University of Wroclaw, Faculty of Chemistry, ul. F. Joliot-Curie 14, 50-383 Wroclaw, Poland.
University of Wroclaw, Faculty of Chemistry, ul. F. Joliot-Curie 14, 50-383 Wroclaw, Poland.
Colloids Surf B Biointerfaces. 2019 Sep 1;181:119-124. doi: 10.1016/j.colsurfb.2019.04.068. Epub 2019 May 2.
Development of protocols for transferring of hydrophobic quantum dots (QDs) into aqueous solution is of special importance for their biomedical applications. Particularly, hydrophilization of AgS without quenching of photoluminescence is a great challenge. Application of standard protocol for amphiphilic polymer coating of hydrophobic AgS nanocrystals failed, whereas ligand exchange and direct synthesis of AgS in aqueous solution leads to poorly emitting materials. In this paper we present the facile method for transferring of hydrophobic AgS QDs into aqueous solution employing the phase transfer catalysed hydrolysis of a commercially available polymer - poly(maleic anhydride-alt-1-octadecene), (PMAO) in the presence of tetramethylammonium hydroxide. Because the original surface ligands are retained and we do not use solvents (like THF) detrimental for AgS emission, the modification does not deteriorate photoluminescence properties and quantum yield of modified QDs in aqueous solution reaches 60% of that for hydrophobic QDs in chloroform. The hydrodynamic diameter of modified, water soluble AgS QDs is about 10 nm and is only slightly larger than their original size. Moreover, the polymer coated nanocrystals are not aggregated and are stable for months. Surface characterization of QDs by NMR and IR spectroscopy indicates that polymer chains intercalate alkyl chains of dodecanethiol (DDT) bound to the surface of AgS. The cytotoxicity studies indicate that the presented method should be regarded as a notable progress towards the biocompatible AgS NIR-II emitting nanoprobes.
发展将疏水性量子点 (QD) 转移到水溶液中的方案对于它们的生物医学应用非常重要。特别是,在不猝灭光致发光的情况下使 AgS 亲水化是一个巨大的挑战。应用标准的两亲聚合物涂覆疏水性 AgS 纳米晶体的方案失败了,而直接在水溶液中合成 AgS 或配体交换会导致发光性能较差的材料。在本文中,我们提出了一种简便的方法,通过在四甲基氢氧化铵存在下,用商业可得的聚合物聚(马来酸酐-alt-1-十八烯)(PMAO)的相转移催化水解,将疏水性 AgS QD 转移到水溶液中。由于保留了原始的表面配体,并且我们不使用对 AgS 发射有害的溶剂(如 THF),因此修饰不会恶化修饰后的 QD 在水溶液中的光致发光性能和量子产率,修饰后的 QD 在水溶液中的量子产率达到了在氯仿中疏水性 QD 的 60%。修饰后的水溶性 AgS QD 的水动力直径约为 10nm,仅略大于其原始尺寸。此外,聚合物包覆的纳米晶体不会聚集并且可以稳定数月。通过 NMR 和 IR 光谱对 QD 的表面特性进行表征表明,聚合物链插入与 AgS 表面结合的十二硫醇 (DDT) 的烷基链。细胞毒性研究表明,所提出的方法应被视为朝着生物相容的 AgS NIR-II 发射纳米探针的显著进展。