We present the research results of the use of plasma modification for the fabrication of carbon nanotube-based devices for chemical and biological sensing. The oxygen plasma treatment of multiwalled carbon nanotubes (MWCNTs) effectively grafts oxygen atoms onto the CNT surface. For investigating the impact of plasma modification on the MWCNT-based sensor performance, three different sensors are fabricated: NH3 gas sensors, humidity sensors, and immunosensors. The plasma-modified MWCNTs (p-MWCNTs) exhibit a sensitivity to NH3 that is approximately twice that of the corresponding untreated sensor. The humidity sensor with a p-MWCNT top electrode exhibits a much faster response time compared with the untreated MWCNT electrodes. The p-MWCNT immunosensor exhibits a detection limit almost 1000 times lower than that of the standard ELISA assay, while the untreated MWCNTs exhibit no detectable signal. These results imply that the oxygen-containing functional groups on the CNT surface significantly affect the performance of the CNT-based chemical and biological sensors.

Selective removal of t-Boc protecting groups in a polymer film imbedded, pyrene-containing calixarene derivative results in the generation of a patterned fluorescence image without employing wet developing processes.

Three-dimensional (3D) printing shows potential for use as an advanced technology for forming biomimetic tissue and other complex structures. However, there are limits and restrictions on selection of conventional bioinks. Here we report the first 3D-printable platelet lysate (PLMA)-based hydrogel, which consists of platelet lysate from whole blood of humans that can simulate the 3D structure of tissues and can be formed into a crosslinked hydrogel layer-by-layer to build cell-laden hydrogel constructs through methacrylated photo-polymerization. Furthermore, it can be customized for use with various tissues by controlling the physical properties according to irradiation time and concentration. In particular, different cells can be mixed and printed, and the integrity of the 3D printed structure can maintain its shape after crosslinking. The bio-ink exhibits excellent cell diffusion and proliferation at low concentrations, which improves moldability and biocompatibility. The 3D-printable PLMA bioinks may constitute a new strategy to create customized microenvironments for the repair of various tissues in vivo using materials derived from the human body.

Ginseng-derived extracellular nanovesicles effectively blocked bone loss both in vitro and in vivo by inhibiting osteoclast differentiation through RANKL-induced IκBα, JNK, and ERK activation.

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