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How nanotechnology can enhance docetaxel therapy

Docetaxel has been recognized as one of the most efficient anticancer drugs over the past decade; however, its poor water solubility and systemic toxicity have greatly limited its clinical application. In recent decades, the emergence of nanotechnology has provided new drug delivery systems for doce...

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Detalles Bibliográficos
Autores principales: Zhang, Li, Zhang, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742154/
https://www.ncbi.nlm.nih.gov/pubmed/23950643
http://dx.doi.org/10.2147/IJN.S46921
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author Zhang, Li
Zhang, Na
author_facet Zhang, Li
Zhang, Na
author_sort Zhang, Li
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description Docetaxel has been recognized as one of the most efficient anticancer drugs over the past decade; however, its poor water solubility and systemic toxicity have greatly limited its clinical application. In recent decades, the emergence of nanotechnology has provided new drug delivery systems for docetaxel, which can improve its water solubility, minimize the side effects and increase the tumor-targeting distribution by passive or active targeting. This review focuses on the research progress in nanoformulations related to docetaxel delivery – such as polymer-based, lipid-based, and lipid-polymer hybrid nanocarriers, as well as inorganic nanoparticles – addressing their structures, characteristics, preparation, physicochemical properties, methods by which drugs are loaded into them, and their in vitro and in vivo efficacies. Further, the targeted ligands used in the docetaxel nanoformulations, such as monoclonal antibodies, peptides, folic acid, transferrin, aptamers and hyaluronic acid, are described. The issues to overcome before docetaxel nanoformulations can be used in clinical and commercial applications are also discussed.
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spelling pubmed-37421542013-08-15 How nanotechnology can enhance docetaxel therapy Zhang, Li Zhang, Na Int J Nanomedicine Review Docetaxel has been recognized as one of the most efficient anticancer drugs over the past decade; however, its poor water solubility and systemic toxicity have greatly limited its clinical application. In recent decades, the emergence of nanotechnology has provided new drug delivery systems for docetaxel, which can improve its water solubility, minimize the side effects and increase the tumor-targeting distribution by passive or active targeting. This review focuses on the research progress in nanoformulations related to docetaxel delivery – such as polymer-based, lipid-based, and lipid-polymer hybrid nanocarriers, as well as inorganic nanoparticles – addressing their structures, characteristics, preparation, physicochemical properties, methods by which drugs are loaded into them, and their in vitro and in vivo efficacies. Further, the targeted ligands used in the docetaxel nanoformulations, such as monoclonal antibodies, peptides, folic acid, transferrin, aptamers and hyaluronic acid, are described. The issues to overcome before docetaxel nanoformulations can be used in clinical and commercial applications are also discussed. Dove Medical Press 2013 2013-08-07 /pmc/articles/PMC3742154/ /pubmed/23950643 http://dx.doi.org/10.2147/IJN.S46921 Text en © 2013 Zhang and Zhang, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Zhang, Li
Zhang, Na
How nanotechnology can enhance docetaxel therapy
title How nanotechnology can enhance docetaxel therapy
title_full How nanotechnology can enhance docetaxel therapy
title_fullStr How nanotechnology can enhance docetaxel therapy
title_full_unstemmed How nanotechnology can enhance docetaxel therapy
title_short How nanotechnology can enhance docetaxel therapy
title_sort how nanotechnology can enhance docetaxel therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742154/
https://www.ncbi.nlm.nih.gov/pubmed/23950643
http://dx.doi.org/10.2147/IJN.S46921
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