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Dual-Drug Loaded Separable Microneedles for Efficient Rheumatoid Arthritis Therapy
Although the inhibitors of the interleukin-6 receptor (IL-6R) and tumor necrosis factor-α (TNF-α) have achieved a certain success in the clinical treatment of rheumatoid arthritis (RA), great effort should be made to overcome side effects and to improve patient compliance. The present research aimed...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324764/ https://www.ncbi.nlm.nih.gov/pubmed/35890412 http://dx.doi.org/10.3390/pharmaceutics14071518 |
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author | An, Mengchen Shi, Mengxiao Su, Jingjing Wei, Yueru Luo, Rongrong Sun, Pengchao Zhao, Yongxing |
author_facet | An, Mengchen Shi, Mengxiao Su, Jingjing Wei, Yueru Luo, Rongrong Sun, Pengchao Zhao, Yongxing |
author_sort | An, Mengchen |
collection | PubMed |
description | Although the inhibitors of the interleukin-6 receptor (IL-6R) and tumor necrosis factor-α (TNF-α) have achieved a certain success in the clinical treatment of rheumatoid arthritis (RA), great effort should be made to overcome side effects and to improve patient compliance. The present research aimed to address these problems by the co-delivery of tocilizumab (TCZ)—an inhibitor of IL-6R—and an aptamer Apt1-67, which specifically inhibits TNF receptor 1 via separable microneedles (MN). MN were featured with a sustained release of TCZ from needle tips and a rapid release of Apt1-67 from needle bodies by using methacrylate groups grafted hyaluronic acid as the fillings of needle tips and polyvinyl alcohol/polyvinyl pyrrolidone as the fillings of needle bodies. Our results demonstrated that TCZ and Apt1-67 were distributed in MN as expected, and they could be released to the surroundings in the skin. In vivo studies revealed that combined medication via MN (TCZ/Apt1-67@MN) was superior to MN loaded with a single drug. Compared with subcutaneous injection, TCZ/Apt1-67@MN was of great advantage in inhibiting bone erosion and alleviating symptoms of CIA mice. This study not only provides a novel approach for combined medication with different release properties but also supplies a strategy for improving drug efficacy. |
format | Online Article Text |
id | pubmed-9324764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93247642022-07-27 Dual-Drug Loaded Separable Microneedles for Efficient Rheumatoid Arthritis Therapy An, Mengchen Shi, Mengxiao Su, Jingjing Wei, Yueru Luo, Rongrong Sun, Pengchao Zhao, Yongxing Pharmaceutics Article Although the inhibitors of the interleukin-6 receptor (IL-6R) and tumor necrosis factor-α (TNF-α) have achieved a certain success in the clinical treatment of rheumatoid arthritis (RA), great effort should be made to overcome side effects and to improve patient compliance. The present research aimed to address these problems by the co-delivery of tocilizumab (TCZ)—an inhibitor of IL-6R—and an aptamer Apt1-67, which specifically inhibits TNF receptor 1 via separable microneedles (MN). MN were featured with a sustained release of TCZ from needle tips and a rapid release of Apt1-67 from needle bodies by using methacrylate groups grafted hyaluronic acid as the fillings of needle tips and polyvinyl alcohol/polyvinyl pyrrolidone as the fillings of needle bodies. Our results demonstrated that TCZ and Apt1-67 were distributed in MN as expected, and they could be released to the surroundings in the skin. In vivo studies revealed that combined medication via MN (TCZ/Apt1-67@MN) was superior to MN loaded with a single drug. Compared with subcutaneous injection, TCZ/Apt1-67@MN was of great advantage in inhibiting bone erosion and alleviating symptoms of CIA mice. This study not only provides a novel approach for combined medication with different release properties but also supplies a strategy for improving drug efficacy. MDPI 2022-07-21 /pmc/articles/PMC9324764/ /pubmed/35890412 http://dx.doi.org/10.3390/pharmaceutics14071518 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article An, Mengchen Shi, Mengxiao Su, Jingjing Wei, Yueru Luo, Rongrong Sun, Pengchao Zhao, Yongxing Dual-Drug Loaded Separable Microneedles for Efficient Rheumatoid Arthritis Therapy |
title | Dual-Drug Loaded Separable Microneedles for Efficient Rheumatoid Arthritis Therapy |
title_full | Dual-Drug Loaded Separable Microneedles for Efficient Rheumatoid Arthritis Therapy |
title_fullStr | Dual-Drug Loaded Separable Microneedles for Efficient Rheumatoid Arthritis Therapy |
title_full_unstemmed | Dual-Drug Loaded Separable Microneedles for Efficient Rheumatoid Arthritis Therapy |
title_short | Dual-Drug Loaded Separable Microneedles for Efficient Rheumatoid Arthritis Therapy |
title_sort | dual-drug loaded separable microneedles for efficient rheumatoid arthritis therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324764/ https://www.ncbi.nlm.nih.gov/pubmed/35890412 http://dx.doi.org/10.3390/pharmaceutics14071518 |
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