Korsholmaldridge1220

Phosphatidylinositol mannosides (PIMs) have been investigated as lipidic antigens for a new subunit tuberculosis vaccine. A non-natural diacylated phosphatidylinositol mannoside (Ac2PIM2) was designed and synthesized by mimicking the natural PIM6 processing procedure in dentritic cells. This synthetic Ac2PIM2 was achieved from α-methyl d-glucopyranoside 1 in 17 steps in 2.5% overall yield. A key feature of the strategy was extending the use of the chiral myo-inositol building block A to the O-2 and O-6 positions of the inositol unit to allow for introducing the mannose building blocks B1 and B2, and to the O-1 position for the phosphoglycerol building block C. Building block A, being a flexible core unit, may facilitate future access to other higher-order PIM analogues. A preliminary antigenic study showed that the synthetic PIM epitope (Ac2PIM2) was significantly more active than natural Ac2PIM2, which indicated that the synthetic Ac2PIM2 can be strongly immunoactive and may be developed as a potential vaccine.The interfacial topology of block copolymer cubic mesophases opens only one of two internal water channel networks for diffusion. Utilizing this topology selection, single and double diamond cubic crystalline networks of Ni were synthesized from cubic block copolymer (BCP) mesophase templates via electroless plating, in which the lattice structures were converted to the polymer cubosome (PC) internal pore networks by selective metal-ion diffusion. This was accomplished by manipulating the BCP molecular weight, which consequently allowed for selective access to the PC internal pore networks. This work provides a selective protocol for highly defined transition-metal cubic networks that are suitable for application in catalysis, electrochemistry, and synthesis of metamaterials with photonic and magnetic properties.Liquid metals are a promising functional material due to their unique combination of metallic properties and fluidity at room temperature. They are of interest in wide-ranging fields including stretchable and flexible electronics, reconfigurable devices, microfluidics, biomedicine, material synthesis, and catalysis. Transformation of bulk liquid metal into particles has enabled further advances by allowing access to a broader palette of fabrication techniques for device manufacture or by increasing area available for surface-based applications. For gallium-based liquid metal alloys, particle stabilization is typically achieved by the oxide that forms spontaneously on the surface, even when only trace amounts of oxygen are present. The utility of the particles formed is governed by the chemical, electrical, and mechanical properties of this oxide. To overcome some of the intrinsic limitations of the native oxide, it is demonstrated here for the first time that 2D graphene-based materials can encapsulate liquid metal particles during fabrication and imbue them with previously unattainable properties. This outer encapsulation layer is used to physically stabilize particles in a broad range of pH environments, modify the particles' mechanical behavior, and control the electrical behavior of resulting films. This demonstration of graphene-based encapsulation of liquid metal particles represents a first foray into the creation of a suite of hybridized 2D material coated liquid metal particles.The triangulenes and their closed-shell ions are a family of polycyclic aromatic hydrocarbons (PAH) that have possible applications in fields as different as spintronics or catalysis. However, the electron delocalization in such systems is not well understood because there are several differences to classical PAHs. We found that the triangulene cations are always more delocalized than the radicals or the anions, independently of the π e- count. Contrary to any other PAHs, the π e- of triangulenes and their ions are delocalized throughout the whole molecule and are even more delocalized than acenes. The π sextet aromaticity does not play a central role in the stabilization of triangulenes like for other PAHs. Interestingly, neither the radicals nor the ions follow Clar's rule, which makes them a unique type of PAH.An indirect electrochemical detoxification and detection platform has been demonstrated for toxic hexavalent chromium (Cr(vi)) based on the biologically important N-4 macrocycle. The research work describes a simple, green, low-cost and potential way for the synthesis of a new N-4 macrocyclic molecule and the molecule is characterized by various analytical and spectroscopic techniques like elemental analysis, TGA, FT-IR, UV-visible, mass spectrometry and NMR spectroscopies, and cyclic voltammetry. The synthesized molecule was explored for the electrochemical reduction of Cr(vi) using both voltammetric and amperometric methods. Amperometric studies exhibited 50 to 2500 nM linear range and the detection limit and quantification limit are 18 and 50 nM, respectively. The common coexisting metal ions did not interfere with Cr(vi) even in the presence of 40-fold excess interfering ions. The real sample analysis was carried out with the fabricated sensor and successfully quantified a recovery result (98-104%) of Cr(vi) in water. This proposed sensor is helpful in the detection of chromium ions in drinking water and is capable of detecting Cr(vi) in the limits set by the World Health Organization (WHO). In addition, this sensor satisfactorily demonstrated considerable stability and reproducibility.Calcium looping (CaL) is a CO2 capture technique based on the reversible carbonation/calcination of CaO that is considered promising to reduce anthropogenic CO2 emissions. However, the rapid decay of the CO2 uptake of CaO over repeated cycles of carbonation and calcination due to sintering limits its implementation at the industrial scale. Thus, the development of material design strategies to stabilize the CO2 uptake capacity of CaO is paramount. The addition of alkali metal salts to CaO has been proposed as a strategy to mitigate the rapid loss of its cyclic CO2 uptake capacity. However, there are conflicting results concerning the effect of the addition of alkali metal carbonates on the structure and CO2 capacity of CaO. In this work, we aim at understanding the effect of the addition of Na2CO3 to CaO on the sorbent's structure and its CO2 uptake capacity. We demonstrate that under industrially-relevant conditions the addition of as little as 1 wt% of Na2CO3 reduces severely the CO2 uptake of CaO. Combining TGA, XAS and FIB-SEM analysis allowed us to attribute the performance degradation to the formation of the double salt Na2Ca(CO3)2 that induces strong sintering leading to a significant loss in the sorbent's pore volume. In addition, during the carbonation step the formation of a dense layer of Na2Ca(CO3)2 that covers unreacted CaO prevents its full carbonation to CaCO3.Wastewater entering sewer networks represents a unique source of pooled epidemiological information. In this study, we coupled online solid-phase extraction with liquid chromatography-high resolution mass spectrometry to achieve high-throughput analysis of health and lifestyle-related substances in untreated municipal wastewater during the coronavirus disease 2019 (COVID-19) pandemic. Twenty-six substances were identified and quantified in influent samples collected from six wastewater treatment plants during the COVID-19 pandemic in central New York. Over a 12 week sampling period, the mean summed consumption rate of six major substance groups (i.e., antidepressants, antiepileptics, antihistamines, antihypertensives, synthetic opioids, and central nervous system stimulants) correlated with disparities in household income, marital status, and age of the contributing populations as well as the detection frequency of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA in wastewater and the COVID-19 test positivity in the studied sewersheds. Nontarget screening revealed the covariation of piperine, a nontarget substance, with SARS-CoV-2 RNA in wastewater collected from one of the sewersheds. Overall, this proof-of-the-concept study demonstrated the utility of high-throughput wastewater analysis for assessing the population-level substance use patterns during a public health crisis such as COVID-19.Limited sample loading capacity is one of the major reasons that prevents the utility of capillary electrophoresis (CE) as a routine separation method as compared to liquid chromatography (LC). In our previous study, separation voltage polarity switching transient capillary isotachophoresis (PS-tCITP) was proposed. Both sample loading capacity and separation resolution could be improved using a single PS-tCITP instead of routine transient capillary isotachophoresis (tCITP). Cell Cycle inhibitor In this study, a detailed investigation on the optimization strategy of the PS-tCITP method was performed systematically. A possible mechanism of sample preconcentration in multiple PS-tCITP was first proposed to better understand the multiple PS-tCITP process. Several optimization experiments were then performed, including single PS-tCITP, paused PS-tCITP and multiple PS-tCITP, sequentially using a mixture of five peptides. By selecting an optimum polarity switching time, sample loading capacity of 100% capillary volume could be achieved in a single PS-tCITP. Introducing an additional pause between each polarity switching in a single PS-tCITP further improved the separation resolution. Experimental results showed a baseline separation of five selected peptide standards at 100% sample loading volume using a 100 min pause in a single PS-tCITP. To further improve separation efficiency while still maintaining 100% sample loading volume, a multiple PS-tCITP technique was developed through this study. Compared to the separation performance of the optimal single PS-tCITP at 100% sample loading volume with a 10 min pause, the separation window was improved by 54% and the peak capacity was improved by 48% in the optimal four PS-tCITP with the same sample loading volume and pause.The effects of whole grain highland barley (WGH) with rich phenolics on glucose metabolism, the insulin pathway, and microRNA (miRNA) expression in db/db mice were explored in the present study. Supplementation with WGH decreased the levels of blood glucose, glycosylated serum protein (GSP), insulin, and inflammatory cytokines in db/db mice. Furthermore, WGH administration triggered a remarkable amelioration of glucose intolerance and insulin resistance. The hepatic glucose-6-phosphatase (G6Pase) and phosphoenolpyruvate carboxylase (PEPCK) activities and the G6PC, PEPCK, and forkhead transcription factor 1 (FOXO1) mRNA levels in the WGH-treated group were also reduced. Moreover, WGH promoted the glycogen storage in the liver via up-regulating the activities of hexokinase (HK) and glycogen synthase (GS) and the phosphorylation of glycogen synthase kinase 3β (GSK3β) protein, while down-regulating the GSK3β mRNA level. The protein expression of phosphatidylinositol 3-kinase (PI3K), the phosphorylation of protein kinase B (Akt), and the mRNA levels of insulin receptor substrate-1 (IRS-1), PI3K and Akt were also up-regulated by WGH treatment. Moreover, WGH significantly augmented the expression of miRNA-26a and miRNA-451, but reduced those of miRNA-126a and miRNA-29a. These results demonstrated that WGH exhibits a hypoglycemic effect through regulating the IRS-1/PI3K/Akt pathway and related miRNAs, further modulating the expression of G6PC, PEPCK, and FOXO1 mRNAs and p-GSK3β protein, thus inhibiting hepatic gluconeogenesis, improving glycogen synthesis and alleviating insulin resistance. Therefore, this study suggested WGH as an effective candidate to ameliorate the hyperglycemia of type 2 diabetes mellitus.