Stable aqueous dispersions of citrate-stabilized gold nanorods (cit-GNRs) have been prepared in scalable fashion by surfactant exchange from cetyltrimethylammonium bromide (CTAB)-stabilized GNRs, using polystyrenesulfonate (PSS) as a detergent. The surfactant exchange process was monitored by infrared spectroscopy, surface-enhanced Raman scattering (SERS), and X-ray photoelectron spectroscopy (XPS). The latter established the quantitative displacement of CTAB (by PSS) and of PSS (by citrate). The Cit-GNRs are indefinitely stable at low ionic strength, and are conducive to further ligand exchange without loss of dispersion stability. The reliability of the surface exchange process supports the systematic analysis of ligand structure on the hydrodynamic size of GNRs, as described in a companion paper.

Ternary noble metal–semiconductor nanocomposites (NCs) with core–shell–satellite nanostructures have received widespread attention due to their outstanding performance in detecting pollutants through surface-enhanced Raman scattering (SERS) and photodegradation of organic pollutants. In this work, ternary Au@Cu2O–Ag NCs were designed and prepared by a galvanic replacement method. The effect of different amounts of Ag nanocrystals adsorbed on the surfaces of Au@Cu2O on the SERS activity was investigated based on the SERS detection of 4-mercaptobenzoic acid (4-MBA) reporter molecules. Based on electromagnetic field simulations and photoluminescence (PL) results, a possible SERS enhancement mechanism was proposed and discussed. Moreover, Au@Cu2O–Ag NCs served as SERS substrates, and highly sensitive SERS detection of malachite green (MG) with a detection limit as low as 10−9 M was achieved. In addition, Au@Cu2O–Ag NCs were recycled due to their superior self-cleaning ability and could catalyze the degradation of MG driven by visible light. This work demonstrates a wide range of possibilities for the integration of recyclable SERS detection and photodegradation of organic dyes and promotes the development of green testing techniques.

Crude oil deposition in oil transfer pipelines and bore wells afflicts many oil reservoirs. Asphaltenes play a major role in this process because of their tendency to precipitate in pipelines upon changes in temperature and/or pressure. Asphaltenes are defined by their lack of solubility in n-alkane solvents, which means that they likely contain many compounds that do not actively contribute to the deposition of crude oil in pipelines. The preponderance of studies in the literature have focused on asphaltenes derived from crude oil, whereas far fewer investigations have focused on asphaltenes derived from oil deposits. In this study, structural parameters of oil-deposit asphaltenes were examined using Raman spectroscopy and tandem mass spectrometry and compared to results reported previously for petroleum asphaltenes. On the basis of D1 and G band intensities in the Raman spectrum of oil-deposit asphaltenes, the average aromatic sheet size of these molecules was 21.0 Å, slightly larger than earlier values reported for petroleum asphaltenes (15.2−18.8 Å). Mass spectrometric experiments of oildeposit asphaltenes ionized via atmospheric pressure chemical ionization (APCI) using CS 2 solvent were used to measure the molecular weight distribution (MWD), saturated carbon content, and the number of fused aromatic rings in the cores of the asphaltene molecules. The MWD was found to be 150−1050 Da with an average molecular weight (average M W ) of 497 Da, which are significantly lower than those reported previously for petroleum asphaltenes (200−1500 Da and 570−700 Da, respectively). Aromatic core sizes were estimated to contain 8 fused rings on average for the most abundant species in oil-deposit asphaltenes, with 5−15 carbons in their alkyl side chains, as compared to averages of 3−7 aromatic rings and 17−41 alkyl carbons for petroleum asphaltenes.

Nanoparticle (NP)-based approaches to cancer drug delivery are challenged by the heterogeneity of the enhanced permeability and retention (EPR) effect in tumors and the premature attrition of payload from drug carriers during circulation. Here we show that such challenges can be overcome by a magnetophoretic approach to accelerate NP delivery to tumors. Payload-bearing poly(lactic-co-glycolic acid) NPs were converted into polymer–iron-oxide nanocomposites (PINCs) by attaching colloidal Fe3O4 onto the surface, via a simple surface modification method using dopamine polymerization. PINCs formed stable dispersions in serum-supplemented medium and responded quickly to magnetic field gradients above 1 kG/cm. Under the field gradients, PINCs were rapidly transported across physical barriers and into cells and captured under flow conditions similar to those encountered in postcapillary venules, increasing the local concentration by nearly three orders of magnitude. In vivo magnetophoretic delivery enabled PINCs to accumulate in poorly vascularized subcutaneous SKOV3 xenografts that did not support the EPR effect. In vivo magnetic resonance imaging, ex vivo fluorescence imaging, and tissue histology all confirmed that the uptake of PINCs was higher in tumors exposed to magnetic field gradients, relative to negative controls.

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