5 research outputs found

    A Study on Edible Polymer Films for Food Packaging Industry: Current Scenario and Advancements

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    Over the past two decades, food packaging and packaging industry have paid close attention to create biodegradable and edible polymer films and coatings. In a broad way, edible polymers emerged as a new class of materials that garnered significant properties due to their advantages over synthetic petroleum-based films. When compared to conventional packaging materials, edible polymer films can fundamentally simplify products, improving their potential to be recycled. This work aims to give readers a thorough introduction to edible polymer films, by discussing present research trends, classification, functionality and composition, fabrication, and characterization. The work also emphasizes the advantages and disadvantages of edible polymer films based on meat, poultry, dairy products, fruits, nuts, and vegetables

    West syndrome: a comprehensive review

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    Since its first clinical description (on his son) by William James West (1793-1848) in 1841, and the definition of the classical triad of (1) infantile spasms; (2) hypsarrhythmia, and (3) developmental arrest or regression as "West syndrome", new and relevant advances have been recorded in this uncommon disorder. New approaches include terminology of clinical spasms (e.g., infantile (IS) vs. epileptic spasms (ES)), variety of clinical and electroencephalographic (EEG) features (e.g., typical ictal phenomena without EEG abnormalities), burden of developmental delay, spectrum of associated genetic abnormalities, pathogenesis, treatment options, and related outcome and prognosis. Aside the classical manifestations, IS or ES may present with atypical electroclinical phenotypes (e.g., subtle spasms; modified hypsarrhythmia) and may have their onset outside infancy. An increasing number of genes, proteins, and signaling pathways play crucial roles in the pathogenesis. This condition is currently regarded as a spectrum of disorders: the so-called infantile spasm syndrome (ISs), in association with other causal factors, including structural, infectious, metabolic, syndromic, and immunologic events, all acting on a genetic predisposing background. Hormonal therapy and ketogenic diet are widely used also in combination with (classical and recent) pharmacological drugs. Biologically targeted and gene therapies are increasingly studied. The present narrative review searched in seven electronic databases (primary MeSH terms/keywords included West syndrome, infantile spasms and infantile spasms syndrome and were coupled to 25 secondary clinical, EEG, therapeutic, outcomes, and associated conditions terms) including MEDLINE, Embase, Cochrane Central, Web of Sciences, Pubmed, Scopus, and OMIM to highlight the past knowledge and more recent advances

    Treatment Strategies for Dravet Syndrome

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    West syndrome: a comprehensive review

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