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Layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis

Psoriatic arthritis (PsA) is a complicated psoriasis comorbidity with manifestations of psoriatic skin and arthritic joints, and tailoring specific treatment strategies for simultaneously delivering different drugs to different action sites in PsA remains challenging. We developed a need-based layer...

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Autores principales: Yu, Kaiyue, Yu, Xiuming, Cao, Sisi, Wang, Yixuan, Zhai, Yuanhao, Yang, Fengdie, Yang, Xiaoyuan, Lu, Yi, Wu, Chuanbin, Xu, Yuehong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893142/
https://www.ncbi.nlm.nih.gov/pubmed/33643827
http://dx.doi.org/10.1016/j.apsb.2020.08.008
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author Yu, Kaiyue
Yu, Xiuming
Cao, Sisi
Wang, Yixuan
Zhai, Yuanhao
Yang, Fengdie
Yang, Xiaoyuan
Lu, Yi
Wu, Chuanbin
Xu, Yuehong
author_facet Yu, Kaiyue
Yu, Xiuming
Cao, Sisi
Wang, Yixuan
Zhai, Yuanhao
Yang, Fengdie
Yang, Xiaoyuan
Lu, Yi
Wu, Chuanbin
Xu, Yuehong
author_sort Yu, Kaiyue
collection PubMed
description Psoriatic arthritis (PsA) is a complicated psoriasis comorbidity with manifestations of psoriatic skin and arthritic joints, and tailoring specific treatment strategies for simultaneously delivering different drugs to different action sites in PsA remains challenging. We developed a need-based layered dissolving microneedle (MN) system loading immunosuppressant tacrolimus (TAC) and anti-inflammatory diclofenac (DIC) in different layers of MNs, i.e., TD-MN, which aims to specifically deliver TAC and DIC to skin and articular cavity, achieving simultaneous alleviation of psoriatic skin and arthritic joint lesions in PsA. In vitro and in vivo skin permeation demonstrated that the inter-layer retained TAC within the skin of ∼100 μm, while the tip-layer delivered DIC up to ∼300 μm into the articular cavity. TD-MN not only efficiently decreased the psoriasis area and severity index scores and recovered the thickened epidermis of imiquimod-induced psoriasis but also alleviated carrageenan/kaolin-induced arthritis even better than DIC injection through reducing joint swelling, muscle atrophy, and cartilage destruction. Importantly, TD-MN significantly inhibited the serum TNF-α and IL-17A in psoriatic and arthritic rats. The results support that this approach represents a promising alternative to multi-administration of different drugs for comorbidity, providing a convenient and effective strategy for meeting the requirements of PsA treatment.
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spelling pubmed-78931422021-02-25 Layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis Yu, Kaiyue Yu, Xiuming Cao, Sisi Wang, Yixuan Zhai, Yuanhao Yang, Fengdie Yang, Xiaoyuan Lu, Yi Wu, Chuanbin Xu, Yuehong Acta Pharm Sin B Original Article Psoriatic arthritis (PsA) is a complicated psoriasis comorbidity with manifestations of psoriatic skin and arthritic joints, and tailoring specific treatment strategies for simultaneously delivering different drugs to different action sites in PsA remains challenging. We developed a need-based layered dissolving microneedle (MN) system loading immunosuppressant tacrolimus (TAC) and anti-inflammatory diclofenac (DIC) in different layers of MNs, i.e., TD-MN, which aims to specifically deliver TAC and DIC to skin and articular cavity, achieving simultaneous alleviation of psoriatic skin and arthritic joint lesions in PsA. In vitro and in vivo skin permeation demonstrated that the inter-layer retained TAC within the skin of ∼100 μm, while the tip-layer delivered DIC up to ∼300 μm into the articular cavity. TD-MN not only efficiently decreased the psoriasis area and severity index scores and recovered the thickened epidermis of imiquimod-induced psoriasis but also alleviated carrageenan/kaolin-induced arthritis even better than DIC injection through reducing joint swelling, muscle atrophy, and cartilage destruction. Importantly, TD-MN significantly inhibited the serum TNF-α and IL-17A in psoriatic and arthritic rats. The results support that this approach represents a promising alternative to multi-administration of different drugs for comorbidity, providing a convenient and effective strategy for meeting the requirements of PsA treatment. Elsevier 2021-02 2020-08-28 /pmc/articles/PMC7893142/ /pubmed/33643827 http://dx.doi.org/10.1016/j.apsb.2020.08.008 Text en © 2021 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://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 Original Article
Yu, Kaiyue
Yu, Xiuming
Cao, Sisi
Wang, Yixuan
Zhai, Yuanhao
Yang, Fengdie
Yang, Xiaoyuan
Lu, Yi
Wu, Chuanbin
Xu, Yuehong
Layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis
title Layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis
title_full Layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis
title_fullStr Layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis
title_full_unstemmed Layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis
title_short Layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis
title_sort layered dissolving microneedles as a need-based delivery system to simultaneously alleviate skin and joint lesions in psoriatic arthritis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893142/
https://www.ncbi.nlm.nih.gov/pubmed/33643827
http://dx.doi.org/10.1016/j.apsb.2020.08.008
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