In the field of bone defect repair, 3D printed scaffolds have the characteristics of personalized customization and accurate internal structure. However, how to construct a well-structured vascular network quickly and effectively inside the scaffold is essential for bone repair after transplantation. Herein, inspired by the unique biological structure of "lotus seedpod", hydrogel microspheres encapsulating deferoxamine (DFO) liposomes were prepared through microfluidic technology as "lotus seeds", and skillfully combined with a three-dimensional (3D) printed bioceramic scaffold with biomimetic "lotus" biological structure which can internally grow blood vessels. In this composite scaffold system, DFO was effectively released by 36% in the first 6 h, which was conducive to promote the growth of blood vessels inside the scaffold quickly. In the following 7 days, the release rate of DFO reached 69%, which was fundamental in the formation of blood vessels inside the scaffold as well as osteogenic differentiation of bone mesenchymal stem cells (BMSCs). It was confirmed that the composite scaffold could significantly promote the human umbilical vein endothelial cells (HUVECs) to form the vascular morphology within 6 h . , the composite scaffold increased the expression of vascularization and osteogenic related proteins Hif1-α, CD31, OPN, and OCN in the rat femoral defect model, significantly cutting down the time of bone repair. To sum up, this "lotus seedpod" inspired porous bioceramic 3D printed scaffold with internal vascularization functionality has broad application prospects in the future.
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http://dx.doi.org/10.1016/j.bioactmat.2020.11.019 | DOI Listing |
Nanomaterials (Basel)
February 2025
CNRS, Institut de Physique de Rennes (IPR), UMR 6251, Université de Rennes, 35000 Rennes, France.
Osteosarcoma is medically defined as a bone-forming tumor with associated bone-degrading activity. There is a lack of knowledge about the network that generates the overproduction of bone. We studied the early stage of osteosarcoma development with mice enduring a periosteum injection of osteosarcoma cells at the proximal third of the tibia.
View Article and Find Full Text PDFBiotechnol Prog
March 2025
Department of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, DC, USA.
The organ transplantation field requires new approaches for replacing and regenerating tissues due to the lack of adequate transplant methods. Three-dimensional (3D) extrusion-based bioprinting is a rapid prototyping approach that can engineer 3D scaffolds for tissue regeneration applications. In this process, 3D printed cell-based constructs, consisting of biomaterials, growth factors, and cells, are formed by the extrusion of bioinks from nozzles.
View Article and Find Full Text PDFMacromolecules
January 2025
Department of Chemistry, Stony Brook University, Stony Brook, New York 11794, United States.
To understand the relationship between the intermolecular structure of aromatic polyamide (PA) scaffold and the water molecules in the barrier layers of reverse osmosis (RO) membranes, a grazing incidence wide-angle X-ray scattering (GIWAXS) study was carried out on freestanding PA thin films at varying relative humidity (RH) conditions. The scattering results were analyzed by an interference scattering model, containing a phase factor between a PA chain and an adsorbed water molecule. This model yielded good fits to the GIWAXS profiles where the water adsorption was found to vary linearly with RH.
View Article and Find Full Text PDFJ Enzyme Inhib Med Chem
December 2025
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.
In light of searching for new breast cancer therapies, DNA-targeted small molecules were rationally designed to simultaneously bind DNA and inhibit human dihydrofolate reductase (DHFR). Fourteen new arylidene-hydrazinyl-1,3-thiazoles () were synthesised and their dual DNA groove binding potential and DHFR inhibition were performed. Two compounds, and , proved their dual efficacy.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
February 2025
Nanophotonics Centre, Cavendish Laboratory, University of Cambridge, Cambridge CB3 0HE, U.K.
Coherent coupling of light and single molecules enables the development of next-generation room temperature-capable nanophotonic devices. Small mode-volume optical fields can be achieved with plasmonics, but challenges remain in placing oriented emitter molecules inside plasmonic cavities to access strong coupling consistently in emission. Using DNA origami, single-emitter molecules can be aligned inside subnanometric cavities created between a gold nanoparticle and a gold mirror.
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