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WHO prescribed shelf life assessment of Syzygium cumini extract through chromatographic and biological activity analyses
BACKGROUND: Regulatory guidelines recommend shelf life of herbal products to be established through systematic stability studies. OBJECTIVE: The study was designed to establish shelf life of Syzygium cumini extract through accelerated and long-term stability testing as per WHO guidelines. MATERIAL A...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527807/ https://www.ncbi.nlm.nih.gov/pubmed/31759785 http://dx.doi.org/10.1016/j.jaim.2019.01.003 |
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author | Kaur, Jasmeen Bansal, Gulshan |
author_facet | Kaur, Jasmeen Bansal, Gulshan |
author_sort | Kaur, Jasmeen |
collection | PubMed |
description | BACKGROUND: Regulatory guidelines recommend shelf life of herbal products to be established through systematic stability studies. OBJECTIVE: The study was designed to establish shelf life of Syzygium cumini extract through accelerated and long-term stability testing as per WHO guidelines. MATERIAL AND METHODS: The extract was stored under accelerated (40°C/75 %RH) and long-term (25°C/60 %RH) stability conditions for 6 and 30 months, respectively. Samples were withdrawn at periodic intervals and analysed through two validated HPLC-UV methods (I and II) for fingerprint and quantitative analysis of markers. Antidiabetic activity of control and stability samples was evaluated by α-glucosidase inhibitory model. RESULTS: Method I generated a well resolved fingerprint of the control sample that was found to contain gallic acid (GA, 1.45 % w/w) and ellagic acid (EA, 3.97 % w/w). The content of GA did not change under both the stability conditions, but that of EA varied insignificantly (3.97–4.77 % w/w) under long-term conditions up to 24 months and subsequently decrease to 3.15 % w/w after 30 months. There was no visible change in LC-UV fingerprint of any stability sample with respect to control. α-Glucosidase inhibitory activity of all stability samples also remained unaltered as compared to control sample (IC(50) 1.48 mg/mL). GA and EA did not elicit any activity at the concentrations present in the extract. CONCLUSION: Phytochemical composition and antidiabetic efficacy of S. cumini extract remain unchanged during its storage under both accelerated and long-term stability conditions, which suggest its shelf life to be 30 months. Also, GA and EA are not appropriate anti-diabetic markers. |
format | Online Article Text |
id | pubmed-7527807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75278072020-10-05 WHO prescribed shelf life assessment of Syzygium cumini extract through chromatographic and biological activity analyses Kaur, Jasmeen Bansal, Gulshan J Ayurveda Integr Med Original Research Article (Experimental) BACKGROUND: Regulatory guidelines recommend shelf life of herbal products to be established through systematic stability studies. OBJECTIVE: The study was designed to establish shelf life of Syzygium cumini extract through accelerated and long-term stability testing as per WHO guidelines. MATERIAL AND METHODS: The extract was stored under accelerated (40°C/75 %RH) and long-term (25°C/60 %RH) stability conditions for 6 and 30 months, respectively. Samples were withdrawn at periodic intervals and analysed through two validated HPLC-UV methods (I and II) for fingerprint and quantitative analysis of markers. Antidiabetic activity of control and stability samples was evaluated by α-glucosidase inhibitory model. RESULTS: Method I generated a well resolved fingerprint of the control sample that was found to contain gallic acid (GA, 1.45 % w/w) and ellagic acid (EA, 3.97 % w/w). The content of GA did not change under both the stability conditions, but that of EA varied insignificantly (3.97–4.77 % w/w) under long-term conditions up to 24 months and subsequently decrease to 3.15 % w/w after 30 months. There was no visible change in LC-UV fingerprint of any stability sample with respect to control. α-Glucosidase inhibitory activity of all stability samples also remained unaltered as compared to control sample (IC(50) 1.48 mg/mL). GA and EA did not elicit any activity at the concentrations present in the extract. CONCLUSION: Phytochemical composition and antidiabetic efficacy of S. cumini extract remain unchanged during its storage under both accelerated and long-term stability conditions, which suggest its shelf life to be 30 months. Also, GA and EA are not appropriate anti-diabetic markers. Elsevier 2020 2019-11-20 /pmc/articles/PMC7527807/ /pubmed/31759785 http://dx.doi.org/10.1016/j.jaim.2019.01.003 Text en © 2019 The Authors http://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/). |
spellingShingle | Original Research Article (Experimental) Kaur, Jasmeen Bansal, Gulshan WHO prescribed shelf life assessment of Syzygium cumini extract through chromatographic and biological activity analyses |
title | WHO prescribed shelf life assessment of Syzygium cumini extract through chromatographic and biological activity analyses |
title_full | WHO prescribed shelf life assessment of Syzygium cumini extract through chromatographic and biological activity analyses |
title_fullStr | WHO prescribed shelf life assessment of Syzygium cumini extract through chromatographic and biological activity analyses |
title_full_unstemmed | WHO prescribed shelf life assessment of Syzygium cumini extract through chromatographic and biological activity analyses |
title_short | WHO prescribed shelf life assessment of Syzygium cumini extract through chromatographic and biological activity analyses |
title_sort | who prescribed shelf life assessment of syzygium cumini extract through chromatographic and biological activity analyses |
topic | Original Research Article (Experimental) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527807/ https://www.ncbi.nlm.nih.gov/pubmed/31759785 http://dx.doi.org/10.1016/j.jaim.2019.01.003 |
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