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Design, Synthesis and Applications of Hyaluronic Acid-Paclitaxel Bioconjugates†
Paclitaxel (1a), a well known antitumor agent adopted mainly for the treatment of breast and ovarian cancer, suffers from significant disadvantages such as low solubility, certain toxicity and specific drug-resistance of some tumor cells. To overcome these problems extensive research has been carrie...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245481/ https://www.ncbi.nlm.nih.gov/pubmed/18305424 http://dx.doi.org/10.3390/molecules13020360 |
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author | Leonelli, Francesca La Bella, Angela Migneco, Luisa Maria Bettolo, Rinaldo Marini |
author_facet | Leonelli, Francesca La Bella, Angela Migneco, Luisa Maria Bettolo, Rinaldo Marini |
author_sort | Leonelli, Francesca |
collection | PubMed |
description | Paclitaxel (1a), a well known antitumor agent adopted mainly for the treatment of breast and ovarian cancer, suffers from significant disadvantages such as low solubility, certain toxicity and specific drug-resistance of some tumor cells. To overcome these problems extensive research has been carried out. Among the various proposed strategies, the conjugation of paclitaxel (1a) to a biocompatible polymer, such as hyaluronic acid (HA, 2), has also been considered. Coupling a bioactive compound to a biocompatible polymer offers, in general, many advantages such as better drug solubilization, better stabilization, specific localization and controlled release. Hereafter the design, synthesis and applications of hyaluronic acid-paclitaxel bioconjugates are reviewed. An overview of HA-paclitaxel combinations is also given. |
format | Online Article Text |
id | pubmed-6245481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62454812018-11-26 Design, Synthesis and Applications of Hyaluronic Acid-Paclitaxel Bioconjugates† Leonelli, Francesca La Bella, Angela Migneco, Luisa Maria Bettolo, Rinaldo Marini Molecules Review Paclitaxel (1a), a well known antitumor agent adopted mainly for the treatment of breast and ovarian cancer, suffers from significant disadvantages such as low solubility, certain toxicity and specific drug-resistance of some tumor cells. To overcome these problems extensive research has been carried out. Among the various proposed strategies, the conjugation of paclitaxel (1a) to a biocompatible polymer, such as hyaluronic acid (HA, 2), has also been considered. Coupling a bioactive compound to a biocompatible polymer offers, in general, many advantages such as better drug solubilization, better stabilization, specific localization and controlled release. Hereafter the design, synthesis and applications of hyaluronic acid-paclitaxel bioconjugates are reviewed. An overview of HA-paclitaxel combinations is also given. MDPI 2008-02-12 /pmc/articles/PMC6245481/ /pubmed/18305424 http://dx.doi.org/10.3390/molecules13020360 Text en © 2008 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes. |
spellingShingle | Review Leonelli, Francesca La Bella, Angela Migneco, Luisa Maria Bettolo, Rinaldo Marini Design, Synthesis and Applications of Hyaluronic Acid-Paclitaxel Bioconjugates† |
title | Design, Synthesis and Applications of Hyaluronic Acid-Paclitaxel Bioconjugates† |
title_full | Design, Synthesis and Applications of Hyaluronic Acid-Paclitaxel Bioconjugates† |
title_fullStr | Design, Synthesis and Applications of Hyaluronic Acid-Paclitaxel Bioconjugates† |
title_full_unstemmed | Design, Synthesis and Applications of Hyaluronic Acid-Paclitaxel Bioconjugates† |
title_short | Design, Synthesis and Applications of Hyaluronic Acid-Paclitaxel Bioconjugates† |
title_sort | design, synthesis and applications of hyaluronic acid-paclitaxel bioconjugates† |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245481/ https://www.ncbi.nlm.nih.gov/pubmed/18305424 http://dx.doi.org/10.3390/molecules13020360 |
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