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Berberine nanoparticles for promising sonodynamic therapy of a HeLa xenograft tumour
Here, we show that berberine (BBR) nanoparticles (BBRNPs, ∼300 nm hydrodynamic diameter) are a promising sonosensitizer for cancer sonodynamic therapy (SDT). HeLa cells were cultured for in vitro investigation, and a HeLa xenograft tumor model was established with BALB/c nude mice (∼20 g, female) fo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062522/ https://www.ncbi.nlm.nih.gov/pubmed/35515276 http://dx.doi.org/10.1039/c8ra09172b |
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author | Liu, Hanqing Zheng, Tingting Zhou, Ziqian Hu, Azhen Li, Minghua Zhang, Zhuxia Yu, Guangyin Feng, Huanhuan An, Yawen Peng, Jiao Chen, Yun |
author_facet | Liu, Hanqing Zheng, Tingting Zhou, Ziqian Hu, Azhen Li, Minghua Zhang, Zhuxia Yu, Guangyin Feng, Huanhuan An, Yawen Peng, Jiao Chen, Yun |
author_sort | Liu, Hanqing |
collection | PubMed |
description | Here, we show that berberine (BBR) nanoparticles (BBRNPs, ∼300 nm hydrodynamic diameter) are a promising sonosensitizer for cancer sonodynamic therapy (SDT). HeLa cells were cultured for in vitro investigation, and a HeLa xenograft tumor model was established with BALB/c nude mice (∼20 g, female) for in vivo study. Significant effects of BBRNP-mediated SDT were observed in both in vitro and in vivo experiments. Cell counting kit-8 (CCK-8) cell proliferation and cytotoxicity assays were performed to confirm if BBRNPs-SDT has cytotoxicity against HeLa cells in vitro. The mechanism for inhibition of tumor proliferation by BBRNPs-SDT was investigated via flow cytometry, photoluminescence spectroscopy, dynamic light scattering, scanning electron microscopy, ultrasonic contrast imaging, tumour pathological analysis, western blot and anatomical analysis. We identified two ongoing assumptive mechanisms. One is due to the tumor angioembolism effect, which blocks oxygen and nutrient supply in situ, leading to early-stage HeLa apoptosis. The other domino effect is due to ultrasonic energy-activated BBRNP cavitation and reactive oxygen species release, which leads to tumor vascular injury and finally induces HeLa apoptosis, resulting in tumour shrinkage. Both pathways synergistically helped with HeLa xenograft tumor supression. In conclusion, we posit that BBRNPs are a promising agent for tumor SDT. |
format | Online Article Text |
id | pubmed-9062522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90625222022-05-04 Berberine nanoparticles for promising sonodynamic therapy of a HeLa xenograft tumour Liu, Hanqing Zheng, Tingting Zhou, Ziqian Hu, Azhen Li, Minghua Zhang, Zhuxia Yu, Guangyin Feng, Huanhuan An, Yawen Peng, Jiao Chen, Yun RSC Adv Chemistry Here, we show that berberine (BBR) nanoparticles (BBRNPs, ∼300 nm hydrodynamic diameter) are a promising sonosensitizer for cancer sonodynamic therapy (SDT). HeLa cells were cultured for in vitro investigation, and a HeLa xenograft tumor model was established with BALB/c nude mice (∼20 g, female) for in vivo study. Significant effects of BBRNP-mediated SDT were observed in both in vitro and in vivo experiments. Cell counting kit-8 (CCK-8) cell proliferation and cytotoxicity assays were performed to confirm if BBRNPs-SDT has cytotoxicity against HeLa cells in vitro. The mechanism for inhibition of tumor proliferation by BBRNPs-SDT was investigated via flow cytometry, photoluminescence spectroscopy, dynamic light scattering, scanning electron microscopy, ultrasonic contrast imaging, tumour pathological analysis, western blot and anatomical analysis. We identified two ongoing assumptive mechanisms. One is due to the tumor angioembolism effect, which blocks oxygen and nutrient supply in situ, leading to early-stage HeLa apoptosis. The other domino effect is due to ultrasonic energy-activated BBRNP cavitation and reactive oxygen species release, which leads to tumor vascular injury and finally induces HeLa apoptosis, resulting in tumour shrinkage. Both pathways synergistically helped with HeLa xenograft tumor supression. In conclusion, we posit that BBRNPs are a promising agent for tumor SDT. The Royal Society of Chemistry 2019-04-04 /pmc/articles/PMC9062522/ /pubmed/35515276 http://dx.doi.org/10.1039/c8ra09172b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Liu, Hanqing Zheng, Tingting Zhou, Ziqian Hu, Azhen Li, Minghua Zhang, Zhuxia Yu, Guangyin Feng, Huanhuan An, Yawen Peng, Jiao Chen, Yun Berberine nanoparticles for promising sonodynamic therapy of a HeLa xenograft tumour |
title | Berberine nanoparticles for promising sonodynamic therapy of a HeLa xenograft tumour |
title_full | Berberine nanoparticles for promising sonodynamic therapy of a HeLa xenograft tumour |
title_fullStr | Berberine nanoparticles for promising sonodynamic therapy of a HeLa xenograft tumour |
title_full_unstemmed | Berberine nanoparticles for promising sonodynamic therapy of a HeLa xenograft tumour |
title_short | Berberine nanoparticles for promising sonodynamic therapy of a HeLa xenograft tumour |
title_sort | berberine nanoparticles for promising sonodynamic therapy of a hela xenograft tumour |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062522/ https://www.ncbi.nlm.nih.gov/pubmed/35515276 http://dx.doi.org/10.1039/c8ra09172b |
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