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Targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke
BACKGROUND: Our previous studies suggest that human fat extract (FE) contains a variety of angiogenic factors and may provide an alternative treatment option for stroke. However, the therapeutic effect is largely limited due to its short half-life, and inaccurate targeting. RESULTS: Herein, we lever...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153102/ https://www.ncbi.nlm.nih.gov/pubmed/35642036 http://dx.doi.org/10.1186/s12951-022-01461-2 |
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author | Wang, Cheng Yang, Xuewei Jiang, Yixu Qi, Lin Zhuge, Deli Xu, Tongtong Guo, Yiyan Deng, Mingwu Zhang, Wenjie Tian, Dongyan Yin, Qingqing Li, Li Zhang, Zhijun Wang, Yongting Yang, Guo-Yuan Chen, Yijie Tang, Yaohui |
author_facet | Wang, Cheng Yang, Xuewei Jiang, Yixu Qi, Lin Zhuge, Deli Xu, Tongtong Guo, Yiyan Deng, Mingwu Zhang, Wenjie Tian, Dongyan Yin, Qingqing Li, Li Zhang, Zhijun Wang, Yongting Yang, Guo-Yuan Chen, Yijie Tang, Yaohui |
author_sort | Wang, Cheng |
collection | PubMed |
description | BACKGROUND: Our previous studies suggest that human fat extract (FE) contains a variety of angiogenic factors and may provide an alternative treatment option for stroke. However, the therapeutic effect is largely limited due to its short half-life, and inaccurate targeting. RESULTS: Herein, we leverage the targeting abilities of platelets (PLTs) to the lesion area of stroke and Arg-Gly-Asp (RGD) peptides to the angiogenic blood vessels to develop a biomimetic nanocarrier that capable of delivering FE precisely to treat stroke. The biomimetic nanocarriers are comprised of FE-encapsulated PLGA (poly(lactic-co-glycolic acid)) core enclosed by RGD peptides decorated plasma membrane of PLTs, namely RGD-PLT@PLGA-FE. We found that RGD-PLT@PLGA-FE not only targeted damaged and inflamed blood vessels but also achieved rapid accumulation in the lesion area of ischemic brain. In addition, RGD-PLT@PLGA-FE kept a sustained release behavior of FE at the lesion site, effectively increased its half-life and promoted angiogenesis and neurogenesis with delivering neurotrophic factors including BDNF, GDNF and bFGF to the brain, that ultimately resulted in blood flow increase and neurobehavioral recovery. CONCLUSIONS: In conclusion, our study provides a new strategy to design a biomimetic system for FE delivery and it is a promising modality for stroke therapy. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01461-2. |
format | Online Article Text |
id | pubmed-9153102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91531022022-06-01 Targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke Wang, Cheng Yang, Xuewei Jiang, Yixu Qi, Lin Zhuge, Deli Xu, Tongtong Guo, Yiyan Deng, Mingwu Zhang, Wenjie Tian, Dongyan Yin, Qingqing Li, Li Zhang, Zhijun Wang, Yongting Yang, Guo-Yuan Chen, Yijie Tang, Yaohui J Nanobiotechnology Research BACKGROUND: Our previous studies suggest that human fat extract (FE) contains a variety of angiogenic factors and may provide an alternative treatment option for stroke. However, the therapeutic effect is largely limited due to its short half-life, and inaccurate targeting. RESULTS: Herein, we leverage the targeting abilities of platelets (PLTs) to the lesion area of stroke and Arg-Gly-Asp (RGD) peptides to the angiogenic blood vessels to develop a biomimetic nanocarrier that capable of delivering FE precisely to treat stroke. The biomimetic nanocarriers are comprised of FE-encapsulated PLGA (poly(lactic-co-glycolic acid)) core enclosed by RGD peptides decorated plasma membrane of PLTs, namely RGD-PLT@PLGA-FE. We found that RGD-PLT@PLGA-FE not only targeted damaged and inflamed blood vessels but also achieved rapid accumulation in the lesion area of ischemic brain. In addition, RGD-PLT@PLGA-FE kept a sustained release behavior of FE at the lesion site, effectively increased its half-life and promoted angiogenesis and neurogenesis with delivering neurotrophic factors including BDNF, GDNF and bFGF to the brain, that ultimately resulted in blood flow increase and neurobehavioral recovery. CONCLUSIONS: In conclusion, our study provides a new strategy to design a biomimetic system for FE delivery and it is a promising modality for stroke therapy. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01461-2. BioMed Central 2022-05-31 /pmc/articles/PMC9153102/ /pubmed/35642036 http://dx.doi.org/10.1186/s12951-022-01461-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wang, Cheng Yang, Xuewei Jiang, Yixu Qi, Lin Zhuge, Deli Xu, Tongtong Guo, Yiyan Deng, Mingwu Zhang, Wenjie Tian, Dongyan Yin, Qingqing Li, Li Zhang, Zhijun Wang, Yongting Yang, Guo-Yuan Chen, Yijie Tang, Yaohui Targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke |
title | Targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke |
title_full | Targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke |
title_fullStr | Targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke |
title_full_unstemmed | Targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke |
title_short | Targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke |
title_sort | targeted delivery of fat extract by platelet membrane-cloaked nanocarriers for the treatment of ischemic stroke |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153102/ https://www.ncbi.nlm.nih.gov/pubmed/35642036 http://dx.doi.org/10.1186/s12951-022-01461-2 |
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