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Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration
An accurate, sensitive, precise, reliable, and quick method for the determination of cholesterol content by high-performance thin layer chromatography is developed. In this method, aluminum-backed precoated silica gel 60 F(254) plates were used as the stationary phase and the samples were sprayed wi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taiwan Food and Drug Administration
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351763/ https://www.ncbi.nlm.nih.gov/pubmed/28911376 http://dx.doi.org/10.1016/j.jfda.2014.07.006 |
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author | John, Jinu Reghuwanshi, Ankit Aravind, Usha K. Aravindakumar, C.T. |
author_facet | John, Jinu Reghuwanshi, Ankit Aravind, Usha K. Aravindakumar, C.T. |
author_sort | John, Jinu |
collection | PubMed |
description | An accurate, sensitive, precise, reliable, and quick method for the determination of cholesterol content by high-performance thin layer chromatography is developed. In this method, aluminum-backed precoated silica gel 60 F(254) plates were used as the stationary phase and the samples were sprayed with the help of CAMAG sample applicator Linomat 5. The chromatogram was developed with the mobile phase consisting of chloroform:methanol (9.5:0.5, v/v). The samples were detected using CAMAG Scanner 4 and evaluated using the method developed on winCATS software. Densitometric analysis of cholesterol was performed in absorbance mode at 200 nm. In this solvent system, cholesterol gave a compact spot with an R(f) value of 0.63 ± 0.03. The linear regression analysis of data for the calibration curve showed good linearity over a concentration range of 2–7 μg/spot with a regression value of 0.99933 and standard deviation of 1.44%. The limit of detection and limit of quantification were found to be 100 ng/spot and 500 ng/spot, respectively. Using the developed method, the concentration of cholesterol in the saponified and unsaponified egg yolk sample was determined. This method was found to be reproducible and can even be used for samples containing complex matrices. |
format | Online Article Text |
id | pubmed-9351763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Taiwan Food and Drug Administration |
record_format | MEDLINE/PubMed |
spelling | pubmed-93517632022-08-09 Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration John, Jinu Reghuwanshi, Ankit Aravind, Usha K. Aravindakumar, C.T. J Food Drug Anal Original Article An accurate, sensitive, precise, reliable, and quick method for the determination of cholesterol content by high-performance thin layer chromatography is developed. In this method, aluminum-backed precoated silica gel 60 F(254) plates were used as the stationary phase and the samples were sprayed with the help of CAMAG sample applicator Linomat 5. The chromatogram was developed with the mobile phase consisting of chloroform:methanol (9.5:0.5, v/v). The samples were detected using CAMAG Scanner 4 and evaluated using the method developed on winCATS software. Densitometric analysis of cholesterol was performed in absorbance mode at 200 nm. In this solvent system, cholesterol gave a compact spot with an R(f) value of 0.63 ± 0.03. The linear regression analysis of data for the calibration curve showed good linearity over a concentration range of 2–7 μg/spot with a regression value of 0.99933 and standard deviation of 1.44%. The limit of detection and limit of quantification were found to be 100 ng/spot and 500 ng/spot, respectively. Using the developed method, the concentration of cholesterol in the saponified and unsaponified egg yolk sample was determined. This method was found to be reproducible and can even be used for samples containing complex matrices. Taiwan Food and Drug Administration 2014-08-23 /pmc/articles/PMC9351763/ /pubmed/28911376 http://dx.doi.org/10.1016/j.jfda.2014.07.006 Text en © 2015 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Original Article John, Jinu Reghuwanshi, Ankit Aravind, Usha K. Aravindakumar, C.T. Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration |
title | Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration |
title_full | Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration |
title_fullStr | Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration |
title_full_unstemmed | Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration |
title_short | Development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration |
title_sort | development and validation of a high-performance thin layer chromatography method for the determination of cholesterol concentration |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351763/ https://www.ncbi.nlm.nih.gov/pubmed/28911376 http://dx.doi.org/10.1016/j.jfda.2014.07.006 |
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