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Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy
[Image: see text] Ursolic acid is widely used as an effective anticancer drug for the treatment of various cancers. However, its poor water solubility, short circulation time in vivo, and lack of targeting have made it a burden for clinical applications. We report a self-assembled folate-modified pe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818303/ https://www.ncbi.nlm.nih.gov/pubmed/33490781 http://dx.doi.org/10.1021/acsomega.0c04350 |
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author | Liu, Yanxue Kong, Tianjiao Yang, Zixuan Zhang, Yawen Lei, Jiandu Zhao, Peng |
author_facet | Liu, Yanxue Kong, Tianjiao Yang, Zixuan Zhang, Yawen Lei, Jiandu Zhao, Peng |
author_sort | Liu, Yanxue |
collection | PubMed |
description | [Image: see text] Ursolic acid is widely used as an effective anticancer drug for the treatment of various cancers. However, its poor water solubility, short circulation time in vivo, and lack of targeting have made it a burden for clinical applications. We report a self-assembled folate-modified pectin nanoparticle for loading ursolic acid (HCPT@F-Pt-PU NPs) and embed the anticancer drug hydroxycamptothecin to achieve synergistic treatment with ursolic acid. In addition, the galactose residue of the pectin molecule can be recognized by the asialoglycoprotein receptor on the surface of the liver cancer cell, promoting the rapid penetration and release of HCPT@F-Pt-PU NPs intracellularly. In particular, the introduction of multiarm polyethylene glycol can improve the uniformity (106 nm) and concealment of the nanoparticles and avoid the early release of the drug or the toxicity to normal cells. HCPT@F-Pt-PU NPs have a high drug loading (7.27 wt %) and embedding efficiency (19.84 wt %) and continuous circulation up to 80 h, leading to more apoptosis (91.61%). HCPT@F-Pt-PU NP intracellular drug delivery will be a promising strategy. |
format | Online Article Text |
id | pubmed-7818303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78183032021-01-22 Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy Liu, Yanxue Kong, Tianjiao Yang, Zixuan Zhang, Yawen Lei, Jiandu Zhao, Peng ACS Omega [Image: see text] Ursolic acid is widely used as an effective anticancer drug for the treatment of various cancers. However, its poor water solubility, short circulation time in vivo, and lack of targeting have made it a burden for clinical applications. We report a self-assembled folate-modified pectin nanoparticle for loading ursolic acid (HCPT@F-Pt-PU NPs) and embed the anticancer drug hydroxycamptothecin to achieve synergistic treatment with ursolic acid. In addition, the galactose residue of the pectin molecule can be recognized by the asialoglycoprotein receptor on the surface of the liver cancer cell, promoting the rapid penetration and release of HCPT@F-Pt-PU NPs intracellularly. In particular, the introduction of multiarm polyethylene glycol can improve the uniformity (106 nm) and concealment of the nanoparticles and avoid the early release of the drug or the toxicity to normal cells. HCPT@F-Pt-PU NPs have a high drug loading (7.27 wt %) and embedding efficiency (19.84 wt %) and continuous circulation up to 80 h, leading to more apoptosis (91.61%). HCPT@F-Pt-PU NP intracellular drug delivery will be a promising strategy. American Chemical Society 2021-01-07 /pmc/articles/PMC7818303/ /pubmed/33490781 http://dx.doi.org/10.1021/acsomega.0c04350 Text en © 2021 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Liu, Yanxue Kong, Tianjiao Yang, Zixuan Zhang, Yawen Lei, Jiandu Zhao, Peng Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy |
title | Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm
Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy |
title_full | Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm
Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy |
title_fullStr | Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm
Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy |
title_full_unstemmed | Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm
Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy |
title_short | Self-Assembled Folic Acid-Targeted Pectin-Multi-Arm
Polyethylene Glycol Nanoparticles for Tumor Intracellular Chemotherapy |
title_sort | self-assembled folic acid-targeted pectin-multi-arm
polyethylene glycol nanoparticles for tumor intracellular chemotherapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818303/ https://www.ncbi.nlm.nih.gov/pubmed/33490781 http://dx.doi.org/10.1021/acsomega.0c04350 |
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