Design of Cationic Lipids with Acetal Linkers: Conformational Preferences,Hydrolytic Stability,and High Drug-Loading Abilities

Lipids are key constituents of numerous biomedical drug delivery technologies. Here, we present the design, synthesis and biophysical characterizations of a library of cationic lipids containing an acetal residue in their linker region. These cationic acetal lipids (CALs) were conveniently prepared through a trans-acetalization protocol from commercially available precursors. NMR studies highlighted the conformational rigidity at the acetal residue and the high hydrolytic stability of these CALs. Fluorescence anisotropy studies revealed that the CAL with a pyridinium headgroup (CAL1) formed highly cohesive vesicular aggregates in water. These structural and self-assembly features of the CAL1 allowed up to 196 % w/w loading of curcumin (Cur) as a representative hydrophobic drug. A reconstitutable formulation of Cur was obtained as a result, which could deliver the drug inside mammalian cells with very high efficiency. The hemocompatibility and cytocompatibility of CAL1 was significantly enhanced by creating a coating of polydopamine (PDA) onto its vesicular assemblies to produce hybrid lipid-polymer nanocapsules. This work demonstrates rapid access to the useful synthetic lipid formulations with high potential in drug and gene delivery applications.     

Characterization of Barley β-Amylase for Application in Maltose Production

A simple procedure is devised to extract β-amylase preparation in a form suitable for commercial applications from germinated barley. α-Amylase activity in the β-amylase preparation was negligible to warrant its further purification. This preparation showed enzymatic activity over a broad pH and temperature range, suitable for conversion of starch to high purity maltose.     

EEG based personality prediction using genetic programming

The reliable correlation between personality and brain signal ensures that inferences from cognitive processes can be achieved. This research aims primarily to predict one's personality using brain signals. On grounds of Psychology, the inference of personality in this work is performed on the basis of the Myers–Briggs Type Indicator (MBTI) personality inventory. Personality consists of different types of thinking, feeling and behavior patterns. EEG signals are produced when a person is exposed to situations or scenarios via visual information and experiences various emotions or sentiments. In this study, by evaluating brain waves while a person watches personality traits elicitation materials, the identification of the personality traits of an individual is done. The elicitation materials used for the collection of the dataset comprise approximately 50 videos with the pre-defined personality of the dramatic personae and therefore, it is considered to be the ground truth for the experimental procedure of this work. For creating a dataset, sixty participants contributed and gave brain signals. The GP model with the proposed BSH crossover, known as the BSHGP model, is implemented. The maximum performance of the BSHGP model for a 10-fold partition scheme is 84.34%.     

Human iPSC-Derived Proinflammatory Macrophages cause Insulin Resistance in an Isogenic White Adipose Tissue Microphysiological System

Chronic white adipose tissue (WAT) inflammation has been recognized as a critical early event in the pathogenesis of obesity-related disorders. This process is characterized by the increased residency of proinflammatory M1 macrophages in WAT. However, the lack of an isogenic human macrophage-adipocyte model has limited biological studies and drug discovery efforts, highlighting the need for human stem cell-based approaches. Here, human induced pluripotent stem cell (iPSC) derived macrophages (iMACs) and adipocytes (iADIPOs) are cocultured in a microphysiological system (MPS). iMACs migrate toward and infiltrate into the 3D iADIPOs cluster to form crown-like structures (CLSs)-like morphology around damaged iADIPOs, recreating classic histological features of WAT inflammation seen in obesity. Significantly more CLS-like morphologies formed in aged and palmitic acid-treated iMAC-iADIPO-MPS, showing the ability to mimic inflammatory severity. Importantly, M1 (proinflammatory) but not M2 (tissue repair) iMACs induced insulin resistance and dysregulated lipolysis in iADIPOs. Both RNAseq and cytokines analyses revealed a reciprocal proinflammatory loop in the interactions of M1 iMACs and iADIPOs. This iMAC-iADIPO-MPS thus successfully recreates pathological conditions of chronically inflamed human WAT, opening a door to study the dynamic inflammatory progression and identify clinically relevant therapies.