Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo Studies

<p>Early in this study, CdTe/ZnS core/shell quantum dots (QDs) were encapsulated in carboxylated Pluronic F127 triblock polymeric micelle, to preserve the optical and colloidal stability of QDs in biological fluids. Folic acid (FA) was then conjugated to the surface of QDs for the targeted del...

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Main Author: Liwei Liu, Ken-Tye Yong, Indrajit Roy, Wing-Cheung Law, Ling Ye, Jianwei Liu, Jing Liu, Rajiv Kumar, Xihe Zhang, Paras N. Prasad
Format: Article
Language:English
Published: Ivyspring International Publisher 2012-01-01
Series:Theranostics
Online Access:http://www.thno.org/v02p0705.htm
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spelling doaj-c396b511ca9a426ea8d1d0f8da1efaa62020-11-24T23:14:35ZengIvyspring International PublisherTheranostics1838-76402012-01-0127705713Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo StudiesLiwei Liu, Ken-Tye Yong, Indrajit Roy, Wing-Cheung Law, Ling Ye, Jianwei Liu, Jing Liu, Rajiv Kumar, Xihe Zhang, Paras N. Prasad<p>Early in this study, CdTe/ZnS core/shell quantum dots (QDs) were encapsulated in carboxylated Pluronic F127 triblock polymeric micelle, to preserve the optical and colloidal stability of QDs in biological fluids. Folic acid (FA) was then conjugated to the surface of QDs for the targeted delivery of the QD formulation to the tumor site, by exploiting the overexpressed FA receptors (FARs) on the tumor cells. Cytotoxicity study demonstrated that the QD formulation has negligible <i>in vitro</i> toxicity. The <i>in vitro</i> study showed that the bioconjugated micelle-encapsulated QDs, but not the unconjugated QDs, were able to efficiently label Panc-1 cancer cells. <i>In vivo</i> imaging study showed that bioconjugated QDs were able to target tumor site after intravenous injection of the formulation in tumor-bearing mice.</p>http://www.thno.org/v02p0705.htm
collection DOAJ
language English
format Article
sources DOAJ
author Liwei Liu, Ken-Tye Yong, Indrajit Roy, Wing-Cheung Law, Ling Ye, Jianwei Liu, Jing Liu, Rajiv Kumar, Xihe Zhang, Paras N. Prasad
spellingShingle Liwei Liu, Ken-Tye Yong, Indrajit Roy, Wing-Cheung Law, Ling Ye, Jianwei Liu, Jing Liu, Rajiv Kumar, Xihe Zhang, Paras N. Prasad
Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo Studies
Theranostics
author_facet Liwei Liu, Ken-Tye Yong, Indrajit Roy, Wing-Cheung Law, Ling Ye, Jianwei Liu, Jing Liu, Rajiv Kumar, Xihe Zhang, Paras N. Prasad
author_sort Liwei Liu, Ken-Tye Yong, Indrajit Roy, Wing-Cheung Law, Ling Ye, Jianwei Liu, Jing Liu, Rajiv Kumar, Xihe Zhang, Paras N. Prasad
title Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo Studies
title_short Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo Studies
title_full Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo Studies
title_fullStr Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo Studies
title_full_unstemmed Bioconjugated Pluronic Triblock-Copolymer Micelle-Encapsulated Quantum Dots for Targeted Imaging of Cancer: In Vitro and In Vivo Studies
title_sort bioconjugated pluronic triblock-copolymer micelle-encapsulated quantum dots for targeted imaging of cancer: in vitro and in vivo studies
publisher Ivyspring International Publisher
series Theranostics
issn 1838-7640
publishDate 2012-01-01
description <p>Early in this study, CdTe/ZnS core/shell quantum dots (QDs) were encapsulated in carboxylated Pluronic F127 triblock polymeric micelle, to preserve the optical and colloidal stability of QDs in biological fluids. Folic acid (FA) was then conjugated to the surface of QDs for the targeted delivery of the QD formulation to the tumor site, by exploiting the overexpressed FA receptors (FARs) on the tumor cells. Cytotoxicity study demonstrated that the QD formulation has negligible <i>in vitro</i> toxicity. The <i>in vitro</i> study showed that the bioconjugated micelle-encapsulated QDs, but not the unconjugated QDs, were able to efficiently label Panc-1 cancer cells. <i>In vivo</i> imaging study showed that bioconjugated QDs were able to target tumor site after intravenous injection of the formulation in tumor-bearing mice.</p>
url http://www.thno.org/v02p0705.htm
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