Alkilany Alaaldin M, Caravana Aidan C, Hamaly Majd A, Lerner Kevin T, Thompson Lucas B
Department of Pharmaceutics & Pharmaceutical Technology, Faculty of Pharmacy, The University of Jordan, Amman 11942, Jordan.
Department of Chemistry, Gettysburg College, 300 North Washington Street, Gettysburg, PA 17325, USA.
J Colloid Interface Sci. 2016 Jan 1;461:39-44. doi: 10.1016/j.jcis.2015.09.010. Epub 2015 Sep 10.
Many synthetic approaches for gold nanoparticles rely on an aqueous media, resulting in water-soluble nanoparticles, which limits the ability to incorporate gold nanoparticles into other organic solvents or hydrophobic polymeric composites. Surface functionalization and phase transfer approaches using alkylthiols or alkylamines, which strongly bind the gold surface, are common routes to overcome this limitation, however they are typically challenging methods. In this paper we report an approach to transport citrate capped gold nanoparticles into a variety of solvents, including ones that are hydrophobic and not miscible with water without the need for phase transfer agents. We suspend gold nanoparticles in a water-miscible polar organic solvent that also is a solvent for a hydrophobic polymer. After drying, polymer-stabilized gold nanoparticles were found to be dispersible in various hydrophobic solvents with maintained colloidal stability. This work investigates two hydrophobic polymers, namely (polymethylmethacrylate and polyvinylacetate), which share common chemical motifs but have significantly different physiochemical properties. Interestingly, a significant difference in their ability to stabilize the transferred gold nanoparticles is observed and discussed.
许多用于金纳米颗粒的合成方法依赖于水性介质,从而产生水溶性纳米颗粒,这限制了将金纳米颗粒掺入其他有机溶剂或疏水性聚合物复合材料中的能力。使用能强烈结合金表面的烷基硫醇或烷基胺进行表面功能化和相转移的方法是克服这一限制的常用途径,然而这些方法通常具有挑战性。在本文中,我们报告了一种将柠檬酸盐包覆的金纳米颗粒转移到多种溶剂中的方法,包括那些疏水性且与水不混溶的溶剂,而无需相转移剂。我们将金纳米颗粒悬浮在一种与水混溶的极性有机溶剂中,该溶剂也是一种疏水性聚合物的溶剂。干燥后,发现聚合物稳定的金纳米颗粒可分散在各种疏水性溶剂中,并保持胶体稳定性。这项工作研究了两种疏水性聚合物,即聚甲基丙烯酸甲酯和聚醋酸乙烯酯,它们具有共同的化学基序,但具有显著不同的物理化学性质。有趣的是,观察并讨论了它们在稳定转移的金纳米颗粒能力方面的显著差异。