Microbial biofilm growth vs. tissue integration: "the race for the surface" experimentally studied

Biomaterial-associated infections constitute a major clinical problem. Unfortunately, microorganisms are frequently introduced onto an implant surface during surgery and start the race for the surface before tissue integration can occur. So far, no method has been forwarded to study biofilm formation and tissue integration simultaneously. The aim of this study is to describe an in vitro method to investigate this “race for the surface”. First, a suitable growth medium was prepared that allowed both bacterial and tissue growth in a parallel plate flow chamber. Staphylococci were deposited on the glass bottom plate of the flow chamber in different surface densities, after which U2OS osteosarcoma cells were seeded. U2OS cells did not grow in the absence of flow, possibly due to poisoning by bacterial endotoxins, but under flow both staphylococci and U2OS cells grew. The number of adhering cells and area per spread cell were determined after 48 h in relation to the initial number of bacteria present. Both the number and spread area per cell decreased with increasing density of adhering staphylococci. This demonstrates that the outcome of the race for the surface between bacteria and tissue cells is dependent on the number of bacteria present prior to cell seeding.\u

Ultrasound-assisted lipase catalyzed hydrolysis of aspirin methyl ester

Supplementary data associated with this article can be found, in the online version, at http://dx.doi.org/10.1016/j.ultsonch.2017.08.004.The ultrasound-assisted hydrolysis of aspirin methyl ester (AME) was investigated using immobilized Candida antarctica lipase B (CALB) (1%) in the presence of solvents like triolein, chloroform (CHCl3) and dichloromethane (DCM). The effect of ultrasound and the role of water on the conversion rates have also been investigated. Proton nuclear magnetic resonance spectroscopic (1H NMR) was chosen to calculate hydrolysis convertion rates. We observed that lipase-ultrasound assisted hydrolysis of AME in the presence of triolein and water showed the highest hydrolysis conversion rate (65.3%). Herein low water amount played an important role as a nucleophile being crucial for the hydrolysis yields obtained. Lipase activity was affected by the conjugated action of ultrasound and solvents (35.75% of decrease), however not disturbing its hydrolytic efficiency. It was demonstrated that lipase is able to hydrolyse AME to methyl 2-hydroxy benzoate (methyl salicylate), which applications include fragrance agents in food, beverages and cosmetics, or analgesic agent in liniments.All authors gratefully acknowledge the financial support provided by International Joint Research Laboratory for Textile and Fibre Bioprocesses at Jiangnan University. The authors are also thankful to the Department of Oils, Oleochemicals and Surfactants technology, Institute of Chemical Technology, Mumbai, India and to the Bioprocess and Bio nanotechnology Research Group (BBRG) of University of Minho. Authors would like also to acknowledge the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit and COMPETE 2020 (POCI-01-0145-FEDER-006684) and BioTecNorte operation (NORTE01-0145-FEDER-000004) funded by European Regional Development Fund under the scope of Norte2020 – Programa Operacional Regional do Norte and to the Fundamental Research Funds for the Central Universities (No. JUSRP51622 A and No. JUSRP115A03), and to the Jiangsu Province Scientific Research Innovation Project for Academic Graduate Students in 2016 (No. KYLX16_0788).info:eu-repo/semantics/publishedVersio

Heterogeneous catalysis for sustainable biodiesel production via esterification and transesterification

Concern over the economics of accessing fossil fuel reserves, and widespread acceptance of the anthropogenic origin of rising CO2 emissions and associated climate change from combusting such carbon sources, is driving academic and commercial research into new routes to sustainable fuels to meet the demands of a rapidly rising global population. Here we discuss catalytic esterification and transesterification solutions to the clean synthesis of biodiesel, the most readily implemented and low cost, alternative source of transportation fuels to meet future societal demands

Characterization of Self-Assembled Functional Polymeric Nanostructures: I. Magnetic Nanostructures from Metallopolymers II. Zwitterionic Polymer Vesicles in Ionic Liquid

Two diverse projects illustrate the application of various materials characterization techniques to investigate the structure and properties of nanostructured functional materials formed in both bulk as well as in solutions. In the first project, ordered magnetic nanostructures were formed within polymer matrix by novel metallopolymers. The novel metal-functionalized block copolymers (BCPs) enabled the confinement of cobalt metal ions within nanostructured BCP domains, which upon simple heat treatment resulted in room temperature ferromagnetic (RTFM) materials. On the contrary, cobalt functionalized homopolymer having similar chemical structure and higher loading of metal-ion are unstructured and exhibited superparamagnetic (SPM) behavior at room temperature. Based on a series of detailed investigations, using various materials characterization techniques, it was hypothesized that the SPM cobalt particles within BCP microdomains exhibited a collective behavior due to increased dipolar interactions between them under the nanoconfinement of cylindrical domains in BCP, resulting in RTFM behavior. On contrary, the same SPM cobalt particles formed within homopolymer, without any confinement exhibited SPM behavior either due to lack of interactions or random interactions between them. To further support this hypothesis, a series of BCPs were prepared in which the BCP morphology was varied between the cylindrical, lamellar, and inverted cylindrical phases and their magnetic properties were compared. All these BCPs, which are nanostructured, exhibited RTFM behavior, further supporting the proposed hypothesis. Different dimensionality or degree of nanoconfinement in BCP morphologies affected the magnetization reversal processes in these BCPs, yielding different macroscopic magnetic properties. Most strongly constrained cylindrical morphology has shown best magnetic properties (highest coercivity) among other BCP morphologies. Inverted cylindrical morphology, in which a 3-D matrix is confined between the non-magnetic cylinders, had second highest and lamellar morphology with least confinement among BCPs, exhibited lowest coercivity. The proposed hypothesis was further tested by systematically varying the dipolar interactions between the SPM cobalt nanoparticles by reducing the density of cobalt within the cylindrical domains and varying the dimensions of the cylindrical domains (i.e. diameter). A series of novel ferrocene-cobalt containing block copolymers were developed and cobalt density within the cylindrical domains of BCP was varied by changing the chemical composition of the metal functionalized block. Further, the diameter of the cylindrical domains was varied by varying the molecular weight of the cobalt-containing BCPs. These studies allowed us to understand the fundamental correlations between the self-assembled nanostructures and their macroscopic magnetic properties. In the second part of the thesis, a novel amphiphilic block copolymer (ABC), composed of a hydrophilic zwitterionic block and a hydrophobic PS block, was synthesized by ROMP. The formation of zwitterionic vesicles in an ionic liquid, as well as in PBS buffer, was confirmed by TEM and DLS characterization. The dispersion of vesicles within ionic liquid enabled the usage of conventional, room temperature TEM to visualize them in their solution state. This technique of materials characterization could be extended for the visualization of other hydrophilic soft matter

A highly efficient separation and physicochemical characteristics of saturated fatty acids from crude palm oil fatty acids mixture using methanol crystallisation method

The objective of the current study was to separate saturated fatty acids (SFAs) from high free fatty acid crude palm oil fatty acid mixture using the methanol crystallisation method. The development of methanol crystallisation method procedure was based on various parameters. The fatty acid composition was determined by using gas chromatography-flame ionisation detector (GC-FID) as Fatty Acid Methyl Esters. The highest percentage of SFAs was more than 89% with the percentage yield of 48.9% under the optimal conditions of the fatty acids-to-methanol ratio of 1:15 (w/v), the crystallisation temperature of −15 °C, and the crystallisation time of 24 hours, respectively. After a double crystallisation, the composition of separated SFAs contains 90% of palmitic acid (C16:0) as a major component and 5.8% of stearic acid (C18:0), respectively. Moreover, almost 4.2% of oleic acid (C18:1) was observed in the saturated solid product. Based on the results, the use of methanol as a crystallisation solvent is recommended because of its high efficiency, low cost, stability, obtainability, and comparative ease of recovery