Deproteinization as a Rapid Method of Saliva Purification for the Determination of Carbamazepine and Carbamazepine-10,11 Epoxide

Saliva is a valuable diagnostic material that, in some cases, may replace blood. However, because of its different composition, its use requires the development of new, or the modification of existing, extraction procedures. Therefore, the aim of the study was to develop a method of saliva purificat...

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Main Authors: Ewelina Dziurkowska, Marek Wesolowski
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/9/4/915
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spelling doaj-a085cd9b39e14133bcd27069adb6a94e2020-11-25T02:09:54ZengMDPI AGJournal of Clinical Medicine2077-03832020-03-01991591510.3390/jcm9040915Deproteinization as a Rapid Method of Saliva Purification for the Determination of Carbamazepine and Carbamazepine-10,11 EpoxideEwelina Dziurkowska0Marek Wesolowski1Department of Analytical Chemistry, Medical University of Gdansk, Gen. J. Hallera 107, 80-416 Gdansk, PolandDepartment of Analytical Chemistry, Medical University of Gdansk, Gen. J. Hallera 107, 80-416 Gdansk, PolandSaliva is a valuable diagnostic material that, in some cases, may replace blood. However, because of its different composition, its use requires the development of new, or the modification of existing, extraction procedures. Therefore, the aim of the study was to develop a method of saliva purification that would enable the determination of carbamazepine and its metabolite, carbamazepine-10,11 epoxide. When comparing two methods of sample purification (Solid Phase Extration (SPE) and deproteinization), it was found that the second method yielded more favorable results. A 1% formic acid solution in acetonitrile was used for extraction. The samples were shaken and centrifuged, and the supernatant obtained was evaporated and dissolved in a mobile phase, then chromatographically analyzed. The developed method was validated by determining its linearity in the range of 10–5000 ng/mL for both analytes. Intra- and inter-day precision did not exceed 14%. In order to check the usefulness of the method, both analytes were determined in the saliva samples from 20 patients treated with carbamazepine. The content of both analytes was detected and determined in all of the tested samples of saliva. It was found that the method developed is rapid, sensitive, reliable, and can be used to monitor the concentration of carbamazepine and metabolite in patients’ saliva.https://www.mdpi.com/2077-0383/9/4/915salivadeproteinizationcarbamazepinecarbamazepine-10,11 epoxide
collection DOAJ
language English
format Article
sources DOAJ
author Ewelina Dziurkowska
Marek Wesolowski
spellingShingle Ewelina Dziurkowska
Marek Wesolowski
Deproteinization as a Rapid Method of Saliva Purification for the Determination of Carbamazepine and Carbamazepine-10,11 Epoxide
Journal of Clinical Medicine
saliva
deproteinization
carbamazepine
carbamazepine-10,11 epoxide
author_facet Ewelina Dziurkowska
Marek Wesolowski
author_sort Ewelina Dziurkowska
title Deproteinization as a Rapid Method of Saliva Purification for the Determination of Carbamazepine and Carbamazepine-10,11 Epoxide
title_short Deproteinization as a Rapid Method of Saliva Purification for the Determination of Carbamazepine and Carbamazepine-10,11 Epoxide
title_full Deproteinization as a Rapid Method of Saliva Purification for the Determination of Carbamazepine and Carbamazepine-10,11 Epoxide
title_fullStr Deproteinization as a Rapid Method of Saliva Purification for the Determination of Carbamazepine and Carbamazepine-10,11 Epoxide
title_full_unstemmed Deproteinization as a Rapid Method of Saliva Purification for the Determination of Carbamazepine and Carbamazepine-10,11 Epoxide
title_sort deproteinization as a rapid method of saliva purification for the determination of carbamazepine and carbamazepine-10,11 epoxide
publisher MDPI AG
series Journal of Clinical Medicine
issn 2077-0383
publishDate 2020-03-01
description Saliva is a valuable diagnostic material that, in some cases, may replace blood. However, because of its different composition, its use requires the development of new, or the modification of existing, extraction procedures. Therefore, the aim of the study was to develop a method of saliva purification that would enable the determination of carbamazepine and its metabolite, carbamazepine-10,11 epoxide. When comparing two methods of sample purification (Solid Phase Extration (SPE) and deproteinization), it was found that the second method yielded more favorable results. A 1% formic acid solution in acetonitrile was used for extraction. The samples were shaken and centrifuged, and the supernatant obtained was evaporated and dissolved in a mobile phase, then chromatographically analyzed. The developed method was validated by determining its linearity in the range of 10–5000 ng/mL for both analytes. Intra- and inter-day precision did not exceed 14%. In order to check the usefulness of the method, both analytes were determined in the saliva samples from 20 patients treated with carbamazepine. The content of both analytes was detected and determined in all of the tested samples of saliva. It was found that the method developed is rapid, sensitive, reliable, and can be used to monitor the concentration of carbamazepine and metabolite in patients’ saliva.
topic saliva
deproteinization
carbamazepine
carbamazepine-10,11 epoxide
url https://www.mdpi.com/2077-0383/9/4/915
work_keys_str_mv AT ewelinadziurkowska deproteinizationasarapidmethodofsalivapurificationforthedeterminationofcarbamazepineandcarbamazepine1011epoxide
AT marekwesolowski deproteinizationasarapidmethodofsalivapurificationforthedeterminationofcarbamazepineandcarbamazepine1011epoxide
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