTROMETRY ION SOURCES - MODELING AND SENSITIVITY [J].
BUSMAN, M ;
SUNNER, J ;
VOGEL, CR .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1991, 2 (01) :1-10
[4]   SIMULATION METHOD FOR POTENTIAL AND CHARGE-DISTRIBUTIONS IN SPACE-CHARGE DOMINATED ION SOURCES [J].
BUSMAN, M ;
SUNNER, J .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1991, 108 (2-3) :165-178
[5]   Relating electrospray ionization response to nonpolar character of small peptides [J].
Cech, NB ;
Enke, CG .
ANALYTICAL CHEMISTRY, 2000, 72 (13) :2717-2723
[6]   Predicting electrospray response from chromatographic retention time [J].
Cech, NB ;
Krone, JR ;
Enke, CG .
ANALYTICAL CHEMISTRY, 2001, 73 (02) :208-213
[7]   Challenges in achieving a fundamental model for ESI [J].
Constantopoulos, TL ;
Jackson, GS ;
Enke, CG .
ANALYTICA CHIMICA ACTA, 2000, 406 (01) :37-52
[8]  
COOK KD, 1998, P 45 ASMS C MASS SPE, P425
[9]   High resolution size analysis of nanoparticles and ions: Running a Vienna DMA of near optimal length at Reynolds numbers up to 5000 [J].
de Juan, L ;
de la Mora, JF .
JOURNAL OF AEROSOL SCIENCE, 1998, 29 (5-6) :617-626
[10]   Differential mobility analysis of molecular ions and nanometer particles [J].
de la Mora, JF ;
de Juan, L ;
Eichler, T ;
Rosell, J .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 1998, 17 (06) :328-339