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Automated sugaring-out liquid-liquid extraction based on flow system coupled with HPLC-UV for the determination of procainamide in urine. / Nugbienyo, Lawrence; Malinina, Yulia; Garmonov, Sergei; Kamencev, Mikhail; Salahov, Ilgiz; Andruch, Vasil; Moskvin, Leonid; Bulatov, Andrey.

в: Talanta, Том 167, 15.05.2017, стр. 709-713.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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@article{9abf6b22c73245aa90e07b7ec3e05209,
title = "Automated sugaring-out liquid-liquid extraction based on flow system coupled with HPLC-UV for the determination of procainamide in urine",
abstract = "A fully automated sugaring-out assisted liquid-liquid extraction procedure was suggested. The procedure was based on the separation of the acetonitrile phase, containing a target analyte from the homogeneous sample solution after injection of sugaring-out reagent (glucose) into a mixing chamber of the flow system. Air bubbling was used to promote the extraction process and phase separation. After the fast phase separation in the mixing chamber, the acetonitrile phase containing the target analyte was transferred to an HPLC-UV system. Under the optimal conditions, the detector response of procainamide was linear in the concentration range of 6×10−7–4×10−5 mol L−1. The limit of detection, calculated from a blank test based on 3σ, was 2×10−7 mol L−1. The proposed method was successfully applied for the determination of procainamide in human urine samples and the analytical results agreed fairly well with the results obtained by reference CE method.",
keywords = "Automated sugaring-out assisted liquid-liquid extraction, Flow analysis, High-performance liquid chromatography, Procainamide, Urine",
author = "Lawrence Nugbienyo and Yulia Malinina and Sergei Garmonov and Mikhail Kamencev and Ilgiz Salahov and Vasil Andruch and Leonid Moskvin and Andrey Bulatov",
year = "2017",
month = may,
day = "15",
doi = "10.1016/j.talanta.2017.02.051",
language = "English",
volume = "167",
pages = "709--713",
journal = "Talanta",
issn = "0039-9140",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Automated sugaring-out liquid-liquid extraction based on flow system coupled with HPLC-UV for the determination of procainamide in urine

AU - Nugbienyo, Lawrence

AU - Malinina, Yulia

AU - Garmonov, Sergei

AU - Kamencev, Mikhail

AU - Salahov, Ilgiz

AU - Andruch, Vasil

AU - Moskvin, Leonid

AU - Bulatov, Andrey

PY - 2017/5/15

Y1 - 2017/5/15

N2 - A fully automated sugaring-out assisted liquid-liquid extraction procedure was suggested. The procedure was based on the separation of the acetonitrile phase, containing a target analyte from the homogeneous sample solution after injection of sugaring-out reagent (glucose) into a mixing chamber of the flow system. Air bubbling was used to promote the extraction process and phase separation. After the fast phase separation in the mixing chamber, the acetonitrile phase containing the target analyte was transferred to an HPLC-UV system. Under the optimal conditions, the detector response of procainamide was linear in the concentration range of 6×10−7–4×10−5 mol L−1. The limit of detection, calculated from a blank test based on 3σ, was 2×10−7 mol L−1. The proposed method was successfully applied for the determination of procainamide in human urine samples and the analytical results agreed fairly well with the results obtained by reference CE method.

AB - A fully automated sugaring-out assisted liquid-liquid extraction procedure was suggested. The procedure was based on the separation of the acetonitrile phase, containing a target analyte from the homogeneous sample solution after injection of sugaring-out reagent (glucose) into a mixing chamber of the flow system. Air bubbling was used to promote the extraction process and phase separation. After the fast phase separation in the mixing chamber, the acetonitrile phase containing the target analyte was transferred to an HPLC-UV system. Under the optimal conditions, the detector response of procainamide was linear in the concentration range of 6×10−7–4×10−5 mol L−1. The limit of detection, calculated from a blank test based on 3σ, was 2×10−7 mol L−1. The proposed method was successfully applied for the determination of procainamide in human urine samples and the analytical results agreed fairly well with the results obtained by reference CE method.

KW - Automated sugaring-out assisted liquid-liquid extraction

KW - Flow analysis

KW - High-performance liquid chromatography

KW - Procainamide

KW - Urine

UR - http://www.scopus.com/inward/record.url?scp=85013766360&partnerID=8YFLogxK

U2 - 10.1016/j.talanta.2017.02.051

DO - 10.1016/j.talanta.2017.02.051

M3 - Article

AN - SCOPUS:85013766360

VL - 167

SP - 709

EP - 713

JO - Talanta

JF - Talanta

SN - 0039-9140

ER -

ID: 9517259