Publication:
Capillary electrophoresis-UV analysis using silica-layer coated capillary for separation of seven phenolic acids and caffeine and its application to tea analysis

dc.contributor.authorPattamaporn Hemwechen_US
dc.contributor.authorApinya Obmaen_US
dc.contributor.authorSasinun Detsangiamsaken_US
dc.contributor.authorSupa Wirasateen_US
dc.contributor.authorPimchai Chaiyenen_US
dc.contributor.authorPrapin Wilairaten_US
dc.contributor.authorRattikan Chantiwasen_US
dc.contributor.otherVidyasirimedhi Institute of Science and Technologyen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2022-08-04T08:17:55Z
dc.date.available2022-08-04T08:17:55Z
dc.date.issued2021-12-01en_US
dc.description.abstractAbstract: This work presents an innovative silica-layer coated capillary with comparison study of the silica-layer coated capillary and the fused-silica capillary for the separation of seven phenolic acids viz. p-hydroxyphenylacetic acid (PHPA), p-coumaric acid (PCA), p-hydroxybenzoic acid (PHBA), caffeic acid (CFA), (3,4-dihydroxyphenyl)acetic acid (DHPA), gallic acid (GLA), and 2,3,4-trihydroxybenzoic acid (THBA), together with caffeine (CF), by capillary electro-chromatography (CEC) and micellar electrokinetic chromatography (MEKC), respectively. The running buffer was 25.0 mM borate at pH 9.0, with addition of 50.0 mM sodium dodecyl sulfate for the MEKC mode. The non-coated capillary could not separate all seven phenolic acids by CEC or MEKC. This was achieved using the coated capillary for both CEC and MEKC. The innovative coated capillary with CEC had plate number N ≥ 2.0 × 104 m−1 and resolution Rs ≥ 1.6 for all adjacent pairs of peaks. The capillary was also able to separate GLA and THBA which are structural isomers. Although MEKC mode provided comparable efficiency and selectivity, the reduced EOF of the coated capillary led to longer separation time. The linear calibration range of the seven phenolic acids and caffeine were different but the coefficients of determinations (r2) were all > 0.9965. The precisions of the relative migration times and peak area ratios of analyte to internal standard were 0.1–1.8% and 1.8–6.8%, respectively. There were no statistical differences in the efficiency of separation of the phenolic acids and caffeine for three coated capillaries. It was applied to the analysis of caffeine and phenolic acids in brewed tea using tyramine as the internal standard. The tea samples were diluted prior to analysis by CEC. The separation was less than 15 min. Caffeine, gallic acid and p-coumaric acid were detected and quantified. Caffeine and gallic acid contents were 10.8–15.0 and 2.6–4.8 mg g−1 dry tea leaves, respectively. p-Coumaric acid was detected in only one of the samples with a content of 0.4 mg g−1. Percent recoveries of spiked diluted samples were 90 ± 9 to 106 ± 13%, respectively. Article highlights: Silica-layer coated capillary is first reported for simultaneous separation of seven phenolic acids by non-MEKC analysis.Performance between coated, and non-coated capillaries with analysis by CEC and MEKC were compared.Plate number, resolution, capillary reproducibility, and electroosmotic flow mobility are investigated. Graphical abstract: [Figure not available: see fulltext.].en_US
dc.identifier.citationSN Applied Sciences. Vol.3, No.12 (2021)en_US
dc.identifier.doi10.1007/s42452-021-04849-1en_US
dc.identifier.issn25233971en_US
dc.identifier.other2-s2.0-85119092765en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/76489
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85119092765&origin=inwarden_US
dc.subjectChemical Engineeringen_US
dc.subjectEarth and Planetary Sciencesen_US
dc.subjectEngineeringen_US
dc.subjectEnvironmental Scienceen_US
dc.subjectMaterials Scienceen_US
dc.subjectPhysics and Astronomyen_US
dc.titleCapillary electrophoresis-UV analysis using silica-layer coated capillary for separation of seven phenolic acids and caffeine and its application to tea analysisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85119092765&origin=inwarden_US

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