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Improved Solubility and Bioactivity of Camptothecin Family Antitumor Drugs with Supramolecular Encapsulation by Water-Soluble Pillar[6]arene
[Image: see text] Water-soluble pillar[6]arene (WP6) was used to solubilize camptothecin family antitumor drugs. In the presence of WP6, the solubility of camptothecin (CPT) and 10-hydroxycamptothecin (HCPT) was enhanced by 380 and 40 times, respectively. The solubility enhancement is proved to be t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044948/ https://www.ncbi.nlm.nih.gov/pubmed/30023745 http://dx.doi.org/10.1021/acsomega.7b01032 |
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author | Liu, Yamin Chen, Xi Ding, Jiaming Yu, Lin Ma, Da Ding, Jiandong |
author_facet | Liu, Yamin Chen, Xi Ding, Jiaming Yu, Lin Ma, Da Ding, Jiandong |
author_sort | Liu, Yamin |
collection | PubMed |
description | [Image: see text] Water-soluble pillar[6]arene (WP6) was used to solubilize camptothecin family antitumor drugs. In the presence of WP6, the solubility of camptothecin (CPT) and 10-hydroxycamptothecin (HCPT) was enhanced by 380 and 40 times, respectively. The solubility enhancement is proved to be the result of the host–guest encapsulation by WP6. WP6 has a low cytotoxicity against normal MC 3T3-E1 cells, whereas the bioactivity of CPT and HCPT is substantially improved as a result of the solubility enhancement. |
format | Online Article Text |
id | pubmed-6044948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60449482018-07-16 Improved Solubility and Bioactivity of Camptothecin Family Antitumor Drugs with Supramolecular Encapsulation by Water-Soluble Pillar[6]arene Liu, Yamin Chen, Xi Ding, Jiaming Yu, Lin Ma, Da Ding, Jiandong ACS Omega [Image: see text] Water-soluble pillar[6]arene (WP6) was used to solubilize camptothecin family antitumor drugs. In the presence of WP6, the solubility of camptothecin (CPT) and 10-hydroxycamptothecin (HCPT) was enhanced by 380 and 40 times, respectively. The solubility enhancement is proved to be the result of the host–guest encapsulation by WP6. WP6 has a low cytotoxicity against normal MC 3T3-E1 cells, whereas the bioactivity of CPT and HCPT is substantially improved as a result of the solubility enhancement. American Chemical Society 2017-08-31 /pmc/articles/PMC6044948/ /pubmed/30023745 http://dx.doi.org/10.1021/acsomega.7b01032 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Liu, Yamin Chen, Xi Ding, Jiaming Yu, Lin Ma, Da Ding, Jiandong Improved Solubility and Bioactivity of Camptothecin Family Antitumor Drugs with Supramolecular Encapsulation by Water-Soluble Pillar[6]arene |
title | Improved Solubility and Bioactivity of Camptothecin
Family Antitumor Drugs with Supramolecular Encapsulation by Water-Soluble
Pillar[6]arene |
title_full | Improved Solubility and Bioactivity of Camptothecin
Family Antitumor Drugs with Supramolecular Encapsulation by Water-Soluble
Pillar[6]arene |
title_fullStr | Improved Solubility and Bioactivity of Camptothecin
Family Antitumor Drugs with Supramolecular Encapsulation by Water-Soluble
Pillar[6]arene |
title_full_unstemmed | Improved Solubility and Bioactivity of Camptothecin
Family Antitumor Drugs with Supramolecular Encapsulation by Water-Soluble
Pillar[6]arene |
title_short | Improved Solubility and Bioactivity of Camptothecin
Family Antitumor Drugs with Supramolecular Encapsulation by Water-Soluble
Pillar[6]arene |
title_sort | improved solubility and bioactivity of camptothecin
family antitumor drugs with supramolecular encapsulation by water-soluble
pillar[6]arene |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044948/ https://www.ncbi.nlm.nih.gov/pubmed/30023745 http://dx.doi.org/10.1021/acsomega.7b01032 |
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