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Novel biosensing system for the simultaneous multiplex fluorescent determination of catecholamines and their metabolites in biological liquidsстатья Исследовательская статья
Статья опубликована в высокорейтинговом журнале
Информация о цитировании статьи получена из
Web of Science,
Scopus
Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 10 августа 2018 г.
- Авторы: Македонская М.И., Веселова И.А., Калмыков С.Н., Шеховцова Т.Н.
- Журнал: Journal of Pharmaceutical and Biomedical Analysis
- Том: 156
- Год издания: 2018
- Издательство: Elsevier BV
- Местоположение издательства: Netherlands
- Первая страница: 133
- Последняя страница: 141
- DOI: 10.1016/j.jpba.2018.04.026
- Аннотация: A novel original biosensing system for the simultaneous multiplex determination of general markers of catecholamine-producing diseases – catecholamines (dopamine, epinephrine, norepinephrine) and their metabolites (homovanillic and vanillylmandelic acids) in biological liquids without preliminary separation of analytes, in the absence of specific antibodies and receptors and with minimum pretreatment of a samples has been developed. This outstanding approach includes the unique combination of obtaining highly fluorescent derivatives of the analytes as a result of their interaction with two different amines ̶ benzylamine and 1,2-diphenylethylenediamine in the presence of peroxidase as a catalyst, with the application of first-order derivative fluorescence spectroscopy for the resolution of their spectra. Fluorescence is measured in 96-well microplates, which wells contain a bio-recognizing film consisted of horseradish peroxidase immobilized in the polymer chitosan. Spectra of the solutions are recorded in the range 400–500 nm (λex ~ 305–356 nm). The proposed procedures provide sensitive (in the range of 3–200 nM), selective, and reproducible (RSDs ≤ 1 %, n = 6) multiplex determination of the catecholamines and their metabolites in biological liquids were successfully applied for the rapid simultaneous (20 samples per 15–30 min) screening of human urine and mice blood plasma. The validated results showed good linearity, precision, accuracy and selectivity of this method.
- Добавил в систему: Веселова Ирина Анатольевна