Biocompatible Glycol Chitosan-Coated Gold Nanoparticles for Tumor-Targeting CT Imaging

Authors
Sun, In-CheolNa, Jin HeeJeong, Seo YoungKim, Dong-EogKwon, Ick ChanChoi, KuiwonAhn, Cheol-HeeKim, Kwangmeyung
Issue Date
2014-06
Publisher
SPRINGER/PLENUM PUBLISHERS
Citation
PHARMACEUTICAL RESEARCH, v.31, no.6, pp.1418 - 1425
Abstract
The application of gold nanoparticles (AuNPs) in biomedical field was limited due to the low stability in the biological condition. Herein, to enhance stability and tumor targeting ability of AuNPs, their surface was modified with biocompatible glycol chitosan (GC) and the in vivo biodistribution of GC coated AuNPs (GC-AuNPs) were studied through computed tomography (CT). Polymer-coated gold nanoparticles were produced using GC as a reducing agent and a stabilizer. Their feasibility in biomedical application was explored through CT in tumor-bearing mice. Stability of gold nanoparticles increased in the physiological condition due to the GC coating layer on the surface. Tomographic images of tumor were successfully obtained in the tumor-xenografted animal model when the GC-AuNPs were used as a CT contrast agent. The tumor targeting property of the gold nanoparticles was due to the properties of GC because GC-AuNPs were accumulated in the tumor, while most of heparin-coated nanoparticles were found in the liver and spleen. The polymer properties on the surface played an important role in the behavior of gold nanoparticles in the biological condition and the enhanced stability and tumor targeting property of nanoparticles were inherited from GC on the surface.
Keywords
CONTRAST AGENT; CANCER-THERAPY; PARTICLE-SIZE; DELIVERY; LIVER; CELLS; STABILITY; HEPARIN; BIOLOGY; ORGAN; CONTRAST AGENT; CANCER-THERAPY; PARTICLE-SIZE; DELIVERY; LIVER; CELLS; STABILITY; HEPARIN; BIOLOGY; ORGAN; CTcontrast agent; glycol chitosan; gold nanoparticle; tumor targeting
ISSN
0724-8741
URI
https://pubs.kist.re.kr/handle/201004/126753
DOI
10.1007/s11095-013-1142-0
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KIST Article > 2014
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