Zwitterionic liquids composed of a tethered cation and anion were synthesized and their thermal properties and ionic conductivity were investigated as novel ionic liquids especially for electrochemical applications. We prepared nine zwitterions in this study. In addition, this paper includes 36 kinds of zwitterions already reported in order to discuss the relationship between the zwitterion structure and their properties. Most zwitterions melt above 100°C; their melting points are generally higher than that of simple ionic liquids. When an equimolar amount of lithium salt (LiTFSI, LiBETI, LiCF3SO3, LiBF4, or LiClO4) was added to the zwitterion, the mixture showed only a glass transition temperature Tg. The Tg values of the zwitterionic liquid/salt mixture showed the lowest value of –37°C when mixed with LiTFSI. This mixture also showed the highest ionic conductivity of 8.9 × 10–4 S cm–1 at 100°C. There is a good relationship between Tg and the ionic conductivity of the zwitterionic liquid/lithium salt mixtures.

SummarySkeletal muscle contains two distinct stem/progenitor populations. One is the satellite cell, which acts as a muscle stem cell, and the other is the mesenchymal progenitor, which contributes to muscle pathogeneses such as fat infiltration and fibrosis. Detailed and accurate characterization of these progenitors in humans remains elusive. Here, we performed comprehensive cell-surface protein profiling of the two progenitor populations residing in human skeletal muscle and identified three previously unrecognized markers: CD82 and CD318 for satellite cells and CD201 for mesenchymal progenitors. These markers distinguish myogenic and mesenchymal progenitors, and enable efficient isolation of the two types of progenitors. Functional study revealed that CD82 ensures expansion and preservation of myogenic progenitors by suppressing excessive differentiation, and CD201 signaling favors adipogenesis of mesenchymal progenitors. Thus, cell-surface proteins identified here are not only useful markers but also functionally important molecules, and provide valuable insight into human muscle biology and diseases.

The incorporation of active pharmaceutical ingredients (APIs) into multicomponent solid forms (such as salts and co-crystals) or liquid forms (such as ionic liquids (ILs) or deep eutectic mixtures) is important in optimizing the efficacy and delivery of APIs. However, there is a current debate regarding the classification of these multicomponent systems based on their ionicity which could interfere with their consideration in important applications. Multicomponent systems of intermediate ionicity can show a combination of properties, leading to behavior that is neither strictly typical of either purely ionic or purely neutral compounds, nor easily described as intermediate between the two. In this perspective, we attempt to illustrate the problems in classifying multicomponent APIs based on one of two categories by discussing selected literature regarding solid and liquid multicomponent APIs and presenting the crystal structures of some relevant systems as case studies. It is clear that a focus on restrictive nomenclature carries with it the risk that a thorough examination of the physicochemical properties of the compounds will be overlooked.

No abstract

No abstract