Polyimide stripping device for producing detection windows on fused-silica tubing used in capillary electrophoresis

1991 ◽  
Vol 63 (7) ◽  
pp. 750-752 ◽  
Author(s):  
Randy M. McCormick ◽  
Robert J. Zagursky
Keyword(s):  
Capillary Electrophoresis ◽  
Fused Silica

Variation of zeta-potential with temperature in fused-silica capillaries used for capillary electrophoresis

2006 ◽  
Vol 27 (3) ◽  
pp. 672-676 ◽  
Author(s):  
Christopher J. Evenhuis ◽  
Rosanne M. Guijt ◽  
Miroslav Macka ◽  
Philip J. Marriott ◽  
Paul R. Haddad
Keyword(s):  
Capillary Electrophoresis ◽  
Zeta Potential ◽  
Fused Silica ◽  
Fused Silica Capillaries ◽  
Silica Capillaries

Capillary electrophoresis of wheat gliadin proteins and its potential for wheat varietal identification using pattern matching software

2001 ◽  
Vol 52 (8) ◽  
pp. 839 ◽  
Author(s):  
S. Siriamornpun ◽  
M. Wootton ◽  
J. M. Cox ◽  
F. Bekes ◽  
C. W. Wrigley
Keyword(s):  
Capillary Electrophoresis ◽  
Pattern Matching ◽  
Processing Parameters ◽  
Peak Height ◽  
Fused Silica ◽  
Constant Current ◽  
Good Resolution ◽  
Relative Mobility ◽  
Window Width ◽  
Relative Standard

Gliadins from 11 wheat flours were extracted with 30% ethanol and fractionated by capillary electrophoresis on a 20-µm i.d. untreated fused silica capillary using 0.1 M phosphate buffer (pH 2.5) containing polymer modifier. Capillary electrophoresis conducted at a constant current provided very good resolution and reproducibility (relative standard deviation <0.5) in mp;lt;15 min. Pattern matching of the profiles was performed with the PatMatch program to provide quantitative comparisons, using the relative mobility and intensity data for each gliadin protein. Data processing parameters, including the integration of the electrophoregram, were optimised for separation of gliadins extracted from either whole-grain or flour samples. The reproducibility and repeatability were compared using peak height and/or area percentages. The optimal window width for identifying matching gliadin peaks was 0.80–1.20% relative mobility units. Using these conditions, it was concluded that unknown varieties could be identified with a confidence level of 90–95%.

scholarly journals Development of a Capillary Electrophoresis Method for the Enantioselective Estimation of Primaquine in Pharmaceutical Formulations

2008 ◽  
Vol 91 (3) ◽  
pp. 536-541 ◽  
Author(s):  
Abdalla A Elbashir ◽  
Bahruddin Saad ◽  
Abdussalam Salhin Mohamed Ali ◽  
Muhammad Idiris Saleh
Keyword(s):  
Capillary Electrophoresis ◽  
Applied Voltage ◽  
Pharmaceutical Formulations ◽  
Fused Silica ◽  
Chiral Selector ◽  
Effective Length ◽  
Racemic Mixture ◽  
Injection Time ◽  
Relative Standard ◽  
Capillary Temperature

Abstract A capillary electrophoresis (CE) method has been developed that allows the separation and estimation of primaquine enantiomers using hydroxypropyl--cyclodextrin (HP--CD) as a chiral selector. The influence of chemical and instrumental parameters on the separation, such as type and concentration of CD, buffer concentration, buffer pH, applied voltage, capillary temperature, and injection time, were investigated. Good separation of the racemic mixture of primaquine was achieved using a fused-silica capillary (52.5 cm effective length 50 m id) and a background electrolyte composed of tris-phosphate buffer solution (50 mM, pH 2.5) containing 15 mM HP--CD as a chiral selector. The recommended applied voltage, capillary temperature, and injection time were 15 kV, 25C, and 6 s, respectively. Within-day and interday reproducibility of peak area and migration time gave relative standard deviation values ranging from 1.053.30. Good recoveries (range of 96.8104.9) were obtained from the determination of placebos that were spiked with 0.251.00 mg/L primaquine. The proposed CE method was successfully applied to the assay of primaquine diphosphate in pharmaceutical formulations (tablets).

High Throughput Speciation Analysis of Mercury in Water Environment by Short Column Capillary Electrophoresis On-Line Coupled with Inductively Coupled Plasma Mass Spectrometry

2011 ◽  
Vol 383-390 ◽  
pp. 790-795
Author(s):  
Bao Hui Li ◽  
Bao Juan Tian
Keyword(s):  
Mass Spectrometry ◽  
Capillary Electrophoresis ◽  
High Throughput ◽  
Inductively Coupled Plasma ◽  
Speciation Analysis ◽  
Fused Silica ◽  
Short Column ◽  
Inductively Coupled ◽  
Icp Ms ◽  
Plasma Mass Spectrometry

A method for mercury high throughput rapid speciation analysis was built by short column capillary electrophoresis (SC-CE) coupled with inductively coupled plasma mass spectrometry (ICP-MS). A micromist nebulizer was employed to increase the nebulization efficiency and a laboratory-made removable SC-CE-ICP-MS interface on the basis of cross design was applied to alleviate buffer contamination of ICP-MS. In less than 60 s methylmercury (MeHg(I)) and inorganic mercury (Hg(II)) were separated in a 16 × 75 μm i.d. short column fused-silica capillary at 21 kV, while a mixture of 30 mmol/L boric aicd + 5% (v/v) CH3OH (pH=8.60) acted as running electrolyte. The precisions (RSD, n=5) of migration time and peak area for MeHg(I) and Hg(II) were in the range of 1.4-2.6% and 3.3-3.4%, respectively. The limits of detection (3σ) mercury species were 9.7 and 12.0 μg/L, respectively. The recoveries for Hg(II) MeHg(I) were in the range of 96-107% and 99-105%.

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