scholarly journals Design of a New Gemini Lipoaminoacid with Immobilized Lipases Based on an Eco-Friendly Biosynthetic Process

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 164
Author(s):  
Patrícia M. Carvalho ◽  
Rita C. Guedes ◽  
Maria R. Bronze ◽  
Célia M. C. Faustino ◽  
Maria H. L. Ribeiro
Keyword(s):  
High Performance ◽  
Transfection Efficiency ◽  
Sol Gel ◽  
Reaction Rates ◽  
Solvent Free ◽  
Bioactive Molecules ◽  
Thermomyces Lanuginosus ◽  
Chemical Production ◽  
Immobilized Lipases ◽  
Free Media

Lipoaminoacids (LAA) are an important group of biosurfactants, formed by a polar hydrophilic part (amino acid) and a hydrophobic tail (lipid). The gemini LAA structures allow the formation of a supramolecular complex with bioactive molecules, like DNA, which provides them with good transfection efficiency. Since lipases are naturally involved in lipid and protein metabolism, they are an alternative to the chemical production of LAA, offering an eco-friendly biosynthetic process option. This work aimed to design the production of novel cystine derived gemini through a bioconversion system using immobilized lipases. Three lipases were used: porcine pancreatic lipase (PPL); lipase from Thermomyces lanuginosus (TLL); and lipase from Rizhomucor miehei (RML). PPL was immobilized in sol-gel lenses. L-cystine dihydrochloride and dodecylamine were used as substrates for the bioreaction. The production of LAA was evaluated by thin layer chromatography (TLC), and colorimetric reaction with eosin. The identification and quantification was carried out by High Performance Liquid Chromatographer-Mass Spectrometry (HPLC-MS/MS). The optimization of media design included co-solvent (methanol, dimethylsulfoxide), biphasic (n-hexane and 2-propanol) or solvent-free media, in order to improve the biocatalytic reaction rates and yields. Moreover, a new medium was tested where dodecylamine was melted and added to the cystine and to the biocatalyst, building a system of mainly undissolved substrates, leading to 5 mg/mL of LAA. Most of the volume turned into foam, which indicated the production of the biosurfactant. For the first time, the gemini derived cystine lipoaminoacid was produced, identified, and quantified in both co-solvent and solvent-free media, with the lipases PPL, RML, and TLL.

scholarly journals A simple approach to prepare fluorescent molecularly imprinted nanoparticles

RSC Advances ◽  
2021 ◽  
Vol 11 (13) ◽  
pp. 7732-7737
Author(s):  
Fenying Wang ◽  
Dan Wang ◽  
Tingting Wang ◽  
Yu Jin ◽  
Baoping Ling ◽  
...  
Keyword(s):  
High Performance ◽  
Low Cost ◽  
Sol Gel ◽  
Silica Sol ◽  
Simple Approach ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Low Toxicity ◽  
Good Biocompatibility ◽  
Molecularly Imprinted Nanoparticles

Fluorescent molecularly imprinted polymer (FMIP) gains great attention in many fields due to their low cost, good biocompatibility and low toxicity. Here, a high-performance FMIP was prepared based on the autocatalytic silica sol–gel reaction.

scholarly journals Elucidation of the Crystal Growth Characteristics of SnO2 Nanoaggregates Formed by Sequential Low-Temperature Sol-Gel Reaction and Freeze Drying

Nanomaterials ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1738
Author(s):  
Saeid Vafaei ◽  
Alexander Wolosz ◽  
Catlin Ethridge ◽  
Udo Schnupf ◽  
Nagisa Hattori ◽  
...  
Keyword(s):  
Crystal Growth ◽  
Low Temperature ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Freeze Drying ◽  
Sno2 Nanoparticles ◽  
Sol Gel ◽  
Functional Materials ◽  
Cost Effective ◽  
High Concentration

SnO2 nanoparticles are regarded as attractive, functional materials because of their versatile applications. SnO2 nanoaggregates with single-nanometer-scale lumpy surfaces provide opportunities to enhance hetero-material interfacial areas, leading to the performance improvement of materials and devices. For the first time, we demonstrate that SnO2 nanoaggregates with oxygen vacancies can be produced by a simple, low-temperature sol-gel approach combined with freeze-drying. We characterize the initiation of the low-temperature crystal growth of the obtained SnO2 nanoaggregates using high-resolution transmission electron microscopy (HRTEM). The results indicate that Sn (II) hydroxide precursors are converted into submicrometer-scale nanoaggregates consisting of uniform SnO2 spherical nanocrystals (2~5 nm in size). As the sol-gel reaction time increases, further crystallization is observed through the neighboring particles in a confined part of the aggregates, while the specific surface areas of the SnO2 samples increase concomitantly. In addition, X-ray photoelectron spectroscopy (XPS) measurements suggest that Sn (II) ions exist in the SnO2 samples when the reactions are stopped after a short time or when a relatively high concentration of Sn (II) is involved in the corresponding sol-gel reactions. Understanding this low-temperature growth of 3D SnO2 will provide new avenues for developing and producing high-performance, photofunctional nanomaterials via a cost-effective and scalable method.

scholarly journals Catalytic production of impurity-free V3.5+ electrolyte for vanadium redox flow batteries

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Jiyun Heo ◽  
Jae-Yun Han ◽  
Soohyun Kim ◽  
Seongmin Yuk ◽  
Chanyong Choi ◽  
...  
Keyword(s):  
High Speed ◽  
High Performance ◽  
Large Scale ◽  
Catalytic Reduction ◽  
Continuous Production ◽  
Vanadium Redox Flow Battery ◽  
Manufacturing Cost ◽  
Chemical Production ◽  
High Manufacturing Cost ◽  
Vanadium Redox

Abstract The vanadium redox flow battery is considered one of the most promising candidates for use in large-scale energy storage systems. However, its commercialization has been hindered due to the high manufacturing cost of the vanadium electrolyte, which is currently prepared using a costly electrolysis method with limited productivity. In this work, we present a simpler method for chemical production of impurity-free V3.5+ electrolyte by utilizing formic acid as a reducing agent and Pt/C as a catalyst. With the catalytic reduction of V4+ electrolyte, a high quality V3.5+ electrolyte was successfully produced and excellent cell performance was achieved. Based on the result, a prototype catalytic reactor employing Pt/C-decorated carbon felt was designed, and high-speed, continuous production of V3.5+ electrolyte in this manner was demonstrated with the reactor. This invention offers a simple but practical strategy to reduce the production cost of V3.5+ electrolyte while retaining quality that is adequate for high-performance operations.

scholarly journals Bioactive Glass as a Nanoporous Drug Delivery System for Teicoplanin

2020 ◽  
Vol 10 (7) ◽  
pp. 2595 ◽  
Author(s):  
Chih-Ling Huang ◽  
Wei Fang ◽  
Bo-Rui Huang ◽  
Yan-Hsiung Wang ◽  
Guo-Chung Dong ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Bioactive Glass ◽  
Drug Delivery System ◽  
Delivery System ◽  
Inductively Coupled Plasma ◽  
High Performance ◽  
Ph Value ◽  
Sol Gel ◽  
Phase Identification ◽  
Bet Analysis

Bioactive glass (BG) was made by the sol–gel method and doped with boron (B) to increase its bioactivity. Microstructures of BG and B-doped BG were observed by scanning electron microscopy, and phase identification was performed using an X-ray diffraction diffractometer. The ion concentrations released after soaking in simulated body fluid (SBF) for 1, 4, and 7 days were measured by inductively coupled plasma mass spectrometry, and the pH value of the SBF was measured after soaking samples to determine the variation in the environment. Brunauer–Emmett–Teller (BET) analysis was performed to further verify the characteristics of mesoporous structures. High performance liquid chromatography was used to evaluate the drug delivery ability of teicoplanin. Results demonstrated that B-doped BG performed significantly better than BG in parameters assessed by the BET analysis. B-doped BG has nanopores and more rough structures, which is advantageous for drug delivery as there are more porous structures available for drug adsorption. Moreover, B-doped BG was shown to be effective for keeping pH values stable and releasing B ions during soaking in SBF. The cumulative release of teicoplanin from BG and B-doped BG reached 20.09% and 3.17% on the first day, respectively. The drug release gradually slowed, reaching 29.43% and 4.83% after 7 days, respectively. The results demonstrate that the proposed bioactive glass has potential as a drug delivery system.

Facile alkali-assisted synthesis of g-C3N4 materials and their high-performance catalytic application in solvent-free cycloaddition of CO2 to epoxides

RSC Advances ◽  
2016 ◽  
Vol 6 (60) ◽  
pp. 55382-55392 ◽  
Author(s):  
Jie Xu ◽  
Jie-Kun Shang ◽  
Quan Jiang ◽  
Yue Wang ◽  
Yong-Xin Li
Keyword(s):  
High Performance ◽  
Alkali Treatment ◽  
Solvent Free ◽  
Catalytic Activities ◽  
Catalytic Application

g-C3N4 materials have been prepared at lower temperatures (450–475 °C) by the aid of alkali treatment. In cycloaddition of CO2 to epoxides, the g-C3N4 materials demonstrated high and stable catalytic activities.

Fast response acetone-sensing properties of SnO2 nanoparticles prepared by the sol-gel method

2021 ◽  
Vol 93 (3) ◽  
pp. 30401
Author(s):  
Jiaxing Wang ◽  
Hai Yu ◽  
Yong Zhang
Keyword(s):  
High Performance ◽  
Gas Sensing ◽  
Sno2 Nanoparticles ◽  
Sol Gel ◽  
Fast Response ◽  
X Ray Diffraction ◽  
Gel Method ◽  
Sol Gel Method ◽  
Short Recovery Time ◽  
Acetone Gas Detection

SnO2 nanoparticle architectures were successfully synthesized using a sol-gel method and developed for acetone gas detection. The morphology and structure of the particles were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The SnO2 nanoparticle architectures were configured as high-performance sensors to detect acetone and showed a very fast response time (<1 s), a short recovery time (10 s), good repeatability and high selectivity at a relatively low working temperature. Thus, SnO2 nanoparticles should be promising candidates for designing and fabricating acetone gas sensors with good gas sensing performance. The possible gas sensing mechanism is also presented.

Expansion of Nanosized MgSiO3/Chitosan Nanocomposite Structural and Spectroscopic for Loading Velosef by Nanomaterial Intervention

2021 ◽  
Author(s):  
amal aboelnaga ◽  
talaat Meaz ◽  
amany M elnahrawy
Keyword(s):  
Antimicrobial Activity ◽  
High Performance ◽  
Sol Gel ◽  
Polymerization Process ◽  
Absorption Bands ◽  
Structural Morphology ◽  
Crystallinity Degree ◽  
Chitosan Matrix ◽  
Antimicrobial Studies ◽  
Sol Gel Process

Abstract The aim of this study is to investigate the effect of different doses of Velosef in magnesium silica/chitosan nanocomposite in terms of structural, morphology, optical properties, and bioactivity. Loading Velosef in fine-sized magnesium silica/chitosan is an efficient engineering approach for drug delivery. The sol-gel process was used to prepare magnesium silica fine-sized before being blended into chitosan matrix, which acts as a potential morphogenetic biomaterial. The Velosef/magnesium silica/chitosan nanocomposites were characterized by XRD, TEM, SEM, FTIR, UV-absorption, and antimicrobial studies. The XRD was characteristic of the crystallinity degree of the MgO-SiO2/chitosan/Velosef nanocomposites with three maximum peaks at 26.37°, 33.34o, 36.9°. FTIR results indicated the structural change occurred with the Velosef sol-gel polymerization process. UV-absorbance reveals that the MgO-SiO2/chitosan nanocomposite appeared a high performance for loading Velosef at two absorption bands at 253 and 347 nm. The MgO-SiO2/Chitosan/Velosef nanocomposites showed considerable antimicrobial activity in opposition to the tested representative microorganisms. The maximum antimicrobial activity was obtained with MgO-SiO2/Chitosan against both Escherichia coli and Candida albicans (37 mm), while the minimum antimicrobial activity (30 mm) was recorded against B. mycoides and E. coli with control.

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