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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...

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Autores principales: Wong, Blenda Chi Kwan, Zhang, Hongqi, Qin, Ling, Chen, Hubiao, Fang, Chen, Lu, Aiping, Yang, Zhijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
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.
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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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