环境水体中叶绿素a、b和β-胡萝卜素的测定:管内固相微萃取-在线纳米液相色谱法减少浪费和分析时间

IF 5.2 Q1 CHEMISTRY, ANALYTICAL
C. Soto, R. Herráez-Hernández, P. Campíns-Falcó
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引用次数: 1

摘要

叶绿素和类胡萝卜素是水质的指标。提出了一种基于管内固相微萃取(IT-SPME)与二极管阵列检测纳米液相色谱(NanoLC-DAD)在线耦合的新方法。本文旨在提供选择性和灵敏度,分析时间约为10分钟,友好溶剂残留量低,5µL/次乙醇:水95:5和250µL乙醇,用于从30 mL水中溶解尼龙过滤器(0.45µm,13 mm)中保留的颜料。IT-SPME毛细管是一种熔融二氧化硅毛细管(10 cm长x 75µm内径,i.d.),带有原硅酸乙酯(TEOS)、掺杂有SiO2纳米颗粒(NP)的三乙肟甲基硅烷(MTEOS)涂层,并使用Zorbax 300SB-C18分析柱(50 mm x 75µm.i.d.,3.5µm粒径)。叶绿素a、叶绿素b和β-胡萝卜素的回收率分别为93±8%、92±7%和94±4%。该方法在叶绿素a和β-胡萝卜素高达300µg L−1和叶绿素b高达600µg L‑1的范围内显示出良好的线性。样品中达到的检测限(LOD)为叶绿素a和γ-胡萝卜素0.1µg L‐1,叶绿素b 0.2µg L1。获得的相对标准偏差(RSD)值以%表示,介于2和3之间。颜料在短分析时间内成功测定,在真实水样中的残留量最小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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.

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