Study on antimicrobial activity of aq food packaging material containing potassium sorbate

The feasibility of EVA/LLDPE films containing 1, 2 and 5% (w/w) K-sorbate to inhibit microbial growth and as a consequence prolong shelf-life of foods was investigated. Based on weight loss experiments it was shown that K-sorbate is very suitable for incorporation in LLDPE because of its heat stability during extrusion. After 3 weeks, resp. 6.4, 2.8 and 5.7% of the incorporated sorbic acid was released into distilled water from films containing resp. 1, 2 and 5% (w/w) K-sorbate. The very limited migration of K-sorbate may be explained by the incompatibility of the polar salt with the apolar LLDPE. This limited migration could explain the very small inhibitory effect of the K-sorbate films on the growth of Candida spp., Pichia spp., Trichosporon spp. and Penicillium spp. During storage at 7 °C of cheese packaged in a 5% (w/w) K-sorbate film, no significant differences could be observed for yeast and mould growth on the cheese cubes compared to a reference film. The concentration of sorbic acid in the cheese did not exceed 14 ppm. This is much lower than the 1000 ppm K-sorbate needed to inhibit microbial growth. The results of this study confirm that the K-sorbate incorporated LLDPE film is not able to inhibit microbial growth in vitro on inoculated media and in vivo on cheese due to the insufficient release of K-sorbate from the film

On the Rothe-Galerkin spectral discretisation for a class of variable fractional-order nonlinear wave equations

In this contribution, a wave equation with a time-dependent variable-order fractional damping term and a nonlinear source is considered. Avoiding the circumstances of expressing the nonlinear variable-order fractional wave equations via closed-form expressions in terms of special functions, we investigate the existence and uniqueness of this problem with Rothe's method. First, the weak formulation for the considered wave problem is proposed. Then, the uniqueness of a solution is established by employing Gr\"onwall's lemma. The Rothe scheme's basic idea is to use Rothe functions to extend the solutions on single-time steps over the entire time frame. Inspired by that, we next introduce a uniform mesh time-discrete scheme based on a discrete convolution approximation in the backward sense. By applying some reasonable assumptions to the given data, we can predict a priori estimates for the time-discrete solution. Employing these estimates side by side with Rothe functions leads to proof of the solution's existence over the whole time interval. Finally, the full discretisation of the problem is introduced by invoking Galerkin spectral techniques in the spatial direction, and numerical examples are given

Effect of vacuum induced nucleation on the final product homogeneity

In the field of freeze drying of pharmaceutics the homogeneity of the sublimation flux during drying is fundamental to allow a final product with the same characteristics. Previous studies have shown that the control of freezing stage, in addition to a dramatic reduction of cycle duration, can also improve the homogeneity of the final batch. In this framework, this study is focused on the investigation of the effects of the Vacuum Induced Nucleation control method (modified in a previous work)[1,2] on the final structure of the product. Two aspects will be taken into consideration: the uniformity among vials of the same batch (inter-vial) and the uniformity of the structure along the height of the product (intra-vial). It has to be pointed out that a non-uniform product structure can have an impact on the protein aggregation and redistribution, and cause a partial cake collapse or micro-collapse. This investigation is really useful to define some limits of the control method used in this work

In-line near infrared spectroscopy during freeze-drying as a tool to measure efficiency of hydrogen bond formation between protein and sugar, predictive of protein storage stability

Sugars are often used as stabilizers of protein formulations during freeze-drying. However, not all sugars are equally suitable for this purpose. Using in-line near-infrared spectroscopy during freeze-drying, it is shown here that hydrogen bond formation during freeze-drying, under secondary drying conditions in particular, can be related to the preservation of the functionality and structure of proteins during storage. The disaccharide trehalose was best capable of forming hydrogen bonds with the model protein, lactate dehydrogenase, thereby stabilizing it, followed by the molecularly flexible oligosaccharide inulin 4kDa. The molecularly rigid oligo- and polysaccharides dextran 5kDa and 70kDa, respectively, formed the least amount of hydrogen bonds and provided least stabilization of the protein. It is concluded that smaller and molecularly more flexible sugars are less affected by steric hindrance, allowing them to form more hydrogen bonds with the protein, thereby stabilizing it better

On a Reconstruction of a Solely Time-Dependent Source in a Time-Fractional Diffusion Equation with Non-smooth Solutions

An inverse source problem for a non-automonous time fractional diffusion equation of order (0 < β< 1) is considered in a bounded Lipschitz domain in Rd. The missing solely time-dependent source is recovered from an additional integral measurement. The existence, uniqueness and regularity of a weak solution is studied. We design two numerical algorithms based on Rothe’s method over uniform and graded grids, derive a priori estimates and prove convergence of iterates towards the exact solution. An essential feature of the fractional subdiffusion problem is that the solution lacks the smoothness near the initial time, although it would be smooth away from t= 0. Rothe’s method on a uniform grid addresses the existence of a such a solution (non-smooth with tγ term where 1 > γ> β) under low regularity assumptions, whilst Rothe’s method over graded grids has the advantage to cope better with the behaviour at t= 0 (also here tβ is included in the class of admissible solutions) for the considered problems. The theoretical obtained results are supported by numerical experiments and stay valid in case of smooth solutions to the problem. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.106016/12P2919N; Universiteit Gent; Russian Science Foundation, RSF: 22-21-00075A. S. Hendy wishes to acknowledge the support of the RSF grant, project 22-21-00075. K. Van Bockstal is supported by a postdoctoral fellowship of the Research Foundation - Flanders (106016/12P2919N).The authors are grateful to the handling editor and the anonymous referees for their constructive feedback and helpful suggestions, which highly improved the paper. The authors would also like to thank Professor Vladimir G. Pimenov of Ural Federal University and Professor Mari?n Slodi?ka of Ghent University, for their generosity and guidance, which has always been so valuable to them

Two-component approach for thermodynamic properties in diluted magnetic semiconductors

We examine the feasibility of a simple description of Mn ions in III-V diluted magnetic semiconductors (DMSs) in terms of two species (components), motivated by the expectation that the Mn-hole exchange couplings are widely distributed, expecially for low Mn concentrations. We find, using distributions indicated by recent numerical mean field studies, that the thermodynamic properties (magnetization, susceptibility, and specific heat) cannot be fit by a single coupling as in a homogeneous model, but can be fit well by a two-component model with a temperature dependent number of ``strongly'' and ``weakly'' coupled spins. This suggests that a two-component description may be a minimal model for the interpretation of experimental measurements of thermodynamic quantities in III-V DMS systems.Comment: 10 pages, 9 figures, 1 new figure, substantial revision

Ebola virus glycoprotein stimulates IL-18 dependent natural killer cell responses

BACKGROUNDNK cells are activated by innate cytokines and viral ligands to kill virus-infected cells. These functions are enhanced during secondary immune responses and after vaccination by synergy with effector T cells and virus-specific antibodies. In human Ebola virus infection, clinical outcome is strongly associated with the initial innate cytokine response, but the role of NK cells has not been thoroughly examined.METHODSThe novel 2-dose heterologous Adenovirus type 26.ZEBOV (Ad26.ZEBOV) and modified vaccinia Ankara-BN-Filo (MVA-BN-Filo) vaccine regimen is safe and provides specific immunity against Ebola glycoprotein, and is currently in phase 2 and 3 studies. Here, we analyzed NK cell phenotype and function in response to Ad26.ZEBOV, MVA-BN-Filo vaccination regimen and in response to in vitro Ebola glycoprotein stimulation of PBMCs isolated before and after vaccination.RESULTSWe show enhanced NK cell proliferation and activation after vaccination compared with baseline. Ebola glycoprotein-induced activation of NK cells was dependent on accessory cells and TLR-4-dependent innate cytokine secretion (predominantly from CD14+ monocytes) and enriched within less differentiated NK cell subsets. Optimal NK cell responses were dependent on IL-18 and IL-12, whereas IFN-γ secretion was restricted by high concentrations of IL-10.CONCLUSIONThis study demonstrates the induction of NK cell effector functions early after Ad26.ZEBOV, MVA-BN-Filo vaccination and provides a mechanism for the activation and regulation of NK cells by Ebola glycoprotein.TRIAL REGISTRATIONClinicalTrials.gov NCT02313077.FUNDINGUnited Kingdom Medical Research Council Studentship in Vaccine Research, Innovative Medicines Initiative 2 Joint Undertaking, EBOVAC (grant 115861) and Crucell Holland (now Janssen Vaccines and Prevention B.V.), European Union's Horizon 2020 research and innovation programme and European Federation of Pharmaceutical Industries and Associations (EFPIA)

Antibody-Dependent Natural Killer Cell Activation after Ebola Vaccination

BACKGROUND:Antibody Fc-mediated functions, such as antibody-dependent cellular cytotoxicity, contribute to vaccine-induced protection against viral infections. Fc-mediated function of anti-Ebola glycoprotein antibodies suggest that Fc-dependent activation of effector cells, including NK cells, could play a role in vaccination against Ebola virus disease. METHODS:We analysed the effect of anti-Ebola glycoprotein antibody in the serum of U.K.-based volunteers vaccinated with the novel 2-dose heterologous Adenovirus type 26.ZEBOV, Modified Vaccinia Ankara-BN-Filo vaccine regimen, on primary human NK cell activation. RESULTS:We demonstrate primary human NK cell CD107a and IFN-γ expression, combined with downregulation of CD16, in response to recombinant Ebola virus glycoprotein and post-vaccine dose 1 and dose 2 sera. These responses varied significantly with vaccine regimen and NK cell activation was found to correlate with anti-glycoprotein antibody concentration. We also reveal an impact of NK cell differentiation phenotype on antibody-dependent NK cell activation, with highly differentiated CD56dimCD57+ NK cells being the most responsive. CONCLUSIONS:This study thus highlights the dual importance of vaccine-induced antibody concentration and NK cell differentiation status in promoting Fc-mediated activation of NK cells after vaccination, raising a potential role for antibody-mediated NK cell activation in vaccine-induced immune responses

Histological interpretation of differentiated vulvar intraepithelial neoplasia (dVIN) remains challenging-observations from a bi-national ring-study

Differentiated vulvar intraepithelial neoplasia (dVIN) is a premalignant lesion that is known to progress rapidly to invasive carcinoma. Accurate histological diagnosis is therefore crucial to allow appropriate treatment. To identify reliable diagnostic features, we evaluated the inter-observer agreement in the histological assessment of dVIN, among a bi-national, multi-institutional group of pathologists. Two investigators from Erasmus MC selected 36 hematoxylin-eosin-stained glass slides of dVIN and no-dysplasia, and prepared a list of 15 histological features of dVIN. Nine participating pathologists (i) diagnosed each slide as dVIN or no-dysplasia, (ii) indicated which features they used for the diagnosis, and (iii) rated these features in terms of their diagnostic usefulness. Diagnoses rendered by > 50% participants were taken as the consensus (gold standard). p53-immunohistochemistry (IHC) was performed for all cases, and the expression patterns were correlated with the consensus diagnoses. Kappa statistics were computed to measure inter-observer agreements, and concordance of the p53-IHC patterns with the consensus diagnoses. For the diagnosis of dVIN, overall agreement was moderate (= 0.42), and pair-wise agreements ranged from slight (= 0.10) to substantial (= 0.73). Based on the levels of agreement and ratings of usefulness, the most helpful diagnostic features were parakeratosis, cobblestone appearance, chromatin abnormality, angulated nuclei, atypia discernable under x 100, and altered cellular alignment. p53-IHC patterns showed substantial concordance (= 0.67) with the consensus diagnoses. Histological interpretation of dVIN remains challenging with suboptimal inter-observer agreement. We identified the histological features that may facilitate the diagnosis of dVIN. For cases with a histological suspicion of dVIN, consensus-based pathological evaluation may improve the reliability of the diagnosis