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Primary Amine-Included Coacervation in Alkyl Polyglucoside Micellar Solution for Supramolecular Solvent-Based Microextraction. / Ковальчук, Янина Андреевна; Вах, Кристина Степановна; Булатов, Андрей Васильевич; Сафонова, Евгения Алексеевна.

в: ACS Sustainable Chemistry and Engineering, Том 11, № 16, 24.04.2023, стр. 6302-6310.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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@article{0d6d9d57cbef42e19ca8b2c336db64ad,
title = "Primary Amine-Included Coacervation in Alkyl Polyglucoside Micellar Solution for Supramolecular Solvent-Based Microextraction",
abstract = "A phenomenon of supramolecular solvent formation in a micellar solution of alkyl polyglucoside in the presence of primary amine is presented for the first time. Primary amines were investigated as coacervation agents for supramolecular solvent formation based on alkyl polyglucosides (C8-C10 and C8-C14). It was found that addition of primary amine promoted in situ formation of tiny supramolecular solvent droplets in alkaline media followed by the separation of a water-immiscible liquid phase. The phenomenon of the formation of supramolecular solvents from an alkyl polyglucoside in an alkaline medium is presented for the first time. The phase diagrams for ternary systems based on alkyl polyglucoside-primary amine-water and physicochemical properties of the supramolecular solvents were investigated. The proposed supramolecular solvents were studied for the microextraction of sulfonamide antibiotics from biological fluids. The salting-out effect on mass-transfer was also investigated. Alkyl polyglucoside C8-C10 and 1-heptylamine provided more effective preconcentration of the antibiotics in the presence of a salting-out agent (sodium carbonate) among studied amphiphiles and coacervation agents. The microextraction procedure was applied to the chromatographic determination of antibiotics in spiked human plasma and serum samples. The limits of detection, calculated from a blank test based on 3σ, were 20 μg L-1 for all analytes.",
keywords = "HPLC-UV, alkyl polyglucoside (alkyl polyglycoside), biological fluids, microextraction, primary amine, sulfonamides, supramolecular solvent",
author = "Ковальчук, {Янина Андреевна} and Вах, {Кристина Степановна} and Булатов, {Андрей Васильевич} and Сафонова, {Евгения Алексеевна}",
year = "2023",
month = apr,
day = "24",
doi = "10.1021/acssuschemeng.2c07522",
language = "English",
volume = "11",
pages = "6302--6310",
journal = "ACS Sustainable Chemistry and Engineering",
issn = "2168-0485",
publisher = "American Chemical Society",
number = "16",

}

RIS

TY - JOUR

T1 - Primary Amine-Included Coacervation in Alkyl Polyglucoside Micellar Solution for Supramolecular Solvent-Based Microextraction

AU - Ковальчук, Янина Андреевна

AU - Вах, Кристина Степановна

AU - Булатов, Андрей Васильевич

AU - Сафонова, Евгения Алексеевна

PY - 2023/4/24

Y1 - 2023/4/24

N2 - A phenomenon of supramolecular solvent formation in a micellar solution of alkyl polyglucoside in the presence of primary amine is presented for the first time. Primary amines were investigated as coacervation agents for supramolecular solvent formation based on alkyl polyglucosides (C8-C10 and C8-C14). It was found that addition of primary amine promoted in situ formation of tiny supramolecular solvent droplets in alkaline media followed by the separation of a water-immiscible liquid phase. The phenomenon of the formation of supramolecular solvents from an alkyl polyglucoside in an alkaline medium is presented for the first time. The phase diagrams for ternary systems based on alkyl polyglucoside-primary amine-water and physicochemical properties of the supramolecular solvents were investigated. The proposed supramolecular solvents were studied for the microextraction of sulfonamide antibiotics from biological fluids. The salting-out effect on mass-transfer was also investigated. Alkyl polyglucoside C8-C10 and 1-heptylamine provided more effective preconcentration of the antibiotics in the presence of a salting-out agent (sodium carbonate) among studied amphiphiles and coacervation agents. The microextraction procedure was applied to the chromatographic determination of antibiotics in spiked human plasma and serum samples. The limits of detection, calculated from a blank test based on 3σ, were 20 μg L-1 for all analytes.

AB - A phenomenon of supramolecular solvent formation in a micellar solution of alkyl polyglucoside in the presence of primary amine is presented for the first time. Primary amines were investigated as coacervation agents for supramolecular solvent formation based on alkyl polyglucosides (C8-C10 and C8-C14). It was found that addition of primary amine promoted in situ formation of tiny supramolecular solvent droplets in alkaline media followed by the separation of a water-immiscible liquid phase. The phenomenon of the formation of supramolecular solvents from an alkyl polyglucoside in an alkaline medium is presented for the first time. The phase diagrams for ternary systems based on alkyl polyglucoside-primary amine-water and physicochemical properties of the supramolecular solvents were investigated. The proposed supramolecular solvents were studied for the microextraction of sulfonamide antibiotics from biological fluids. The salting-out effect on mass-transfer was also investigated. Alkyl polyglucoside C8-C10 and 1-heptylamine provided more effective preconcentration of the antibiotics in the presence of a salting-out agent (sodium carbonate) among studied amphiphiles and coacervation agents. The microextraction procedure was applied to the chromatographic determination of antibiotics in spiked human plasma and serum samples. The limits of detection, calculated from a blank test based on 3σ, were 20 μg L-1 for all analytes.

KW - HPLC-UV

KW - alkyl polyglucoside (alkyl polyglycoside)

KW - biological fluids

KW - microextraction

KW - primary amine

KW - sulfonamides

KW - supramolecular solvent

UR - https://www.mendeley.com/catalogue/9d58b522-1119-3bff-840c-b2ba446a0b9d/

U2 - 10.1021/acssuschemeng.2c07522

DO - 10.1021/acssuschemeng.2c07522

M3 - Article

VL - 11

SP - 6302

EP - 6310

JO - ACS Sustainable Chemistry and Engineering

JF - ACS Sustainable Chemistry and Engineering

SN - 2168-0485

IS - 16

ER -

ID: 105409152