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We have previously developed a regenerative engineering approach to repair irregularly shaped craniomaxillofacial bone defects utilizing "self-fitting" shape memory polymer (SMP) scaffolds based on cross-linked poly(ε-caprolactone) (PCL). However, a slow rate of degradation may hinder neotissue infiltration, and a lack of innate antimicrobial activity creates vulnerability to postoperative infection stemming from biofilm formation. Introduction of chitosan (CS), a hydrophilic natural polymer with known antimicrobial behavior, to PCL SMP scaffolds could provide a synergistic combination of desirable properties. Herein, for the first time, we report the development of hybrid (i.e., formed from a synthetic and a naturally derived polymer) CS/PCL SMP scaffolds. A series of eight highly porous PCL/CS--PCL scaffolds were formed as semi-interpenetrating networks (semi-IPNs) using cross-linkable PCL-diacrylate (PCL-DA) and thermoplastic CS--PCL copolymers. Scaffold CS content was tuned by graft copolymer composition and wt % ratio to PCL-DA. A solvent-cast particulate leaching process produced scaffolds with highly interconnected macropores (∼240 μm), which is conducive to osteogenesis. Owing to sufficient retention of PCL crystallinity, all hybrid scaffolds retained excellent shape memory and robust mechanical behavior. Compared with PCL scaffold controls, hybrid scaffolds of sufficient CS content exhibited faster rates of in vitro degradation, which is favorable to osteoinductivity. Accelerated degradation was related to increased hydrophilicity and phase separation effects. Hybrid scaffolds also displayed an ability to reduce biofilm formation by both direct and indirect contact, compared with PCL scaffolds.
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http://dx.doi.org/10.1021/acsbiomaterials.5c01160 | DOI Listing |
Neurochem Res
September 2025
International Translational Neuroscience Research Institute, Zhejiang Chinese Medical University, Hangzhou, 310053, Zhejiang, China.
The concept of the central nervous system (CNS) reserve emerged from the mismatch often observed between the extent of brain pathology and its clinical manifestations. The cognitive reserve reflects an "active" capacity, driven by the plasticity of CNS cellular components and shaped by experience, learning, and memory processes that increase resilience. We propose that neuroglial cells are central to defining this resilience and cognitive reserve.
View Article and Find Full Text PDFThe human mind constructs and updates models of events during comprehension. Event models are multidimensional, multi-timescale, and structured. They enable prediction, shape memory formation, and facilitate action control.
View Article and Find Full Text PDFFood Sci Biotechnol
October 2025
Department of Life Sciences, Somaiya Vidyavihar University, Vidyavihar, Mumbai, India.
Challenges such as a downward trend in cultivation and post-harvest losses lead to increased gap in cocoa bean supply and demand. This review deals with the recent AI models used in farming, processing, and supply chain of cocoa beans. Farming models viz.
View Article and Find Full Text PDFRSC Adv
September 2025
Chemistry Department, Faculty of Science, Cairo University Cairo Egypt
The field of biomaterials has evolved rapidly with the introduction of time as a transformative factor, giving rise to four-dimensional (4D) materials that can dynamically change their structure or function in response to external stimuli. This review presents a comprehensive comparison between traditional three-dimensional (3D) and emerging 4D biomaterials, highlighting the key distinctions in design, adaptability, and functionality. We explore the development of smart biomaterials at the core of 4D systems, including stimuli-responsive polymers, shape-memory materials, and programmable hydrogels.
View Article and Find Full Text PDFFront Immunol
September 2025
Bacterial Scientific Area, GSK Vaccine, Siena, Italy.
Background: Protein-polysaccharide conjugate vaccines rely on the induction of T-cell-dependent responses that support germinal center (GC) reactions to potentiate the expansion of antigen-specific memory B-cell (MBC) populations and high-avidity antibody responses. The effects of adjuvants on B-cell and antibody responses are well described for protein antigens but remain largely unexplored for conjugated polysaccharidic antigens.
Methods: We assessed the effects of five adjuvants present in licensed vaccines (AS01, AS03, AS04, and aluminum hydroxide [Alum]) or under clinical evaluation (AS37) on the magnitude and quality of antigen-specific antibody responses and local/systemic B-cell responses.