Non-targeted analysis (NTA) methods are widely used for chemical discovery but seldom employed for quantitation due to a lack of robust methods to estimate chemical concentrations with confidence limits. Herein, we present and evaluate new statistical methods for quantitative NTA (qNTA) using high-resolution mass spectrometry (HRMS) data from EPA's Non-Targeted Analysis Collaborative Trial (ENTACT). Experimental intensities of ENTACT analytes were observed at multiple concentrations using a semi-automated NTA workflow.
View Article and Find Full Text PDFChemical risk assessments follow a long-standing paradigm that integrates hazard, dose-response, and exposure information to facilitate quantitative risk characterization. Targeted analytical measurement data directly support risk assessment activities, as well as downstream risk management and compliance monitoring efforts. Yet, targeted methods have struggled to keep pace with the demands for data regarding the vast, and growing, number of known chemicals.
View Article and Find Full Text PDFBlended poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-(1,4-benzo-{2,1',3}-thiadiazole)] (PFBT)/poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV) conjugated polymer nanoparticles were prepared and characterized by conventional and single-particle fluorescence spectroscopy. The particles exhibit red emission and improved quantum efficiency resulting from highly efficient energy transfer from donor PFBT to acceptor MEH-PPV as well as suppression of MEH-PPV aggregation. Photobleaching results indicate better photostability in the blended sample compared to undoped MEH-PPV nanoparticles and photoactivation of donor emission, which could be useful for single-molecule localization-based super-resolution microscopy.
View Article and Find Full Text PDFConjugated polymer nanoparticles with incorporated antifade agents were prepared, and ensemble and single particle measurements showed that incorporation of antifade agents effectively improves the fluorescence quantum yield and photostability of the conjugated polymer nanoparticles, likely by a combination of triplet quenching and suppression of processes involved in photogeneration of hole polarons (cations), which act as fluorescence quenchers. The photostability of conjugated polymer nanoparticles and CdSe quantum dots was compared, at both the ensemble and single particle level. The results provide confirmation of the hypothesis that quenching by photogenerated hole polarons is a key factor limiting the fluorescence quantum yield and maximum emission rate in conjugated polymer nanoparticles.
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