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This work has focused on the development of a new analytical alternative based on the laser-induced breakdown spectroscopy (LIBS) technique for the fast, reliable, and economical determination of the gold and silver nanoparticle content in a low linear concentration range between 2.9 and 0.058 μg mL−1 and 2.9–0.116 μg mL−1, respectively, without requiring complicated sample pretreatment procedures or advanced separation techniques. Metallic nanoparticles are currently essential materials for the development of new technologies in different scientific and technical areas. However, numerous studies have pointed out these nanomaterials' toxic and polluting potential and the various health implications for humans, animals, and the ecosystem. The current reality reflects the lack of analytical techniques with low economic, environmental, and health impacts and the capacity to quantify the total metallic nanoparticle content. For this purpose, a novel and simple method for the selective capture of gold and silver nanoparticles, consisting of a chemically functionalized glass surface, has been custom-developed for subsequent analysis with LIBS. The results show that the proposed method, employing a functionalized sample glass support, presents a suitable analytical performance characterized by increased sensitivity, specifically 4.7% and 329.2% for Au-NPs and Ag-NPs, and proportionally decreased error in the slope and intercept of the calibration curves, 68% for Au-NPs and 87% for Ag-NPs, respectively. [ABSTRACT FROM AUTHOR]

Single-cell analysis using inductively coupled plasma mass spectrometry (SC-ICP-MS) is an analytical methodology that allows to obtain qualitative and quantitative information of the element content of bioparticles (cells, bacteria, unicellular algae, yeasts...) on a cell-by-cell basis. In this study, two commercially available nebulisation systems for introduction of intact bioparticles were evaluated, showing similar performance. Bacteria (E. coli) exposed to Ag(I) and 10 nm Ag nanoparticles were detected and their complete silver content distributions successfully recorded. Analysis of the corresponding spheroplasts, obtained after enzymatic digestion of the bacterial outer membrane with lysozyme, allowed information about the intracellular silver to be obtained, providing an insight into the biodistribution of silver in the bacteria. Likewise, validity of the quantitative information obtained by SC-ICP-MS was evaluated by applying methodology based on the estimation of silver mass per bioparticle critical values and successive dilutions. The quantitative information obtained by SC-ICP-MS for the total content of silver in bacteria and spheroplasts was confirmed by acid digestion followed by conventional ICP-MS analysis. Bacteria exposed to silver nanoparticles accumulated lower amounts of silver than those exposed to ionic silver, the latter being totally internalized, showing the higher bioavailability of ionic silver. This study proves for the first time the suitability of SC-ICP-MS for the quantitative determination of silver in bacteria, as well as in spheroplasts when combined with lysozyme digestion. Limits of detection of 7 ag of Ag per bioparticle, 500 bioparticles per mL and 38 ng of total Ag per litre of bacteria/spheroplast suspension were achieved. [ABSTRACT FROM AUTHOR]