Bhawawet Nakara, Polo-Parada Luis, Ishtaweera Piyuni, Larm Nathaniel E, Baker Gary A
Department of Chemistry, Chulalongkorn University, Bangkok 10330, Thailand.
Department of Medical Pharmacology and Physiology, University of Missouri, Columbia, Missouri 65211, United States.
ACS Omega. 2023 Oct 23;8(44):41633-41640. doi: 10.1021/acsomega.3c05795. eCollection 2023 Nov 7.
Three new cationic surfactants--cetyl-bis(2-dimethylaminoethyl)ether bromide (CBDEB), dodecyl-bis(2-dimethylaminoethyl)ether bromide (DBDEB), and -hexyl-bis(2-dimethylaminoethyl)ether bromide (HBDEB)-have been designed herein using a simple and tailorable synthesis route. CBDEB and DBDEB, the 16- and 12-carbon chain surfactants, demonstrate facile, rapid, and controllable aqueous syntheses of gold nanoparticles (AuNPs) as dual-action reducing and capping agents. The synthesis strategy, using only surfactant and HAuCl salt, and 4 min of heating at 80 °C, results in spherical AuNPs (average diameters of 13.4 ± 3.8 nm for CBDEB and 12.0 ± 3.8 nm for DBDEB). Microwave irradiation was also investigated as a heating method and produces AuNPs in as little as 30 s. Control over the size and shape of AuNPs was proven to be feasible (toward populations of Euclidean shapes) by appropriately tuning reaction parameters, such as the molar ratio of surfactant to Au, temperature, incorporation of a time delay before heating, or shape control agents, such as Cu. Frustratingly, the cytotoxicity of CBDEB is similar to that of cetyltrimethylammonium bromide (CTAB), a popular 16-carbon chain cationic surfactant. Notably, while the shorter HBDEB (6-carbon chain) does not produce AuNPs under the applied conditions, it does appear to improve cell viability upon cytotoxicity evaluation and may be favorable as a new biological surfactant.
本文采用简单且可定制的合成路线设计了三种新型阳离子表面活性剂——十六烷基 - 双(2 - 二甲基氨基乙基)醚溴化物(CBDEB)、十二烷基 - 双(2 - 二甲基氨基乙基)醚溴化物(DBDEB)和己基 - 双(2 - 二甲基氨基乙基)醚溴化物(HBDEB)。CBDEB和DBDEB,即具有16个和12个碳链的表面活性剂,作为双功能还原剂和封端剂,能实现金纳米颗粒(AuNP)在水中简便、快速且可控的合成。该合成策略仅使用表面活性剂和HAuCl盐,并在80℃加热4分钟,可得到球形AuNP(CBDEB合成的AuNP平均直径为13.4±3.8nm,DBDEB合成的为12.0±3.8nm)。还研究了微波辐射作为加热方法,在短短30秒内就能制备出AuNP。通过适当调整反应参数,如表面活性剂与金的摩尔比、温度、加热前引入的时间延迟或形状控制剂(如铜),已证明对AuNP的尺寸和形状进行控制是可行的(针对欧几里得形状的群体)。令人沮丧的是,CBDEB的细胞毒性与十六烷基三甲基溴化铵(CTAB,一种常见的16碳链阳离子表面活性剂)相似。值得注意的是,虽然较短的HBDEB(6碳链)在所应用的条件下不会产生AuNP,但在细胞毒性评估中它似乎确实能提高细胞活力,可能作为一种新型生物表面活性剂具有优势。