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Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery
BACKGROUND AND PURPOSE: Benjakul (BJK) is a combination of five botanical herbal constituents widely used in Thai traditional medicine as an anti-inflammatory remedy. This study aimed to develop a novel topical microemulsion containing BJK for clinical use. EXPERIMENTAL APPROACH: The microemulsions...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860110/ https://www.ncbi.nlm.nih.gov/pubmed/35280840 http://dx.doi.org/10.4103/1735-5362.335170 |
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author | Kuropakornpong, Pranporn Itharat, Arunporn Ooraikul, Buncha Loebenberg, Raimar Davies, Neal M. |
author_facet | Kuropakornpong, Pranporn Itharat, Arunporn Ooraikul, Buncha Loebenberg, Raimar Davies, Neal M. |
author_sort | Kuropakornpong, Pranporn |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Benjakul (BJK) is a combination of five botanical herbal constituents widely used in Thai traditional medicine as an anti-inflammatory remedy. This study aimed to develop a novel topical microemulsion containing BJK for clinical use. EXPERIMENTAL APPROACH: The microemulsions were produced by a phase inversion temperature (PIT) methodology. Physicochemical properties and stability were evaluated to determine an optimal formula. The stable BJK-loaded microemulsion formulas were then subjected to in vitro studies for their anti-inflammatory activity, skin cell toxicity, drug permeation, and stability. FINDING/RESULTS: Two novel formulations containing isopropyl myristate (ME1-BJK and ME2-BJK) passed the compendial stability test. BJK constituents were completely dissolved in the oil phase and incorporated into the microemulsion base Transcutol® and Labrasol® avoiding the use of alcohol, both microemulsion formulations demonstrated high anti-inflammatory activity with IC(50) values of 3.41 ± 0.36 and 3.95 ± 1.73 μg/mL, respectively. However, dissolution of ME1-BJK showed a superior release profile through both lipophilic and hydrophilic membranes with the highest accumulated amount at 4 h of 25.13% and 38.06%, respectively. All tested formulations of BJK extract demonstrated no apparent skin cell toxicity at concentrations up to 50 μg/mL. After six-month storage under accelerated conditions, there were no significant changes in anti-inflammatory activity. CONCLUSIONS AND IMPLICATIONS: A novel and stable BJK-loaded microemulsion formulation was successfully developed with excellent release and stability properties. Further clinical research to evaluate pain reduction, edema, and skin irritation using this formulation in animal models is ongoing. |
format | Online Article Text |
id | pubmed-8860110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-88601102022-03-10 Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery Kuropakornpong, Pranporn Itharat, Arunporn Ooraikul, Buncha Loebenberg, Raimar Davies, Neal M. Res Pharm Sci Original Article BACKGROUND AND PURPOSE: Benjakul (BJK) is a combination of five botanical herbal constituents widely used in Thai traditional medicine as an anti-inflammatory remedy. This study aimed to develop a novel topical microemulsion containing BJK for clinical use. EXPERIMENTAL APPROACH: The microemulsions were produced by a phase inversion temperature (PIT) methodology. Physicochemical properties and stability were evaluated to determine an optimal formula. The stable BJK-loaded microemulsion formulas were then subjected to in vitro studies for their anti-inflammatory activity, skin cell toxicity, drug permeation, and stability. FINDING/RESULTS: Two novel formulations containing isopropyl myristate (ME1-BJK and ME2-BJK) passed the compendial stability test. BJK constituents were completely dissolved in the oil phase and incorporated into the microemulsion base Transcutol® and Labrasol® avoiding the use of alcohol, both microemulsion formulations demonstrated high anti-inflammatory activity with IC(50) values of 3.41 ± 0.36 and 3.95 ± 1.73 μg/mL, respectively. However, dissolution of ME1-BJK showed a superior release profile through both lipophilic and hydrophilic membranes with the highest accumulated amount at 4 h of 25.13% and 38.06%, respectively. All tested formulations of BJK extract demonstrated no apparent skin cell toxicity at concentrations up to 50 μg/mL. After six-month storage under accelerated conditions, there were no significant changes in anti-inflammatory activity. CONCLUSIONS AND IMPLICATIONS: A novel and stable BJK-loaded microemulsion formulation was successfully developed with excellent release and stability properties. Further clinical research to evaluate pain reduction, edema, and skin irritation using this formulation in animal models is ongoing. Wolters Kluwer - Medknow 2022-01-15 /pmc/articles/PMC8860110/ /pubmed/35280840 http://dx.doi.org/10.4103/1735-5362.335170 Text en Copyright: © 2022 Research in Pharmaceutical Sciences https://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 Kuropakornpong, Pranporn Itharat, Arunporn Ooraikul, Buncha Loebenberg, Raimar Davies, Neal M. Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery |
title | Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery |
title_full | Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery |
title_fullStr | Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery |
title_full_unstemmed | Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery |
title_short | Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery |
title_sort | development and optimization of benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860110/ https://www.ncbi.nlm.nih.gov/pubmed/35280840 http://dx.doi.org/10.4103/1735-5362.335170 |
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