Anionic Functionalized Gold Nanoparticle Continuous Full Filling Separations: Importance of Sample Concentration

Abstract

Electrically driven separations which contain nanoparticles offer detection and separation advantages but are often difficult to reproduce. To address possible sources of separation inconsistencies, anionic functionalized gold nanoparticles are thoroughly characterized and subsequently included in continuous full filling capillary electrophoresis separations of varying concentrations of three small molecules. Citrate stabilized gold nanospheres are functionalized with 11-mercaptoundecanoic acid, 6-mercaptohexanoic acid, or thioctic acid self-assembled monolayers (SAMs) and characterized using dynamic light scattering, extinction spectroscopy, zeta potential, and X-ray photoelectron spectroscopy prior to use in capillary electrophoresis. Several important trends are noted. First, the stability of these anionic nanoparticles in the capillary improves with increased ligand packing density as indicated by a ratio of absorbance collected at 520 to 600 nm. Second, increasing nanoparticle concentration from 0 to 2 nM (0-0.002(5)%, w/w) minimally impacts analyte migration times; however, when higher nanoparticle concentrations are included within the capillary, nanoparticle aggregation occurs which induces separation inconsistencies. Third, analyte peak areas are most significantly impacted as their concentration decreases. These trends are attributed to both sample enrichment and electrostatic interactions between the anionic carboxylic acid functionalized gold nanoparticles and sample. These important findings suggest that sample concentration-induced conductivity differences between the sample matrix and separation buffer as well as SAM packing density are important parameters to both characterize and consider when nanoparticles are used during continuous full filling separations and their subsequent use to enhance spectroscopic signals to improve in-capillary analyte detection limits.