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Neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy
BACKGROUND: Neutrophil-based drug delivery system possesses excellent advantages in targeting at tumour because neutrophils are easily recruited by chemotactic factor in tumor microenvironment. Herein, we developed a novel tactic of multistage neutrophils-based nanoparticle delivery system for promo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523400/ https://www.ncbi.nlm.nih.gov/pubmed/32993684 http://dx.doi.org/10.1186/s12951-020-00682-7 |
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author | Ye, Bo Zhao, Bao Wang, Kun Guo, Yilong Lu, Qinguo Zheng, Longpo Li, Ang Qiao, Jianou |
author_facet | Ye, Bo Zhao, Bao Wang, Kun Guo, Yilong Lu, Qinguo Zheng, Longpo Li, Ang Qiao, Jianou |
author_sort | Ye, Bo |
collection | PubMed |
description | BACKGROUND: Neutrophil-based drug delivery system possesses excellent advantages in targeting at tumour because neutrophils are easily recruited by chemotactic factor in tumor microenvironment. Herein, we developed a novel tactic of multistage neutrophils-based nanoparticle delivery system for promoting photothermal therapy (PTT) of lung cancer. RESULTS: Au nanorod (AuNR) was successfully modified with bovine serum albumin (AuNRB) and further conjugated with RGD (AuNRBR), followed by neutrophil internalisation to obtain neutrophils-based delivery system (AuNRBR/N). The engineered neutrophils efficiently migrated across the epithelial cells due to inflammatory signal. They exhibited better toxicity against Lewis cells with laser irradiation in vitro. Moreover, AuNRBR/N showed significantly more targetability to tumour tissue compared with cell carrier-free AuNRBR, as demonstrated in Lewis tumour-bearing mice. The enhanced tumour homing efficiency of AuNRBR/N together with subsequently released AuNRBR from the neutrophils was favourable for further deep tissue diffusion and contributed to the inhibition of the tumour growth in PTT and improved survival rate (over 120 days). CONCLUSIONS: Overall results illustrated that the design of cell-based nanoparticle delivery system for PTT of cancer is promising. [Image: see text] |
format | Online Article Text |
id | pubmed-7523400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75234002020-09-30 Neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy Ye, Bo Zhao, Bao Wang, Kun Guo, Yilong Lu, Qinguo Zheng, Longpo Li, Ang Qiao, Jianou J Nanobiotechnology Research BACKGROUND: Neutrophil-based drug delivery system possesses excellent advantages in targeting at tumour because neutrophils are easily recruited by chemotactic factor in tumor microenvironment. Herein, we developed a novel tactic of multistage neutrophils-based nanoparticle delivery system for promoting photothermal therapy (PTT) of lung cancer. RESULTS: Au nanorod (AuNR) was successfully modified with bovine serum albumin (AuNRB) and further conjugated with RGD (AuNRBR), followed by neutrophil internalisation to obtain neutrophils-based delivery system (AuNRBR/N). The engineered neutrophils efficiently migrated across the epithelial cells due to inflammatory signal. They exhibited better toxicity against Lewis cells with laser irradiation in vitro. Moreover, AuNRBR/N showed significantly more targetability to tumour tissue compared with cell carrier-free AuNRBR, as demonstrated in Lewis tumour-bearing mice. The enhanced tumour homing efficiency of AuNRBR/N together with subsequently released AuNRBR from the neutrophils was favourable for further deep tissue diffusion and contributed to the inhibition of the tumour growth in PTT and improved survival rate (over 120 days). CONCLUSIONS: Overall results illustrated that the design of cell-based nanoparticle delivery system for PTT of cancer is promising. [Image: see text] BioMed Central 2020-09-29 /pmc/articles/PMC7523400/ /pubmed/32993684 http://dx.doi.org/10.1186/s12951-020-00682-7 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Ye, Bo Zhao, Bao Wang, Kun Guo, Yilong Lu, Qinguo Zheng, Longpo Li, Ang Qiao, Jianou Neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy |
title | Neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy |
title_full | Neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy |
title_fullStr | Neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy |
title_full_unstemmed | Neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy |
title_short | Neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy |
title_sort | neutrophils mediated multistage nanoparticle delivery for prompting tumor photothermal therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523400/ https://www.ncbi.nlm.nih.gov/pubmed/32993684 http://dx.doi.org/10.1186/s12951-020-00682-7 |
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