Enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells

Here, a set of novel and personalized nanocarriers are presented for controlled nucleus-targeted antitumor drug delivery and real-time imaging of intracellular drug molecule trafficking by integrating an enzyme activatable cell penetrating peptide (CPP) with mesoporous silica coated quantum dots nan...

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Main Authors: Costa, Marianne, Yeow, Edwin K. L., Li, Jinming, Liu, Fang, Shao, Qing, Min, Yuanzeng, Xing, Bengang
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2014
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Online Access:https://hdl.handle.net/10356/102852
http://hdl.handle.net/10220/19217
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1028522020-03-07T12:31:22Z Enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells Costa, Marianne Yeow, Edwin K. L. Li, Jinming Liu, Fang Shao, Qing Min, Yuanzeng Xing, Bengang School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Biochemistry Here, a set of novel and personalized nanocarriers are presented for controlled nucleus-targeted antitumor drug delivery and real-time imaging of intracellular drug molecule trafficking by integrating an enzyme activatable cell penetrating peptide (CPP) with mesoporous silica coated quantum dots nanoparticles. Upon loading of antitumor drug, doxorubicin (DOX) and further exposure to proteases in tumor cell environment, the enzymatic cleavage of peptide sequence activates oligocationic TAT residues on the QDs@mSiO2 surface and direct the DOX delivery into cellular nucleus. The systematic cell imaging and cytotoxicity studies confirm that the enzyme responsive DOX-loaded CPP-QDs@mSiO2 nanoparticles can selectively release DOX in the tumor cells with high cathepsin B enzyme expression and greatly facilitate DOX accumulation in targeted nucleus, thus exhibiting enhanced antitumor activity in these cells. As contrast, there is limited nuclear-targeted drug accumulation and lower tumor cytotoxicity observed in the cells without enzyme expression. More importantly, significant antitumor DOX accumulation and higher tumor inactivation is also found in the drug resistant tumor cells with targeted enzyme expression. Such simple and specific enzyme responsive mesoporous silica-QDs nanoconjugates provide great promise for rational design of targeted drug delivery into biological system, and may thus greatly facilitate the medical theranostics in the near future. 2014-04-10T04:18:45Z 2019-12-06T21:01:11Z 2014-04-10T04:18:45Z 2019-12-06T21:01:11Z 2014 2014 Journal Article Li, J., Liu, F., Shao, Q., Min, Y., Costa, M., Yeow, E. K. L., et al. (2014). Enzyme-Responsive Cell-Penetrating Peptide Conjugated Mesoporous Silica Quantum Dot Nanocarriers for Controlled Release of Nucleus-Targeted Drug Molecules and Real-Time Intracellular Fluorescence Imaging of Tumor Cells. Advanced Healthcare Materials, 3(8), 1230-1239. 2192-2640 https://hdl.handle.net/10356/102852 http://hdl.handle.net/10220/19217 10.1002/adhm.201300613 en Advanced healthcare materials © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science::Chemistry::Biochemistry
spellingShingle DRNTU::Science::Chemistry::Biochemistry
Costa, Marianne
Yeow, Edwin K. L.
Li, Jinming
Liu, Fang
Shao, Qing
Min, Yuanzeng
Xing, Bengang
Enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells
description Here, a set of novel and personalized nanocarriers are presented for controlled nucleus-targeted antitumor drug delivery and real-time imaging of intracellular drug molecule trafficking by integrating an enzyme activatable cell penetrating peptide (CPP) with mesoporous silica coated quantum dots nanoparticles. Upon loading of antitumor drug, doxorubicin (DOX) and further exposure to proteases in tumor cell environment, the enzymatic cleavage of peptide sequence activates oligocationic TAT residues on the QDs@mSiO2 surface and direct the DOX delivery into cellular nucleus. The systematic cell imaging and cytotoxicity studies confirm that the enzyme responsive DOX-loaded CPP-QDs@mSiO2 nanoparticles can selectively release DOX in the tumor cells with high cathepsin B enzyme expression and greatly facilitate DOX accumulation in targeted nucleus, thus exhibiting enhanced antitumor activity in these cells. As contrast, there is limited nuclear-targeted drug accumulation and lower tumor cytotoxicity observed in the cells without enzyme expression. More importantly, significant antitumor DOX accumulation and higher tumor inactivation is also found in the drug resistant tumor cells with targeted enzyme expression. Such simple and specific enzyme responsive mesoporous silica-QDs nanoconjugates provide great promise for rational design of targeted drug delivery into biological system, and may thus greatly facilitate the medical theranostics in the near future.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Costa, Marianne
Yeow, Edwin K. L.
Li, Jinming
Liu, Fang
Shao, Qing
Min, Yuanzeng
Xing, Bengang
format Article
author Costa, Marianne
Yeow, Edwin K. L.
Li, Jinming
Liu, Fang
Shao, Qing
Min, Yuanzeng
Xing, Bengang
author_sort Costa, Marianne
title Enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells
title_short Enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells
title_full Enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells
title_fullStr Enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells
title_full_unstemmed Enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells
title_sort enzyme-responsive cell-penetrating peptides conjugated mesoporous silica quantum dots nanocarriers for controlled release of nucleus-targeted drug molecules and real-time intracellular fluorescence imaging of tumor cells
publishDate 2014
url https://hdl.handle.net/10356/102852
http://hdl.handle.net/10220/19217
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