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Cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation
Current drug delivery approaches for the treatment of cartilage disorders such as osteoarthritis (OA) remain inadequate to achieve sufficient drug penetration and retention in the dense cartilage matrix. Herein, we synthesize sub‐30 nm lipid‐polymer hybrid nanoparticles functionalized with collagen‐...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7823131/ https://www.ncbi.nlm.nih.gov/pubmed/33532587 http://dx.doi.org/10.1002/btm2.10187 |
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author | Ai, Xiangzhao Duan, Yaou Zhang, Qiangzhe Sun, Derrick Fang, Ronnie H. Liu‐Bryan, Ru Gao, Weiwei Zhang, Liangfang |
author_facet | Ai, Xiangzhao Duan, Yaou Zhang, Qiangzhe Sun, Derrick Fang, Ronnie H. Liu‐Bryan, Ru Gao, Weiwei Zhang, Liangfang |
author_sort | Ai, Xiangzhao |
collection | PubMed |
description | Current drug delivery approaches for the treatment of cartilage disorders such as osteoarthritis (OA) remain inadequate to achieve sufficient drug penetration and retention in the dense cartilage matrix. Herein, we synthesize sub‐30 nm lipid‐polymer hybrid nanoparticles functionalized with collagen‐targeting peptides for targeted drug delivery to the cartilage. The nanoparticles consist of a polymeric core for drug encapsulation and a lipid shell modified with a collagen‐binding peptide. By combining these design features, the nanoparticles can penetrate deep and accumulate preferentially in the cartilage. Using MK‐8722, an activator of 5′‐adenosine monophosphate‐activated protein kinase (AMPK), as a model drug, the nanoparticles can encapsulate the drug molecules in high capacity and release them in a sustained and controllable manner. When injected into the knee joints of the mice with collagenase‐induced OA, the drug‐loaded nanoparticles can effectively reduce cartilage damage and alleviate the disease severity. Overall, the ultrasmall targeted nanoparticles represent a promising delivery platform to overcome barriers of dense tissues for the treatment of various indications, including cartilage disorders. |
format | Online Article Text |
id | pubmed-7823131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78231312021-02-01 Cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation Ai, Xiangzhao Duan, Yaou Zhang, Qiangzhe Sun, Derrick Fang, Ronnie H. Liu‐Bryan, Ru Gao, Weiwei Zhang, Liangfang Bioeng Transl Med Research Reports Current drug delivery approaches for the treatment of cartilage disorders such as osteoarthritis (OA) remain inadequate to achieve sufficient drug penetration and retention in the dense cartilage matrix. Herein, we synthesize sub‐30 nm lipid‐polymer hybrid nanoparticles functionalized with collagen‐targeting peptides for targeted drug delivery to the cartilage. The nanoparticles consist of a polymeric core for drug encapsulation and a lipid shell modified with a collagen‐binding peptide. By combining these design features, the nanoparticles can penetrate deep and accumulate preferentially in the cartilage. Using MK‐8722, an activator of 5′‐adenosine monophosphate‐activated protein kinase (AMPK), as a model drug, the nanoparticles can encapsulate the drug molecules in high capacity and release them in a sustained and controllable manner. When injected into the knee joints of the mice with collagenase‐induced OA, the drug‐loaded nanoparticles can effectively reduce cartilage damage and alleviate the disease severity. Overall, the ultrasmall targeted nanoparticles represent a promising delivery platform to overcome barriers of dense tissues for the treatment of various indications, including cartilage disorders. John Wiley & Sons, Inc. 2020-09-10 /pmc/articles/PMC7823131/ /pubmed/33532587 http://dx.doi.org/10.1002/btm2.10187 Text en © 2020 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Reports Ai, Xiangzhao Duan, Yaou Zhang, Qiangzhe Sun, Derrick Fang, Ronnie H. Liu‐Bryan, Ru Gao, Weiwei Zhang, Liangfang Cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation |
title |
Cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation |
title_full |
Cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation |
title_fullStr |
Cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation |
title_full_unstemmed |
Cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation |
title_short |
Cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation |
title_sort | cartilage‐targeting ultrasmall lipid‐polymer hybrid nanoparticles for the prevention of cartilage degradation |
topic | Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7823131/ https://www.ncbi.nlm.nih.gov/pubmed/33532587 http://dx.doi.org/10.1002/btm2.10187 |
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