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Benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: A transdermal strategy for botanicals

Indigo naturalis (IN) has been extensively used as a topical treatment for psoriasis. However, clinical applications of IN in ointment were hampered by its limited transdermal efficiency and dark stains. To address the aforementioned issues, nanopatches carrying IN were fabricated using poly(ε-capro...

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Autores principales: Wang, Pengyu, Gao, Junwei, Guo, Shijie, Liu, Hongmei, Cao, Can, Hong, Shihao, Sun, Yu, Wang, Chen, Xiao, Wei, Song, Ping, Li, Ning, Xu, Ruodan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430593/
https://www.ncbi.nlm.nih.gov/pubmed/37593218
http://dx.doi.org/10.1016/j.mtbio.2023.100756
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author Wang, Pengyu
Gao, Junwei
Guo, Shijie
Liu, Hongmei
Cao, Can
Hong, Shihao
Sun, Yu
Wang, Chen
Xiao, Wei
Song, Ping
Li, Ning
Xu, Ruodan
author_facet Wang, Pengyu
Gao, Junwei
Guo, Shijie
Liu, Hongmei
Cao, Can
Hong, Shihao
Sun, Yu
Wang, Chen
Xiao, Wei
Song, Ping
Li, Ning
Xu, Ruodan
author_sort Wang, Pengyu
collection PubMed
description Indigo naturalis (IN) has been extensively used as a topical treatment for psoriasis. However, clinical applications of IN in ointment were hampered by its limited transdermal efficiency and dark stains. To address the aforementioned issues, nanopatches carrying IN were fabricated using poly(ε-caprolactone, PCL)/poly(ethylene oxide, PEO) and topically applied to psoriasiform skin. The ideal ratio of 5% PCL/PEO was established to be 80:20 (w/w), and 15% IN as payload was confirmed. Investigations on the three principal active components of IN release indicated that indirubin and tryptanthrin were released in bursts, while indigo was released in a limited and controlled manner. Further biological analyses confirmed a favorable biocompatibility of amphiphilic IN-PCL/PEO, which coincided with the intended therapeutic outcomes as measured by severity index scoring and pathological evaluations in vivo. The advantages of IN as nanopatches over ointment could be due to improved transdermal distribution of indirubin and tryptanthrin, resulting in effective management of epidermal hyperplasia and blood vessel remodeling. Meanwhile, due to the lower preservation of epidermal indigo, IN-PCL/PEO nanopatches caused no skin coloration. Similarly, during a 4-week topical treatment of IN-PCL/PEO nanopatches, the safety and anti-psoriatic benefits were obtained in an initial human test. The conversion of IN from topical cream to electrospun nanofibers opens up new avenues for bench-to-bedside translation of this herbal therapy and provides mechanistic insight into IN's roles in the management of psoriasis.
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spelling pubmed-104305932023-08-17 Benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: A transdermal strategy for botanicals Wang, Pengyu Gao, Junwei Guo, Shijie Liu, Hongmei Cao, Can Hong, Shihao Sun, Yu Wang, Chen Xiao, Wei Song, Ping Li, Ning Xu, Ruodan Mater Today Bio Full Length Article Indigo naturalis (IN) has been extensively used as a topical treatment for psoriasis. However, clinical applications of IN in ointment were hampered by its limited transdermal efficiency and dark stains. To address the aforementioned issues, nanopatches carrying IN were fabricated using poly(ε-caprolactone, PCL)/poly(ethylene oxide, PEO) and topically applied to psoriasiform skin. The ideal ratio of 5% PCL/PEO was established to be 80:20 (w/w), and 15% IN as payload was confirmed. Investigations on the three principal active components of IN release indicated that indirubin and tryptanthrin were released in bursts, while indigo was released in a limited and controlled manner. Further biological analyses confirmed a favorable biocompatibility of amphiphilic IN-PCL/PEO, which coincided with the intended therapeutic outcomes as measured by severity index scoring and pathological evaluations in vivo. The advantages of IN as nanopatches over ointment could be due to improved transdermal distribution of indirubin and tryptanthrin, resulting in effective management of epidermal hyperplasia and blood vessel remodeling. Meanwhile, due to the lower preservation of epidermal indigo, IN-PCL/PEO nanopatches caused no skin coloration. Similarly, during a 4-week topical treatment of IN-PCL/PEO nanopatches, the safety and anti-psoriatic benefits were obtained in an initial human test. The conversion of IN from topical cream to electrospun nanofibers opens up new avenues for bench-to-bedside translation of this herbal therapy and provides mechanistic insight into IN's roles in the management of psoriasis. Elsevier 2023-08-02 /pmc/articles/PMC10430593/ /pubmed/37593218 http://dx.doi.org/10.1016/j.mtbio.2023.100756 Text en © 2023 The Authors https://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 Full Length Article
Wang, Pengyu
Gao, Junwei
Guo, Shijie
Liu, Hongmei
Cao, Can
Hong, Shihao
Sun, Yu
Wang, Chen
Xiao, Wei
Song, Ping
Li, Ning
Xu, Ruodan
Benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: A transdermal strategy for botanicals
title Benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: A transdermal strategy for botanicals
title_full Benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: A transdermal strategy for botanicals
title_fullStr Benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: A transdermal strategy for botanicals
title_full_unstemmed Benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: A transdermal strategy for botanicals
title_short Benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: A transdermal strategy for botanicals
title_sort benefits of topical indigo naturalis nanofibrous patch on psoriatic skin: a transdermal strategy for botanicals
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430593/
https://www.ncbi.nlm.nih.gov/pubmed/37593218
http://dx.doi.org/10.1016/j.mtbio.2023.100756
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