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Implantable devices powered by batteries have been used for sixty years. In recent devices, lithium-based batteries are the most widely used power source. However, lithium batteries have many disadvantages in terms of safety, reliability, and longevity and require regular monitoring and substitution. Implantable glucose biofuel cells (BFCs) are increasingly seen as a potential future technology for replacing lithium-based batteries because they do not require surgical replacement after 8-10 years and have a theoretically unlimited lifetime thanks to the continued recovery of glucose and oxygen present in the human body. This paper shows the fabrication of flexible implantable abiotic cathodes, based on a nitrogen/iron-doped graphene catalyst, for glucose/oxygen biofuel cell application. An ink, based on nitrogen-iron doped graphene as the abiotic catalyst and chitosan as a binder, was prepared and coated on a flexible teflonated gas diffusion layer using doctor blade coating. The characterization of the biocathode shows an open potential circuit corresponding to the potential of the abiotic catalyst and a high oxygen reduction current density of up to 66 μA cm -2 under physiological conditions. Those cathodes remain stable for up to two years with a current density loss of only 25%. The flexible abiotic electrode cytotoxicity was evaluated by cell culture experiments showing living cells' high tolerance on the biocathode surface. This work demonstrates that this abiotic catalyst can be a promising alternative for the development of implantable glucose BFCs due to its stability and its cytocompatibility., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (This journal is © The Royal Society of Chemistry.)

Water-based inks were formulated using cellulose nanofibers as a binder in order to directly front/reverse print lithium ion cells on a paper separator. Moreover, the high cohesion of electrodes as provided by cellulose nanofibers allowed for the embedding metallic current collectors in the electrodes during the printing stage, in order to develop a one-step printing and assembling process. Positive and negative inks based on LiFePO₄, or graphite, respectively, and cellulose nanofibers, displayed rheological properties complying with a variety of printing processes, as well as with screen printing. Printed cells exhibited high electrical conductivity and adhesion between current collectors and inks, i.e., up to 64 ± 1 J/m². Electrochemical cycling tests at C/10 showed a reversible capacity during the first cycle of about 80 mAh/g, which slightly decayed upon cycling. Preliminary results and assembling strategies can be considered as promising, and they represent a quick solution for the manufacturing of lithium ion batteries. Work is in progress to improve these processing issues and the cycling performances of Li-ion cells.

Nucleic acid amplification testing is a very powerful method to perform efficient and early diagnostics. However, the integration of a DNA amplification reaction with its associated detection in a low-cost, portable, and autonomous device remains challenging. Addressing this challenge, the use of screen-printed electrochemical sensor is reported. To achieve the detection of the DNA amplification reaction, a real-time monitoring of the hydronium ions concentration, a byproduct of this reaction, is performed. Such measurements are done by potentiometry using polyaniline (PAni)-based working electrodes and silver/silver chloride reference electrodes. The developed potentiometric sensor is shown to enable the real-time monitoring of a loop-mediated isothermal amplification (LAMP) reaction with an initial number of DNA strands as low as 10 copies. In addition, the performance of this PAni-based sensor is compared to fluorescence measurements, and it is shown that similar results are obtained for both methods.

The use of capillary systems in space and biotechnology applications requires the regulation of the capillary flow velocity. It has been observed that constricted sections act as flow resistors. In this work, we also show that enlarged sections temporarily reduce the velocity of the flow. In this work, the theory of the dynamics of capillary flows passing through a constricted or an enlarged channel section is presented. It is demonstrated that the physics of a capillary flow in a channel with a constriction or an enlargement is different and that a constriction acts as a global flow resistor and an enlargement as a local flow resistor. The theoretical results are checked against experimental approaches.

We demonstrate a novel combined chitosan-carbon-nanotube-enzyme biocathode with a greatly enhanced and stable long-term current density of -0.19 mA mL(-1). The fibrous microstructure of the electrode improves the performance of the biocathode by creating a protective microenvironment, preventing the loss of the electrocatalytic activity of the enzyme, and providing good oxygen diffusion.

An industrial pressure-sensitive adhesive was microencapsulated by spray-drying using an aqueous colloidal ethylcellulose dispersion (Aquacoat® ECD) plasticised by triacetin to form the wall material. Unloaded (0:100) and adhesive-loaded (25:75) particles were produced in a Büchi B-191 mini spray-dryer with product yields of 62% and 57%, respectively. Microparticles were spherical and narrow sized with mean D₃,₂ diameters of 3.165 ± 0.001 and 5.544 ± 0.105 µm, respectively. The microparticles were found to redisperse well in water and exhibit enough stability in neutral and alkaline aqueous media to be further used in a coating slip. Crush tests on single microparticles with diameters ranging from 2 to 12 µm were performed using a nanoindenter. They revealed that the crushing force of both kinds of microparticles increased linearly with their diameter and that the adhesive loading reduced the mechanical strength of the prepared microparticles.

This work describes a very simple, rapid, and efficient approach to the hydrophobization and lipophobization of cellulose fibers through their reaction with gaseous trichloromethylsilane (TCMS). The characterization of the modified surface involved FTIR-ATR and solid-state (29)Si NMR spectroscopy, scanning electron microscopy (SEM), and contact angle measurements with different liquids. The modification generated an inorganic coating around the fibers, associated with the construction of a three-dimensional network of Si-O-Si bridges partly bound to the polysaccharide macromolecules. This coating conferred both a high hydrophobicity and a lipophobicity to the samples even when the treatments applied modest TCMS quantities and reaction times as short as 30 s. The green connotation of this novel process constitutes an additional positive feature., (2010 Elsevier Inc. All rights reserved.)