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Cytosine-phosphodiester-guanine oligodeoxynucleotide (CpG ODN)-capped hollow mesoporous silica particles for enzyme-triggered drug delivery

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/49727

Title: Cytosine-phosphodiester-guanine oligodeoxynucleotide (CpG ODN)-capped hollow mesoporous silica particles for enzyme-triggered drug delivery
Authors: Zhu, Yufang Browse this author
Meng, Wenjun Browse this author
Hanagata, Nobutaka Browse this author →KAKEN DB
Keywords: Hollow mesoporous silica
Controlled release
CpG ODN
Drug delivery
Issue Date: 21-Oct-2011
Publisher: Royal Society of Chemistry
Journal Title: Dalton Transactions
Volume: 40
Issue: 39
Start Page: 10203
End Page: 10208
Publisher DOI: 10.1039/c1dt11114k
Abstract: We designed, for the first time, an enzyme-triggered drug delivery system that is based on cytosine-phosphodiester-guanine oligodeoxynucleotide (CpG ODN)-capped hollow mesoporous silica (HMS) particles as carriers. Fluorescein dye was used as a model drug, and the fluorescein loading, amino-grafting and CpG ODN capping were evaluated by UV/Vis analysis, zeta potential and N2 adsorption-desorption measurements and gel electrophoresis. The fluorescein loading capacity and CpG ODN capping amount were 37.7 and 39.6 μg mg, respectively at the weight ratio of 10 Dye/HMS-NH2/CpG ODN. Importantly, fluorescein release can be triggered by the addition of deoxyribonuclease I (DNase I) for CpG ODN degradation, and the release rate can also be controlled by changing the DNase I concentration. Therefore, it might be a promising controlled drug delivery system for application in the field of biomedicine and cancer therapy.
Rights: Dalton Trans., 2011, 40, 10203-10208 - Reproduced by permission of The Royal Society of Chemistry (RSC)
Type: article (author version)
URI: http://hdl.handle.net/2115/49727
Appears in Collections:生命科学院・先端生命科学研究院 (Graduate School of Life Science / Faculty of Advanced Life Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 花方 信孝

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