Cargando…
The formulation of lozenge using black mulberries (Morus nigra L.) leaf extract as an α-glucosidase inhibitor
BACKGROUND: Diabetes mellitus is a chronic metabolic disease, which possibly leads to kidney, brain, heart failure, and other organ complications, subsequently harming human health. These symptoms have been prevented using the leaf of black mulberry (BM), as a traditional medicine, because the pheno...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373108/ https://www.ncbi.nlm.nih.gov/pubmed/32742116 http://dx.doi.org/10.4103/jpbs.JPBS_219_19 |
_version_ | 1783561444902567936 |
---|---|
author | Budiman, Arif Sofian, Ferry F Santi, Ni Made W S Aulifa, Diah L |
author_facet | Budiman, Arif Sofian, Ferry F Santi, Ni Made W S Aulifa, Diah L |
author_sort | Budiman, Arif |
collection | PubMed |
description | BACKGROUND: Diabetes mellitus is a chronic metabolic disease, which possibly leads to kidney, brain, heart failure, and other organ complications, subsequently harming human health. These symptoms have been prevented using the leaf of black mulberry (BM), as a traditional medicine, because the phenolic compounds contained are able to decrease blood glucose concentration. Meanwhile, previous reports have shown that BM contains 1-deoxynojirimycin, with strong activity as an α-glucosidase inhibitor. The aim of this study, therefore, was to formulate and evaluate BM leaf extract in lozenge dosage form as an α-glucosidase inhibitor. MATERIALS AND METHODS: The leaves of BM were extracted using the maceration method, where ethanol (70%) served as a solvent, and the inhibitory activity of the sourced α-glucosidase enzyme was determined through in vitro study. Subsequently, the extract was formulated into lozenge dosage form and evaluated for physical stability and also the effect of α-glucosidase enzyme. RESULTS: The result showed an inhibitory activity of BM leaf extract against the enzyme α-glucosidase, with a half maximal inhibitory concentration (IC(50)) value of 357.6 μg/mL, whereas the lozenge formulation containing 43% of extract as well as 5% polyvinylpyrrolidone showed the best physical stability as compared to other formulas. However, the lozenge inhibits α-glucosidase enzyme with an IC(50) value of 549.7 μg/mL. CONCLUSION: It was established that the lozenge of BM leaf extract possesses activity as an α-glucosidase inhibitor. |
format | Online Article Text |
id | pubmed-7373108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-73731082020-07-30 The formulation of lozenge using black mulberries (Morus nigra L.) leaf extract as an α-glucosidase inhibitor Budiman, Arif Sofian, Ferry F Santi, Ni Made W S Aulifa, Diah L J Pharm Bioallied Sci Original Article BACKGROUND: Diabetes mellitus is a chronic metabolic disease, which possibly leads to kidney, brain, heart failure, and other organ complications, subsequently harming human health. These symptoms have been prevented using the leaf of black mulberry (BM), as a traditional medicine, because the phenolic compounds contained are able to decrease blood glucose concentration. Meanwhile, previous reports have shown that BM contains 1-deoxynojirimycin, with strong activity as an α-glucosidase inhibitor. The aim of this study, therefore, was to formulate and evaluate BM leaf extract in lozenge dosage form as an α-glucosidase inhibitor. MATERIALS AND METHODS: The leaves of BM were extracted using the maceration method, where ethanol (70%) served as a solvent, and the inhibitory activity of the sourced α-glucosidase enzyme was determined through in vitro study. Subsequently, the extract was formulated into lozenge dosage form and evaluated for physical stability and also the effect of α-glucosidase enzyme. RESULTS: The result showed an inhibitory activity of BM leaf extract against the enzyme α-glucosidase, with a half maximal inhibitory concentration (IC(50)) value of 357.6 μg/mL, whereas the lozenge formulation containing 43% of extract as well as 5% polyvinylpyrrolidone showed the best physical stability as compared to other formulas. However, the lozenge inhibits α-glucosidase enzyme with an IC(50) value of 549.7 μg/mL. CONCLUSION: It was established that the lozenge of BM leaf extract possesses activity as an α-glucosidase inhibitor. Wolters Kluwer - Medknow 2020 2020-04-10 /pmc/articles/PMC7373108/ /pubmed/32742116 http://dx.doi.org/10.4103/jpbs.JPBS_219_19 Text en © 2020 Journal of Pharmacy and Bioallied Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Budiman, Arif Sofian, Ferry F Santi, Ni Made W S Aulifa, Diah L The formulation of lozenge using black mulberries (Morus nigra L.) leaf extract as an α-glucosidase inhibitor |
title | The formulation of lozenge using black mulberries (Morus nigra L.) leaf extract as an α-glucosidase inhibitor |
title_full | The formulation of lozenge using black mulberries (Morus nigra L.) leaf extract as an α-glucosidase inhibitor |
title_fullStr | The formulation of lozenge using black mulberries (Morus nigra L.) leaf extract as an α-glucosidase inhibitor |
title_full_unstemmed | The formulation of lozenge using black mulberries (Morus nigra L.) leaf extract as an α-glucosidase inhibitor |
title_short | The formulation of lozenge using black mulberries (Morus nigra L.) leaf extract as an α-glucosidase inhibitor |
title_sort | formulation of lozenge using black mulberries (morus nigra l.) leaf extract as an α-glucosidase inhibitor |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373108/ https://www.ncbi.nlm.nih.gov/pubmed/32742116 http://dx.doi.org/10.4103/jpbs.JPBS_219_19 |
work_keys_str_mv | AT budimanarif theformulationoflozengeusingblackmulberriesmorusnigralleafextractasanaglucosidaseinhibitor AT sofianferryf theformulationoflozengeusingblackmulberriesmorusnigralleafextractasanaglucosidaseinhibitor AT santinimadews theformulationoflozengeusingblackmulberriesmorusnigralleafextractasanaglucosidaseinhibitor AT aulifadiahl theformulationoflozengeusingblackmulberriesmorusnigralleafextractasanaglucosidaseinhibitor AT budimanarif formulationoflozengeusingblackmulberriesmorusnigralleafextractasanaglucosidaseinhibitor AT sofianferryf formulationoflozengeusingblackmulberriesmorusnigralleafextractasanaglucosidaseinhibitor AT santinimadews formulationoflozengeusingblackmulberriesmorusnigralleafextractasanaglucosidaseinhibitor AT aulifadiahl formulationoflozengeusingblackmulberriesmorusnigralleafextractasanaglucosidaseinhibitor |