Surface-Initiated Atom Transfer Polymerized Anionic Corona on Gold Nanoparticles for Anti-Cancer Therapy

Surface initiated atom transfer radical polymerization (SI-ATRP) documented a simple but efficient technique to grow a dense polymer layer on any surface. Gold nanoparticles (AuNPs) give a broad surface to immobilize sulfhyryl group-containing initiators for SI-ATRP; in addition, AuNPs are the major...

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Main Authors: Wei Mao, Sol Lee, Ji Un Shin, Hyuk Sang Yoo
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/12/3/261
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spelling doaj-1bad3e41b1e54fb7b2663c821cfd38a52020-11-25T02:38:46ZengMDPI AGPharmaceutics1999-49232020-03-0112326110.3390/pharmaceutics12030261pharmaceutics12030261Surface-Initiated Atom Transfer Polymerized Anionic Corona on Gold Nanoparticles for Anti-Cancer TherapyWei Mao0Sol Lee1Ji Un Shin2Hyuk Sang Yoo3Department of Biomedical Materials Engineering, Kangwon National University, Chuncheon 24341, KoreaDepartment of Biomedical Materials Engineering, Kangwon National University, Chuncheon 24341, KoreaDepartment of Biomedical Materials Engineering, Kangwon National University, Chuncheon 24341, KoreaDepartment of Biomedical Materials Engineering, Kangwon National University, Chuncheon 24341, KoreaSurface initiated atom transfer radical polymerization (SI-ATRP) documented a simple but efficient technique to grow a dense polymer layer on any surface. Gold nanoparticles (AuNPs) give a broad surface to immobilize sulfhyryl group-containing initiators for SI-ATRP; in addition, AuNPs are the major nanoparticulate carriers for delivery of anti-cancer therapeutics, since they are biocompatible and bioinert. In this work, AuNPs with a disulfide initiator were polymerized with sulfoethyl methacrylate by SI-ATRP to decorate the particles with anionic corona, and branched polyethyeleneimine (PEI) and siRNA were sequentially layered onto the anionic corona of AuNP by electrostatic interaction. The in vitro anti-cancer effect confirmed that AuNP with anionic corona showed higher degrees of apoptosis as well as suppression of the oncogene expression in a siRNA dose-dependent manner. The in vivo study of tumor-bearing nude mice revealed that mice treated with c-Myc siRNA-incorporated AuNPs showed dramatically decreased tumor size in comparison to those with free siRNA for 4 weeks. Furthermore, histological examination and gene expression study revealed that the decorated AuNP significantly suppressed c-Myc expression. Thus, we envision that the layer-by-layer assembly on the anionic brushes can be potentially used to incorporate nucleic acids onto metallic particles with high transfection efficiency.https://www.mdpi.com/1999-4923/12/3/261surface-initiated atom transfer radical polymerizationgold nanoparticlec-myc sirnaanti-cancer therapy
collection DOAJ
language English
format Article
sources DOAJ
author Wei Mao
Sol Lee
Ji Un Shin
Hyuk Sang Yoo
spellingShingle Wei Mao
Sol Lee
Ji Un Shin
Hyuk Sang Yoo
Surface-Initiated Atom Transfer Polymerized Anionic Corona on Gold Nanoparticles for Anti-Cancer Therapy
Pharmaceutics
surface-initiated atom transfer radical polymerization
gold nanoparticle
c-myc sirna
anti-cancer therapy
author_facet Wei Mao
Sol Lee
Ji Un Shin
Hyuk Sang Yoo
author_sort Wei Mao
title Surface-Initiated Atom Transfer Polymerized Anionic Corona on Gold Nanoparticles for Anti-Cancer Therapy
title_short Surface-Initiated Atom Transfer Polymerized Anionic Corona on Gold Nanoparticles for Anti-Cancer Therapy
title_full Surface-Initiated Atom Transfer Polymerized Anionic Corona on Gold Nanoparticles for Anti-Cancer Therapy
title_fullStr Surface-Initiated Atom Transfer Polymerized Anionic Corona on Gold Nanoparticles for Anti-Cancer Therapy
title_full_unstemmed Surface-Initiated Atom Transfer Polymerized Anionic Corona on Gold Nanoparticles for Anti-Cancer Therapy
title_sort surface-initiated atom transfer polymerized anionic corona on gold nanoparticles for anti-cancer therapy
publisher MDPI AG
series Pharmaceutics
issn 1999-4923
publishDate 2020-03-01
description Surface initiated atom transfer radical polymerization (SI-ATRP) documented a simple but efficient technique to grow a dense polymer layer on any surface. Gold nanoparticles (AuNPs) give a broad surface to immobilize sulfhyryl group-containing initiators for SI-ATRP; in addition, AuNPs are the major nanoparticulate carriers for delivery of anti-cancer therapeutics, since they are biocompatible and bioinert. In this work, AuNPs with a disulfide initiator were polymerized with sulfoethyl methacrylate by SI-ATRP to decorate the particles with anionic corona, and branched polyethyeleneimine (PEI) and siRNA were sequentially layered onto the anionic corona of AuNP by electrostatic interaction. The in vitro anti-cancer effect confirmed that AuNP with anionic corona showed higher degrees of apoptosis as well as suppression of the oncogene expression in a siRNA dose-dependent manner. The in vivo study of tumor-bearing nude mice revealed that mice treated with c-Myc siRNA-incorporated AuNPs showed dramatically decreased tumor size in comparison to those with free siRNA for 4 weeks. Furthermore, histological examination and gene expression study revealed that the decorated AuNP significantly suppressed c-Myc expression. Thus, we envision that the layer-by-layer assembly on the anionic brushes can be potentially used to incorporate nucleic acids onto metallic particles with high transfection efficiency.
topic surface-initiated atom transfer radical polymerization
gold nanoparticle
c-myc sirna
anti-cancer therapy
url https://www.mdpi.com/1999-4923/12/3/261
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AT sollee surfaceinitiatedatomtransferpolymerizedanioniccoronaongoldnanoparticlesforanticancertherapy
AT jiunshin surfaceinitiatedatomtransferpolymerizedanioniccoronaongoldnanoparticlesforanticancertherapy
AT hyuksangyoo surfaceinitiatedatomtransferpolymerizedanioniccoronaongoldnanoparticlesforanticancertherapy
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