Decontamination of aflatoxin B1‐contaminated corn by ammonium persulphate during fermentation

The decontamination of aflatoxin B₁(AFB₁)‐contaminated corn, which is required if the corn is to be suitable for alternative use, by an ammoniation–fermentation integrated process was studied. This process could be used for the production of fuel ethanol from aflatoxin‐containing corn. Different concentrations (0.25, 0.50, 1.00, 1.5 and 2.0% w/w) of ammonium persulphate were tested in the detoxification of AFB₁‐contaminated corn during fermentation. In order to increase the decontamination of corn, 0.5 and 1.0% (w/w) azodicarbonamide, benzoyl peroxide and hydrogen peroxide were tested. Peroxides were added at three different stages of the fermentation process: liquefaction, saccharification and fermentation. Levels of AFB₁ and ethanol were determined after each fermentation process. Treated corn was tested for mutagenic potential using the Ames test with TA100 tester strain and pure AFB₁ as positive control. Addition of 2.0% (w/w) ammonium persulphate caused the highest level of decontamination without affecting ethanol production. Addition of peroxides did not significantly (P < 0.05) increase ethanol production or significantly (P < 0.05) improve the decontamination process. The best processes for decontamination of corn and for ethanol production included the addition of 2.0% (w/w) ammonium persulphate for both and of 1.0 and 0.5% (w/w) benzoyl peroxide respectively. All treated corn samples showed no mutagenic potential. Possible industrial use of these processes is discussed. © 2002 Society of Chemical Industry     

Pupil center detection with a single webcam for gaze tracking

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Skin colour assessment in safety testing of cosmetics. An overview

Synopsis
Few subjects are as problematical to dermatologists, cosmetologists and related experimenters involved in safety testing as the clinical assessment of skin colour. At the core of the problem is the word erythema, which does not communicate a sense for the nuance of red. In addition, light shades of red are not visible in dark-skinned people. Human assays aiming at evaluating the irritancy and allergic potential of cosmetics take advantage to use instrumental assessments of skin colour. However, there are pitfalls related to the complex biological aspects of the cutaneous reactivity, to the design of the in vivo assay, and to technical aspects bound to the principle of the measuring methods. Sound information can only be reached when these concerns are solved.
Résumé
Peu de sujets sont aussi problématiques pour les dermatologues, cosmétologues et autres expérimentateurs impliqués dans les tests de sûreté que l'évaluation clinique des couleurs cutanées. Au centre du problème est le mot érythème qui ne communique pas la notion des nuances de rouge. De plus, un érythème discret peut ne pas être visible chez des individus à la peau foncée. Les tests humains visant àévaluer les potentialités d'irritation et d'allergie aux cosmétiques bénéficient des évaluations instrumentales de la couleur cutanée. Cependant, il existe des pièges liés aux aspects biologiques complexes de la réactivité cutanée, au choix du test in vivo et à des aspects techniques en relation avec le principe du système de mesure. Une information adéquate ne peut être obtenue qu'après avoir résolu ces problèmes.     

Severe inhibition of maize wall degradation by synthetic lignins formed with coniferaldehyde

Although the enzymatic or ruminal degradability of plants deficient in cinnamyl alcohol dehydrogenase (CAD) is often greater than their normal counterparts, factors responsible for these degradability differences have not been identified. Since lignins in CAD deficient plants often contain elevated concentrations of aldehydes, we used a cell-wall model system to evaluate what effect aldehyde-containing lignins have on the hydrolysis of cell walls by fungal enzymes. Varying ratios of coniferaldehyde and coniferyl alcohol were polymerised into non-lignified primary walls of maize (Zea mays L) by wall-bound peroxidase and exogenously supplied H₂O₂. Coniferaldehyde lignins formed fewer cross-linked structures with other wall components, but they were much more inhibitory to cell wall degradation than lignins formed with coniferyl alcohol. This suggests that the improved degradability of CAD deficient plants is not related to the incorporation of p-hydroxycinnamaldehyde units into lignin. Degradability differences were diminished if enzyme loadings were increased and if hydrophobic aldehyde groups in lignins were reduced to their corresponding alcohols by ethanolic sodium borohydride. © 1998 Society of Chemical Industry.     

An Empirical Testing of the Economic Base Theory

Most central cities must at present bargain with other units of their regions and the nation for the residents and industry they need; and their bargaining power is so weak as to threaten their viability unless aid from state and federal governments is supplied. Both in order to serve the disadvantaged residents they do attract, and to cultivate their attractiveness to other residents and to industry, cities must re-define “urban renewal” as consisting of large investments in the development of human, land, and transportation potentialities. Such investments must, as all investments, come from “surpluses” which are controlled by the states and the nation, not the cities.     

The effect of physiologically relevant additives on the rheological properties of concentrated Pluronic copolymer gels

The high concentration triblock copolymer poly(ethylene oxide)₉₉-poly(propylene oxide)₆₉-poly(ethylene oxide)₉₉ (Pluronic F127) aqueous solutions with the addition of different components commonly used in physiologically relevant applications were characterized by rheological measurements, differential scanning calorimetry (DSC) and small angle X-ray/neutron scattering. The sol-gel transition temperature, as well as the storage modulus of the F127 solution depend both on the concentration of polymer and of clay. Above the gel transition, the storage modulus of the solutions increased with clay concentration. Yield strain is independent of polymer and clay concentrations. Two different kinds of inorganic salts, sodium chloride (NaCl) and calcium chloride (CaCl₂) were added into the polymer and polymer-clay solutions. The sol-gel transition temperature decreased noticeably, but the storage modulus decreased only a small amount with increasing concentration of inorganic salts. Addition of salts to polymer-clay solutions resulted in precipitation of the clays which decreased the modulus. No effect on the mechanical properties was observed with the addition of common serum proteins. However, addition of 0.5-10% glucose decreased the transition temperature between 3° and 7°, without significantly affecting the modulus. The depression of the transition temperature by glucose was similar to that found with salts and indicated that the mechanism, namely competition for water, may be similar.     

Platelet-Released Growth Factors Influence Wound Healing-Associated Genes in Human Keratinocytes and Ex Vivo Skin Explants

Platelet-released growth factors (PRGFs) or other thrombocyte concentrate products, e.g., Platelet-Rich Fibrin (PRF), have become efficient tools of regenerative medicine in many medical disciplines. In the context of wound healing, it has been demonstrated that treatment of chronic or complicated wounds with PRGF or PRF improves wound healing in the majority of treated patients. Nevertheless, the underlying cellular and molecular mechanism are still poorly understood. Therefore, we aimed to analyze if PRGF-treatment of human keratinocytes caused the induction of genes encoding paracrine factors associated with successful wound healing. The investigated genes were Semaphorin 7A (SEMA7A), Angiopoietin-like 4 (ANGPLT4), Fibroblast Growth Factor-2 (FGF-2), Interleukin-32 (IL-32), the CC-chemokine-ligand 20 (CCL20), the matrix-metalloproteinase-2 (MMP-2), the chemokine C-X-C motif chemokine ligand 10 (CXCL10) and the subunit B of the Platelet-Derived Growth Factor (PDGFB). We observed a significant gene induction of SEMA7A, ANGPLT4, FGF-2, IL-32, MMP-2 and PDGFB in human keratinocytes after PRGF treatment. The CCL20- and CXCL10 gene expressions were significantly inhibited by PRGF therapy. Signal transduction analyses revealed that the PRGF-mediated gene induction of SEMA7A, ANGPLT4, IL-32 and MMP-2 in human keratinocytes was transduced via the IL-6 receptor pathway. In contrast, EGF receptor signaling was not involved in the PRGF-mediated gene expression of analyzed genes in human keratinocytes. Additionally, treatment of ex vivo skin explants with PRGF confirmed a significant gene induction of SEMA7A, ANGPLT4, MMP-2 and PDGFB. Taken together, these results describe a new mechanism that could be responsible for the beneficial wound healing properties of PRGF or related thrombocytes concentrate products such as PRF.