Analysis of vitamin formulations by electrokinetic chromatography utilizing tetradecylammonium ions as the pseudostationary phase

Research output: Contribution to journalJournal articleResearchpeer-review

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Analysis of vitamin formulations by electrokinetic chromatography utilizing tetradecylammonium ions as the pseudostationary phase. / Næss, Øystein; Tilander, Tuija; Pedersen-Bjergaard, Stig; Rasmussen, Knut Einar.

In: Electrophoresis, Vol. 19, No. 16-17, 01.11.1998, p. 2912-2917.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Næss, Ø, Tilander, T, Pedersen-Bjergaard, S & Rasmussen, KE 1998, 'Analysis of vitamin formulations by electrokinetic chromatography utilizing tetradecylammonium ions as the pseudostationary phase', Electrophoresis, vol. 19, no. 16-17, pp. 2912-2917.

APA

Næss, Ø., Tilander, T., Pedersen-Bjergaard, S., & Rasmussen, K. E. (1998). Analysis of vitamin formulations by electrokinetic chromatography utilizing tetradecylammonium ions as the pseudostationary phase. Electrophoresis, 19(16-17), 2912-2917.

Vancouver

Næss Ø, Tilander T, Pedersen-Bjergaard S, Rasmussen KE. Analysis of vitamin formulations by electrokinetic chromatography utilizing tetradecylammonium ions as the pseudostationary phase. Electrophoresis. 1998 Nov 1;19(16-17):2912-2917.

Author

Næss, Øystein ; Tilander, Tuija ; Pedersen-Bjergaard, Stig ; Rasmussen, Knut Einar. / Analysis of vitamin formulations by electrokinetic chromatography utilizing tetradecylammonium ions as the pseudostationary phase. In: Electrophoresis. 1998 ; Vol. 19, No. 16-17. pp. 2912-2917.

Bibtex

@article{c8bd1730d8464449bec1e35444558738,
title = "Analysis of vitamin formulations by electrokinetic chromatography utilizing tetradecylammonium ions as the pseudostationary phase",
abstract = "A recently proposed method for the separation of fat-soluble vitamins by electrokinetic chromatography was further developed and investigated in the present study. The separation medium consisted of acetonitrile-water (80:20 v/v) and contained 80 mM tetradecylammonium bromide (TDA+); the content of acetonitrile served to maintain the hydrophobic vitamins dissolved during electrophoresis, while the TDA+ ions served as the pseudostationary phase. With the cathode placed at the outlet of the capillary, the fat-soluble vitamins were separated based on different hydrophobic interactions to the TDA+ ions and migrated in order of decreasing hydrophobicity prior to the electroosmotic flow. Migration time stability was significantly enhanced by the addition of 4 mu borate to the separation medium. The separation system was validated for the determination of vitamin E acetate in commercial tablets; quantitative results deviated by less than 3.5% from specified values, varying by less than 2.5% relative standard deviation (RSD) for within-day experiments, and by less than 6.5% RSD during between-day experiments. The separation system was compatible with injection solvents ranging in polarity from water to tetrahydrofuran, and was even capable of separating the water-soluble vitamins B1, B2, B12, and nicotinamide.",
keywords = "Electrokinetic chromatography, Fat-soluble vitamins, Pharmaceutical products, Tetradecylammonium bromide, Water-soluble vitamins",
author = "{\O}ystein N{\ae}ss and Tuija Tilander and Stig Pedersen-Bjergaard and Rasmussen, {Knut Einar}",
year = "1998",
month = nov,
day = "1",
language = "English",
volume = "19",
pages = "2912--2917",
journal = "Electrophoresis",
issn = "0173-0835",
publisher = "Wiley - V C H Verlag GmbH & Co. KGaA",
number = "16-17",

}

RIS

TY - JOUR

T1 - Analysis of vitamin formulations by electrokinetic chromatography utilizing tetradecylammonium ions as the pseudostationary phase

AU - Næss, Øystein

AU - Tilander, Tuija

AU - Pedersen-Bjergaard, Stig

AU - Rasmussen, Knut Einar

PY - 1998/11/1

Y1 - 1998/11/1

N2 - A recently proposed method for the separation of fat-soluble vitamins by electrokinetic chromatography was further developed and investigated in the present study. The separation medium consisted of acetonitrile-water (80:20 v/v) and contained 80 mM tetradecylammonium bromide (TDA+); the content of acetonitrile served to maintain the hydrophobic vitamins dissolved during electrophoresis, while the TDA+ ions served as the pseudostationary phase. With the cathode placed at the outlet of the capillary, the fat-soluble vitamins were separated based on different hydrophobic interactions to the TDA+ ions and migrated in order of decreasing hydrophobicity prior to the electroosmotic flow. Migration time stability was significantly enhanced by the addition of 4 mu borate to the separation medium. The separation system was validated for the determination of vitamin E acetate in commercial tablets; quantitative results deviated by less than 3.5% from specified values, varying by less than 2.5% relative standard deviation (RSD) for within-day experiments, and by less than 6.5% RSD during between-day experiments. The separation system was compatible with injection solvents ranging in polarity from water to tetrahydrofuran, and was even capable of separating the water-soluble vitamins B1, B2, B12, and nicotinamide.

AB - A recently proposed method for the separation of fat-soluble vitamins by electrokinetic chromatography was further developed and investigated in the present study. The separation medium consisted of acetonitrile-water (80:20 v/v) and contained 80 mM tetradecylammonium bromide (TDA+); the content of acetonitrile served to maintain the hydrophobic vitamins dissolved during electrophoresis, while the TDA+ ions served as the pseudostationary phase. With the cathode placed at the outlet of the capillary, the fat-soluble vitamins were separated based on different hydrophobic interactions to the TDA+ ions and migrated in order of decreasing hydrophobicity prior to the electroosmotic flow. Migration time stability was significantly enhanced by the addition of 4 mu borate to the separation medium. The separation system was validated for the determination of vitamin E acetate in commercial tablets; quantitative results deviated by less than 3.5% from specified values, varying by less than 2.5% relative standard deviation (RSD) for within-day experiments, and by less than 6.5% RSD during between-day experiments. The separation system was compatible with injection solvents ranging in polarity from water to tetrahydrofuran, and was even capable of separating the water-soluble vitamins B1, B2, B12, and nicotinamide.

KW - Electrokinetic chromatography

KW - Fat-soluble vitamins

KW - Pharmaceutical products

KW - Tetradecylammonium bromide

KW - Water-soluble vitamins

UR - http://www.scopus.com/inward/record.url?scp=0031798020&partnerID=8YFLogxK

M3 - Journal article

C2 - 9870388

AN - SCOPUS:0031798020

VL - 19

SP - 2912

EP - 2917

JO - Electrophoresis

JF - Electrophoresis

SN - 0173-0835

IS - 16-17

ER -

ID: 231655094