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Acceleration of wound healing by topical application of gel formulation of Barringtonia racemosa (L.) Spreng kernel extract
Background: Phytomedicines are gaining a spotlight in wound management, where much research has suggested the wound healing potential of Barringtonia racemosa. The objective of this study was to investigate the effectiveness of B. racemosa kernel extract in accelerating wound healing process in anim...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933646/ https://www.ncbi.nlm.nih.gov/pubmed/35356313 http://dx.doi.org/10.12688/f1000research.104602.2 |
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author | Sitohang, Nur A. Putra, Effendy D. L. Kamil, Hajjul Musman, Musri |
author_facet | Sitohang, Nur A. Putra, Effendy D. L. Kamil, Hajjul Musman, Musri |
author_sort | Sitohang, Nur A. |
collection | PubMed |
description | Background: Phytomedicines are gaining a spotlight in wound management, where much research has suggested the wound healing potential of Barringtonia racemosa. The objective of this study was to investigate the effectiveness of B. racemosa kernel extract in accelerating wound healing process in animal models. Methods: B. racemosa kernel was extracted using ethanol:water (7:3) solvent and was then used as a bioactive ingredient in a Carbopol 940-based gel formulation in four different concentrations (1, 3, 5 and 7 ppm). A 3 cm diameter wound was made in the dorsal area of Rattus norvegicus rat and wound healing process was assessed up to 12 days using DESIGN (Depth, Exudate, Size of Inflammation/Infection, Granulation tissue, and Necrotic tissue) scoring system. Results: Our data suggested that the DESIGN scores were significantly different among concentration groups after the 3 (rd)day onward suggesting B. racemosa extract accelerated the wound healing process. Rats treated with gel formulation containing 7 ppm of B. racemosa kernel extract had faster wound healing than that treated with topical Metcovazin. On day 6, macroscopic observation on 7 ppm group revealed that the wound had persistent redness, lesion area of < 3 cm (2), and 80% healthy granulation, where presence of exudate and redness were not observable. Conclusion: B. racemosa kernel extract was effective in accelerating wound healing on rats. Further study is warranted to purify the bioactive component and the action mechanism in wound healing process. |
format | Online Article Text |
id | pubmed-8933646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-89336462022-03-29 Acceleration of wound healing by topical application of gel formulation of Barringtonia racemosa (L.) Spreng kernel extract Sitohang, Nur A. Putra, Effendy D. L. Kamil, Hajjul Musman, Musri F1000Res Research Article Background: Phytomedicines are gaining a spotlight in wound management, where much research has suggested the wound healing potential of Barringtonia racemosa. The objective of this study was to investigate the effectiveness of B. racemosa kernel extract in accelerating wound healing process in animal models. Methods: B. racemosa kernel was extracted using ethanol:water (7:3) solvent and was then used as a bioactive ingredient in a Carbopol 940-based gel formulation in four different concentrations (1, 3, 5 and 7 ppm). A 3 cm diameter wound was made in the dorsal area of Rattus norvegicus rat and wound healing process was assessed up to 12 days using DESIGN (Depth, Exudate, Size of Inflammation/Infection, Granulation tissue, and Necrotic tissue) scoring system. Results: Our data suggested that the DESIGN scores were significantly different among concentration groups after the 3 (rd)day onward suggesting B. racemosa extract accelerated the wound healing process. Rats treated with gel formulation containing 7 ppm of B. racemosa kernel extract had faster wound healing than that treated with topical Metcovazin. On day 6, macroscopic observation on 7 ppm group revealed that the wound had persistent redness, lesion area of < 3 cm (2), and 80% healthy granulation, where presence of exudate and redness were not observable. Conclusion: B. racemosa kernel extract was effective in accelerating wound healing on rats. Further study is warranted to purify the bioactive component and the action mechanism in wound healing process. F1000 Research Limited 2022-03-16 /pmc/articles/PMC8933646/ /pubmed/35356313 http://dx.doi.org/10.12688/f1000research.104602.2 Text en Copyright: © 2022 Sitohang NA et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sitohang, Nur A. Putra, Effendy D. L. Kamil, Hajjul Musman, Musri Acceleration of wound healing by topical application of gel formulation of Barringtonia racemosa (L.) Spreng kernel extract |
title | Acceleration of wound healing by topical application of gel formulation of
Barringtonia racemosa (L.) Spreng kernel extract |
title_full | Acceleration of wound healing by topical application of gel formulation of
Barringtonia racemosa (L.) Spreng kernel extract |
title_fullStr | Acceleration of wound healing by topical application of gel formulation of
Barringtonia racemosa (L.) Spreng kernel extract |
title_full_unstemmed | Acceleration of wound healing by topical application of gel formulation of
Barringtonia racemosa (L.) Spreng kernel extract |
title_short | Acceleration of wound healing by topical application of gel formulation of
Barringtonia racemosa (L.) Spreng kernel extract |
title_sort | acceleration of wound healing by topical application of gel formulation of
barringtonia racemosa (l.) spreng kernel extract |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933646/ https://www.ncbi.nlm.nih.gov/pubmed/35356313 http://dx.doi.org/10.12688/f1000research.104602.2 |
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