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Carbonic anhydrase IX-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro
Targeted drug delivery to cancer cells by use of antibody-conjugated liposomes (immunoliposomes) has attracted considerable interest in recent years. Despite increasing efforts in developing immunoliposomes as drug carriers, the investigation of useful tumor-associated antigen targets is far from co...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113570/ https://www.ncbi.nlm.nih.gov/pubmed/25092965 http://dx.doi.org/10.2147/DDDT.S63235 |
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author | Wong, Blenda Chi Kwan Zhang, Hongqi Qin, Ling Chen, Hubiao Fang, Chen Lu, Aiping Yang, Zhijun |
author_facet | Wong, Blenda Chi Kwan Zhang, Hongqi Qin, Ling Chen, Hubiao Fang, Chen Lu, Aiping Yang, Zhijun |
author_sort | Wong, Blenda Chi Kwan |
collection | PubMed |
description | Targeted drug delivery to cancer cells by use of antibody-conjugated liposomes (immunoliposomes) has attracted considerable interest in recent years. Despite increasing efforts in developing immunoliposomes as drug carriers, the investigation of useful tumor-associated antigen targets is far from complete. Carbonic anhydrase IX (CA IX) is a cell surface antigen characterized by hypoxia-induced expression in many solid tumors. This study investigated the feasibility of CA IX-directed immunoliposomes for targeted delivery of docetaxel to human lung cancer cells in vitro. Docetaxel-loaded immunoliposomes targeting CA IX were developed with an encapsulation efficiency of 84.4±3.9% and an average particle size of 143.9±11.1 nm. Using fluorescence-based flow cytometry, the in vitro binding activity of the immunoliposomes was found to be significantly higher (by 1.65-fold) than that of the nontargeted liposomes in CA IX-positive lung cancer cells, whereas no such difference was observed between the two groups when CA IX was not expressed. Furthermore, immunoliposomal docetaxel exhibited the strongest growth inhibitory effect against CA IX-positive lung cancer cells when compared with nontargeted liposomal docetaxel or free docetaxel solution. These data suggested that CA IX-directed immunoliposomes could serve as a promising drug delivery system for targeted killing of lung cancer cells. |
format | Online Article Text |
id | pubmed-4113570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41135702014-08-04 Carbonic anhydrase IX-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro Wong, Blenda Chi Kwan Zhang, Hongqi Qin, Ling Chen, Hubiao Fang, Chen Lu, Aiping Yang, Zhijun Drug Des Devel Ther Original Research Targeted drug delivery to cancer cells by use of antibody-conjugated liposomes (immunoliposomes) has attracted considerable interest in recent years. Despite increasing efforts in developing immunoliposomes as drug carriers, the investigation of useful tumor-associated antigen targets is far from complete. Carbonic anhydrase IX (CA IX) is a cell surface antigen characterized by hypoxia-induced expression in many solid tumors. This study investigated the feasibility of CA IX-directed immunoliposomes for targeted delivery of docetaxel to human lung cancer cells in vitro. Docetaxel-loaded immunoliposomes targeting CA IX were developed with an encapsulation efficiency of 84.4±3.9% and an average particle size of 143.9±11.1 nm. Using fluorescence-based flow cytometry, the in vitro binding activity of the immunoliposomes was found to be significantly higher (by 1.65-fold) than that of the nontargeted liposomes in CA IX-positive lung cancer cells, whereas no such difference was observed between the two groups when CA IX was not expressed. Furthermore, immunoliposomal docetaxel exhibited the strongest growth inhibitory effect against CA IX-positive lung cancer cells when compared with nontargeted liposomal docetaxel or free docetaxel solution. These data suggested that CA IX-directed immunoliposomes could serve as a promising drug delivery system for targeted killing of lung cancer cells. Dove Medical Press 2014-07-22 /pmc/articles/PMC4113570/ /pubmed/25092965 http://dx.doi.org/10.2147/DDDT.S63235 Text en © 2014 Wong et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Wong, Blenda Chi Kwan Zhang, Hongqi Qin, Ling Chen, Hubiao Fang, Chen Lu, Aiping Yang, Zhijun Carbonic anhydrase IX-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro |
title | Carbonic anhydrase IX-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro |
title_full | Carbonic anhydrase IX-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro |
title_fullStr | Carbonic anhydrase IX-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro |
title_full_unstemmed | Carbonic anhydrase IX-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro |
title_short | Carbonic anhydrase IX-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro |
title_sort | carbonic anhydrase ix-directed immunoliposomes for targeted drug delivery to human lung cancer cells in vitro |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113570/ https://www.ncbi.nlm.nih.gov/pubmed/25092965 http://dx.doi.org/10.2147/DDDT.S63235 |
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