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Engineered Protein Polymer-Gold Nanoparticle Hybrid Materials for Small Molecule Delivery

We have fabricated protein polymer-gold nanoparticle (P-GNP) nanocomposites that exhibit enhanced binding and delivery properties of the small hydrophobic molecule drug, curcumin, to the model breast cancer cell line, MCF-7. These hybrid biomaterials are constructed via in situ GNP templated-synthes...

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Autores principales: Dai, Min, Frezzo, JA, Sharma, E, Chen, R, Singh, N, Yuvienco, C, Caglar, E, Xiao, S, Saxena, A, Montclare, JK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828936/
https://www.ncbi.nlm.nih.gov/pubmed/27081576
http://dx.doi.org/10.4172/2157-7439.1000356
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author Dai, Min
Frezzo, JA
Sharma, E
Chen, R
Singh, N
Yuvienco, C
Caglar, E
Xiao, S
Saxena, A
Montclare, JK
author_facet Dai, Min
Frezzo, JA
Sharma, E
Chen, R
Singh, N
Yuvienco, C
Caglar, E
Xiao, S
Saxena, A
Montclare, JK
author_sort Dai, Min
collection PubMed
description We have fabricated protein polymer-gold nanoparticle (P-GNP) nanocomposites that exhibit enhanced binding and delivery properties of the small hydrophobic molecule drug, curcumin, to the model breast cancer cell line, MCF-7. These hybrid biomaterials are constructed via in situ GNP templated-synthesis with genetically engineered histidine tags. The P-GNP nanocomposites exhibit enhanced small molecule loading, sustained release and increased uptake by MCF-7 cells. When compared to the proteins polymers alone, the P-GNPs demonstrate a greater than 7-fold increase in curcumin binding, a nearly 50% slower release profile and more than 2-fold increase in cellular uptake of curcumin. These results suggest that P-GNP nanocomposites serve as promising candidates for drug delivery vehicles.
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spelling pubmed-48289362016-04-12 Engineered Protein Polymer-Gold Nanoparticle Hybrid Materials for Small Molecule Delivery Dai, Min Frezzo, JA Sharma, E Chen, R Singh, N Yuvienco, C Caglar, E Xiao, S Saxena, A Montclare, JK J Nanomed Nanotechnol Article We have fabricated protein polymer-gold nanoparticle (P-GNP) nanocomposites that exhibit enhanced binding and delivery properties of the small hydrophobic molecule drug, curcumin, to the model breast cancer cell line, MCF-7. These hybrid biomaterials are constructed via in situ GNP templated-synthesis with genetically engineered histidine tags. The P-GNP nanocomposites exhibit enhanced small molecule loading, sustained release and increased uptake by MCF-7 cells. When compared to the proteins polymers alone, the P-GNPs demonstrate a greater than 7-fold increase in curcumin binding, a nearly 50% slower release profile and more than 2-fold increase in cellular uptake of curcumin. These results suggest that P-GNP nanocomposites serve as promising candidates for drug delivery vehicles. 2016-02-29 2016-02 /pmc/articles/PMC4828936/ /pubmed/27081576 http://dx.doi.org/10.4172/2157-7439.1000356 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Dai, Min
Frezzo, JA
Sharma, E
Chen, R
Singh, N
Yuvienco, C
Caglar, E
Xiao, S
Saxena, A
Montclare, JK
Engineered Protein Polymer-Gold Nanoparticle Hybrid Materials for Small Molecule Delivery
title Engineered Protein Polymer-Gold Nanoparticle Hybrid Materials for Small Molecule Delivery
title_full Engineered Protein Polymer-Gold Nanoparticle Hybrid Materials for Small Molecule Delivery
title_fullStr Engineered Protein Polymer-Gold Nanoparticle Hybrid Materials for Small Molecule Delivery
title_full_unstemmed Engineered Protein Polymer-Gold Nanoparticle Hybrid Materials for Small Molecule Delivery
title_short Engineered Protein Polymer-Gold Nanoparticle Hybrid Materials for Small Molecule Delivery
title_sort engineered protein polymer-gold nanoparticle hybrid materials for small molecule delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828936/
https://www.ncbi.nlm.nih.gov/pubmed/27081576
http://dx.doi.org/10.4172/2157-7439.1000356
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