The extracellular matrix (ECM) is one of the most striking natural self-assembled landscapes, essential for tissue integrity and cellular functions, where it orchestrates cell fate through a dynamic interplay of noncovalent interactions. Despite decades of research, there is still no scaffold that can replicate its nanostructural elegance and functional dynamic behavior. In this Perspective, we summarize cutting-edge approaches to reconstruct the ECM, putting an emphasis on either dynamic supramolecular designs or naturally sourced biopolymers.
View Article and Find Full Text PDFRecapitulating the biophysical and biochemical complexity of the extracellular matrix (ECM) remains a major challenge in tissue engineering. Hydrogels derived from decellularized ECM provide a unique opportunity to replicate the architecture and bioactivity of native ECM, however, they exhibit limited long-term stability and mechanical integrity. In turn, materials assembled through supramolecular interactions have achieved considerable success in replicating the dynamic biophysical properties of the ECM.
View Article and Find Full Text PDFTissue Eng Part C Methods
July 2022
Cell-based therapies require a large number of cells, as well as appropriate methods to deliver the cells to damaged tissue. Microcarriers provide an optimal platform for large-scale cell culture while also improving cell retention during cell delivery. However, this technology still presents significant challenges due to low-throughput fabrication methods and an inability of the microcarriers to recreate the properties of human tissue.
View Article and Find Full Text PDFThe fabrication of scaffolds that accurately recreate the architecture of living tissues is a major challenge in the field of tissue engineering and regenerative medicine. Core-shell microcapsules hold great potential in this regard, as they can recreate the hierarchical structure of biological systems. The independent modulation of the composition of both core and shell layers allows the design of compartmentalized platforms tailored to the recreation of specific cell niches.
View Article and Find Full Text PDFNew porphyrin-pyrrolidine/pyrroline conjugates were prepared by revisiting 1,3-dipolar cycloaddition reactions between a porphyrinic azomethine ylide and a series of dipolarophiles. Cationic conjugates obtained by alkylation of the pyrrolidine/pyrroline cycloadducts showed ability to generate singlet oxygen and to produce iodine in presence of KI when irradiated with visible light. Some of the cationic derivatives showed photobactericidal properties towards a Gram-negative bioluminescent .
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