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基于石墨烯量子点的荷电反转纳米材料用于靶向细胞核的药物输送和效率可控的光动力疗法。

Graphene quantum dot based charge-reversal nanomaterial for nucleus-targeted drug delivery and efficiency controllable photodynamic therapy.

机构信息

School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore.

Department of Chemistry, Oakland University, Rochester, Michigan.

出版信息

J Biophotonics. 2019 Jun;12(6):e201800367. doi: 10.1002/jbio.201800367. Epub 2019 Mar 4.

Abstract

Graphene quantum dots (GQDs), the new zero-dimensional carbon nanomaterial, have been demonstrated as a promising material for biomedical applications due to its good biocompatibility and low toxicity. However, the integration of multiple therapeutic approaches into a nanosized platform based on the GQD has not been explored yet to our best knowledge. In this report, we regulate the generation of reactive oxygen species (ROS) when using the GQD as a photosensitizer by varying the doping amount of nitrogen atoms to achieve efficiency controllable photodynamic therapy. On the other hand, charge-reversal (3-Aminopropyl) triethoxysilane (APTES) was used to conjugate on the surface of GQD for nucleus targeting drug delivery for the first time. The treatment outcome of produced ROS and nucleus-targeting drug delivery was investigated by fluorescence imaging. The results demonstrated that the N-GQD-DOX-APTES in dual roles as a drug carrier and photosensitizer could achieve nucleus-targeting delivery and strong ROS production simultaneously. This approach provides a promising strategy for the development of multifunctional therapy in one nano platform for biomedical applications.

摘要

石墨烯量子点(GQDs)作为一种新型的零维碳纳米材料,由于其良好的生物相容性和低毒性,已被证明是一种很有前途的生物医学应用材料。然而,据我们所知,尚未有人将多种治疗方法整合到基于 GQD 的纳米级平台中。在本报告中,我们通过改变氮原子的掺杂量来调节 GQD 作为光敏剂时活性氧(ROS)的产生,从而实现效率可控的光动力治疗。另一方面,首次使用带正电荷的(3-氨丙基)三乙氧基硅烷(APTES)修饰 GQD 的表面以进行核靶向药物传递。通过荧光成像研究了产生的 ROS 和核靶向药物传递的治疗效果。结果表明,N-GQD-DOX-APTES 兼具药物载体和光敏剂的双重作用,能够实现核靶向递药和强 ROS 产生的协同作用。该方法为在一个纳米平台上开发用于生物医学应用的多功能治疗方法提供了一个很有前途的策略。

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