Cargando…

In-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction

Cyclodextrins (CDs) as a pseudophase in pseudophase-to-pseudophase microextraction (P(2)ME) in capillary zone electrophoresis (CZE) are proposed. In this P(2)ME mode called CD to admicelle ME, a long plug of dilute analyte solution prepared in cetyltrimethylammonium bromide (CTAB) at the critical mi...

Descripción completa

Detalles Bibliográficos
Autores principales: Vaas, Andaravaas Patabadige Jude P., Yu, Raymond B., Quirino, Joselito P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411250/
https://www.ncbi.nlm.nih.gov/pubmed/35978220
http://dx.doi.org/10.1007/s00216-022-04230-0
_version_ 1784775275149524992
author Vaas, Andaravaas Patabadige Jude P.
Yu, Raymond B.
Quirino, Joselito P.
author_facet Vaas, Andaravaas Patabadige Jude P.
Yu, Raymond B.
Quirino, Joselito P.
author_sort Vaas, Andaravaas Patabadige Jude P.
collection PubMed
description Cyclodextrins (CDs) as a pseudophase in pseudophase-to-pseudophase microextraction (P(2)ME) in capillary zone electrophoresis (CZE) are proposed. In this P(2)ME mode called CD to admicelle ME, a long plug of dilute analyte solution prepared in cetyltrimethylammonium bromide (CTAB) at the critical micellar concentration was injected into the capillary. This formed CTAB admicelles at the interface between the solution and the negatively charged capillary surface, where the analytes were trapped. The injection of CD solution released the admicelles and the analytes from the capillary surface due to the formation of stable CD/CTAB inclusion complexes. The analytes are concentrated at the CD front during injection and voltage separation. Various neutral CDs were found to be effective for CD to admicelle ME. To implement this in-line sample concentration technique in CZE, CD concentration, sample injection time, and sample:CD solution injection ratio were optimized. The optimized conditions for five model anionic analytes, namely, 4-bromophenol, sulindac, sulfamethizole, 4-vinylbenzoic acid, and succinylsulfathiazole, were 20 mM α-CD in 20 mM sodium tetraborate (pH 9.2) solution, sample injection time of 370 s, and CD:sample injection ratio of 1:2. The sensitivity enhancement factors (SEFs) were between 112 and 168. The SEFs of sulindac and sulfamethizole in particular were similar to previously published off-line microextraction techniques, which are typically time-consuming. The calculated values of LOQ, intra-/inter-day (n = 6/n = 10, 3 days) repeatability, and linearity (R(2)) of CD to admicelle ME were 0.0125–0.05 µg/mL, 1.5–4.6%, 1.8–4.8%, and ≥0.999, respectively. Finally, the potential of CD to admicelle ME to the analysis of artificial urine samples was demonstrated. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-022-04230-0.
format Online
Article
Text
id pubmed-9411250
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-94112502022-08-27 In-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction Vaas, Andaravaas Patabadige Jude P. Yu, Raymond B. Quirino, Joselito P. Anal Bioanal Chem Research Paper Cyclodextrins (CDs) as a pseudophase in pseudophase-to-pseudophase microextraction (P(2)ME) in capillary zone electrophoresis (CZE) are proposed. In this P(2)ME mode called CD to admicelle ME, a long plug of dilute analyte solution prepared in cetyltrimethylammonium bromide (CTAB) at the critical micellar concentration was injected into the capillary. This formed CTAB admicelles at the interface between the solution and the negatively charged capillary surface, where the analytes were trapped. The injection of CD solution released the admicelles and the analytes from the capillary surface due to the formation of stable CD/CTAB inclusion complexes. The analytes are concentrated at the CD front during injection and voltage separation. Various neutral CDs were found to be effective for CD to admicelle ME. To implement this in-line sample concentration technique in CZE, CD concentration, sample injection time, and sample:CD solution injection ratio were optimized. The optimized conditions for five model anionic analytes, namely, 4-bromophenol, sulindac, sulfamethizole, 4-vinylbenzoic acid, and succinylsulfathiazole, were 20 mM α-CD in 20 mM sodium tetraborate (pH 9.2) solution, sample injection time of 370 s, and CD:sample injection ratio of 1:2. The sensitivity enhancement factors (SEFs) were between 112 and 168. The SEFs of sulindac and sulfamethizole in particular were similar to previously published off-line microextraction techniques, which are typically time-consuming. The calculated values of LOQ, intra-/inter-day (n = 6/n = 10, 3 days) repeatability, and linearity (R(2)) of CD to admicelle ME were 0.0125–0.05 µg/mL, 1.5–4.6%, 1.8–4.8%, and ≥0.999, respectively. Finally, the potential of CD to admicelle ME to the analysis of artificial urine samples was demonstrated. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-022-04230-0. Springer Berlin Heidelberg 2022-08-18 2022 /pmc/articles/PMC9411250/ /pubmed/35978220 http://dx.doi.org/10.1007/s00216-022-04230-0 Text en © Crown 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Paper
Vaas, Andaravaas Patabadige Jude P.
Yu, Raymond B.
Quirino, Joselito P.
In-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction
title In-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction
title_full In-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction
title_fullStr In-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction
title_full_unstemmed In-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction
title_short In-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction
title_sort in-line sample concentration in capillary electrophoresis by cyclodextrin to admicelle microextraction
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9411250/
https://www.ncbi.nlm.nih.gov/pubmed/35978220
http://dx.doi.org/10.1007/s00216-022-04230-0
work_keys_str_mv AT vaasandaravaaspatabadigejudep inlinesampleconcentrationincapillaryelectrophoresisbycyclodextrintoadmicellemicroextraction
AT yuraymondb inlinesampleconcentrationincapillaryelectrophoresisbycyclodextrintoadmicellemicroextraction
AT quirinojoselitop inlinesampleconcentrationincapillaryelectrophoresisbycyclodextrintoadmicellemicroextraction