Photoluminescent Cationic Carbon Dots as efficient Non-Viral Delivery of Plasmid SOX9 and Chondrogenesis of Fibroblasts.
Photoluminescent Cationic Carbon Dots as efficient Non-Viral Delivery of Plasmid SOX9 and Chondrogenesis of Fibroblasts.
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光致发光阳离子碳点作为质粒 SOX9 的有效非病毒传递和成纤维细胞的软骨形成
DOI:
10.1038/s41598-018-25330-x
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发表时间:
2018-05-04
影响因子:
4.6
通讯作者:
Xu X
中科院分区:
文献类型:
--
作者:
Cao X;Wang J;Deng W;Chen J;Wang Y;Zhou J;Du P;Xu W;Wang Q;Wang Q;Yu Q;Spector M;Yu J;Xu X
With the increasing demand for higher gene carrier performance, a multifunctional vector could immensely simplify gene delivery for disease treatment; nevertheless, the current non- viral vectors lack self-tracking ability. Here, a type of novel, dual-functional cationic carbon dots (CDs), produced through one-step, microwave-assisted pyrolysis of arginine and glucose, have been utilized as both a self-imaging agent and a non-viral gene vector for chondrogenesis from fibroblasts. The cationic CDs could condense the model gene plasmid SOX9 (pSOX9) to form ultra-small (10–30 nm) nanoparticles which possessed several favorable properties, including high solubility, tunable fluorescence, high yield, low cytotoxicity and outstanding biocompatibility. The MTT assay indicated that CDs/pSOX9 nanoparticles had little cytotoxicity against mouse embryonic fibroblasts (MEFs) compared to Lipofectamine2000 and PEI (25 kDa). Importantly, the CDs/pSOX9 nanoparticles with tunable fluorescence not only enabled the intracellular tracking of the nanoparticles, but also could successfully deliver the pSOX9 into MEFs with significantly high efficiency. Furthermore, the CDs/pSOX9 nanoparticles-mediated transfection of MEFs showed obvious chondrogenic differentiation. Altogether, these findings demonstrated that the CDs prepared in this study could serve as a paradigmatic example of the dual-functional reagent for both self-imaging and effective non-viral gene delivery.
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影响因子:
3.1
作者:
Cao, Xia;Deng, Wenwen;Yu, Jiangnan
通讯作者:
Yu, Jiangnan
影响因子:
9.7
作者:
Segovia, Nathaly;Dosta, Pere;Borros, Salvador
通讯作者:
Borros, Salvador
影响因子:
--
作者:
Ikeda, T;Kamekura, S;Chung, UI
通讯作者:
Chung, UI
影响因子:
8
作者:
Deng WW;Cao X;Wang M;Qu R;Su WY;Yang Y;Wei YW;Xu XM;Yu JN
通讯作者:
Yu JN
影响因子:
10.5
作者:
Kadaja M;Keyes BE;Lin M;Pasolli HA;Genander M;Polak L;Stokes N;Zheng D;Fuchs E
通讯作者:
Fuchs E