Publications by authors named "Vijay B Kumar"

Short peptides are attractive building blocks for the fabrication of self-assembled materials with significant biological, chemical, and physical properties. The microscopic and macroscopic properties of assemblies are usually closely related to the dimensionality of formed hydrogen bond networks. Here, two completely different supramolecular architectures connected by distinct hydrogen bond networks were obtained by simply adding a hydroxyl group to switch from cyclo-tryptophan-alanine (cyclo-WA) to cyclo-tryptophan-serine (cyclo-WS).

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Peptide-based nanomaterials can serve as promising drug delivery agents, facilitating the release of active pharmaceutical ingredients while reducing the risk of adverse reactions. We previously demonstrated that Cyclo-Histidine-Histidine (Cyclo-HH), co-assembled with cancer drug Epirubicin, zinc, and nitrate ions, can constitute an attractive drug delivery system, combining drug self-encapsulation, enhanced fluorescence, and the ability to transport the drug into cells. Here, we investigated both computationally and experimentally whether Cyclo-HH could co-assemble, in the presence of zinc and nitrate ions, with other cancer drugs with different physicochemical properties.

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Bacterial infections are of major medical concern due to antibiotic resistance. Carbon quantum dots (CDs) have emerged as potentially excellent biomaterials for multifunctional applications due to their low toxicity, outstanding water solubility, high fluorescence, and high biocompatibility. All of these properties allow CDs to be exceptional biomaterials for inhibiting the growth of bacteria and stopping biofilm formation due to their strong binding affinity, cell wall penetration, and solubilizing biofilm in water.

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Article Synopsis
  • Carbon quantum dots (CQDs) are promising fluorescent nanomaterials known for their water solubility, biocompatibility, and exceptional optical properties, particularly nitrogen-containing CQDs derived from amino acids.
  • Recent efforts have enhanced the preparation of these amino acid-based CQDs, achieving the highest reported quantum yield of 86% and significant improvements in refractive indices, especially for positively charged amino acids like arginine and histidine.
  • These CQDs exhibit photostability, noncytotoxicity, and excitation-dependent emission profiles, making them ideal for applications in live cell imaging, bioimaging, and optoelectronic devices, particularly in studying cellular structures.
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Molten metals have prospective applications as soft fluids with unique physical and chemical properties, yet materials based on them are still in their infancy and have great potential. Ultrasonic irradiation of molten metals in liquid media induces acoustic cavitation and dispersion of the liquid metal into micrometric and nanometric spheres. This review focuses on the synthesis of mmetallic materials via sonochemistry from molten metals with low melting point (< 420 ᴼC): Ga, Hg, In, Sn, Bi, Pb, and Zn, which can be melted in organic or inorganic media or water and of aqueous solutions of metallic ions to form two immiscible liquid phases.

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Ultrasonic irradiation of molten metals in liquid media causes dispersion of the metals into suspensions of micro- and nanoparticles that can be separated. This is applicable mainly to low-m elemental metals or alloys, but higher m elemental metals or alloys were also reported. Among metals, mercury and gallium exhibit especially-low melting points and are thus considered as liquid metals (LMs).

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This review article summarizes the comprehensive work that was done in our laboratory in recent years, as-well-as other reports, on the various aspects of sonochemistry of molten gallium. The low m (29.8 °C) of gallium enables its melting in warm water, aqueous solutions and organic liquids.

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Tissue engineering (TE) is a rapidly expanding field aimed at restoring or replacing damaged tissues. In spite of significant advancements, the implementation of TE technologies requires the development of novel, highly biocompatible three-dimensional tissue structures. In this regard, the use of peptide self-assembly is an effective method for developing various tissue structures and surface functionalities.

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The design of novel cancer drug nanocarriers is critical in the framework of cancer therapeutics. Nanomaterials are gaining increased interest as cancer drug delivery systems. Self-assembling peptides constitute an emerging novel class of highly attractive nanomaterials with highly promising applications in drug delivery, as they can be used to facilitate drug release and/or stability while reducing side effects.

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Carbon quantum dots (CDs) are a class of emerging carbonaceous nanomaterials that have received considerable attention due to their excellent fluorescent properties, extremely small size, ability to penetrate cells and tissues, ease of synthesis, surface modification, low cytotoxicity, and superior water dispersion. In light of these properties, CDs are extensively investigated as candidates for bioimaging probes, efficient drug carriers, and disease diagnostics. Functionalized CDs represent a promising therapeutic candidate for ocular diseases.

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Carbon dots (CDs) are a novel type of carbon-based nanomaterial that has gained considerable attention for their unique optical properties, including tunable fluorescence, stability against photobleaching and photoblinking, and strong fluorescence, which is attributed to a large number of organic functional groups (amino groups, hydroxyl, ketonic, ester, and carboxyl groups, etc.). In addition, they also demonstrate high stability and electron mobility.

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A microporous carboxylate metal-organic framework MIL-100 Fe was prepared as submicron particles by microwave-assisted hydrothermal synthesis (Fe-MOF-MW). This product was explored, for the first time, for the preparation of polylactic acid (PLA) mixed matrix membranes. The produced MOF was characterised by powder X-ray diffraction (PXRD), environmental scanning electron microscopy (ESEM) as well as by thermogravimetric analysis (TGA) and nitrogen adsorption/desorption.

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Tender coconut water is a pure and nutritious drink which play important role as nutraceuticals and pharmaceuticals contributes to the rapid growth of the functional food industry. In the mean-time the safety and shelf-life of the food is crucial for the both product as well as consumers. The intervention or application of nanotechnology gives immense a solution for the prolonged sustainability of the food products.

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The current study explores the formation of active eco-friendly materials capable of preventing microbial contamination using in situ ultrasonic grafting of vanillin, curcumin and a curcumin-vanillin mixture on the surfaces of carboxymethylcellulose (CMC) and chitosan films. Spectroscopic, microscopic, physical and mechanical studies revealed that the films grafted with curcumin-vanillin mixture demonstrate improved mechanical properties and higher degree of order. The bioactivity of the prepared films was tested on food model, fresh-cut melons and films with a deposited curcumin-vanillin mixture showed superior antibacterial properties.

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Carbon-based nanomaterials are gaining more and more interest because of their wide range of applications. Carbon dots (CDs) have shown exclusive interest due to unique and novel physicochemical, optical, electrical, and biological properties. Since their discovery, CDs became a promising material for wide range of research applications from energy to biomedical and tissue engineering applications.

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This work unraveled kinetics, isotherm, and thermodynamic properties of methylene blue (MB) adsorbed on polyaniline (PANI) and polypyrrole (PPY). The two polymers, PANI and PPY, synthesized by a facile C-dot (CD)-initiated polymerization method have been proven as the effective adsorbent materials to remove MB from wastewater. This dye model is also generally employed as a redox indicator in analytical chemistry and exhibits blue in an oxidizing environment, but it is colorless when exposed to a reducing agent.

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We report the osteogenic potential of silver (Ag), gold (Au), or silver-gold doped hydroxyapatite nanoparticles (Ag-Au-HA) in zebrafish (ZF) jawbone regeneration (JBR) model. The hydroxyapatite (HA, Ca(PO)(OH)), Ag-HA, Au-HA, and Ag-Au-HA nanomaterials were synthesized by the co-precipitation procedure. The surface structures of Ag-HA, Au-HA, HA, and Ag-Au-HA were analysed by scanning electron microscopy, transmission-electron microscopy (TEM), x-ray diffraction, Fourier transform infrared (FTIR), UV-vis, energy dispersive x-ray spectroscopy (EDS), elemental mapping, and laser fluorescent spectroscopy.

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The delivery of therapeutic nanoparticles (NPs) represents a potentially powerful tool that can significantly alter the biological effects of pharmaceutically active compounds. Here, we report on sensitization of tumors to chemotherapy by ammonium trichloro(dioxoethylene-,')tellurate (AS101) encapsulated in NPs, termed AS101-NPs, developed as a composite with the biocompatible and biodegradable copolymer of poly(d,l-lactic--glycolic acid)--poly(ethylene glycol) (PLGA--PEG). AS101 is a potent immunomodulating agent (both and ) currently undergoing phase II clinical trials for antitumor activity and sensitization of tumors to chemotherapy.

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Furfural is a versatile biomass-derived platform compound used for the synthesis of several strategic chemicals. The sonochemically synthesized Zn doped CuO nanoparticles (NPs) were used for the production of furfural. The catalytic activity of the Zn doped CuO NPs was examined, as a model, during the dehydration reaction of xylose to furfural.

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There is a growing need for biocompatible nanocomposites that may efficiently interact with biological tissues through multiple modalities. Carbon dots (CDs) could serve as biocompatible fluorescence nanomaterials for targeted tissue/cell imaging. Important goals toward this end are to enhance the fluorescence quantum yields of the CDs and to increase their targetability to cells.

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In this work, we describe a low-cost, two-step synthesis of composites of nitrogen-doped carbon quantum dots (NCDs) with γ-FeO (NCDs/γ-FeO), which is based on a hydrothermal cum co-precipitation method. The product is a fine powder of particles having an average diameter of 9 ± 3 nm. The physical and chemical properties of NCDs/γ-FeO were studied, as well as the superconducting quantum interference device and Mossbauer analysis of the magnetic properties of these nanocomposites.

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Carbon dots (CDs) can generate free radicals in aqueous solutions which lead to their unique properties and many applications. The main goal of the current study is to employ CDs as initiators for the polymerization of the monomer 4,4'-diaminodiphenylmethane. Efforts have been recently focused on developing a polymerization process by using a facile one-step synthesis using HNO, CDs, and UV light as initiators.

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Concentrated suspensions of silver and copper salts in silicone oil were heated to 200 °C and irradiated with ultrasonic energy for different time durations. Characterization of the products was done using X-ray powder diffraction. In most cases, metallic Ag or Cu were obtained, together with their oxide forms AgO and CuO.

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We investigated the osteogenic potential of nitrogen-doped carbon dots (NCDs) conjugated with hydroxyapatite (HA) nanoparticles on the MC3T3-E1 osteoblast cell functions and in a zebrafish (ZF) jawbone regeneration (JBR) model. The NCDs-HA nanoparticles were fabricated by a hydrothermal cum co-precipitation technique. The surface structures of NCDs-HA nanoparticles were characterized by X-ray diffraction; Fourier transform infrared (FTIR), UV-vis, and laser fluorescence spectroscopies; and scanning electron microscopy, transmission electron microscopy (TEM), energy-dispersive spectrometry (EDS), and NMR analyses.

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Enantiospecific total syntheses of (+)-hapalindole H and (-)-12-epi-hapalindole U as well as the formal syntheses of (+)-hapalindole Q and (+)-12-epi-fischerindole U isothiocyanate have been described. Key steps of our approach feature expedient, highly regio- and diastereoselective Lewis acid catalyzed Friedel-Crafts reaction of indole with cyclic allylic alcohols and intramolecular reductive Heck reaction. Efficiency of the synthetic route also relies on an alkynyl aluminate complex driven regioselective nucleophilic epoxide opening from a sterically hindered site.

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