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一步还原和聚乙二醇化氧化石墨烯用于光热控制药物递送。

One-step reduction and PEGylation of graphene oxide for photothermally controlled drug delivery.

机构信息

MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.

Department of Pain Management, The First Affiliated Hospital of Jinan University, Guangzhou 510632, China.

出版信息

Biomaterials. 2014 Jun;35(18):4986-95. doi: 10.1016/j.biomaterials.2014.02.032. Epub 2014 Mar 20.

Abstract

Here, we developed one-step green reduction and PEGylation of nanosized graphene oxide (NGO) to obtain NrGO/PEG as a photothermally controllable drug delivery system. NrGO/PEG was synthesized by bathing methoxypolyethylene glycol amine (mPEG-NH2) and NGO at 90 °C for 24 h. The NrGO/PEG kept water stability for at least two months, and had ~14-fold increment in near-infrared (NIR) absorbance and ~2-fold increment in resveratrol (RV) loading over the unreduced NGO/PEG via π-π and hydrophobic interactions. Exposure of 4T1 cells to NrGO/PEG for 2 h showed 53.6% uptake ratio, and localization of NrGO/PEG in lysosomes instead of mitochondria. NIR irradiation (808 nm laser at 0.6 W/cm(2)) for 3 min potently enhanced RV release from NrGO/PEG-RV and the cytotoxicity of NrGO/PEG-RV against 4T1 cells, including decrease of cell viability, loss of mitochondrial membrane potential (ΔΨm) and cell apoptosis. Finally, NIR irradiation dramatically enhanced the efficacy of NrGO/PEG-RV in suppressing tumor growth in animal tumor models, further proving the remarkable synergistic action between photothermal effect of NrGO/PEG and RV loaded on NrGO/PEG.

摘要

在这里,我们开发了一步绿色还原和聚乙二醇化纳米氧化石墨烯(NGO),以获得 NrGO/PEG 作为光热可控的药物传递系统。NrGO/PEG 通过在 90°C 下将甲氧基聚乙二醇胺(mPEG-NH2)和 NGO 浸泡 24 小时合成。NrGO/PEG 至少保持两个月的水稳定性,并且通过 π-π 和疏水性相互作用,近红外(NIR)吸收增加了14 倍,白藜芦醇(RV)负载增加了2 倍。4T1 细胞暴露于 NrGO/PEG 2 小时后,摄取率为 53.6%,NrGO/PEG 定位于溶酶体而不是线粒体。NIR 照射(808nm 激光,0.6W/cm²)3 分钟可显著增强 NrGO/PEG-RV 中 RV 的释放以及 NrGO/PEG-RV 对 4T1 细胞的细胞毒性,包括细胞活力降低、线粒体膜电位(ΔΨm)丧失和细胞凋亡。最后,NIR 照射显著增强了 NrGO/PEG-RV 在动物肿瘤模型中抑制肿瘤生长的疗效,进一步证明了 NrGO/PEG 的光热效应与 NrGO/PEG 上负载的 RV 之间的协同作用非常显著。

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