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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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 |
work_keys_str_mv |
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