Stretchable and reflective displays: materials, technologies and strategies

Displays play a significant role in delivering information and providing visual data across all media platforms. Among displays, the prominence of reflective displays is increasing, in the form of E-paper, which has features distinct from emissive displays. These unique features include high visibility under daylight conditions, reduced eye strain and low power consumption, which make them highly effective for outdoor use. Furthermore, such characteristics enable reflective displays to achieve high synergy in combination with wearable devices, which are frequently used for outdoor activities. However, as wearable devices must stretch to conform to the dynamic surfaces of the human body, the issue of how to fabricate stretchable reflective displays should be tackled prior to merging them with wearable devices. In this paper, we discuss stretchable and reflective displays. In particular, we focus on reflective displays that can be divided into two types, passive and active, according to their responses to stretching. Passive displays, which consist of dyes or pigments, exhibit consistent colors under stretching, while active displays, which are based on mechanochromic materials, change their color under the same conditions. We will provide a comprehensive overview of the materials and technologies for each display type, and present strategies for stretchable and reflective displays.This research was supported by Nano Material Technology Development Program through the National Research Foundation of Korea(NRF) funded by Ministry of Science and ICT (NRF2018M3A7B4089670). D.Y.K. is supported by the National Research Foundation of Korea (NRF) Grant funded by the Korean Government (NRF-2016-Global Ph.D. Fellowship Program)

Trichloroethanol, an active metabolite of chloral hydrate, modulates tetrodotoxin-resistant Na+ channels in rat nociceptive neurons

Abstract Background Chloral hydrate is a sedative-hypnotic drug widely used for relieving fear and anxiety in pediatric patients. However, mechanisms underlying the chloral hydrate-mediated analgesic action remain unexplored. Therefore, we investigated the effect of 2′,2′,2′-trichloroethanol (TCE), the active metabolite of chloral hydrate, on tetrodotoxin-resistant (TTX-R) Na+ channels expressed in nociceptive sensory neurons. Methods The TTX-R Na+ current (INa) was recorded from acutely isolated rat trigeminal ganglion neurons using the whole-cell patch-clamp technique. Results Trichloroethanol decreased the peak amplitude of transient TTX-R INa in a concentration-dependent manner and potently inhibited persistent components of transient TTX-R INa and slow voltage-ramp-induced INa at clinically relevant concentrations. Trichloroethanol exerted multiple effects on various properties of TTX-R Na+ channels; it (1) induced a hyperpolarizing shift on the steady-state fast inactivation relationship, (2) increased use-dependent inhibition, (3) accelerated the onset of inactivation, and (4) retarded the recovery of inactivated TTX-R Na+ channels. Under current-clamp conditions, TCE increased the threshold for the generation of action potentials, as well as decreased the number of action potentials elicited by depolarizing current stimuli. Conclusions Our findings suggest that chloral hydrate, through its active metabolite TCE, inhibits TTX-R INa and modulates various properties of these channels, resulting in the decreased excitability of nociceptive neurons. These pharmacological characteristics provide novel insights into the analgesic efficacy exerted by chloral hydrate