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影响碳点安全性的物理化学特性:来自纳米颗粒文库综合研究的教训。

Physicochemical characteristics that affect carbon dot safety: Lessons from a comprehensive study on a nanoparticle library.

机构信息

Laboratoire de Conception et Application de Molécules Bioactives, UMR 7199, CNRS-Université de Strasbourg, Faculté de Pharmacie, Illkirch, France.

Laboratoire de Conception et Application de Molécules Bioactives, UMR 7199, CNRS-Université de Strasbourg, Faculté de Pharmacie, Illkirch, France.

出版信息

Int J Pharm. 2019 Oct 5;569:118521. doi: 10.1016/j.ijpharm.2019.118521. Epub 2019 Jul 16.

DOI:10.1016/j.ijpharm.2019.118521
PMID:31323371
Abstract

Carbon dots (CDs) are emerging nanomaterial in medicine and pharmacy. To explore the impact of physicochemical characteristics on their safety, we synthesized a library of 35 CDs exhibiting different size, charge, chemical composition and surface coating, using various starting materials (carbon source and passivation reagent) and carbonization procedures. The 35 CDs triggered different levels of viability loss when incubated with human macrophages at 3-200 µg/mL for 24 h. The smaller NPs (10-20 nm) were more toxic that larger ones (40-100 nm), whereas NPs that aggregated in culture medium were more toxic than dispersed ones. A positive correlation was found between CD charge or nitrogen content and toxicity. Furthermore, a greater toxicity was observed for CDs prepared from high molecular weight polyamines, suggesting a role of the CD global density of positive charges, rather than the charge at the CD surface, in the CD toxicity. At last, PEG decoration decreased the toxicity of cationic NPs. In conclusion, the size, aggregation in culture medium, charge, nitrogen content, nature of the passivation agent and synthesis procedure were found to influence CD toxicity, making it difficult to predict CD safety from a single characteristic.

摘要

碳点(CDs)是医学和药学领域新兴的纳米材料。为了探究理化特性对其安全性的影响,我们使用不同的起始材料(碳源和钝化试剂)和碳化程序,合成了具有不同尺寸、电荷、化学成分和表面涂层的 35 个 CD 文库。当以 3-200μg/mL 的浓度在 24h 内与人类巨噬细胞共孵育时,这 35 个 CD 引发了不同程度的细胞活力丧失。较小的 NPs(10-20nm)比较大的 NPs(40-100nm)毒性更大,而在培养基中聚集的 NPs 比分散的 NPs 毒性更大。CD 电荷或氮含量与毒性之间存在正相关关系。此外,我们发现,由高分子量聚胺制备的 CDs 毒性更大,这表明 CD 整体正电荷密度而不是 CD 表面的电荷在 CD 毒性中起作用。最后,PEG 修饰降低了阳离子 NPs 的毒性。总之,大小、在培养基中的聚集、电荷、氮含量、钝化剂的性质和合成程序都会影响 CD 的毒性,因此,仅从单一特性预测 CD 的安全性是很困难的。

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