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Ion-pair dispersive liquid–liquid microextraction solidification of floating organic droplets method for the rapid and sensitive detection of phenolic acids in wine samples using liquid chromatography combined with a core–shell particle column
Institution:1. College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea;2. College of Pharmacy, Research Institute of Pharmaceutical Sciences and Plant Genomics and Breeding Institute, Seoul National University, Seoul 08826, Republic of Korea;3. School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea;1. Department of Biotechnology, Chemistry and Environmental Engineering, Aalborg University, Sohngaardsholmsvej 49, 9000 Aalborg, Denmark;2. Department of Chemical and Biochemical Engineering, Technical University of Denmark, Søltofts Plads, Building 227, 2800 Kgs. Lyngby, Denmark;1. Department of Chemical Engineering and Biotechnology, National Taipei University of Technology, Taipei 10608, Taiwan;2. Department of Opto-Electronic Nano Hybrid Materials Research, Material and Chemical Research Laboratories, Industrial Technology Research Institute, Hsinchu 31040, Taiwan;1. Institute of Organic Chemistry, National Academy of Sciences of Ukraine, 5, Murmanska, 02094 Kiev, Ukraine;2. Institute of Bioorganic Chemistry & Petrochemistry, National Academy of Sciences of Ukraine, 1, Murmanska, 02660 Kiev, Ukraine
Abstract:This study describes a novel sample preparation method for extraction of phenolic acids from wine using ion pair dispersive liquid–liquid microextraction based on the solidification of a floating organic droplet (IP-DLLME-SFO). The ion-pairing technique combined with DLLME-SFO dramatically enhanced the extraction efficiency for very polar phenolic acids, such as gallic acid and protocatechuic acid, which could not be extracted by DLLME-SFO in the absence of an ion-pairing reagent. The effects of the parameters that can affect the extraction efficiency were systematically investigated, including the type and concentration of ion-pairing reagent, type and volume of extraction and dispersive solvents, extraction time, sample pH, and ion strength. The method linearity was constructed in the range of 0.01–15 μg/mL, and the sensitivity expressed as limit of detection was as low as 10 ng/mL. The method that we developed was applied for the analysis of commercial wine samples, revealing different levels of phenolic acids among these products.
Keywords:Phenolic acids  Food analysis  Food composition  Dispersive liquid–liquid microextraction  Solidification of organic droplets  Ion pairing  Wine  Core–shell particle column  Gallic acid (PubChem CID 370)  Protocatechuic acid (PubChem CID 72)  Vanillic acid (PubChem CID 8468)  Caffeic acid (PubChem CID 689043)  Ferulic acid (PubChem CID 445858)  Sinapic acid (PubChem CID 637775)  Cinnamic acid (PubChem CID 444538)
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