Analysis of dimeric cyanine–nucleic acid dyes by capillary zone electrophoresis in N, N-dimethylacetamide as non-aqueous organic solvent

A method based on capillary zone electrophoresis is presented for the determination of the purity of commercial dimeric cyanine dyes (TOTO, YOYO, BOBO, all -1 and -3 species, LOLO-1, POPO-1) that are common as fluorescent probes for nucleic acid staining. These dyes are tetracharged cations, and hav...

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Veröffentlicht in:Journal of Chromatography A 2002-03, Vol.950 (1), p.249-255
Hauptverfasser: Muzikar, Jan, Rozing, Gerard, van de Goor, Tom, Eberwein, Christine, Kenndler, Ernst
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container_issue 1
container_start_page 249
container_title Journal of Chromatography A
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creator Muzikar, Jan
Rozing, Gerard
van de Goor, Tom
Eberwein, Christine
Kenndler, Ernst
description A method based on capillary zone electrophoresis is presented for the determination of the purity of commercial dimeric cyanine dyes (TOTO, YOYO, BOBO, all -1 and -3 species, LOLO-1, POPO-1) that are common as fluorescent probes for nucleic acid staining. These dyes are tetracharged cations, and have a strong tendency to interact with negatively charged centres, where they are rapidly adsorbed, especially from aqueous solutions. Thus anionic sites at the capillary wall must be avoided, and aqueous buffers are not suitable. The method introduced here avoids both complications, using non-aqueous N, N-dimethylacetamide as solvent, and suppressing the dissociation of silanol groups at the capillary surface due to selection of acidic separation conditions (20 mmol/l perchloric acid as background electrolyte). The present method enables the determination of the purity of all 10 dyes in less than 15 min. The selectivity of the method allows separation of at least five main and differentiating a number of unresolved minor contaminants as demonstrated in detail for TOTO-3 as an example. Quantitation (with 100% normalisation of the peak areas) of nine lots of this dye results in a purity between 33 and 87%.
doi_str_mv 10.1016/S0021-9673(02)00055-9
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These dyes are tetracharged cations, and have a strong tendency to interact with negatively charged centres, where they are rapidly adsorbed, especially from aqueous solutions. Thus anionic sites at the capillary wall must be avoided, and aqueous buffers are not suitable. The method introduced here avoids both complications, using non-aqueous N, N-dimethylacetamide as solvent, and suppressing the dissociation of silanol groups at the capillary surface due to selection of acidic separation conditions (20 mmol/l perchloric acid as background electrolyte). The present method enables the determination of the purity of all 10 dyes in less than 15 min. The selectivity of the method allows separation of at least five main and differentiating a number of unresolved minor contaminants as demonstrated in detail for TOTO-3 as an example. 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subjects Acetamides - chemistry
Analytical, structural and metabolic biochemistry
Biological and medical sciences
Carbocyanines - chemistry
Coloring Agents - chemistry
Cyanine-nucleic acid dyes
Cyanine–nucleic acid
Dimerization
Dyes
Electrophoresis, Capillary - methods
Fundamental and applied biological sciences. Psychology
General aspects, investigation methods
N, N-Dimethylacetamide
Nucleic acid dyes
Nucleic acids
Nucleic Acids - chemistry
Photochemistry
title Analysis of dimeric cyanine–nucleic acid dyes by capillary zone electrophoresis in N, N-dimethylacetamide as non-aqueous organic solvent
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