Highly Permeable Polylactic Acid Membrane Grafted with Quaternary Ammonium Salt for Effective and Durable Water Disinfection.

Given the increasing usage of drinking water purifiers, highly permeable membranes with strong antimicrobial functions are desperately desirable for effective and durable water disinfection. Hereby, we prepared such antimicrobial membranes by chemical grafting of quaternary ammonium salt (QAS) molecules, 3-(trimethoxysilyl)propyldimethyloctadecyl ammonium chloride (TPMMC), onto air plasma pretreated biodegradable polylactic acid (PLA) substrates. The high chemical grafting density promoted very strong and positive zeta potential charge of the resulted PLA-QAS membrane, contributing to effective and broad-spectrum antimicrobial efficiencies (>99.99%) against different microbes, including fungi and conventional and drug-resistant bacteria. The solid grafting of QAS molecules produced a durable antimicrobial performance of the PLA-QAS membrane. In addition, the pleated filter (0.45 m2) of PLA-QAS membrane showed outstanding bacteria rejection properties (>99.99%) and excellent washing durability (up to 20 m3 water) even at very high water filtration rates (up to 4 L/min). The disinfection mechanism was clarified that negatively charged bacteria could be rapidly adsorbed to positively charged PLA-QAS spinnings, followed by devastating cell membrane damage to bacterial debris, leaving a clean environment without significant biofilm and biofouling formation.

Effective Antibacterial Glass Fiber Membrane Prepared by Plasma-Enhanced Chemical Grafting.

This paper reports a novel glass fiber membrane with an effective antibacterial performance by chemical grafting of quaternary ammonium salt (QAS) which is enhanced by a plasma bombardment technique. Plasma bombardment as a pretreatment of the membrane can increase the QAS anchored on the membrane from 0.8 to 1.3 wt %. The chemical grafting technique can increase the membrane zeta potential from negative values to positive values in aqueous solutions at various pHs. Furthermore, the plasma-enhanced chemical-grafting membrane has more positive zeta potentials (49.0 mV at pH = 7) than the chemical-grafting membrane without the plasma bombardment technique (38.9 mV at pH = 7). In the antibacterial performance evaluation, the Escherichia coli survival rate decreased from 127.0% of the pristine membrane to 4.1 and 11.3% of the plasma-enhanced chemical-grafting membrane and the chemical-grafting membrane, respectively. In addition, the plasma-enhanced chemical-grafting membrane shows durable antibacterial activity against E. coli with copious water rinsing as much as 3 L·cm-2.

Bone Marrow-Derived CD44+ Cells Migrate to Tissue-Engineered Constructs via SDF-1/CXCR4-JNK Pathway and Aid Bone Repair.

BACKGROUND AND AIMS: Host-derived cells play crucial roles in the regeneration process of tissue-engineered constructs (TECs) during the treatment of large segmental bone defects (LSBDs). However, their identity, source, and cell recruitment mechanisms remain elusive. METHODS: A complex model was created using mice by combining methods of GFP+ bone marrow transplantation (GFP-BMT), parabiosis (GFP+-BMT and wild-type mice), and femoral LSBD, followed by implantation of TECs or DBM scaffolds. Postoperatively, the migration of host BM cells was detected by animal imaging and immunofluorescent staining. Bone repair was evaluated by micro-CT. Signaling pathway repressors including AMD3100 and SP600125 associated with the migration of BM CD44+ cells were further investigated. In vitro, transwell migration and western-blotting assays were performed to verify the related signaling pathway. In vivo, the importance of the SDF-1/CXCR4-JNK pathway was validated by ELISA, fluorescence-activated cell sorting (FACS), immunofluorescent staining, and RT-PCR. RESULTS: First, we found that host cells recruited to facilitate TEC-mediated bone repair were derived from bone marrow and most of them express CD44, indicating the significance of CD44 in the migration of bone marrow cells towards donor MSCs. Then, the predominant roles of SDF-1/CXCR4 and downstream JNK in the migration of BM CD44+ cells towards TECs were demonstrated. CONCLUSION: Together, we demonstrated that during bone repair promoted by TECs, BM-derived CD44+ cells were essential and their migration towards TECs could be regulated by the SDF-1/CXCR4-JNK signaling pathway.

Free-Radical Copolymerization of Dibenzofulvene with (Meth)acrylates Leading to π-Stacked Copolymers.

Copolymerizations of dibenzofulvene (DBF) with methyl methacrylate (MMA), 2-hydroxyethyl methacrylate (HEMA), methyl acrylate (MA), and 2-hydroxyethyl acrylate (HEA) were conducted under free radical conditions in toluene using α,α'-azobisisobutylonitrile (AIBN) as the initiator. In the copolymerizations, DBF indicated much higher reactivity than the comonomers, and the products comprised mainly of DBF units. NMR, UV, and fluorescence spectra, as well as electrochemical features indicated that the copolymers possess both isolated and rather short, sequential (meth)acrylate units, as well as π-stacked and unstacked DBF sequences. Isolated (meth)acrylate units are proposed to be sandwiched between DBF units. The ratios of π-stacked and unstacked side-chain fluorene groups of DBF units in excited states were accurately determined on the basis of fluorescent emission spectra; DBF units are mostly π-stacked in excited states as disclosed by fluorescence spectra. Two types of π-stacked sequences were suggested to be present in the ground state by electrochemical analysis. The copolymers exhibited higher solubility than pure poly(DBF).

Nanofibrous polymeric beads from aramid fibers for efficient bilirubin removal.

Polymer based hemoperfusion has been developed as an effective therapy to remove the extra bilirubin from patients. However, the currently applied materials suffer from either low removal efficiency or poor blood compatibility. In this study, we report the development of a new class of nanofibrous absorbent that exhibited high bilirubin removal efficiency and good blood compatibility. The Kevlar nanofiber was prepared by dissolving micron-sized Kevlar fiber in proper solvent, and the beads were prepared by dropping Kevlar nanofiber solutions into ethanol. Owing to the nanofiborous structure of the Kevlar nanofiber, the beads displayed porous structures and large specific areas, which would facilitate the adsorption of toxins. In the adsorption test, it was noticed that the beads possessed an adsorption capacity higher than 40 mg g(-1) towards bilirubin. In plasma mimetic solutions, the beads still showed high bilirubin removal efficiency. Furthermore, after incorporating with carbon nanotubes, the beads were found to have increased adsorption capacity for human degradation waste. Moreover, the beads showed excellent blood compatibility in terms of a low hemolysis ratio, prolonged clotting times, suppressed coagulant activation, limited platelet activation, and inhibited blood related inflammatory activation. Additionally, the beads showed good compatibility with endothelial cells. In general, the Kevlar nanofiber beads, which integrated with high adsorption capacity, good blood compatibility and low cytotoxicity, may have great potential for hemoperfusion and some other applications in biomedical fields.