Publications by authors named "Lu-Chen Yeh"

A major challenge in the use of chemotherapy and immunotherapy is hypoxia-induced progression of tumor cells. We aim to curb hypoxia using metal-based O-producing nanomedicine. The key focus is therapeutic targeting of hypoxia-inducible factor 1α (HIF-1α), a major reactive oxygen species (ROS)-activated player that drives hypoxia-dependent tumor progression.

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The progress of wound regeneration relies on inflammation management, while neovascular angiogenesis is a critical aspect of wound healing. In this study, the bioactive core and corona synergism of quantized gold (QG) were developed to simultaneously address these complicated issues, combining the abilities to eliminate endotoxins and provide oxygen. The QG was constructed from ultrasmall nanogold and a loosely packed amine-based corona via a simple process, but it could nonetheless eliminate endotoxins (a vital factor in inflammation also called lipopolysaccharides) and provide oxygen in situ for the remodeling of wound sites.

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Article Synopsis
  • Bio-inert biomaterials are essential for applications like biosensors and medical implants, requiring materials that are hydrophilic and electrically neutral.
  • This study introduced a new zwitterionic copolymer with a catechol group that can effectively coat different materials without being limited to a specific substrate.
  • The research determined the critical number of catechol groups needed for successful modification, achieving up to 95% reduction in non-specific biological interactions like protein and cell attachment when tested with human blood.
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The field of bioinert materials is relatively mature, as unique molecular designs for antifouling have been regularly presented over the past 30 years. However, the effect of steam sterilization, a common procedure in hospitals for sterilizing biomedical devices in clinical uses, on the stability of antifouling and hemocompatible biomaterials remains unexplored. The only available set of data indicates that poly(sulfobetaine methacrylate) (SBMA) is unstable and loses its antifouling properties when exposed to hot humid air, depriving it of its attractiveness.

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Despite a set of properties ideal to the design of wound dressings, bioinert membranes are seldom applied as wound-healing systems. This work presents a unique series of random copolymers of glycidyl methacrylate (GMA) and poly(ethylene glycol) methacrylate (PEGMA), namely GMA--PEGMA, used to surface-modify by grafting onto method polytetrafluorethylene membranes, with the aim of developing wound dressings for quick and efficient wound closure. It is shown that the membrane modified with G50P50 copolymer combines high surface hydrophilicity, high porosity, protein resistance, bacterial resistance, and hemocompatibility, essential properties to wound dressings.

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Article Synopsis
  • Titanium and stainless steel are commonly used in devices, but their biocompatibility issues limit their use in biomedical applications.
  • This study explores attaching triblock copolymers made of zwitterionic sulfobetaine and glycidyl methacrylate to these metals to boost their biofouling resistance.
  • The optimal copolymer design, specifically with 50 repeat units in each block, showed the best antifouling properties on steel and titanium surfaces, making it a promising option for modifying biomedical devices.
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This work discusses the impact of the charge bias and the hydrophilicity on the human blood compatibility of pseudozwitterionic biomaterial gels. Four series of hydrogels were prepared, all containing negatively-charged 3-sulfopropyl methacrylate (SA), and either acrylamide, N-isopropylacrylamide, 2-dimethylaminoethyl methacrylate (DMAEMA) or [2-(methacryloyloxy)ethyl]trimethylammonium (TMA), to form SA, SN, SD or ST hydrogels, respectively. An XPS analysis proved that the polymerization was well controlled from the initial monomer ratios.

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In this manuscript, neat electrospun poly(o-methoxyaniline) (POMA) fibers were applied for the first time in the growth of neural stem cells. POMA was synthesized by chemical oxidative polymerization, followed by dissolving in tetrahydrofuran/dimethylformamide to prepare electrospinning solution. Subsequently, the solution was electrospun to produce polymeric fibers.

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