Fabrication of a Flexible Photodetector Based on a Liquid Eutectic Gallium Indium

A fluidic gallium-based liquid metal (LM) is an interesting material for producing flexible and stretchable electronics. A simple and reliable method developed to facilitate the fabrication of a photodetector based on an LM is presented. A large and thin conductive eutectic gallium indium (EGaIn) film can be fabricated with compressed EGaIn microdroplets. A solution of LM microdroplets can be synthesized by ultrasonication after mixing with EGaIn and ethanol and then dried on a PDMS substrate. In this study, a conductive LM film was obtained after pressing with another substrate. The film was sufficiently conductive and stretchable, and its electrical conductivity was 2.2 × 10⁶ S/m. The thin film was patterned by a fiber laser marker, and the minimum line width of the pattern was approximately 20 μm. Using a sticky PDMS film, a Ga₂O₃ photo-responsive layer was exfoliated from the fabricated LM film. With the patterned LM electrode and the transparent photo-responsive film, a flexible photodetector was fabricated, which yielded photo-response-current ratios of 30.3%, 14.7%, and 16.1% under 254 nm ultraviolet, 365 nm ultraviolet, and visible light, respectively.     

Antiplatelet Effect of Clopidogrel Can Be Reduced by Calcium-Channel Blockers

Purpose

Clopidogrel is metabolized by the hepatic cytochrome P450 (CYP) system into its active thiol metabolite. CYP3A4 is involved in the metabolism of both clopidogrel and dihydropyridine calcium channel blockers (CCBs). A few reports have suggested an inhibitory interaction between CCBs and clopidogrel. Accordingly, the aim of this study was to determine the effect of CCBs on the antiplatelet activity of clopidogrel by serial P2Y12 reaction unit (PRU) measurements.

Materials and Methods

We assessed changes in antiplatelet activity in patients receiving both clopidogrel and CCBs for at least 2 months prior to enrollment in the study. The antiplatelet activity of clopidogrel was measured by VerifyNow P2Y12 assay in the same patient while medicated with CCBs and at 8 weeks after discontinuation of CCBs. After discontinuation of the CCBs, angiotensin receptor blockers were newly administered to the patients or dosed up for control of blood pressure.

Results

Thirty patients finished this study. PRU significantly decreased after discontinuation of CCBs (238.1±74.1 vs. 215.0±69.3; p=0.001). Of the 11 patients with high post-treatment platelet reactivity to clopidogrel (PRU≥275), PRU decreased in nine patients, decreasing below the cut-off value in seven of these nine patients after 8 weeks. Decrease in PRU was not related to CYP2C19 genotype.

Conclusion

CCBs inhibit the antiplatelet activity of clopidogrel.     

Neuropathic Pain Model of Peripheral Neuropathies Mediated by Mutations of Glycyl-tRNA Synthetase

Charcot-Marie-Tooth disease (CMT) is the most common inherited motor and sensory neuropathy. Previous studies have found that, according to CMT patients, neuropathic pain is an occasional symptom of CMT. However, neuropathic pain is not considered to be a significant symptom associated with CMT and, as a result, no studies have investigated the pathophysiology underlying neuropathic pain in this disorder. Thus, the first animal model of neuropathic pain was developed by our laboratory using an adenovirus vector system to study neuropathic pain in CMT. To this end, glycyl-tRNA synthetase (GARS) fusion proteins with a FLAG-tag (wild type [WT], L129P and G240R mutants) were expressed in spinal cord and dorsal root ganglion (DRG) neurons using adenovirus vectors. It is known that GARS mutants induce GARS axonopathies, including CMT type 2D (CMT2D) and distal spinal muscular atrophy type V (dSMA-V). Additionally, the morphological phenotypes of neuropathic pain in this animal model of GARS-induced pain were assessed using several possible markers of pain (Iba1, pERK1/2) or a marker of injured neurons (ATF3). These results suggest that this animal model of CMT using an adenovirus may provide information regarding CMT as well as a useful strategy for the treatment of neuropathic pain.

Graphical Abstract

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