1,394 research outputs found

    Nanofluids with optimised thermal properties based on metal chalcogenides with different morphology

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    Over the last decades, the interest around renewable energies has increased considerably because of the growing energy demand and the environmental problems derived from fossil fuels combustion. In this scenario, concentrating solar power (CSP) is a renewable energy with a high potential to cover the global energy demand. However, improving the efficiency and reducing the cost of technologies based on this type of energy to make it more competitive is still a work in progress. One of the current lines of research is the replacement of the heat transfer fluid used in the absorber tube of parabolic trough collectors with nano-colloidal suspensions of nanomaterials in a base fluid, typically named nanofluids. Nanofluids are considered as a new generation of heat transfer fluids since they exhibit thermophysical properties improvements compared with conventional heat transfer fluids. But there are still some barriers to overcome for the implementation of nanofluids. For example, obtaining nanofluids with high stability is a priority challenge for this kind of system. Also ensuring that nanoparticles will not clog pipes or cause pressure drops. In this Doctoral Thesis, the use of transition metal dichalcogenide-based nanofluids as a heat transfer fluid in solar power plants has been investigated for the first time. Specifically, nanofluids based on one-dimensional, two-dimensional and three-dimensional MoS2 , WS2 and WSe2 nanostructures have been researched. The base fluid used in the preparation of these nanofluids is the eutectic mixture of biphenyl and diphenyl oxide typically employed as heat transfer fluid in concentrating solar power plants. Mainly two preparation methods have been explored: the liquid phase exfoliation method, and the solvothermal synthesis of the nanomaterial and its subsequent dispersion in the thermal oil by ultrasound. Experimental parameters such as surfactant concentration, time and sonication frequency for preparation of nanofluids have also been analysed. The nanofluids have been subjected to an extensive characterisation which includes the study of colloidal stability over time, characterisation of thermal properties such as isobaric specific heat or thermal conductivity, rheological properties and optical properties. The results have revealed that nanofluids based on 1D and 2D nanostructures of transition metal dichalcogenides are colloidally stable over time and exhibit improved thermal properties compared to the typical thermal fluid used in solar power plants. The most promising nanofluids are those based on MoS 2 nanosheets and those based on WSe 2 nanosheets with heat transfer coefficient improvements of 36.2% and 34.1% respectively with respect to thermal oil. Furthermore, the dramatic role of WSe2 nanosheets in enhancing optical extinction of the thermal oil suggests the use of these nanofluids in direct absorption solar collectors. In conclusion, the present work demonstrates the feasibility of using nanofluids based on transition metal dichalcogenide nanostructures as heat transfer fluids in concentrating solar power plants based on parabolic trough collectors.En las últimas décadas, el interés en torno a las energías renovables ha aumentado considerablemente debido a la creciente demanda energética y a los problemas medioambientales derivados de la combustión de combustibles fósiles. En este escenario, la energía solar de concentración (CSP) es una energía renovable con un alto potencial para cubrir la demanda energética mundial. Sin embargo, es necesario trabajar para mejorar la eficiencia y reducir el coste de las tecnologías basadas en este tipo de energía con el objetivo de hacerla más competitiva. Una de las líneas de investigación actuales es la sustitución del fluido caloportador utilizado en el tubo absorbedor de los colectores cilindroparabólicos por suspensiones nanocoloidales de nanomateriales en un fluido base, típicamente denominados nanofluidos. Los nanofluidos se consideran una nueva generación de fluidos de transferencia de calor, ya que presentan mejoras en sus propiedades termofísicas en comparación con los fluidos de transferencia de calor convencionales. Pero aún quedan algunos obstáculos por superar para la aplicación de los nanofluidos. Por ejemplo, obtener nanofluidos con alta estabilidad es un reto prioritario en este tipo de sistemas. También garantizar que las nanopartículas no obstruyan las tuberías ni provoquen caídas de presión. En esta Tesis Doctoral se ha investigado por primera vez el uso de nanofluidos basados en dicalcogenuros de metales de transición como fluido caloportador en centrales solares. En concreto, se han investigado nanofluidos basados en nanoestructuras unidimensionales, bidimensionales y tridimensionales de MoS2, WS2 y WSe2. El fluido base utilizado en la preparación de estos nanofluidos es la mezcla eutéctica de bifenilo y óxido de difenilo empleada habitualmente como fluido de transferencia de calor en las centrales de concentración de energía solar. Se han explorado principalmente dos métodos de preparación: el método de exfoliación en fase líquida y la síntesis solvotermal del nanomaterial y su posterior dispersión en el aceite térmico mediante ultrasonidos. También se han analizado parámetros experimentales como la concentración de surfactante, el tiempo y la frecuencia de sonicación para la preparación de los nanofluidos. Los nanofluidos han sido sometidos a una extensa caracterización que incluye el estudio de la estabilidad coloidal a lo largo del tiempo, la caracterización de propiedades térmicas como el calor específico isobárico o la conductividad térmica, propiedades reológicas y propiedades ópticas. Los resultados han revelado que los nanofluidos basados en nanoestructuras 1D y 2D de dicalcogenuros de metales de transición son coloidalmente estables en el tiempo y presentan propiedades térmicas mejoradas en comparación con el fluido térmico típico utilizado en las centrales solares. Los nanofluidos más prometedores son los basados en nanoláminas de MoS2 y los basados en nanoláminas de WSe2, con mejoras del coeficiente de transferencia térmica del 36,2% y el 34,1%, respectivamente, con respecto al aceite térmico. Además, el espectacular papel de las nanoláminas de WSe2 en la mejora de la extinción óptica del aceite térmico sugiere el uso de estos nanofluidos en colectores solares de absorción directa. En conclusión, el presente trabajo demuestra la viabilidad del uso de nanofluidos basados en nanoestructuras de dicalcogenuros de metales de transición como fluidos de transferencia de calor en centrales solares de concentración basadas en colectores cilindro-parabólicos

    Rational development of stabilized cyclic disulfide redox probes and bioreductive prodrugs to target dithiol oxidoreductases

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    Countless biological processes allow cells to develop, survive, and proliferate. Among these, tightly balanced regulatory enzymatic pathways that can respond rapidly to external impacts maintain dynamic physiological homeostasis. More specifically, redox homeostasis broadly affects cellular metabolism and proliferation, with major contributions by thiol/disulfide oxidoreductase systems, in particular, the Thioredoxin Reductase Thioredoxin (TrxR/Trx) and the Glutathione Reductase-Glutathione-Glutaredoxin (GR/GSH/Grx) systems. These cascades drive vital cellular functions in many ways through signaling, regulating other proteins' activity by redox switches, and by stoichiometric reductant transfers in metabolism and antioxidant systems. Increasing evidence argues that there is a persistent alteration of the redox environment in certain pathological states, such as cancer, that heavily involve the Trx system: upregulation and/or overactivity of the Trx system may support or drive cancer progression, making both TrxR and Trx promising targets for anti-cancer drug development. Understanding the biochemical mechanisms and connections between certain redox cascades requires research tools that interact with them. The state-of-the-art genetic tools are mostly ratiometric reporters that measure reduced:oxidized ratios of selected redox pairs or the general thiol pool. However, the precise cellular roles of the central oxidoreductase systems, including TrxR and Trx, remain inaccessible due to the lack of probes to selectively measure turnover by either of these proteins. However, such probes would allow measuring their effective reductive activity apart from expression levels in native systems, including in cells, animals, or patient samples. They are also of high interest to identify chemical inhibitors for TrxR/Trx in cells and to validate their potential use as anti-cancer agents (to date, there is no selective cellular Trx inhibitor, and most known TrxR inhibitors were not comprehensively evaluated considering selectivity and potential off-targets). However, small molecule redox imaging tools are underdeveloped: their protein specificity, spectral properties, and applicability remain poorly precedented. This work aimed to address this opportunity gap and develop novel, small molecule diagnostic and therapeutic tools to selectively target the Trx system based on a modular trigger cargo design: artificial cyclic disulfide substrates (trigger) for oxidoreductases are tethered to molecular agents (cargo) such that the cargo’s activity is masked and is re-established only through reduction by a target protein. The rational design of these novel reduction sensors to target the cell's strongest disulfide-reducing enzymes was driven by the following principles: (i) cyclic disulfide triggers with stabilized ring systems were used to gain low reduction potentials that should resist reduction except by the strongest cellular reductases, such as Trx; and (ii) the cyclic topology also offers the potential for kinetic reversibility that should select for dithiol-type redox proteins over the cellular monothiol background. Creating imaging agents based on such two-component designs to selectively measure redox protein activity in native cells required to combine the correct trigger reducibility, probe activation kinetics, and imaging modalities and to consider the overall molecular architecture. The major prior art in this field has applied cyclic 5-membered disulfides (1,2 dithiolanes) as substrates for TrxR in a similar way to create such tools. However, this motif was described elsewhere as thermodynamically instable and was due to widely used for dynamic covalent cascade reactions. By comparing a novel 1,2 dithiolane-based probe to the state-of-the-art probes, including commercial TrxR sensors, by screening a conclusive assay panel of cellular TrxR modulations, I clarified that 1,2 dithiolanes are not selective substrates for TrxR in biological settings (Nat Commun 2022). Instead, aiming for more stable ring systems and thus more robust redox probes, during this work, I developed bicyclic 6 membered disulfides (piperidine fused 1,2 dithianes) with remarkably low reduction potentials. I showed that molecular probes using them as reduction sensors can be mostly processed by thioredoxins while being stable against reduction by GSH. The thermodynamically stabilized decalin like topology of the cis-annelated 1,2 dithianes requires particularly strong reductants to be cleaved. They also select for dithiol type redox proteins, like Trx, based on kinetic reversibility and offer fast cyclization due to the preorganization by annelation (JACS 2021). This work further expanded the system’s modularity with structural cores based on piperazine-fused 1,2 dithianes with the two amines allowing independent derivatization. Diagnostic tools using them as reduction sensors proved equally robust but with highly improved activation kinetics and were thus cellularly activated. Cellular studies evolved that they are substrates for both Trxs and their protein cousins Grxs, so measuring the cellular dithiol protein pool rather than solely Trx activity (preprint 2023). Finally, a trigger based on a slightly adapted reduction sensor, a desymmetrized 1,2 thiaselenane, was designed for selective reduction by TrxR’s selenol/thiol active site, then combined with a precipitating large Stokes’ shift fluorophore and a solubilizing group, to evolve the first selective probe RX1 to measure cellular TrxR activity, which even allowed high throughput inhibitor screening (Chem 2022). The central principle of this work was further advanced to therapeutic prodrugs based on the duocarmycin cargo (CBI) with tunable potency (JACS Au 2022) that can be used to create off-to-on therapeutic prodrugs. Such CBI prodrugs employing stabilized 1,2 dichalcogenide triggers proved to be cytotoxins that depend on Trx system activity in cells. They could further be exploited for cell-line dependent reductase activity profiling by screening their redox activation indices, the reduction-dependent part of total prodrug activation, in 177 cell lines. Beyond that, these prodrugs were well-tolerated in animals and showed anti-cancer efficacy in vivo in two distinct mouse tumor models (preprint 2022). Taken together, I introduced unique monothiol-resistant reducible motifs to target the cellular Trx system with chemocompatible units for each for TrxR and Trx/Grx, where the cyclic nature of the dichalcogenides avoids activation by GSH. By using them with distinct molecular cargos, I developed novel selective fluorescent reporter probes; and introduced a new class of bioreductive therapeutic constructs based on a common modular design. These were either applied to selectively measure cellular reductase activity or to deliver cytotoxic anti cancer agents in vivo. Ongoing work aims to differentiate between the two major redox effector proteins Trx and Grx, requiring additional layers of selectivity that may be addressed by tuned molecular recognition. The flexible use of various molecular cargos allows harnessing the same cellular redox machinery by either probes or prodrugs. This allows predictive conclusions from diagnostics to be directly translated into therapy and offers great potential for future adaptation to other enzyme classes and therapeutic venues.Die zelluläre Redox-Homöostase hängt von Thiol/Disulfid-Oxidoreduktasen ab, die den Stoffwechsel, die Proliferation und die antioxidative Antwort von Zellen beeinflussen. Die wichtigsten Netzwerke sind die Thioredoxin Reduktase-Thioredoxin (TrxR/Trx) und Glutathion Reduktase-Glutathion-Glutaredoxin (GR/GSH/Grx) Systeme, die über Redox-Schalter in Substratproteinen lebenswichtige zelluläre Funktionen steuern und so an der Redox-Regulation und -Signalübertragung beteiligt sind. Persistente Veränderungen des Redoxmilieus in pathologischen Zuständen, wie z. B. bei Krebs, sind in hohem Maße mit dem Trx-System verbunden. Eine Hochregulierung und/oder Überaktivität des Trx-Systems, die bei vielen Krebsarten auftreten, unterstützt zudem das Fortschreiten des Krebswachstums, was TrxR/Trx zu vielversprechenden Zielproteinen für die Entwicklung neuer Krebsmedikamente macht. Um die biochemischen Prozesse dahinter zu erforschen, sind spezielle Techniken zur Visualisierung und Messung enzymatischer Aktivität nötig. Die hierzu geeigneten, meist genetischen Sensoren messen ratiometrisch das Verhältnis reduzierter/oxidierter Spezies in zellulärem Umfeld oder spezifisch ausgewählte Redoxpaare. Die weitere Erforschung der exakten Funktion von TrxR/Trx und deren Substrate ist jedoch durch mangelnde Nachweismethoden limitiert. Diese sind außerdem zur Validierung chemischer Hemmstoffe für TrxR/Trx in Zellen und deren potenziellen Verwendung als Krebsmittel von großem Interesse. Bislang gibt es keinen selektiven zellulären Trx-Inhibitor und potenzielle Off-Target-Effekte der bekannten TrxR-Inhibitoren wurden nicht abschließend bewertet. Ziel dieser Arbeit ist die Entwicklung niedermolekularer, diagnostischer und therapeutischer Werkzeuge, die selektiv auf das Trx-System abzielen und auf einem modularen Trigger-Cargo Design basieren. Hierzu werden zyklische Disulfid-Substrate (Trigger) für Oxidoreduktasen so mit molekularen Wirkstoffen (Cargo) verknüpft, dass dabei die Wirkstoffaktivität maskiert, und erst nach Reduktion durch ein Zielprotein wiederhergestellt wird. Diese neuartigen, synthetischen Reduktionssensoren basieren auf den folgenden Grundprinzipien: (i) Zyklische Disulfide sind thermodynamisch stabilisiert und können nur durch die stärksten Reduktasen gespalten werden; und (ii) die zyklische Topologie ermöglicht die kinetische Reversibilität der zwei Thiol-Disulfid-Austauschreaktionen, die eine erste Reaktion mit Monothiolen, wie z. B. GSH, sofort umkehrt und so eine vollständige Reduktion verhindert. Die meisten früheren Arbeiten auf diesem Gebiet verwendeten ein zyklisches, fünfgliedriges Disulfid (1,2 Dithiolan) als Substrat für TrxR. Das gleiche Strukturmotiv wurde jedoch an anderer Stelle als thermodynamisch instabil beschrieben und aufgrund dieser Eigenschaft explizit für dynamische Kaskadenreaktionen verwendet. Deshalb vergleicht diese Arbeit zu Beginn einen neuen 1,2 Dithiolan basierten fluorogenen Indikator mit bestehenden, z. T. kommerziellen, Redox Sonden für TrxR in einer Reihe von Zellkultur-Experimenten unter Modulation der zellulären TrxR Aktivität und stellt so einen Widerspruch in der Literatur klar: 1,2 Dithiolane eignen sich nicht als selektive Substrate für TrxR, da sie labil sowohl gegen die Reduktion durch andere Redoxproteine, als auch gegen den Monothiol Hintergrund in Zellen sind (Nat. Commun. 2022). Als alternatives Strukturmotiv wird in dieser Arbeit ein bizyklisches sechsgliedriges Disulfid (anneliertes 1,2 Dithian) etabliert. Durch sein niedriges Reduktionspotenzial, also seine hohe Resistenz gegen Reduktion, werden molekulare Sonden basierend auf diesem 1,2 Dithian als Reduktionssensor fast ausschließlich von Trx aktiviert, nicht aber von TrxR oder GSH (JACS 2021). Dieses Kernmotiv bestimmt dabei die Reduzierbarkeit, und damit die Enzymspezifität, durch seine zyklische Natur und die Annelierung, auch unter Verwendung unterschiedlicher Farb-/Wirkstoffe. Auf dieser Grundlage konnte die molekulare Struktur durch einen weiteren Modifikationspunkt für die flexible Verwendung weiterer funktioneller Einheiten ergänzt werden. Obwohl zelluläre Studien ergaben, dass diese neuartigen 1,2 Dithian Einheiten in Zellen sowohl Trx als auch das strukturell verwandte Grx adressieren, sind die daraus resultierenden diagnostischen Moleküle wertvoll, um den katalytischen Umsatz zellulärer Dithiol-Reduktasen, der sogenannten Trx Superfamilie, selektiv anzuzeigen (Preprint 2023). Begünstigt durch das modulare Moleküldesign stellt diese Arbeit zudem das erste Reportersystem RX1 zum selektiven Nachweis der TrxR-Aktivität in Zellen vor. Es basiert auf der Verwendung eines zyklischen, unsymmetrischen Selenenylsulfid-Sensors (1,2 Thiaselenan), der selektiv von dem einzigartigen Selenolat der TrxR angegriffen wird, und dadurch letztlich nur von TrxR reduziert werden kann. RX1 eignete sich zudem für eine Hochdurchsatz-Validierung bestehender TrxR Inhibitoren und unterstreicht dadurch den kommerziellen Nutzen derartiger Diagnostika (Chem 2022). Das zentrale Trigger-Cargo Konzept dieser Arbeit wurde für therapeutische Zwecke weiterentwickelt und nutzt dabei den einzigartigen Wirkmechanismus der Duocarmycin-Naturstoffklasse (CBI) (JACS Au 2022) zur Entwicklung reduktiv aktivierbarer Therapeutika. CBI Prodrugs basierend auf stabilisierten Redox-Schaltern (1,2 Dithiane für Trx; 1,2 Thiaselenan für TrxR) reagierten signifikant auf TrxR-Modulation in Zellen. Sie wurden darüber hinaus durch das Referenzieren ihrer Aktivität gegenüber nicht-reduzierbaren Kontrollmoleküle für die Erstellung zelllinienabhängiger Profile der Reduktaseaktivität in 177 Zelllinien genutzt. Schließlich waren diese neuen Krebsmittel im Tiermodell gut verträglich und zeigten in zwei verschiedenen Mausmodellen eine krebshemmende Wirkung (Preprint 2022b). Zusammenfassend präsentiert diese Dissertation monothiol-resistente reduzierbare Trigger-Einheiten für das zelluläre Trx-System zur Entwicklung neuartiger, selektiver Reporter-Sonden, sowie eine neue Klasse reduktiv aktivierbarer Krebsmittel auf Basis eines adaptierbaren Trigger-Cargo Designs. Diese fanden entweder zur selektiven Messung zellulärer Proteinaktivität oder zum Einsatz als Antikrebsmittel Verwendung. Es wurden chemokompatible Motive sowohl für TrxR als auch für Trx/Grx identifiziert, wobei deren zyklische Natur eine Aktivierung durch GSH verhindert. Eine weitere Differenzierung zwischen den beiden Redox-Proteinen Trx und Grx und anderen Proteinen der Trx-Superfamilie erfordert eine zusätzliche Ebene der Selektierung, z. B. durch molekulare Erkennung, und ist Gegenstand laufender Arbeiten. Die flexible Verwendung verschiedener molekularer Wirkstoffe ermöglicht dabei die „Pipeline-Entwicklung“ von Diagnostika und Therapeutika, die von der zellulären Redox-Maschinerie analog umgesetzt werden, und dadurch Schlussfolgerungen aus der Diagnostik direkt auf eine Therapie übertragbar machen. Dies birgt großes Potenzial für künftige Entwicklungen bei einer potenziellen Übertragung des modularen Konzepts auf andere Enzymklassen und therapeutische Einsatzgebiete

    Modern meat: the next generation of meat from cells

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    Modern Meat is the first textbook on cultivated meat, with contributions from over 100 experts within the cultivated meat community. The Sections of Modern Meat comprise 5 broad categories of cultivated meat: Context, Impact, Science, Society, and World. The 19 chapters of Modern Meat, spread across these 5 sections, provide detailed entries on cultivated meat. They extensively tour a range of topics including the impact of cultivated meat on humans and animals, the bioprocess of cultivated meat production, how cultivated meat may become a food option in Space and on Mars, and how cultivated meat may impact the economy, culture, and tradition of Asia

    Multi-Fidelity Bayesian Optimization for Efficient Materials Design

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    Materials design is a process of identifying compositions and structures to achieve desirable properties. Usually, costly experiments or simulations are required to evaluate the objective function for a design solution. Therefore, one of the major challenges is how to reduce the cost associated with sampling and evaluating the objective. Bayesian optimization is a new global optimization method which can increase the sampling efficiency with the guidance of the surrogate of the objective. In this work, a new acquisition function, called consequential improvement, is proposed for simultaneous selection of the solution and fidelity level of sampling. With the new acquisition function, the subsequent iteration is considered for potential selections at low-fidelity levels, because evaluations at the highest fidelity level are usually required to provide reliable objective values. To reduce the number of samples required to train the surrogate for molecular design, a new recursive hierarchical similarity metric is proposed. The new similarity metric quantifies the differences between molecules at multiple levels of hierarchy simultaneously based on the connections between multiscale descriptions of the structures. The new methodologies are demonstrated with simulation-based design of materials and structures based on fully atomistic and coarse-grained molecular dynamics simulations, and finite-element analysis. The new similarity metric is demonstrated in the design of tactile sensors and biodegradable oligomers. The multi-fidelity Bayesian optimization method is also illustrated with the multiscale design of a piezoelectric transducer by concurrently optimizing the atomic composition of the aluminum titanium nitride ceramic and the device’s porous microstructure at the micrometer scale.Ph.D

    Towards Predicting Equilibrium Distributions for Molecular Systems with Deep Learning

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    Advances in deep learning have greatly improved structure prediction of molecules. However, many macroscopic observations that are important for real-world applications are not functions of a single molecular structure, but rather determined from the equilibrium distribution of structures. Traditional methods for obtaining these distributions, such as molecular dynamics simulation, are computationally expensive and often intractable. In this paper, we introduce a novel deep learning framework, called Distributional Graphormer (DiG), in an attempt to predict the equilibrium distribution of molecular systems. Inspired by the annealing process in thermodynamics, DiG employs deep neural networks to transform a simple distribution towards the equilibrium distribution, conditioned on a descriptor of a molecular system, such as a chemical graph or a protein sequence. This framework enables efficient generation of diverse conformations and provides estimations of state densities. We demonstrate the performance of DiG on several molecular tasks, including protein conformation sampling, ligand structure sampling, catalyst-adsorbate sampling, and property-guided structure generation. DiG presents a significant advancement in methodology for statistically understanding molecular systems, opening up new research opportunities in molecular science.Comment: 80 pages, 11 figure

    Orvosképzés 2023

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    2008 GREAT Day Program

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    SUNY Geneseo’s Second Annual GREAT Day.https://knightscholar.geneseo.edu/program-2007/1002/thumbnail.jp

    DEFINITION OF AN ADVANCED PROCESS FOR THE PRODUCTION OF LOW ENVIRONMENTAL IMPACT CONTAINERS AS POTENTIAL ALTERNATIVE TO PLASTICS

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    For decades, petroleum-based synthetic polymers, commonly known as plastics, have become one of the most appealing materials used for a wide variety of applications. Nevertheless, currently, conventional petroleum-based plastics represent a serious problem for global pollution because remain for hundreds of years in the environment when discarded. In order to reduce dependence on fossil resources, bioplastic materials are being proposed as safer and more sustainable alternatives. Bioplastics are bio-based and/or biodegradable materials, typically derived from renewable sources. Among different resources, food waste is attracting more and more attention in the research field of bioplastics’ production. The sources of food waste include household, commercial, industrial and agricultural residues. In fact, every year, around one-third of all food resources produced for human consumption are lost or wasted. Although European Union guidelines stated that food waste should preferentially be used as animal feed, in some cases, it became illegal because of disease control concerns and other times its nutritional value is very poor. On the other hand, the production of bioplastics from food waste is a renewable, sustainable process, in which materials are fabricated from carbon neutral resources, thus aligning itself with the principles of the circular bioeconomy. However, the conversion of fruit and vegetable by-products into eco-friendly materials with mechanical and hydrodynamic performances comparable to those of fuel-based plastics still remains a challenge. In this thesis, different approaches have been investigated for the valorization of fruit and vegetable wastes to produce low environmental impact materials, as a potential alternative to plastics with application in the field of food packaging. In the first section, apple waste and tomato peel by-products have been used as fillers to fabricate starch-based biocomposites. The mechanical characterization of the samples showed their suitability for covering purposes, since a ductile and soft behaviour was exhibited. In the second section, an avocado by-product extract has been incorporated to an ethyl cellulose matrix for the production of impregnated paper with enhanced durability. Since fruit wastes can contain potential pathogens and physical and chemical contaminants which can be released when used as additive for active packaging, a preliminary untargeted metabolomic characterization of the extract was conducted by LC-ESI(-)-Q Exactive-Orbitrap- MS/MS. The lipid components detected in the extract proved to be useful additives to improve paper hydrophobicity, preventing food browning and moisture loss. In general, the addition of all tested wastes (apple waste, tomato peel and avocado by-products) has proved to be useful to increase the biodegradability of the fabricated biomaterials. Hence, the environmental benefits associated with their recovery are proposed as a driving force to expand their further use for these purposes. The upcycling of food waste through the production of value-added products is an ideal and practical end use, allowing to save huge economic and energy losses

    Nanoprobes for Tumor Theranostics

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    This book reports cutting-edge technology in nanoprobes or nanobiomaterials used for the accurate diagnosis and therapy of tumors, involving a multidisciplinary of chemistry, materials science, oncology, biology, and medicine
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