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Kwon, Tae-Hyuk
Energy Recognition Lab.
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MOF × Biopolymer: Collaborative Combination of Metal–Organic Framework and Biopolymer for Advanced Anticancer Therapy

Author(s)
Kim, KibeomLee, SungminJin, EunjiPalanikumar, L.Lee, Jeong HyeonKim, Jin ChulNam, Jung SeungJana, BatakrishnaKwon, Tae-HyukKwak, Sang KyuChoe, WonyoungRyu, Ja-Hyoung
Issued Date
2019-08
DOI
10.1021/acsami.9b05736
URI
https://scholarworks.unist.ac.kr/handle/201301/33043
Fulltext
https://pubs.acs.org/doi/abs/10.1021/acsami.9b05736
Citation
ACS APPLIED MATERIALS & INTERFACES, v.11, no.31, pp.27512 - 27520
Abstract
Metal-organic framework (MOF) nanoparticles with high porosity and greater tunability have emerged as new drug delivery vehicles. However, premature drug release still remains a challenge in the MOF delivery system. Here, we report an enzyme-responsive, polymer-coated MOF gatekeeper system using hyaluronic acid (HA) and PCN-224 nanoMOF. The external surface of nanoMOF can be stably covered by HA through multivalent coordination bonding between the Zr cluster and carboxylic acid of HA, which acts as a gatekeeper. HA allows selective accumulation of drug carriers in CD44 overexpressed cancer cells and enzyme-responsive drug release in the cancer cell environment. In particular, inherent characteristics of PCN-224, which is used as a drug carrier, facilitates the transfer of the drug to cancer cells more stably and allows photodynamic therapy. This HA-PCN system enables a dual chemo and photodynamic therapy to enhance the cancer therapy effect.
Publisher
American Chemical Society
ISSN
1944-8244
Keyword (Author)
metal-organic frameworkgatekeeper systemcolloidal stabilitycancer targetingcombined therapy
Keyword
MESOPOROUS SILICA NANOPARTICLESTARGETED DRUG-DELIVERYRATIONAL DESIGNPLATFORMRELEASECONSTRUCTIONMOLECULESPROTEINSCARRIERSSIZE

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