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The Treatment of Breast Cancer Using Liposome Technology

Liposome-based chemotherapeutics used in the treatment of breast cancer can in principle enhance the therapeutic index of otherwise unencapsulated anticancer drugs. This is partially attributed to the fact that encapsulation of cytotoxic agents within liposomes allows for increased concentrations of...

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Detalles Bibliográficos
Autores principales: Brown, Sarah, Khan, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312267/
https://www.ncbi.nlm.nih.gov/pubmed/22506119
http://dx.doi.org/10.1155/2012/212965
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author Brown, Sarah
Khan, David R.
author_facet Brown, Sarah
Khan, David R.
author_sort Brown, Sarah
collection PubMed
description Liposome-based chemotherapeutics used in the treatment of breast cancer can in principle enhance the therapeutic index of otherwise unencapsulated anticancer drugs. This is partially attributed to the fact that encapsulation of cytotoxic agents within liposomes allows for increased concentrations of the drug to be delivered to the tumor site. In addition, the presence of the phospholipid bilayer prevents the encapsulated active form of the drug from being broken down in the body prior to reaching tumor tissue and also serves to minimize exposure of the drug to healthy sensitive tissue. While clinically approved liposome-based chemotherapeutics such as Doxil have proven to be quite effective in the treatment of breast cancer, significant challenges remain involving poor drug transfer between the liposome and cancerous cells. In this review, we discuss the recent advancements made in the development of liposome-based chemotherapeutics with respect to improved drug transfer for use in breast cancer therapy.
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spelling pubmed-33122672012-04-13 The Treatment of Breast Cancer Using Liposome Technology Brown, Sarah Khan, David R. J Drug Deliv Review Article Liposome-based chemotherapeutics used in the treatment of breast cancer can in principle enhance the therapeutic index of otherwise unencapsulated anticancer drugs. This is partially attributed to the fact that encapsulation of cytotoxic agents within liposomes allows for increased concentrations of the drug to be delivered to the tumor site. In addition, the presence of the phospholipid bilayer prevents the encapsulated active form of the drug from being broken down in the body prior to reaching tumor tissue and also serves to minimize exposure of the drug to healthy sensitive tissue. While clinically approved liposome-based chemotherapeutics such as Doxil have proven to be quite effective in the treatment of breast cancer, significant challenges remain involving poor drug transfer between the liposome and cancerous cells. In this review, we discuss the recent advancements made in the development of liposome-based chemotherapeutics with respect to improved drug transfer for use in breast cancer therapy. Hindawi Publishing Corporation 2012 2012-02-21 /pmc/articles/PMC3312267/ /pubmed/22506119 http://dx.doi.org/10.1155/2012/212965 Text en Copyright © 2012 S. Brown and D. R. Khan. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Brown, Sarah
Khan, David R.
The Treatment of Breast Cancer Using Liposome Technology
title The Treatment of Breast Cancer Using Liposome Technology
title_full The Treatment of Breast Cancer Using Liposome Technology
title_fullStr The Treatment of Breast Cancer Using Liposome Technology
title_full_unstemmed The Treatment of Breast Cancer Using Liposome Technology
title_short The Treatment of Breast Cancer Using Liposome Technology
title_sort treatment of breast cancer using liposome technology
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312267/
https://www.ncbi.nlm.nih.gov/pubmed/22506119
http://dx.doi.org/10.1155/2012/212965
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