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Naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation

Glucosamine-6-Phosphate synthase enzyme has been targeted for development of better and safe preservative due to its role in microbial cell wall synthesis. In recent year’s demand of preservatives for the food, cosmetics and pharmaceuticals have increased. Although, the available synthetic preservat...

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Autores principales: Lather, Amit, Sharma, Sunil, Khatkar, Anurag
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686335/
https://www.ncbi.nlm.nih.gov/pubmed/33235242
http://dx.doi.org/10.1038/s41598-020-77511-2
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author Lather, Amit
Sharma, Sunil
Khatkar, Anurag
author_facet Lather, Amit
Sharma, Sunil
Khatkar, Anurag
author_sort Lather, Amit
collection PubMed
description Glucosamine-6-Phosphate synthase enzyme has been targeted for development of better and safe preservative due to its role in microbial cell wall synthesis. In recent year’s demand of preservatives for the food, cosmetics and pharmaceuticals have increased. Although, the available synthetic preservatives have associated unwanted adverse effects, soa chain of naringin derivatives were schemed synthesized and judged for antioxidant, antimicrobial, preservative efficacy, stability study and topical evaluation. Molecular docking resulted with excellent dock score and binding energy for compound 7, compound 6 and compound 1 as compared to standard drugs. Resultant data of antimicrobial activity revealed compound 7as most potent antimicrobial compound for P. mirabilis, P. aeruginosa, S. aureus, E. coli, C. albicans, and A. niger, respectively, as compared to the standard drugs. The preservative efficacy test of compound 7 in White Lotion USP showed the log cfu/mL value within prescribed limit of USP standard. Compound 7 stabilize the White lotion USP from microbial growth for a period of six months under accelerated storage condition. Compound 7 was further evaluated for toxicity by using the Draize test in rabbits and showed no sign of eye and skin irritation. The outcome demonstrated that synthesized naringin compounds showed glorious antioxidant, antimicrobial, preservative efficacy, stable and safe as compared to standards.
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spelling pubmed-76863352020-11-27 Naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation Lather, Amit Sharma, Sunil Khatkar, Anurag Sci Rep Article Glucosamine-6-Phosphate synthase enzyme has been targeted for development of better and safe preservative due to its role in microbial cell wall synthesis. In recent year’s demand of preservatives for the food, cosmetics and pharmaceuticals have increased. Although, the available synthetic preservatives have associated unwanted adverse effects, soa chain of naringin derivatives were schemed synthesized and judged for antioxidant, antimicrobial, preservative efficacy, stability study and topical evaluation. Molecular docking resulted with excellent dock score and binding energy for compound 7, compound 6 and compound 1 as compared to standard drugs. Resultant data of antimicrobial activity revealed compound 7as most potent antimicrobial compound for P. mirabilis, P. aeruginosa, S. aureus, E. coli, C. albicans, and A. niger, respectively, as compared to the standard drugs. The preservative efficacy test of compound 7 in White Lotion USP showed the log cfu/mL value within prescribed limit of USP standard. Compound 7 stabilize the White lotion USP from microbial growth for a period of six months under accelerated storage condition. Compound 7 was further evaluated for toxicity by using the Draize test in rabbits and showed no sign of eye and skin irritation. The outcome demonstrated that synthesized naringin compounds showed glorious antioxidant, antimicrobial, preservative efficacy, stable and safe as compared to standards. Nature Publishing Group UK 2020-11-24 /pmc/articles/PMC7686335/ /pubmed/33235242 http://dx.doi.org/10.1038/s41598-020-77511-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lather, Amit
Sharma, Sunil
Khatkar, Anurag
Naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation
title Naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation
title_full Naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation
title_fullStr Naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation
title_full_unstemmed Naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation
title_short Naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation
title_sort naringin derivatives as glucosamine-6-phosphate synthase inhibitors based preservatives and their biological evaluation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686335/
https://www.ncbi.nlm.nih.gov/pubmed/33235242
http://dx.doi.org/10.1038/s41598-020-77511-2
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