University of North Florida
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Contact Info

Stuart Chalk, Ph.D.
Department of Chemistry
University of North Florida
Phone: 1-904-620-1938
Fax: 1-904-620-3535
Email: schalk@unf.edu
Website: @unf

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Barry L. Karger

Abbrev:
Karger, B.L.
Other Names:
Address:
Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA, USA
Phone:
617-373-2867
Fax:
617-373-8795

Citations 2

"Continuous-flow Automated HPLC Analysis Of Fat-soluble Vitamins In Tablets"
J. Chromatogr. Sci. 1978 Volume 16, Issue 12 Pages 616-623
J.W. Dolan, J.R. Gant, N. Tanaka, R.W. Giese and B.L. Karger

Abstract: A prototype automated system involving continuous-flow analysis and high performance liquid chromatography (CFA/ HPLC) has been developed for the analysis of fat-soluble vitamins in individual pharmaceutical tablets. The novel features are the front-end coupling of CFA to HPLC, injection of hexane solutions on reversed phase columns, separation/quantitation of vitamins A, D2 and E within single chromatographic runs for a wide variety of tablets, and a dynamic range sufficient to accommodate the 1000-fold higher levels of vitamins A and E over D2 in the same tablets. The analysis rate is 10 samples per hour, the precision better than 6% for all three vitamins, and the recovery is 70-90% of that obtained by the standard AOAC method. Although the system is a prototype, it already greatly outperforms current manual analyzes which are time consuming, tedious, and demanding in terms of the level of skill and experience of the experimenter. Included in this work are some retention comparisons of commercial columns.
Vitamin A Vitamin D2 Vitamin E Pharmaceutical HPLC Interface Method comparison

"Automated Microanalysis Using Magnetic Beads With Commercial Capillary Electrophoretic Instrumentation"
J. Chromatogr. A 1997 Volume 781, Issue 1-2 Pages 197-204
Leonid G. Rashkovetsky, Yelena V. Lyubarskaya, Frantisek Foret, Dallas E. Hughes and Barry L. Karger*

Abstract: The potential of a new microanalytical method using magnetic beads (MBs) and commercial capillary electrophoresis (CE) instrumentation for performing enzymatic and inhibition assays, as well as for analysis of biological molecules such as antigens, substrates, etc., has been explored. A small quantity of magnetic beads containing immobilized biomolecules was injected into a neutral hydrophilic-coated fused-silica capillary. The short plug (2-3 mm) of beads was held fixed by a magnet placed in the cartridge of the CE system, without the use of frits. The beads could be replaced after each run, eliminating the need to regenerate the solid support. Two protocols were used for analysis: sequential injection (SI) and SI followed by isotachophoretic (ITP) focusing. Alkaline phosphatase (AP) and HIV-protease were used to demonstrate the SI procedure for enzymatic and inhibition assays. The second protocol, SI/ITP, was employed to quantitate an antigen (mouse mAB) using antibodies (sheep IgG towards mouse AB) immobilized on the beads. The MB-CE method, requiring only femtomole (fmol) quantities of material, can potentially be employed in diagnostic and forensic assays, kinetic studies and searching for inhibitors, ligands, receptors, etc.
Enzyme, alkaline phosphatase Enzyme, alkaline protease, HIV Antigen, mAB, mouse Blood Electrophoresis Magnetic particles Interface Sequential injection Renewable surface Immobilized antibody