The extent of protein hydration dictates the preference for heterogeneous or homogeneous nucleation generating either parallel or antiparallel β-sheet α-synuclein aggregates

α-Synuclein amyloid self-assembly is the hallmark of a number of neurodegenerative disorders, including Parkinson''s disease, although there is still very limited understanding about the factors and mechanisms that trigger this process. Primary nucleation has been observed to be initiated in vitro at hydrophobic/hydrophilic interfaces by heterogeneous nucleation generating parallel β-sheet aggregates, although no such interfaces have yet been identified in vivo. In this work, we have discovered that α-synuclein can self-assemble into amyloid aggregates by homogeneous nucleation, without the need of an active surface, and with a preference for an antiparallel β-sheet arrangement. This particular structure has been previously proposed to be distinctive of stable toxic oligomers and we here demonstrate that it indeed represents the most stable structure of the preferred amyloid pathway triggered by homogeneous nucleation under limited hydration conditions, including those encountered inside α-synuclein droplets generated by liquid–liquid phase separation. In addition, our results highlight the key role that water plays not only in modulating the transition free energy of amyloid nucleation, and thus governing the initiation of the process, but also in dictating the type of preferred primary nucleation and the type of amyloid polymorph generated depending on the extent of protein hydration. These findings are particularly relevant in the context of in vivo α-synuclein aggregation where the protein can encounter a variety of hydration conditions in different cellular microenvironments, including the vicinity of lipid membranes or the interior of membraneless compartments, which could lead to the formation of remarkably different amyloid polymorphs by either heterogeneous or homogeneous nucleation.     

Ultra‐performance liquid chromatography MS/MS method for the determination of parabens in compost from sewage sludge: Comparison of the efficiency of two extraction techniques

The efficiency of two extraction techniques—ultrasound‐assisted extraction and pressurized liquid extraction—are compared and evaluated in the determination of parabens in compost samples. The extraction parameters for each technique were accurately optimized. The selected compounds were detected and quantified using ultra‐performance LC MS/MS, operating in negative ESI and in SRM mode. The analytes were separated in less than 5 min. Ethylparaben (ring‐¹³C₆ labeled) was used as an internal standard. Two selective, sensitive, and accurate analytical methods were developed and validated. The LODs of the methods ranged from 3 to 7 ng/g and the LOQs from 10 to 23 ng/g, while inter‐ and intraday variability was under 6% in all cases. The methods were validated separately by using matrix‐matched calibration and recovery assays with spiked samples. Recovery rates ranged from 94.0 to 105.0%. Compost samples were taken from different composting plants. Although the statistical comparison demonstrated no statistically significant differences between the two extraction techniques, the method based on pressurized liquid extraction was more sensitive than the ultrasound extraction based method.     

Layer-by-layer assembly of silica-based flame retardant thin film on PET fabric

A novel method to improve flame retardant properties of textile fabric using multilayered thin films was evaluated. In this work, PET fabrics were coated with silica nanoparticles using layer-by-layer assembly. Five bilayers of positively and negatively charged colloidal silica (<10 nm average thickness) increased time to ignition and decreased heat release rate peak of PET fabric by 45% and 20%, respectively. In vertical burn test, this same nanocoating dramatically reduced burn time and eliminated melt dripping. This study demonstrates the ability to impart flame retardant behavior using a water-based, environmentally-friendly protective coating.     

The use of thermographic technique in the evaluation of polymers combustion and fire retardants performance

The combustion behaviour of polymeric materials either fire retarded or not, burning in the Glow Wire and UL 94 tests, was characterised by means of thermography. It is shown that the distribution of temperatures in the gas and condensed phase of the burning specimen thus recorded, supplies fundamental complementary information for the characterisation of the combustion process.     

The use of fluorinated additives in fire retardance of polymers

Polytetrafluoroethylene (PTFE) is shown to improve fire retardance characteristics of brominated compounds/antimony trioxide systems added to polymers burning with or without dripping, as for example high-impact polystyrene or acrylonitrilebutadiene-styrene terpolymer, respectively. The action of PTFE seems to be the reduction of intrinsic flammability of the material as shown by parallel improvement of Underwriters Laboratories (UL94) tests and oxygen index parameters. A mechanistic interpretation is tentatively proposed which takes into account the very high effectiveness of PTFE.