Plastic pollution is a global problem affecting the environment and, consequently, people's well-being. Careful and timely end-of-life plastic recycling is certainly a way, albeit a partial one, to remedy the problem. The immediate identification and selection of the different types of plastic materials in the recycling process certainly facilitate its recovery and reuse, allowing the damage caused by plastic emission into the environment to be limited. Recently, new technologies for automatic sorting of plastics based upon fluorescent tagging have been considered. This article reports the synthesis and characterization of fluorescent copolymers of poly(methyl methacrylate) (PMMA) that could be potentially used as fluorescent markers of commercial PMMA. Poly(methylmetacrylate--2-(9-carbazolyl)ethyl methacrylate) (P(MMA--CEMA)) and poly(methylmetacrylate--7-methacryloyloxycoumarin) (P(MMA--MAOC)) samples containing a small number of fluorescent units (<4%) were synthesized by free-radical polymerization. All copolymer samples show chemico-physical properties like those of pure PMMA and produce fluorescence emission under 290 nm wavelength excitation. P(MMA--CEMA)s and P(MMA--MAOC)s were also tested as fluorescent dyes for PMMA identification. The experimental results demonstrate that PMMA/P(MMA--CEMA) and PMMA/P(MMA--MAOC) blends prepared using 1% by weight of fluorescent copolymer show a homogeneous morphology completely similar to pure PMMA and are still optically active.
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http://dx.doi.org/10.3390/molecules29245940 | DOI Listing |
RSC Chem Biol
January 2025
Department of Pharmaceutical Sciences, University of California Irvine California 92697 USA
The architecture of cells and the tissue they form within multicellular organisms are highly complex and dynamic. Cells optimize their function within tissue microenvironments by expressing specific subsets of RNAs. Advances in cell tagging methods enable spatial understanding of RNA expression when merged with transcriptomics.
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January 2025
Centre for Research Impact & Outcome, Chitkara College of Pharmacy, Chitkara University, Rajpura 140401, Punjab, India.
Exosomes are small extracellular vesicles secreted by various cell types, playing a crucial role in intercellular communication by carrying proteins, lipids, and nucleic acids, thus holding significant potential in diagnostics and therapeutics. Accurate labeling of exosomes is vital for studying their biogenesis, trafficking, and functional properties, enabling precise tracking and manipulation. This review examines current labeling techniques, including metabolic glycan labeling, chemical tagging, membrane fluorescent dyes, bio-conjugation, non-covalent labeling, and cell-engineering approaches.
View Article and Find Full Text PDFBiophys J
January 2025
Department of Physiology & Biophysics, UC Irvine, Irvine, California; Department of Biomedical Engineering, UC Irvine, Irvine, California; Center for Complex Biological Systems, UC Irvine, Irvine, California; Sue and Bill Gross Stem Cell Research Center, UC Irvine, Irvine, California. Electronic address:
The mechanically-activated ion channel PIEZO1 is critical to numerous physiological processes, and is activated by diverse mechanical cues. The channel is gated by membrane tension and has been found to be mobile in the plasma membrane. We employed single particle tracking (SPT) of endogenous, tdTomato-tagged PIEZO1 using Total Internal Reflection Fluorescence Microscopy in live cells.
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January 2025
Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University.
Live imaging techniques have revolutionized our understanding of paracrine signaling, a crucial form of cell-to-cell communication in biological processes. This review examines recent advances in visualizing and tracking paracrine factors through four key stages: secretion from producing cells, diffusion through extracellular space, binding to target cells, and activation of intracellular signaling within target cells. Paracrine factor secretion can be directly visualized by fluorescent protein tagging to ligand, or indirectly by visualizing the cleavage of the transmembrane pro-ligands or plasma membrane fusion of endosomes comprising the paracrine factors.
View Article and Find Full Text PDFSci Adv
January 2025
Center for Alzheimer's and Neurodegenerative Diseases, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Distinct tau amyloid assemblies underlie diverse tauopathies but defy rapid classification. Cell and animal experiments indicate tau functions as a prion, as different strains propagated in cells cause unique, transmissible neuropathology after inoculation. Strain amplification requires compatibility of the monomer and amyloid template.
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