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Non-iridescent photonic glass pigments of block copolymers show great potential for sustainable structural coloration. However, the ability to create accurate RGB color mixtures for real-world applications is limited by the prevalent use of non-degradable, fossil oil-derived components and the difficulty in achieving pure red hues. This work presents an alternative strategy for achieving more sustainable structural coloration by fabricating composite photonic pigments through controlled self-assembly of water, vegetable oil, and biodegradable bottlebrush block copolymers (BBCPs) in a complex emulsion system. The obtained photonic balls feature unprecedented multicompartment structures characterized by a short-range ordered assembly of water nanodroplets stabilized by the BBCPs, along with oil droplets stabilized by these nanodroplets, which substantially enhances resistance to Ostwald ripening. Furthermore, a new structural model is introduced to eliminate disordered scattering, successfully creating a pure red structural color and overcoming a long-standing limitation in versatile chromatic engineering.
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http://dx.doi.org/10.1002/adma.202501303 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology, Ulju-gun, UNIST-gil 50, Ulsan, 44919, Republic of Korea.
Structurally colored colloids, or photonic pigments, offer a sustainable alternative to conventional dyes, yet existing systems are constrained by limited morphologies and complex synthesis. In particular, achieving angle-independent color typically relies on disordered inverse architectures formed from synthetically demanding bottlebrush block copolymers (BCPs), hindering scalability and functional diversity. Here, we report a conceptually distinct strategy to assemble three-dimensional inverse photonic glass microparticles using amphiphilic linear BCPs (poly(styrene-block-4-vinylpyridine), PS-b-P4VP) via an emulsion-templated process.
View Article and Find Full Text PDFBioresour Technol
September 2025
Université Paris-Saclay, CentraleSupélec, Laboratoire de Génie des Procédés et Matériaux, Centre Européen de Biotechnologie et de Bioéconomie (CEBB), 3 rue des Rouges Terres, 51110 Pomacle, France. Electronic address:
Trophic conversion - a sequential cultivation strategy combining heterotrophic and phototrophic growth - offers a promising route for large-scale microalgae production by coupling the high biomass yields of heterotrophy with the biochemical advantages of phototrophy. Despite its potential, the cellular mechanisms governing this transition remain poorly understood. Here is presented the first mechanistic dissection of trophic conversion in Chlorella vulgaris, using isoactinic light conditions (30-600 µmol photons/m/s) and inocula with varied physiological states.
View Article and Find Full Text PDFNat Commun
August 2025
Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Crop leaves absorb approximately 90% of visible photons (400 - 700 nm) but transmit or reflect most far-red (FR) photons (700 - 800 nm). However, some cyanobacteria use FR photons up to 800 nm by incorporating chlorophyll (Chl) d or/and f into their photosystems. Here, we use a 3D canopy model to evaluate whether introducing these pigments could improve photosynthetic performance of field grown soybean.
View Article and Find Full Text PDFAntioxidants (Basel)
August 2025
Faculty of Biotechnology and Drug Development, University of Rijeka, Radmile Matejčić 2, 51000 Rijeka, Croatia.
One of the main limitations of photodynamic therapy (PDT) is hypoxia, which is caused by increased tumour proliferation creating a hypoxic tumour microenvironment (TME), as well as oxygen consumption by PDT. Hypoxia-activated prodrugs (HAPs), such as molecules containing aliphatic or aromatic -oxide functionalities, are non-toxic prodrugs that are activated in hypoxic regions, where they are reduced into their cytotoxic form. The (oxido)pyridylporphyrins tested in this work were synthesised as potential HAPs from their AB pyridylporphyrin precursors, using -chloroperbenzoic acid (-CPBA) as an oxidising reagent.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Gavin Herbert Eye Institute-Robert M. Brunson Center for Translational Vision Research, Department of Ophthalmology and Visual Sciences, University of California Irvine, Irvine, CA 92697.
In vivo genome editing has the potential to address many inherited and environmental disorders. However, a major hurdle for the clinical translation of genome editing is safe, efficient delivery to disease-relevant tissues. A modality-agnostic reporter animal model that facilitates rapid, precise, and quantifiable assessment of functional delivery and editing could greatly enhance the evaluation and translation of delivery technologies.
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