Recent progress in polymeric non-invasive insulin delivery

The design of carriers for insulin delivery has recently attracted major research attentions in the biomedical field. In general, the release of drug from polymers is driven via a variety of polymers. Several mechanisms such as matrix release, leaching of drug, swelling, and diffusion are usually adopted for the release of drug through polymers. Insulin is one of the most predominant therapeutic drugs for the treatment of both diabetes mellitus; type-I (insulin-dependent) and type II (insulin-independent). Currently, insulin is administered subcutaneously, which makes the patient feel discomfort, pain, hyperinsulinemia, allergic responses, lipodystrophy surrounding the injection area, and occurrence of miscarried glycemic control. Therefore, significant research interest has been focused on designing and developing new insulin delivery technologies to control blood glucose levels and time, which can enhance the patient compliance simultaneously through alternative routes as non-invasive insulin delivery. The aim of this review is to emphasize various non-invasive insulin delivery mechanisms including oral, transdermal, rectal, vaginal, ocular, and nasal. In addition, this review highlights different smart stimuli-responsive insulin delivery systems including glucose, pH, enzymes, near-infrared, ultrasound, magnetic and electric fields, and the application of various polymers as insulin carriers. Finally, the advantages, limitations, and the effect of each non-invasive route on insulin delivery are discussed in detail

Recent Advances on Nano-Catalysts for Biological Processes

We are honored to serve as the Guest Editors of this Special Issue entitled “Recent Advances on Nano-Catalysts for Biological Processes” for the journal Catalysts [...

Recent Advances on Nano-Catalysts for Biological Processes

We are honored to serve as the Guest Editors of this Special Issue entitled “Recent Advances on Nano-Catalysts for Biological Processes” for the journal Catalysts [...

Valorization of Waste Glycerol to Dihydroxyacetone with Biocatalysts Obtained from <i>Gluconobacter oxydans</i>

Waste glycerol is the main by-product generated during biodiesel production, in an amount reaching up to 10% of the produced biofuel. Is there any method which allows changing this waste into industrial valuable compounds? This manuscript describes a method for valorization of crude glycerol via microbial bioconversion. It has been shown that the use of free and immobilized biocatalysts obtained from Gluconobacter oxydans can enable beneficial valorization of crude glycerol to industrially valuable dihydroxyacetone. The highest concentration of this compound, reaching over 20 g&#183;L&#8722;1, was obtained after 72 h of biotransformation with free G. oxydans cells, in a medium containing 30 or 50 g&#183;L&#8722;1 of waste glycerol. Using a free cell extract resulted in higher concentrations of dihydroxyacetone and a higher valorization efficiency (up to 98%) compared to the reaction with an immobilized cell extract. Increasing waste glycerol concentration to 50 g&#183;L&#8722;1 causes neither a faster nor higher increase in product yield and reaction efficiency compared to its initial concentration of 30 g&#183;L&#8722;1. The proposed method could be an alternative for utilization of a petrochemical waste into industry applicated chemicals

Green Synthesis of Metallic Nanoparticles: Applications and Limitations

The past decade has witnessed a phenomenal rise in nanotechnology research due to its broad range of applications in diverse fields including food safety, transportation, sustainable energy, environmental science, catalysis, and medicine. The distinctive properties of nanomaterials (nano-sized particles in the range of 1 to 100 nm) make them uniquely suitable for such wide range of functions. The nanoparticles when manufactured using green synthesis methods are especially desirable being devoid of harsh operating conditions (high temperature and pressure), hazardous chemicals, or addition of external stabilizing or capping agents. Numerous plants and microorganisms are being experimented upon for an eco–friendly, cost–effective, and biologically safe process optimization. This review provides a comprehensive overview on the green synthesis of metallic NPs using plants and microorganisms, factors affecting the synthesis, and characterization of synthesized NPs. The potential applications of metal NPs in various sectors have also been highlighted along with the major challenges involved with respect to toxicity and translational research

Recent Developments in Lignocellulosic Biofuel Production with Nanotechnological Intervention: An Emphasis on Ethanol

Biofuel, an inexhaustible fuel source, plays a pivotal role in the contemporary era by diminishing the dependence on non-renewable energy sources and facilitating the mitigation of CO2 emissions. Due to the many constraints in existing technology and the resulting increased costs, the production of biofuels on a large scale is a laborious process. Furthermore, the methods used to convert varied feedstock into the intended biofuel may vary based on the specific techniques and materials involved. The demand for bioethanol is increasing worldwide due to the implementation of regulations by world nations that mandates the blending of bioethanol with petrol. In this regard, second-generation bioethanol made from lignocellulosic biomass is emerging at a rapid rate. Pre-treatment, hydrolysis, and fermentation are some of the technical, practical, and economic hurdles that the biochemical conversion method must overcome. Nanoparticles (NPs) provide a very effective approach to address the present obstacles in using biomass, due to their selectivity, energy efficiency, and time management capabilities, while also reducing costs. NPs smaller dimensions allow them to be more effective at interacting with lignocellulosic components at low concentrations to release carbohydrates that can be utilized to produce bioethanol. This article provides a concise overview of various biofuels and the nanotechnological advancements in producing it, with a particular emphasis on ethanol. It provides a detailed discussion on the application of nanotechnology at each stage of ethanol production, with a particular emphasis on understanding the mechanism of how nanoparticles interact with lignocellulose

Modification of Graphite Sheet Anode with Iron (II, III) Oxide-Carbon Dots for Enhancing the Performance of Microbial Fuel Cell

The present study explores the use of carbon dots coated with Iron (II, III) oxide (Fe3O4) for its application as an anode in microbial fuel cells (MFC). Fe3O4@PSA-C was synthesized using a hydrothermal-assisted probe sonication method. Nanoparticles were characterized with XRD, SEM, FTIR, and RAMAN Spectroscopy. Different concentrations of Fe3O4- carbon dots (0.25, 0.5, 0.75, and 1 mg/cm2) were coated onto the graphite sheets (Fe3O4@PSA-C), and their performance in MFC was evaluated. Cyclic voltammetry (CV) of Fe3O4@PSA-C (1 mg/cm2) modified anode indicated oxidation peaks at &minus;0.26 mV and +0.16 mV, respectively, with peak currents of 7.7 mA and 8.1 mA. The fluxes of these anodes were much higher than those of other low-concentration Fe3O4@PSA-C modified anodes and the bare graphite sheet anode. The maximum power density (Pmax) was observed in MFC with a 1 mg/cm2 concentration of Fe3O4@PSA-C was 440.01 mW/m2, 1.54 times higher than MFCs using bare graphite sheet anode (285.01 mW/m2). The elevated interaction area of carbon dots permits pervasive Fe3O4 crystallization providing enhanced cell attachment capability of the anode, boosting the biocompatibility of Fe3O4@PSA-C. This significantly improved the performance of the MFC, making Fe3O4@PSA-C modified graphite sheets a good choice as an anode for its application in MFC

Modification of Graphite Sheet Anode with Iron (II, III) Oxide-Carbon Dots for Enhancing the Performance of Microbial Fuel Cell

The present study explores the use of carbon dots coated with Iron (II, III) oxide (Fe3O4) for its application as an anode in microbial fuel cells (MFC). Fe3O4@PSA-C was synthesized using a hydrothermal-assisted probe sonication method. Nanoparticles were characterized with XRD, SEM, FTIR, and RAMAN Spectroscopy. Different concentrations of Fe3O4- carbon dots (0.25, 0.5, 0.75, and 1 mg/cm2) were coated onto the graphite sheets (Fe3O4@PSA-C), and their performance in MFC was evaluated. Cyclic voltammetry (CV) of Fe3O4@PSA-C (1 mg/cm2) modified anode indicated oxidation peaks at −0.26 mV and +0.16 mV, respectively, with peak currents of 7.7 mA and 8.1 mA. The fluxes of these anodes were much higher than those of other low-concentration Fe3O4@PSA-C modified anodes and the bare graphite sheet anode. The maximum power density (Pmax) was observed in MFC with a 1 mg/cm2 concentration of Fe3O4@PSA-C was 440.01 mW/m2, 1.54 times higher than MFCs using bare graphite sheet anode (285.01 mW/m2). The elevated interaction area of carbon dots permits pervasive Fe3O4 crystallization providing enhanced cell attachment capability of the anode, boosting the biocompatibility of Fe3O4@PSA-C. This significantly improved the performance of the MFC, making Fe3O4@PSA-C modified graphite sheets a good choice as an anode for its application in MFC