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The use of vesicular carriers has recently emerged as a feasible method for minimizing the obstructive effects of the stratum corneum. The use of transferosomes, also known as ultradeformable lipids or elastic liposomes, in cutaneous distribution has attracted a lot of attention. They are generally used to treat a range of chronic skin disorders, but they may also be utilised to guarantee patient compliance via concentrated and controlled distribution. These self-assembled nanocarriers may adjust their pore size to that of the stratum corneum. Edge activators (specific surfactants), phospholipids, buffering agents, and other substances are found in transferosomes. Due to the activity of edge activators and their concentration, constructed vesicles have the requisite flexibility. Drug solubilization, efficient drug loading, and therapeutic molecule permeability may all be improved by elastic liposomes. As nanocarriers, transferosomes have improved reflectivity and provide a diverse platform for effective transdermal applications. These one-of-a-kind nanocarriers also have exceptional elasticity and penetration. These systems are thought to be safe, with effective delivery routes for pharmaceutically and aesthetically active chemical moieties. Recent scientific results highlighting the need for ultradeformable liposomes have revealed that medication penetration is constant and effective. This book contains up-to-date research as well as in-depth updates on crucial issues and the usage of future transferosomes with enhanced bioavailability profiles.

The environment has rapidly looked at proven specialist task forces in the aftermath of the COVID-19 pandemic to build public health policies and measures to mitigate the effects of emerging coronaviruses. According to the researchers, taking 10 μg of 25-hydroxy vitamin D daily is recommended to keep us safe. There have been several studies recently indicating that there is a reduced risk of contracting Coronavirus by 25-hydroxy vitamin D consumption, even though there is no scientific data to prove that one would not affect the COVID-19 viral infection by 25-hydroxy vitamin D consumption. In this regard, the present study investigates the important literature and the role of 25-hydroxy vitamin D to prevent COVID-19 infection by conducting an in-silico study with SARS-CoV-2 spike protein as a target. Lopinavir, a previously reported drug candidate, served as a reference standard for the study. MD simulations were carried out to improve predictions of receptor-ligand complexes which offer novelty and strength to the current study. MD simulation protocols were explored and subjected to 25-hydroxy vitamin D and a known drug, Lopinavir. Comparison of ligands at refined models to the crystal structure led to promising results. Appropriate timescale simulations have been used to understand the activation mechanism, the role of water networks for receptor function, and the ligand binding process. Furthermore, MD simulations in combination with free energy calculations have also been carried out for lead optimization, evaluation of ligand binding modes, and assessment of ligand selectivity. From the results, 25-hydroxy vitamin D was discovered to have the vital interaction and highest potency in LBE, lower RMSD, and lower inhibition intensity similar to the standard. The findings from the current study suggested that 25-hydroxy vitamin D would be more effective in treating COVID-19. Compared with Lopinavir, 25-hydroxy vitamin D had the most potent interaction with the putative binding sites of the SARS-CoV-2 spike protein of COVID-19.

Recently, the demand for fungal pigments has increased due to their several benefits over synthetic dyes. Many species of fungi are known to produce pigments and a large number of fungal strains for pigment production are yet to be extensively investigated. The natural pigment from sustainable natural sources has good economic and industrial value. Many synthetic colorants used in textile and various industries have many harmful effects on the human population and environment. Pigments and coloring agents may be extracted from a wide range of fungal species. These compounds are among the natural compounds having the most significant promise for medicinal, culinary, cosmetics, and textile applications. This study attempts to isolate and optimize the fermentation conditions of Penicillium sclerotiorum strain AK-1 for pigment production. A dark yellow-colored pigment was isolated from the strain with significant extractive value and antioxidant capacity. This study also identifies that the pigment does not have any cytotoxic effect and is multicomponent. The pigment production was optimized for the parameters such as pH, temperature, carbon and nitrogen source. Fabric dyeing experiments showed significant dyeing capacity of the pigment on cotton fabrics. Accordingly, the natural dye isolated from P. sclerotiorum strain AK-1 has a high potential for industrial-scale dyeing of cotton materials.

Trypsin is a protein-digesting enzyme that is essential for the growth and regeneration of bone, muscle, cartilage, skin, and blood. The trypsin inhibitors have various role in diseases such as inflammation, Alzheimer's disease, pancreatitis, rheumatoid arthritis, cancer prognosis, metastasis and so forth. From 10 endophytic fungi isolated, we were able to screen only one strain with the required activity. The fungus with activity was obtained as an endophyte from Dendrophthoe falcata and was later identified as Nigrospora sphaerica. The activity was checked by enzyme assays using trypsin. The fungus was fermented and the metabolites were extracted and further purified by bioassay-guided chromatographic methods and the compound isolated was identified using gas chromatography-mass spectrometry. The compound was identified as quercetin. Docking studies were employed to study the interaction. The absorption, distribution, metabolism, and excretion analysis showed satisfactory results and the compound has no AMES and hepatotoxicity. This study reveals the ability of N. sphaerica to produce bioactive compound quercetin has been identified as a potential candidate for trypsin inhibition. The present communication describes the first report claiming that N. sphaerica strain AVA-1 can produce quercetin and it can be considered as a sustainable source of trypsin active-site inhibitors.

Alzheimer's disease (AD), also called senile dementia is a neurodegenerative disease seen commonly in the elderly and is characterised by the formation of β-amyloid plaques and neurofibrillary tangles (NFT). Though a complete understanding of the disease is lacking, recent studies showed the role of the enzyme acetylcholinesterase (AChE) in pathogenesis. Finding new lead compounds from natural sources has always been a quest for researchers. Endophytic fungi are a set of microbes that reside within plants without causing any harm. This study focuses on screening endophytes for the production of active acetylcholinesterase inhibitors. Five endophytic fungi were isolated from Catharanthus roseus and screened for AChE inhibitory activity. Three isolates were found to inhibit AChE inhibitory activity and were distinguished based on molecular and microscopic methods. The mycelial extract was taken for the bioassay-guided column chromatography and TLC was performed on the active fraction. The GC-MS and NMR analysis identified the active compounds in the extract as 9-hexadecen-1-ol and erucamide. Molecular docking studies revealed that the compounds are thermodynamically feasible and have significant glide scores. Computational studies revealed that the hydroxyl group of 9-hexadecen-1-ol forms a hydrogen bond with Ser 293 in the active site of AChE, whereas the active site interactions were predominantly hydrophobic in the case of erucamide and are reflected in AChE inhibition assays.

The science and technology of electrical equipment for communication experience a rapid growth rate. However, the unwanted interference of electromagnetic waves of different electronic devices brought serious anxiety about human health as well as the lifetime and performance of the systems. To combat these consequences, we need to lessen the electromagnetic wave emission by making our devices more noise-sensitive. Herein, we incorporated carbon nanotubes (CNTs) at different ratios into natural rubber (NR) and chlorobutyl rubber (CIIR) to achieve shielding efficiency, along with carbon nanofibers (CNFs), nanoclay (NC), and carbon black (CB) to manipulate EMI shielding performance. The blend of CIIR/NR in a 70/30 (w/w) ratio also mixed with CNT, CNF, CB and NC. The effect of different fillers and their concentration/combination was analyzed by UV spectroscopy, demonstrating an absorbance peak in CIIR in 320 nm. From FTIR spectroscopy, it was evident that CIIR/CNT (5 phr), NR (30 wt.%)/CIIR (70 wt.%)/CB (5 phr), and NR (30 wt.%)/CIIR (70 wt.%)/CNT (5 phr) new bonding signatures were detected. The dielectric spectroscopic analyses were reflected in dielectric loss, dielectric permittivity and AC conductivity, where NR (30 wt.%)/CIIR (70 wt.%)/CB (5 phr) blend nanocomposite with 5 dB showed significantly higher EMI shielding performance compared to CIIR/CNT (5 phr) and CIIR/CNF (5 phr) with 29 and 15 dB, respectively. The greater the concentration of nanofiller, the lower the electromagnetic interference (EMI) shielding, i.e., CIIR/CNT (10 phr) with 15 dB (≈−48% dB), but with more agglomeration. Surprisingly, even a combination of fillers did not lead to higher EMI performance, such that CIIR/CNT (5 phr)-CB (20 phr) showed an EMI shielding value of 59 dB.

The human body’s contact with the outside world is the skin, which has a total surface area of roughly 1.8 m2. Because it removes many of the difficulties associated with the oral route, the transdermal mode of medicine administration has aroused a lot of interest in pharmaceutical research. Although the skin, particularly the stratum corneum, is a barrier to most medicine absorption, it does provide a large (1.2 m2) and easily accessible surface area for drug diffusion. Several approaches for improving bioactive delivery through transdermal distribution have recently been investigated. Some of the most frequent examples are iontophoresis, electrophoresis, sonophoresis, chemical permeation enhancers, magnetophoresis, microneedles, and vesicular systems (niosomes, liposomes, elastic liposomes such as transfersomes, ethosomes, and transethosomes). Transethosomes seem to be the most promising of the group, since they include both lipophilic and hydrophilic sections and can take therapeutic compounds with a wide range of solubility. Transethosomes may bend and pass through constrictions that are 5 to 10 times smaller in diameter than their own. Intact vesicles may be pierced more readily due to their high deformability. These vesicles may transport analgesics, anesthetics, corticosteroids, sex hormones, anticancer drugs, insulin, and other pharmaceuticals transdermally.

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Cross-linked polyethylene (XLPE) and its nanocomposites have found various application in recent years. As many key factors for HVDC cable insulation design, low conductivity and good mechanical, thermal and electrical stability too are required. Various methods have been used to improve the current challenges of cross-linked polyethylene (XLPE). Addition of nanoparticles (NPs) is been improving the above properties and cleared the pathway for long lifetime application. This chapter includes various strategies for cross-linking PE coupled with different nanofillers to enhance the electrical insulation properties to attain high power transmission. Some of the challenges in dielectric insulation for cables, like partial discharge (PD), space charge accumulation, water trees, volume resistivity, and DC breakdown strength, are addressed.

Coronavirus disease 2019 (COVID-19), a highly contagious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has drastically changed the lifestyle of people around the globe. Due to the lack of specific and effective antiviral drugs, transmission of the disease increases exponentially and makes it more serious and harder to control. Drugs that were assumed to be effective against COVID-19 have failed in various stages of clinical trials and this made the scientific community more disappointed. But, the race of researchers for developing new and effective antiviral to stop the disease progression still continues and our work is one among them. This study is an attempt to analyze the action of Tectoquinone and Acteoside; an important phytocompound, on SARS-CoV2 viral protease via in silico approach. The compounds were selected on the basis of their molecular docking values and they were subjected to molecular dynamics simulations about 50 ns to determine the stability and the thermodynamic feasibility between the target and the ligands. Binding energies like hydrogen bonding, hydrophobic and electrostatic interactions of the complexes were determined after MD simulations. The Pharmacokinetics and drug likeness evaluation of the compounds provide a strong evidence for the use of these compounds in developing drugs for clinical trials. Thus, the current study reveals the potential phytoconstituents present in

The copolymerization of styrene (St) with a bioderived monomer, pentadecylphenyl methacrylate (PDPMA), via atom transfer radical polymerization (ATRP) was studied in this work. The copolymerization reactivity ratio was calculated using the composition data obtained from 1H NMR spectroscopy, applying Kelen-Tudos and Finemann-Ross methods. The reactivity ratio of styrene (r1 = 0.93) and PDPMA (r2 = 0.05) suggested random copolymerization of the two monomers with alternation. The copolymerization conversion increased with increasing PDPMA concentration of the feed, upto 70 wt % PDPMA, but decreased thereafter. The molecular weight determined by gel permeation chromatography was lower than the theoretical values and the polydispersity increased from 1.32 to 2.19, with increasing PDPMA content in the feed. The influence of styrene content on the glass transition and thermal decomposition behavior of the copolymers was studied by differential scanning calorimetry (DSC) and thermogravimetric analysis, respectively. Morphological characterization by transmission electron microscopy (TEM) revealed a phase separated soft core-hard shell type structure. The complex viscosity and adhesion properties like peel strength and lap shear strength of the copolymer on different substrates increased with increasing styrene content.

The plausible interactions of the two novel natural inhibitors; 2-(3,4-dihydroxy-5-methoxyphenyl)-3,5,7-trihydroxychromenylium (1) and 2-(3,4-dihydroxyphenyl)-3-hydroxy-7-methoxy-4H-chromen-4-one (2) (Figure 1) with one of the prominent Coronavirus target (Viral SARS-CoV-2 Spike Glycoprotein) which is involved with the survival of the virus was studied through the Glide (Molecular Docking) module of the Schrodinger (Maestro 9.1) software. The docking scores of both the two natural compounds were reported and a probable conclusion for pharmacotherapeutics was drawn from this exploration.