Evan

Advanced in vitro cell culture or microphysiological systems (MPSs) recapitulate features of human tissues and are increasingly being used for drug development and disease modeling. Still, they are commonly based on standard polymers with minimal real-time stimuli and read-out capacity. This review describes how advanced materials and devices could enable a technology leap in reproducing in vivo-like functionality and real-time tissue monitoring.

Abstract

Advanced in vitro cell culture systems or microphysiological systems (MPSs), including microfluidic organ-on-a-chip (OoC), are breakthrough technologies in biomedicine. These systems recapitulate features of human tissues outside of the body. They are increasingly being used to study the functionality of different organs for applications such as drug evolutions, disease modeling, and precision medicine. Currently, developers and endpoint users of these in vitro models promote how they can replace animal models or even be a better ethically neutral and humanized alternative to study pathology, physiology, and pharmacology. Although reported models show a remarkable physiological structure and function compared to the conventional 2D cell culture, they are almost exclusively based on standard passive polymers or glass with none or minimal real-time stimuli and readout capacity. The next technology leap in reproducing in vivo-like functionality and real-time monitoring of tissue function could be realized with advanced functional materials and devices. This review describes the currently reported electronic and optical advanced materials for sensing and stimulation of MPS models. In addition, an overview of multi-sensing for Body-on-Chip platforms is given. Finally, one gives the perspective on how advanced functional materials could be integrated into in vitro systems to precisely mimic human physiology.

A single‐crystalline gallium nitride (GaN) film with atomic‐step terraces is realized on a complementary metal‐oxide‐semiconductor‐compatible Si(100) substrate by using a one‐atom‐thick single‐crystalline graphene buffer layer. The monolayer single‐crystalline graphene provides an in‐plane driving force for the uniform alignment of nitrides domains. This approach can also enable the growth of wafer‐scale hexagonal single‐crystalline films on amorphous or flexible substrates.

Abstract

Fabricating single‐crystalline gallium nitride (GaN)‐based devices on a Si(100) substrate, which is compatible with the mainstream complementary metal‐oxide‐semiconductor circuits, is a prerequisite for next‐generation high‐performance electronics and optoelectronics. However, the direct epitaxy of single‐crystalline GaN on a Si(100) substrate remains challenging due to the asymmetric surface domains of Si(100), which can lead to polycrystalline GaN with a two‐domain structure. Here, by utilizing single‐crystalline graphene as a buffer layer, the epitaxy of a single‐crystalline GaN film on a Si(100) substrate is demonstrated. The in situ treatment of graphene with NH₃ can generate sp³ CN bonds, which then triggers the nucleation of nitrides. The one‐atom‐thick single‐crystalline graphene provides an in‐plane driving force to align all GaN domains to form a single crystal. The nucleation mechanisms and domain evolutions are further clarified by surface science exploration and first‐principle calculations. This work lays the foundation for the integration of GaN‐based devices into Si‐based integrated circuits and also broadens the choice for the epitaxy of nitrides on unconventional amorphous or flexible substrates.

Abstract

Publication date: 20 August 2014
Source:Tetrahedron Letters, Volume 55, Issue 34
Author(s): Astrid-Caroline Knall , Manuel Hollauf , Christian Slugovc
Inverse electron demand Diels–Alder additions (iEDDA) between 1,2,4,5-tetrazines and olefins have recently found widespread application as a novel ‘click chemistry’ scheme and as a mild technique for the modification of materials. Norbornenes are, due to their straightforward synthetic availability, especially interesting in the latter context. Therefore, the reactivity of different norbornene-based compounds was compared with unsubstituted norbornene and other alkenes using UV-vis measurements for the determination of reaction rates under pseudo first order conditions. Thereby, exo,exo-5-norbornene-2,3-dimethanol was found to be almost as reactive as unsubstituted norbornene whereas (±)-endo,exo-dimethyl-5-norbornene-2,3-dicarboxylate reacted only insignificanty faster than unstrained alkenes.

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