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Drug delivery to redox-disease site using an artificial virus

Drug delivery to redox-disease site using an artificial virus
使用人造病毒将药物递送至氧化还原疾病位点
批准号:
23800045
负责人:
TOITA Riki
金额:
$1.66万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Research Activity Start-up
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2012

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中文摘要
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英文摘要
Traditional drug carriers do not have sufficient selectivity to disease cells. In this research, a naturally occurring protein cage, Hsp16.5, was fabricated to selectively deliver cargos into hepatoma cells through chemical and genetic methods. Resulting fabricated Hsp16.5 cages were selectively taken up by hepatoma cells, but not by normal hepatocyte. When conjugate with doxorubicin (DOX) and hepatoma-targetable Hsp were added to hepatoma and normal hepatocyte, cytotoxicity of this conjugates to hepatoma was comparable with that of free DOX, whereas this conjugates drastically reduced cytotoxicity to normal hepatocyte.
期刊论文(23)
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会议论文
A hydrophilic polymer grafted with a histone tail peptide as an artificial gene regulator
接枝组蛋白尾肽的亲水性聚合物作为人工基因调节剂
DOI: 10.1016/j.bmc.2011.05.011
发表时间: 2011
期刊: Bioorganic and Medicinal Chemistry
影响因子: 3.5
作者: [Shiosaki, S., Kuramoto, M., Toita, R., Mori, T.,Niidome, T., Katayama, Y.]
通讯作者: Y.
DOI: 10.1021/bc300015f
发表时间: 2012-07-01
期刊: BIOCONJUGATE CHEMISTRY
影响因子: 4.7
作者: [Toita, Riki, Murata, Masaharu, Hashizume, Makoto]
通讯作者: Hashizume, Makoto
歯学研究院生体材料学講座
牙科学院生物材料系
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Liver cell specific targeting by the preS1 domain of hepatitis B virus surface antigen displayed in protein nanocages
蛋白质纳米笼中展示的乙型​​肝炎病毒表面抗原的 preS1 结构域对肝细胞的特异性靶向
DOI: --
发表时间: 2012
期刊: International Journal of Nanomedicine
影响因子: 8
作者: [Masaharu Murata, Sayoko Narahara, Kaori Umezaki, Riki Toita, Shigekazu Tabata, Jing Shu Piao, Kana Abe, Joeng-Hun Kang, Kenoki Ohuchida, Lin Cui, Makoto Hashizume]
通讯作者: Makoto Hashizume
17
    海外基金