Lignin-Based High-Performance Fibers by Textile Spinning Techniques.

As a major component of lignocellulosic biomass, lignin is one of the largest natural resources of biopolymers and, thus, an abundant and renewable raw material for products, such as high-performance fibers for industrial applications. Direct conversion of lignin has long been investigated, but the fiber spinning process for lignin is difficult and the obtained fibers exhibit unsatisfactory mechanical performance mainly due to the amorphous chemical structure, low molecular weight of lignin, and broad molecular weight distribution. Therefore, different textile spinning techniques, modifications of lignin, and incorporation of lignin into polymers have been and are being developed to increase lignin's spinnability and compatibility with existing materials to yield fibers with better mechanical performance. This review presents the latest advances in the textile fabrication techniques, modified lignin-based high-performance fibers, and their potential in the enhancement of the mechanical performance.

Lignocellulosic Biomass-Derived Carbon Electrodes for Flexible Supercapacitors: An Overview.

With the increasing demand for high-performance electronic devices in smart textiles, various types of flexible/wearable electronic device (i.e., supercapacitors, batteries, fuel cells, etc.) have emerged regularly. As one of the most promising wearable devices, flexible supercapacitors from a variety of electrode materials have been developed. In particular, carbon materials from lignocellulosic biomass precursor have the characteristics of low cost, natural abundance, high specific surface area, excellent electrochemical stability, etc. Moreover, their chemical structures usually contain a large number of heteroatomic groups, which greatly contribute to the capacitive performance of the corresponding flexible supercapacitors. This review summarizes the working mechanism, configuration of flexible electrodes, conversion of lignocellulosic biomass-derived carbon electrodes, and their corresponding electrochemical properties in flexible/wearable supercapacitors. Technology challenges and future research trends will also be provided.

A Rapid and Quantitative Fluorimetric Method for Protein-Targeting Small Molecule Drug Screening.

We demonstrate a new drug screening method for determining the binding affinity of small drug molecules to a target protein by forming fluorescent gold nanoclusters (Au NCs) within the drug-loaded protein, based on the differential fluorescence signal emitted by the Au NCs. Albumin proteins such as human serum albumin (HSA) and bovine serum albumin (BSA) are selected as the model proteins. Four small molecular drugs (e.g., ibuprofen, warfarin, phenytoin, and sulfanilamide) of different binding affinities to the albumin proteins are tested. It was found that the formation rate of fluorescent Au NCs inside the drug loaded albumin protein under denaturing conditions (i.e., 60 °C or in the presence of urea) is slower than that formed in the pristine protein (without drugs). Moreover, the fluorescent intensity of the as-formed NCs is found to be inversely correlated to the binding affinities of these drugs to the albumin proteins. Particularly, the higher the drug-protein binding affinity, the slower the rate of Au NCs formation, and thus a lower fluorescence intensity of the resultant Au NCs is observed. The fluorescence intensity of the resultant Au NCs therefore provides a simple measure of the relative binding strength of different drugs tested. This method is also extendable to measure the specific drug-protein binding constant (KD) by simply varying the drug content preloaded in the protein at a fixed protein concentration. The measured results match well with the values obtained using other prestige but more complicated methods.