The cosmetic industry has a history of constant modernization, with products that are increasingly sustainable and well tolerated by the customers. In the last years, the growing understanding and knowledge of the potential of marine species, as well as the application of “blue biotechnology” have been motivating new innovative solutions in this area. Marine organisms are important sources of compounds that may be applicable in cosmetics, with biological activities that include depigmentant, anti-aging or anti-bacterial properties, specifically against acne, but also as formulation promoters and facilitators. Several methods can be used to extract these molecules, but these are not free of challenges and implications – possible biological and chemical contamination, and problems with batch reproducibility, which can be associated to the intraspecific variability of the different specimens, should be considered. Alongside these, the legislative and normative framework is increasingly developed and there is a growing concern with this situation. The application of sustainability fundamentals in the production of cosmetics must respect a life cycle approach, critically analyzing each stage. In this sense, “blue biotechnology”, in constant evolution, together with the use of invasive species or marine waste products to obtain new active ingredients, emerge as innovative and sustainable solutions for the future’s cosmetics industry. This review explores various biological properties of marine-derived molecules and discusses the challenges and implications associated with extracting these compounds. It also examines recent advancements in 'blue biotechnology' and their relevance to the sustainable development of innovative cosmetics.

Polymer-based composites reinforced with nanocarbonaceous materials can be tailored for functional applications. Poly(vinylidene fluoride) (PVDF) reinforced with carbon nanotubes (CNT) or graphene with different filler contents have been developed as potential piezoresistive materials. The mechanical properties of the nanocomposites depend of the PVDF matrix, filler type and filler content. PVDF 6010 is a relatively more ductile material, whereas PVDF-HFP shows larger maximum strain near 300% strain for composites with CNT, 10 times higher than the pristine polymer. This behaviour is similar for all composites reinforced with CNT. On the other hand, rGO/PVDF composites decrease the maximum strain compared to neat PVDF. It is shown that the use of different PVDF copolymers does not influence the electrical properties of the composites. On the other hand, CNT as filler leads to composites with percolation threshold around 0.5 wt.%, whereas reduced graphene oxide (rGO) nanocomposites shows percolation threshold at ≈2 wt.%. Both nanocomposites present excellent linearity between applied pressure and resistance variation, with pressure sensibility (PS) decreasing with applied pressure, from PS≈ 1.1 to 0.2 MPa^-1. A proof of concept demonstration is presented, showing the suitability of the materials for industrial pressure sensing applications.

Urinary tract infections (UTIs) caused by Klebsiella pneumoniae can lead to severe clinical complications and even death. An alternative treatment option for infected patients is using bacteriophages (phages). In the present study, we isolated phage KP-1 from sewage water using K. pneumoniae as a host. Whole genome analysis indicated that the genome was a double-stranded linear 176,096-bp long DNA molecule with 41.8% GC content and did not contain virulence or antibiotic resistance genes. The inactivation potential of phage KP-1 was assessed in broth at an MOI of 1 and 10, and a maximum inactivation of 4.9 and 5.4 log CFU/mL was observed after 9 h, respectively. The MOI of 10 efficacy was also assessed in urine to evaluate the phage’s performance in an acidic environment. A maximum inactivation of 3.8 log CFU/mL was observed after 9 h. The results indicate that phage KP-1 could be used to control UTIs caused by K. pneumoniae; however, further studies using phage cocktails to broader the phage’s spectrum of activity and phages in micro- or nanocarriers to avoid the negative effect of the low pH of the urine on phage viability, are necessary.

Human activities continue to degrade oceanic, coastal and inland waters. The generational change in the role of society in actively looking after the health of water resources can be achieved through the expansion of ocean and water literacy in schools. The Network of European Blue Schools established under the EU4Ocean Coalition for Ocean Literacy has improved ocean and water literacy; however, this Network needs to grow and be supported. Here we present ProBleu; a recently funded EU project that will expand and support the Network, partly through the use of citizen science. The core of the proposed methodology is facilitating school activities related to ocean and water literacy through funding calls to sustain and enrich current school activities, and kick-start and support new activities. The outcomes of the project are anticipated to have wide and long-term impacts across society, oceanic, coastal and inland water environments.

The interest on amorphous carbon thin films with low secondary electron yield (SEY) has been increasing in the last years, to mitigate electron multipacting in particle accelerators and in RF devices. Previous works found that the SEY increases with the hydrogen amount and correlates with the Tauc gap. In this work, we analyse films produced by magnetron sputtering with different contents of hydrogen and deuterium, incorporated via target poisoning and sputtering of CxDy molecules. XPS was implemented to estimate the phase composition of the films. The maximal SEY was found to decrease linearly with the fraction of the graphitic phase in the films. These results are supported by Raman scattering and UPS. The graphitic phase decreases almost linearly for hydrogen and deuterium concentrations between 12% and 46% (at.), but abruptly decreases when the concentration reaches 53%. This vanishing of the graphitic phase is accompanied by a strong increase of SEY and of the Tauc gap. These results suggest that the SEY is not dictated directly by the concentration of H/D but by the fraction of graphitic phase. The results are supported by a model used to calculate SEY of films consisting of a mixture of graphitic and polymeric phases.