Determination of chlorophylls a and b and β-carotene in environmental waters: Diminishing wastes and analysis time by in-tube solid-phase microextraction coupled on-line to nano liquid chromatography
{"title":"Determination of chlorophylls a and b and β-carotene in environmental waters: Diminishing wastes and analysis time by in-tube solid-phase microextraction coupled on-line to nano liquid chromatography","authors":"C. Soto, R. Herráez-Hernández, P. Campíns-Falcó","doi":"10.1016/j.sampre.2023.100093","DOIUrl":null,"url":null,"abstract":"<div><p>Chlorophylls and carotenoids are indicators of water quality. A new method based on in-tube solid-phase microextraction (IT-SPME) coupled on-line to nano-liquid chromatography with diode array detection (NanoLC-DAD) was developed. This paper aims to provide selectivity and sensitivity with a short analysis time of about 10 min and low residues of friendly solvents, 5 µL/run of ethanol:water 95:5 and 250 µL of ethanol for dissolving the pigments retained in a nylon filter (0.45 µm, 13 mm) from 30 mL of water. IT-SPME capillary was a fused silica capillary (10 cm length x 75 µm internal diameter, i.d.) with a coating of tetraethyl orthosilicato (TEOS), triethoximethylsilane (MTEOS) doped with SiO<sub>2</sub> nanoparticles (NPs) and an analytical column Zorbax 300SB-C<sub>18</sub> (50 mm x 75 µm i.d., 3.5 µm particle size) was used. The recovery obtained to chlorophyll a, chlorophyll <em>b</em> and β-carotene were 93 ± 8 %, 92 ± 7 % and 94 ± 4 %, respectively. The method shows good linearity in the range up to 300 µg L<sup>−1</sup> for chlorophyll a and β-carotene and up to 600 µg L<sup>−1</sup> for chlorophyll <em>b</em>. The achieved limits of detection (LODs) in samples were 0.1 µg L<sup>−1</sup> to chlorophyll a and β-carotene, and 0.2 µg L<sup>−1</sup> to chlorophyll <em>b</em>. Values of relative standard deviations (RSD) expressed in% between 2 and 3 were obtained. Pigments were successfully determined with a short analysis time and minimal residues in real water samples.</p></div>","PeriodicalId":100052,"journal":{"name":"Advances in Sample Preparation","volume":"8 ","pages":"Article 100093"},"PeriodicalIF":5.2000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Sample Preparation","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772582023000438","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 1
Abstract
Chlorophylls and carotenoids are indicators of water quality. A new method based on in-tube solid-phase microextraction (IT-SPME) coupled on-line to nano-liquid chromatography with diode array detection (NanoLC-DAD) was developed. This paper aims to provide selectivity and sensitivity with a short analysis time of about 10 min and low residues of friendly solvents, 5 µL/run of ethanol:water 95:5 and 250 µL of ethanol for dissolving the pigments retained in a nylon filter (0.45 µm, 13 mm) from 30 mL of water. IT-SPME capillary was a fused silica capillary (10 cm length x 75 µm internal diameter, i.d.) with a coating of tetraethyl orthosilicato (TEOS), triethoximethylsilane (MTEOS) doped with SiO2 nanoparticles (NPs) and an analytical column Zorbax 300SB-C18 (50 mm x 75 µm i.d., 3.5 µm particle size) was used. The recovery obtained to chlorophyll a, chlorophyll b and β-carotene were 93 ± 8 %, 92 ± 7 % and 94 ± 4 %, respectively. The method shows good linearity in the range up to 300 µg L−1 for chlorophyll a and β-carotene and up to 600 µg L−1 for chlorophyll b. The achieved limits of detection (LODs) in samples were 0.1 µg L−1 to chlorophyll a and β-carotene, and 0.2 µg L−1 to chlorophyll b. Values of relative standard deviations (RSD) expressed in% between 2 and 3 were obtained. Pigments were successfully determined with a short analysis time and minimal residues in real water samples.