Cellular Uptake Pathway and Drug Release Characteristics of Drug-Encapsulated Glycol Chitosan Nanoparticles in Live Cells

Authors
Park, SangjinLee, So JinChung, HyunjinHer, SongwookChoi, YongseokKim, KwangmeyungChoi, KuiwonKwon, Ick Chan
Issue Date
2010-09
Publisher
WILEY
Citation
MICROSCOPY RESEARCH AND TECHNIQUE, v.73, no.9, pp.857 - 865
Abstract
Herein, we evaluated the cellular uptake pathways of hydrophobically modified glycol chitosan (HGC) nanoparticles as nano-sized drug carriers using cellular imaging technology. The endocytic pathway of nanocarriers for intracellular drug delivery is of great interest for the design of high efficacy delivery carriers for therapeutic agents. To evaluate the cellular uptake pathways of HGC nanoparticles, HGC was chemically labeled with near infrared (NIR) fluorescence dye, Cy5.5, to visualize the nanoparticle under confocal laser scanning microscopy. The internalization pathways of HGC nanoparticles were evaluated after treatment of specific endocytosis inhibitors. Importantly, HCG nanoparticles showed different cellular uptake efficiency and intracellular fate in cytoplasm according to the internalization pathways. Furthermore, drug distribution also evaluated according to the endocytic pathways after treatment of drug encapsulated HGC nanoparticles. As a model drug, fluorescent photosensitizer, Ce6, was encapsulated into HGC (Ce6-HGC) nanoparticles and the distribution of Ce6 in cytoplasm was evaluated using confocal laser scanning microscopy. The intracellular drug distribution showed different manner through specific endocytic pathways. The cellular imaging technology is highly useful for evaluation of endocytosis pathways and intracellular fate of drug delivery carrier which are closely related to drug distribution and therapeutic efficacy. Microsc. Res. Tech. 73:857-865, 2010. (C) 2010 Wiley-Liss, Inc.
Keywords
SELF-ASSEMBLED NANOPARTICLES; MACROMOLECULAR THERAPEUTICS; MULTIDRUG-RESISTANCE; UPTAKE MECHANISM; EFFICACY; PERMEABILITY; PROSPECTS; DELIVERY; ACID; SELF-ASSEMBLED NANOPARTICLES; MACROMOLECULAR THERAPEUTICS; MULTIDRUG-RESISTANCE; UPTAKE MECHANISM; EFFICACY; PERMEABILITY; PROSPECTS; DELIVERY; ACID; hydrophobically modified glycol chitosan; nanoparticle; cellular uptake; endocytosis; intracellular trafficking; cellular imaging
ISSN
1059-910X
URI
https://pubs.kist.re.kr/handle/201004/131151
DOI
10.1002/jemt.20845
Appears in Collections:
KIST Article > 2010
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