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Application of Butylamine as a Conjugative Reagent to On-Column Derivatization for the Determination of Antioxidant Amino Acids in Brain Tissue, Plasma, and Urine Samples
(1) Antioxidants are involved in body protection mechanisms against reactive oxygen species. Amino acids such as glutathione (GSH) and N-acetylcysteine (NAC) are known to be involved in providing protection against oxidative lethality. A quick and simple method for the determination of NAC and GSH i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651812/ https://www.ncbi.nlm.nih.gov/pubmed/31284671 http://dx.doi.org/10.3390/ijms20133340 |
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author | Borowczyk, Kamila Olejarz, Patrycja Kamińska, Adrianna Głowacki, Rafał Chwatko, Grażyna |
author_facet | Borowczyk, Kamila Olejarz, Patrycja Kamińska, Adrianna Głowacki, Rafał Chwatko, Grażyna |
author_sort | Borowczyk, Kamila |
collection | PubMed |
description | (1) Antioxidants are involved in body protection mechanisms against reactive oxygen species. Amino acids such as glutathione (GSH) and N-acetylcysteine (NAC) are known to be involved in providing protection against oxidative lethality. A quick and simple method for the determination of NAC and GSH in various biological matrices such as urine, plasma, and homogenates of brain tissues has been developed and described in this work. (2) The assay is based on reversed phase high performance liquid chromatography with spectrofluorimetric detection and on-column derivatization. Butylamine and o-phthaldialdehyde have been used as derivatization reagents. Since o-phthaldialdehyde constitutes a part of the mobile phase, the derivatization reaction and chromatographic separation occur simultaneously. (3) Linearity in the detector response for NAC in human urine was observed in the range of 5–200 nmol mL(−1), and NAC and GSH in the brain tissue homogenates were observed in the range of 0.5–5 nmol mL(−1) and 0.5–15 nmol mL(−1), respectively. Human plasma linearity ranges covered 0.25–5.00 nmol mL(−1) and 0.5–15 nmol mL(−1) for NAC and GSH, respectively. The LODs for NAC and GSH were 0.01 and 0.02 nmol mL(−1) while the LOQs were 0.02 and 0.05 nmol mL(−1), respectively. The usefulness of the proposed method was proven through its application to real samples. |
format | Online Article Text |
id | pubmed-6651812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66518122019-08-08 Application of Butylamine as a Conjugative Reagent to On-Column Derivatization for the Determination of Antioxidant Amino Acids in Brain Tissue, Plasma, and Urine Samples Borowczyk, Kamila Olejarz, Patrycja Kamińska, Adrianna Głowacki, Rafał Chwatko, Grażyna Int J Mol Sci Article (1) Antioxidants are involved in body protection mechanisms against reactive oxygen species. Amino acids such as glutathione (GSH) and N-acetylcysteine (NAC) are known to be involved in providing protection against oxidative lethality. A quick and simple method for the determination of NAC and GSH in various biological matrices such as urine, plasma, and homogenates of brain tissues has been developed and described in this work. (2) The assay is based on reversed phase high performance liquid chromatography with spectrofluorimetric detection and on-column derivatization. Butylamine and o-phthaldialdehyde have been used as derivatization reagents. Since o-phthaldialdehyde constitutes a part of the mobile phase, the derivatization reaction and chromatographic separation occur simultaneously. (3) Linearity in the detector response for NAC in human urine was observed in the range of 5–200 nmol mL(−1), and NAC and GSH in the brain tissue homogenates were observed in the range of 0.5–5 nmol mL(−1) and 0.5–15 nmol mL(−1), respectively. Human plasma linearity ranges covered 0.25–5.00 nmol mL(−1) and 0.5–15 nmol mL(−1) for NAC and GSH, respectively. The LODs for NAC and GSH were 0.01 and 0.02 nmol mL(−1) while the LOQs were 0.02 and 0.05 nmol mL(−1), respectively. The usefulness of the proposed method was proven through its application to real samples. MDPI 2019-07-07 /pmc/articles/PMC6651812/ /pubmed/31284671 http://dx.doi.org/10.3390/ijms20133340 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Borowczyk, Kamila Olejarz, Patrycja Kamińska, Adrianna Głowacki, Rafał Chwatko, Grażyna Application of Butylamine as a Conjugative Reagent to On-Column Derivatization for the Determination of Antioxidant Amino Acids in Brain Tissue, Plasma, and Urine Samples |
title | Application of Butylamine as a Conjugative Reagent to On-Column Derivatization for the Determination of Antioxidant Amino Acids in Brain Tissue, Plasma, and Urine Samples |
title_full | Application of Butylamine as a Conjugative Reagent to On-Column Derivatization for the Determination of Antioxidant Amino Acids in Brain Tissue, Plasma, and Urine Samples |
title_fullStr | Application of Butylamine as a Conjugative Reagent to On-Column Derivatization for the Determination of Antioxidant Amino Acids in Brain Tissue, Plasma, and Urine Samples |
title_full_unstemmed | Application of Butylamine as a Conjugative Reagent to On-Column Derivatization for the Determination of Antioxidant Amino Acids in Brain Tissue, Plasma, and Urine Samples |
title_short | Application of Butylamine as a Conjugative Reagent to On-Column Derivatization for the Determination of Antioxidant Amino Acids in Brain Tissue, Plasma, and Urine Samples |
title_sort | application of butylamine as a conjugative reagent to on-column derivatization for the determination of antioxidant amino acids in brain tissue, plasma, and urine samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651812/ https://www.ncbi.nlm.nih.gov/pubmed/31284671 http://dx.doi.org/10.3390/ijms20133340 |
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