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Stimuli-Responsive Amphiphilic Pillar[n]arene Nanovesicles for Targeted Delivery of Cancer Drugs
[Image: see text] Cancer chemotherapeutics face several challenges, including uncontrollable drug release, off-target toxic effects, and poor bioavailability. Recently, supramolecular nanovesicles, such as calix[n]arenes (CXs), cyclodextrins (CDs), cucurbiturils (CBs), and pillar[n]arenes (PRs), hav...
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/PMC8515365/ https://www.ncbi.nlm.nih.gov/pubmed/34660950 http://dx.doi.org/10.1021/acsomega.1c04297 |
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author | Fahmy, Sherif Ashraf Ramzy, Asmaa Saleh, Basma M. El-Said Azzazy, Hassan Mohamed |
author_facet | Fahmy, Sherif Ashraf Ramzy, Asmaa Saleh, Basma M. El-Said Azzazy, Hassan Mohamed |
author_sort | Fahmy, Sherif Ashraf |
collection | PubMed |
description | [Image: see text] Cancer chemotherapeutics face several challenges, including uncontrollable drug release, off-target toxic effects, and poor bioavailability. Recently, supramolecular nanovesicles, such as calix[n]arenes (CXs), cyclodextrins (CDs), cucurbiturils (CBs), and pillar[n]arenes (PRs), have attracted attention as potential smart nanocarriers for chemotherapeutics because of their exceptional cavities that can achieve high encapsulation capacity and accommodate both hydrophilic and hydrophobic drugs. In addition, they can be functionalized with different stimuli-responsive groups, which facilitate controlled drug release. Supramolecular nanovesicles, loaded with drugs and decorated with stimuli-responsive targeting moieties, are designed by either host–guest complexation or self-assembly of amphiphilic cavitands. Pillar[n]arenes, in particular, are novel supramolecular host molecules that have recently been employed in cancer targeted drug delivery because of their symmetric pillar-shaped structure, simplicity of functionalization, and biocompatibility. This review summarizes state-of-the-art strategies for developing single or multiple stimuli-responsive pillar[n]arene nanovesicles for effective cancer treatment. |
format | Online Article Text |
id | pubmed-8515365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85153652021-10-15 Stimuli-Responsive Amphiphilic Pillar[n]arene Nanovesicles for Targeted Delivery of Cancer Drugs Fahmy, Sherif Ashraf Ramzy, Asmaa Saleh, Basma M. El-Said Azzazy, Hassan Mohamed ACS Omega [Image: see text] Cancer chemotherapeutics face several challenges, including uncontrollable drug release, off-target toxic effects, and poor bioavailability. Recently, supramolecular nanovesicles, such as calix[n]arenes (CXs), cyclodextrins (CDs), cucurbiturils (CBs), and pillar[n]arenes (PRs), have attracted attention as potential smart nanocarriers for chemotherapeutics because of their exceptional cavities that can achieve high encapsulation capacity and accommodate both hydrophilic and hydrophobic drugs. In addition, they can be functionalized with different stimuli-responsive groups, which facilitate controlled drug release. Supramolecular nanovesicles, loaded with drugs and decorated with stimuli-responsive targeting moieties, are designed by either host–guest complexation or self-assembly of amphiphilic cavitands. Pillar[n]arenes, in particular, are novel supramolecular host molecules that have recently been employed in cancer targeted drug delivery because of their symmetric pillar-shaped structure, simplicity of functionalization, and biocompatibility. This review summarizes state-of-the-art strategies for developing single or multiple stimuli-responsive pillar[n]arene nanovesicles for effective cancer treatment. American Chemical Society 2021-09-30 /pmc/articles/PMC8515365/ /pubmed/34660950 http://dx.doi.org/10.1021/acsomega.1c04297 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Fahmy, Sherif Ashraf Ramzy, Asmaa Saleh, Basma M. El-Said Azzazy, Hassan Mohamed Stimuli-Responsive Amphiphilic Pillar[n]arene Nanovesicles for Targeted Delivery of Cancer Drugs |
title | Stimuli-Responsive Amphiphilic Pillar[n]arene Nanovesicles
for Targeted Delivery of Cancer Drugs |
title_full | Stimuli-Responsive Amphiphilic Pillar[n]arene Nanovesicles
for Targeted Delivery of Cancer Drugs |
title_fullStr | Stimuli-Responsive Amphiphilic Pillar[n]arene Nanovesicles
for Targeted Delivery of Cancer Drugs |
title_full_unstemmed | Stimuli-Responsive Amphiphilic Pillar[n]arene Nanovesicles
for Targeted Delivery of Cancer Drugs |
title_short | Stimuli-Responsive Amphiphilic Pillar[n]arene Nanovesicles
for Targeted Delivery of Cancer Drugs |
title_sort | stimuli-responsive amphiphilic pillar[n]arene nanovesicles
for targeted delivery of cancer drugs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515365/ https://www.ncbi.nlm.nih.gov/pubmed/34660950 http://dx.doi.org/10.1021/acsomega.1c04297 |
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