Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractMixed amido/imido/guanidinato complexes of niobium: potential precursors for MOCVD of niobium nitride thin films    Next AbstractCooperative binding interactions required for function of the Ty1 sterile responsive element »

J Chromatogr A


Title:Electroosmotic flow variations caused by the volatility of buffer components: diagnosis and therapy
Author(s):Baur L; Sanger-van de Griend C; Watzig H;
Address:"Technical University of Braunschweig, Institute of Pharmaceutical Chemistry, Beethovenstrasse 55, D-38106 Braunschweig, Germany"
Journal Title:J Chromatogr A
Year:2002
Volume:979
Issue:1-Feb
Page Number:97 - 103
DOI: 10.1016/s0021-9673(02)01406-1
ISSN/ISBN:0021-9673 (Print) 0021-9673 (Linking)
Abstract:"In order to separate a polar amine pharmaceutical and its potential impurities, a micellar electrokinetic chromatography method was developed. The main compound and 11 other substances were completely separated using a 20 mM Tris buffer, pH 8.0, containing 50 mM sodium dodecylsulfate (SDS) and 24% (v/v) acetonitrile. However, a strong, continuous reduction in the EOF occurred and quantification was not possible. The EOF reproducibility could not be improved by suitable rinsing procedures. Surface effects or interactions did not cause the EOF changes, but the evaporation of acetonitrile was identified as the major source for EOF instability. However, a high concentration of acetonitrile was decisive for selectivity. Thus a reliable protection against the evaporation of this buffer constituent had to be found. Paraffin and various silicon oils were tested as covering film. In order to quickly test buffer systems if the evaporation of electrophoresis solutions is acceptable, an alternative experimental design without doing CE experiments had to be found. Electrical conductivity was chosen as parameter, because it can be determined simply and fast. The buffers under investigation were placed in a 50-ml beaker with a magnetic stirring rod, placed on a magnetic stirrer. The buffer solution was kept in motion at 120 rev./min. The beaker was covered around the measuring head with laboratory film and in addition to this with paraffin or silicon oil. An acetonitrile content up to 10% (v/v) was acceptable if a coverage was used. The various cover liquids had a similar effect. A content of 15% (v/v) already increased the evaporation effect significantly. Higher acetonitrile contents are not acceptable. A buffer similar to the originally transferred method, 20 mM Tris (pH 8.0), 50 mM SDS containing 10% (v/v) acetonitrile as well as 10% (v/v) isopropanol showed an acceptably low evaporation in the conductivity experiments. With this buffer, a stable EOF was also obtained. Conductivity measurements are generally applicable to quickly test buffers that contain organic solvents"
Keywords:"*Buffers Chromatography, Micellar Electrokinetic Capillary/*methods Osmosis Reproducibility of Results Volatilization;"
Notes:"MedlineBaur, Leonhard Sanger-van de Griend, Cari Watzig, Hermann eng Netherlands 2002/12/25 J Chromatogr A. 2002 Dec 6; 979(1-2):97-103. doi: 10.1016/s0021-9673(02)01406-1"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-12-2024