Ultrasmall Chitosan-Genipin Nanocarriers Fabricated from Reverse Microemulsion Process for Tumor Photothermal Therapy in Mice | |
Song, Xiaojie1,2; Wu, Hao1,2; Li, Shen1,2; Wang, Yanfang1,2; Ma, Xiaojun1; Tan, Mingqian1 | |
刊名 | biomacromolecules |
2015-07-01 | |
卷号 | 16期号:7页码:2080-2090 |
英文摘要 | nanocarriers play an important role in improving the photo- and thermal-stability of photosensitizers to gain better pharmacokinetics behavior in tumor photothermal therapy. herein, pegylated chitosan (cg-peg; peg: polyethylene glycol) nanoparticles with ultrasmall size (similar to 5 nm), were prepared through a water-in-oil reverse microemulsion method using genipin as a cross-linker. particle size and zeta-potential can be tuned by varying the molar ratio between chitosan amino groups and genipin. cg-peg-icg (icg: indocyanine green) nanoparticles were fabricated by adding icg to cg-peg aqueous solution through a self-assembly method via electrostatic interaction. the resultant cg-peg-icg nanoparticles exhibited improved photo- and thermal-stability, good biocompatibility, and low toxicity. when irradiated with a laser, the cells incubated with cg-peg-icg nanoparticles showed very low cell viability (15%), indicating the cg-peg-icg nanoparticles possess high in vitro photothermal toxicity. moreover, the cg-peg nanocarriers can significantly alter the biodistribution and prolong the retention time of icg in the mice body after intravenous injection. in vivo photothermal study of tumors injected with cg-peg-icg nanoparticles containing icg at a concentration greater than 100 mu g.ml(-1) (100 mu l) induced irreversible tissue damage. the growth of u87 tumors was dramatically inhibited by cg-peg-icg nanoparticles, demonstrating that the cg-peg nanoparticles may act as potential icg nanocarriers for effective in vivo tumor photothermal therapy. |
WOS标题词 | science & technology ; life sciences & biomedicine ; physical sciences |
类目[WOS] | biochemistry & molecular biology ; chemistry, organic ; polymer science |
研究领域[WOS] | biochemistry & molecular biology ; chemistry ; polymer science |
关键词[WOS] | indocyanine-green ; silica nanoparticles ; drug-delivery ; in-vitro ; peg ; biodistribution ; hydrogels ; release ; system |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000358026400020 |
公开日期 | 2016-05-09 |
内容类型 | 期刊论文 |
源URL | [http://cas-ir.dicp.ac.cn/handle/321008/146390] |
专题 | 大连化学物理研究所_中国科学院大连化学物理研究所 |
作者单位 | 1.Chinese Acad Sci, Dalian Inst Chem Phys, Div Biotechnol, Dalian 116023, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China |
推荐引用方式 GB/T 7714 | Song, Xiaojie,Wu, Hao,Li, Shen,et al. Ultrasmall Chitosan-Genipin Nanocarriers Fabricated from Reverse Microemulsion Process for Tumor Photothermal Therapy in Mice[J]. biomacromolecules,2015,16(7):2080-2090. |
APA | Song, Xiaojie,Wu, Hao,Li, Shen,Wang, Yanfang,Ma, Xiaojun,&Tan, Mingqian.(2015).Ultrasmall Chitosan-Genipin Nanocarriers Fabricated from Reverse Microemulsion Process for Tumor Photothermal Therapy in Mice.biomacromolecules,16(7),2080-2090. |
MLA | Song, Xiaojie,et al."Ultrasmall Chitosan-Genipin Nanocarriers Fabricated from Reverse Microemulsion Process for Tumor Photothermal Therapy in Mice".biomacromolecules 16.7(2015):2080-2090. |
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