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Self-assembled glycol chitosan nanoparticles for disease-specific theranostics

Authors
Yhee, Ji YoungSon, SoheeKim, Sun HwaPark, KinamChoi, KuiwonKwon, Ick Chan
Issue Date
10-Nov-2014
Publisher
ELSEVIER SCIENCE BV
Keywords
Glycol chitosan; Nanoparticles; Targeted delivery; Theranostics
Citation
JOURNAL OF CONTROLLED RELEASE, v.193, pp.202 - 213
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CONTROLLED RELEASE
Volume
193
Start Page
202
End Page
213
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/96781
DOI
10.1016/j.jconrel.2014.05.009
ISSN
0168-3659
Abstract
Hydrophobically modified glycol chitosan (hGC) conjugates spontaneously form self-assembled nanoparticles (NPs) in aqueous conditions, and glycol chitosan NPs (CNPs) have been extensively studied for the past few decades. For disease-specific theranostics, CNPs could be simply modified with imaging agents, and the hydrophobic domains of hGC are available for encapsulation of various drugs. Based on the excellent physiochemical and biological properties, CNPs have been investigated for multimodal imaging and target specific drug delivery. In particular, a recent application of CNPs has shown great potential as an efficient theranostic system because the CNPs could be utilized for a disease-specific theranostic delivery system of different imaging agents and therapeutics, simultaneously. Furthermore, various therapeutic agents including chemo-drugs, nucleotides, peptides, and photodynamic chemicals could be simply encapsulated into the CNPs through hydrophobic or charge-charge interactions. Under in vivo conditions, the encapsulated imaging agents and therapeutic drugs have been successfully delivered to targeted diseases. In this article, the overall research progress on CNPs is reviewed from early works. The current challenges of CNPs to overcome in theranostics are also discussed, and continuous studies would provide more opportunities for early diagnosis of diseases and personalized medicine. (C) 2014 Elsevier B.V. All rights reserved.
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