Cargando…
Cancer Cell–Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy
PURPOSE: Nanomaterial-based drug-delivery systems allowing for effective targeted delivery of smallmolecule chemodrugs to tumors have revolutionized cancer therapy. Recently, as novel nanomaterials with outstanding physicochemical properties, boron nitride nanospheres (BNs) have emerged as a promisi...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959002/ https://www.ncbi.nlm.nih.gov/pubmed/33731994 http://dx.doi.org/10.2147/IJN.S266948 |
_version_ | 1783664898953183232 |
---|---|
author | Feng, Shini Ren, Yajing Li, Hui Tang, Yunfei Yan, Jinyu Shen, Zeyuan Zhang, Huijie Chen, Fuxue |
author_facet | Feng, Shini Ren, Yajing Li, Hui Tang, Yunfei Yan, Jinyu Shen, Zeyuan Zhang, Huijie Chen, Fuxue |
author_sort | Feng, Shini |
collection | PubMed |
description | PURPOSE: Nanomaterial-based drug-delivery systems allowing for effective targeted delivery of smallmolecule chemodrugs to tumors have revolutionized cancer therapy. Recently, as novel nanomaterials with outstanding physicochemical properties, boron nitride nanospheres (BNs) have emerged as a promising candidate for drug delivery. However, poor dispersity and lack of tumor targeting severely limit further applications. In this study, cancer cell–membrane biomimetic BNs were designed for targeted anticancer drug delivery. METHODS: Cell membrane extracted from HeLa cells (HM) was used to encapsulate BNs by physical extrusion. Doxorubicin (Dox) was loaded onto HM-BNs as a model drug. RESULTS: The cell-membrane coating endowed the BNs with excellent dispersibility and cytocompatibility. The drug-release profile showed that the Dox@HM-BNs responded to acid pH, resulting in rapid Dox release. Enhanced cellular uptake of Dox@HM-BNs by HeLa cells was revealed because of the homologous targeting of cancer-cell membranes. CCK8 and live/dead assays showed that Dox@HM-BNs had stronger cytotoxicity against HeLa cells, due to self-selective cellular uptake. Finally, antitumor investigation using the HeLa tumor model demonstrated that Dox@HM-BNs possessed much more efficient tumor inhibition than free Dox or Dox@BNs. CONCLUSION: These findings indicate that the newly developed HM-BNs are promising as an efficient tumor-selective drug-delivery vehicle for tumor therapy. |
format | Online Article Text |
id | pubmed-7959002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-79590022021-03-16 Cancer Cell–Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy Feng, Shini Ren, Yajing Li, Hui Tang, Yunfei Yan, Jinyu Shen, Zeyuan Zhang, Huijie Chen, Fuxue Int J Nanomedicine Original Research PURPOSE: Nanomaterial-based drug-delivery systems allowing for effective targeted delivery of smallmolecule chemodrugs to tumors have revolutionized cancer therapy. Recently, as novel nanomaterials with outstanding physicochemical properties, boron nitride nanospheres (BNs) have emerged as a promising candidate for drug delivery. However, poor dispersity and lack of tumor targeting severely limit further applications. In this study, cancer cell–membrane biomimetic BNs were designed for targeted anticancer drug delivery. METHODS: Cell membrane extracted from HeLa cells (HM) was used to encapsulate BNs by physical extrusion. Doxorubicin (Dox) was loaded onto HM-BNs as a model drug. RESULTS: The cell-membrane coating endowed the BNs with excellent dispersibility and cytocompatibility. The drug-release profile showed that the Dox@HM-BNs responded to acid pH, resulting in rapid Dox release. Enhanced cellular uptake of Dox@HM-BNs by HeLa cells was revealed because of the homologous targeting of cancer-cell membranes. CCK8 and live/dead assays showed that Dox@HM-BNs had stronger cytotoxicity against HeLa cells, due to self-selective cellular uptake. Finally, antitumor investigation using the HeLa tumor model demonstrated that Dox@HM-BNs possessed much more efficient tumor inhibition than free Dox or Dox@BNs. CONCLUSION: These findings indicate that the newly developed HM-BNs are promising as an efficient tumor-selective drug-delivery vehicle for tumor therapy. Dove 2021-03-11 /pmc/articles/PMC7959002/ /pubmed/33731994 http://dx.doi.org/10.2147/IJN.S266948 Text en © 2021 Feng et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Feng, Shini Ren, Yajing Li, Hui Tang, Yunfei Yan, Jinyu Shen, Zeyuan Zhang, Huijie Chen, Fuxue Cancer Cell–Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy |
title | Cancer Cell–Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy |
title_full | Cancer Cell–Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy |
title_fullStr | Cancer Cell–Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy |
title_full_unstemmed | Cancer Cell–Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy |
title_short | Cancer Cell–Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy |
title_sort | cancer cell–membrane biomimetic boron nitride nanospheres for targeted cancer therapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959002/ https://www.ncbi.nlm.nih.gov/pubmed/33731994 http://dx.doi.org/10.2147/IJN.S266948 |
work_keys_str_mv | AT fengshini cancercellmembranebiomimeticboronnitridenanospheresfortargetedcancertherapy AT renyajing cancercellmembranebiomimeticboronnitridenanospheresfortargetedcancertherapy AT lihui cancercellmembranebiomimeticboronnitridenanospheresfortargetedcancertherapy AT tangyunfei cancercellmembranebiomimeticboronnitridenanospheresfortargetedcancertherapy AT yanjinyu cancercellmembranebiomimeticboronnitridenanospheresfortargetedcancertherapy AT shenzeyuan cancercellmembranebiomimeticboronnitridenanospheresfortargetedcancertherapy AT zhanghuijie cancercellmembranebiomimeticboronnitridenanospheresfortargetedcancertherapy AT chenfuxue cancercellmembranebiomimeticboronnitridenanospheresfortargetedcancertherapy |