Academic literature on the topic 'Nanoparticles'
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Journal articles on the topic "Nanoparticles"
Li, Meng, Liqiang Lin, Ruyan Guo, Amar Bhalla, and Xiaowei Zeng. "Numerical investigation of size effects on mechanical behaviors of Fe nanoparticles through an atomistic field theory." Journal of Micromechanics and Molecular Physics 02, no. 03 (September 2017): 1750010. http://dx.doi.org/10.1142/s2424913017500102.
Full textKaratrantos, Argyrios, Yao Koutsawa, Philippe Dubois, Nigel Clarke, and Martin Kröger. "Miscibility and Nanoparticle Diffusion in Ionic Nanocomposites." Polymers 10, no. 9 (September 10, 2018): 1010. http://dx.doi.org/10.3390/polym10091010.
Full textShannahan, Jonathan. "The biocorona: a challenge for the biomedical application of nanoparticles." Nanotechnology Reviews 6, no. 4 (August 28, 2017): 345–53. http://dx.doi.org/10.1515/ntrev-2016-0098.
Full textVenkateswara Rao, S., E. Anuhya, and K. Padmalatha. "Nanoparticles: A smart drug delivery." Journal of Drug Delivery and Therapeutics 9, no. 2-s (April 15, 2019): 590–93. http://dx.doi.org/10.22270/jddt.v9i2-s.2500.
Full textSutthavas, Pichaporn, Matthias Schumacher, Kai Zheng, Pamela Habibović, Aldo Roberto Boccaccini, and Sabine van Rijt. "Zn-Loaded and Calcium Phosphate-Coated Degradable Silica Nanoparticles Can Effectively Promote Osteogenesis in Human Mesenchymal Stem Cells." Nanomaterials 12, no. 17 (August 24, 2022): 2918. http://dx.doi.org/10.3390/nano12172918.
Full textWang, Shenqing, Xiliang Yan, Gaoxing Su, and Bing Yan. "Cytotoxicity Induction by the Oxidative Reactivity of Nanoparticles Revealed by a Combinatorial GNP Library with Diverse Redox Properties." Molecules 26, no. 12 (June 14, 2021): 3630. http://dx.doi.org/10.3390/molecules26123630.
Full textZhang, Yong, Xiao Jing Zhao, Qiang He, Ye Jun, and Qin Po Niu. "Experimental Study of Nanoparticle as Oil Additives." Advanced Materials Research 230-232 (May 2011): 288–92. http://dx.doi.org/10.4028/www.scientific.net/amr.230-232.288.
Full textWang, Xijun. "The Magnetic Nanoparticle Movement in Magnetic Fluid Characterized by the Laser Dynamic Speckle Interferometry." Journal of Nanomaterials 2014 (2014): 1–7. http://dx.doi.org/10.1155/2014/287813.
Full textCaballero-Florán, Isaac H., Hernán Cortés, Fabiola V. Borbolla-Jiménez, Carla D. Florán-Hernández, María L. Del Prado-Audelo, Jonathan J. Magaña, Benjamín Florán, and Gerardo Leyva-Gómez. "PEG 400:Trehalose Coating Enhances Curcumin-Loaded PLGA Nanoparticle Internalization in Neuronal Cells." Pharmaceutics 15, no. 6 (May 25, 2023): 1594. http://dx.doi.org/10.3390/pharmaceutics15061594.
Full textChandra, Arun, and Nalina C. "Review on nanoparticles technology and applications based on drug delivery." IP International Journal of Comprehensive and Advanced Pharmacology 6, no. 3 (October 15, 2021): 117–20. http://dx.doi.org/10.18231/j.ijcaap.2021.021.
Full textDissertations / Theses on the topic "Nanoparticles"
Lemaître, Caroline. "Contribution à l'étude théorique, numérique et expérimentale des nanoantennes patch optiques." Thesis, Clermont-Ferrand 2, 2016. http://www.theses.fr/2016CLF22742/document.
Full textIn the field of biosensors, efficient absorption of the electromagnetic field in a confined space is essential. The use of metallic nanoparticules comparable to metamaterials is the best way, to date, to amplify the field. In fact, by placing a dielectric film between a metal substrate and these particules, we allow the propagation of a gap-plasmon under these particules. This locates the magnetic field under these particules and the electric field on the edges of these nanoparticules. The resonances of this system are very sensitive to the environment of the gap-plasmon which allows very precise analysis. Although we can explain where these resonances come from, the efficiency to absorb of these structures remains poorly understood. The interferometric control is a response to this efficiency. In this report, I show that interferometric modeling of this system can fully explain the absorption. Indeed, the interferometric control well explains the presence of resonances at specific wavelenghts or the appearance of resonances when the angle of incidence is not normal. This study is very important to understand and master biosensors. In addition, this model can explain the amplification of the field in these structures and will allow us to provide the resonances of a system in various environments
Barbero, Francesco. "Physicochemical characterization of the evolution of metal nanoparticles in biological and environmental media: from synthesis to interaction with living organisms." Doctoral thesis, Universitat Autònoma de Barcelona, 2019. http://hdl.handle.net/10803/670187.
Full textLa creciente producción de nanopartículas (NP) conducirá inevitablemente a un aumento de la exposición humana y ambiental a estos materiales. En consecuencia, han surgido preocupaciones razonables con respecto a sus posibles riesgos de seguridad, dando lugar a la disciplina de nanotoxicología/nanoseguridad. Debido a la alta reactividad, los NP expuestos a diferentes escenarios biológicos y ambientales tienden a alcanzar un estado termodinámico más estable a través de la agregación, la interacción con las moléculas presentes en el medio ambiente, la adsorción a la materia macro-orgánica, las transformaciones químicas y la disolución. Todas estas transformaciones pueden generar una nueva identidad de los nanoobjetos o producir nuevas entidades químicas, cambiando así su comportamiento y, en consecuencia, su riesgo asociado potencial. Por lo tanto, los mismos NP pueden tener un destino totalmente diferente y, en consecuencia, un impacto totalmente diferente en los organismos vivos y el medio ambiente dependiendo del microambiente (por ejemplo, el medio de exposición) en el que se encuentran. Además, las características prístinas del nanomaterial influyen mucho en su destino biológico y medioambiental. Desde esta perspectiva, resulta fundamental comprender las características del objeto final que encontrará organismos vivos y analizar sus propiedades, a fin de correlacionar las características de NP prístinas y finales con los posibles efectos sobre los organismos vivos. En este contexto, el objetivo de esta tesis ha sido el estudio de la transformacion fisicoquímico de NP modelo expuestos a medios biológicos y ambientales. Para estos estudios, se eligieron NPs de Au y Ag, ya que son modelos de NP ampliamente utilizados y debido a sus numerosas aplicaciones. En primer lugar, el estudio se centró en la influencia de la composición de los medios de cultivo celular en el proceso de formación de protein corona, la composición final y el estado de agregación de NP y los efectos consiguientes en la absorción de células NP. También se realizó una caracterización fisicoquímica de la naturaleza de la bicapa CTAB - Au NP para estudiar el impacto de este recubrimiento de superficie NP ampliamente utilizado en la exposición de la partícula a los fluidos biológicos, en la formación de la corona de proteínas y en el diseño e interpretación de Pruebas de toxicidad NP. Finalmente, la evolución de NP en agua dulce natural se exploró mediante la realización de un estudio de la naturaleza de interacción de NP y materia orgánica natural y las características derivadas de NP.
The increasing production of engineered Nanoparticles (NPs) will inevitably lead to an increase of human and environmental exposition to these materials. Consequently reasonable concerns have arisen regarding their potential safety risks, giving rise to the nanotoxicology/nanosafety discipline. Because of the high reactivity, NPs exposed to different biological and environmental scenarios, tend to reach a more stable thermodynamic state via aggregation, interaction with the molecules present in the environment, adsorption to macro-organic matter, chemical transformations and dissolution. All these transformations can generate a new identity of the nano-objects or produce new chemical entities, thereby changing their behaviour and consequently their potential associated risk. Thus, the same NPs can have a totally different fate and consequently a totally different impact on living organisms and the environment depending on the microenvironment (e.g., the exposure medium) in which they are. Furthermore, the pristine features of nano-material highly influence their biological and environmental fate. From this perspective, it becomes fundamental to understand the characteristics of the final object that will encounter living organisms and analyze its properties, in order to correlate the pristine and final NP features with the potential effects on living organisms. In this context, the focus of this thesis has been on the physicochemical transformation of model NPs exposed to biological and environmental media. For these studies, Au and Ag NPs were chosen as they are widely used NP models and because of their numerous applications. Firstly, the study focused on the influence of the cell culture media composition on the protein corona (PC) formation process, final composition and NPs aggregation state and the consequent effects on NP cell uptake. A physicochemical characterization of the nature of the CTAB - Au NP bilayer was also carried out to study the impact of this widely used NP surface coating on the particle’s exposition to biological fluids, on the formation of the protein corona and on the design and interpretation of NP toxicity tests. Finally, the NP evolution in natural fresh water was explored by carrying out a study of the interaction nature of NPs and natural organic matter and the deriving NP features.
Díaz, Ocaña Raquel. "Recombinant self-assembling nanoparticles for cancer therapy based on toxin and venom compounds." Doctoral thesis, Universitat Autònoma de Barcelona, 2020. http://hdl.handle.net/10803/670483.
Full textLa plataforma desarrollada de ingeniería de proteínas autoensamblables permite diseñar nanopartículas únicamente proteicas (NPs) capaces de atacar y actuar selectivamente sobre las células cancerosas mediante la interacción con receptores que se sobreexpresan. Las estructuras esféricas estables de las NPs desarrolladas y su tamaño adecuado, en combinación con los péptidos de direccionamiento involucrados, mejoran su especificidad. Además, la novedosa incorporación de segmentos de toxina y veneno ha mejorado los efectos terapéuticos de estas estructuras que son totalmente biocompatibles y que no tienen ningún portador externo o material agregado, cumpliendo de esta manera con el concepto emergente para medicamentos de precisión que involucra un fármaco recombinante libre de vehículo, autoensamblado, auto-dirigido y eficiente. Una versión modificada de la cadena catalítica de ricina A, con la capacidad de disminuir los efectos secundarios no deseados del síndrome de derrame vascular, pero conservando su citotoxicidad natural, se adaptó a la plataforma de proteínas. El diseño se desarrolló con el péptido T22, que se une a CXCR4, en el extremo N-terminal, y una cola de histidinas en el extremo C-terminal, en combinación con un fragmento del sitio escindible de furina para liberar la proteína intracelularmente, y una secuencia KDEL para evitar secreción del retículo endoplásmico. Las NPs de cadena de ricina A solubles purificadas dirigidas a CXCR4, con un diámetro promedio de 11 nm, alcanzaron un incremento de 100 veces en su citotoxicidad con un IC50 de 13 ± 0,5 x 10 -9 M en células HeLa. Pero también se produjeron por métodos recombinantes y se purificaron cuerpos de inclusión insolubles de 400-600 nm, con resultados citotóxicos parciales. El mecanismo de entrada dependiente del receptor de T22-mRTA-H6 se verificó y evaluó en un modelo de ratón con leucemia mieloide aguda (AML) mediante la inyección sistémica en la vena de la cola, donde se verificó un bloqueo importante de las células leucémicas sin toxicidad sistémica o histológica lateral en los órganos sanos. De manera similar, la clorotoxina (CTX) también se incorporó a la plataforma de proteínas con el fin de aprovechar su direccionamiento y efecto terapéutico en glioblastoma (GBM), ambas funciones en un solo péptido. Se diseñaron dos versiones que se unen a la proteína anexina-2 y la metaloproteinasa de matriz MMP-2; CTX-GFP-H6 y CTX-KRKRK-GFP-H6. Lss NPs solubles, de un diámetro promedio de 12 nm, se incubaron en células HeLa sobreexpresando anexina-2, y en células U87MG, sobreexpresando MMP2. Ambas versiones eran completamente fluorescentes, pero CTX-GFP-H6 presentó efectos citotóxicos leves, mientras que CTX-KRKRK-GFP-H6 mostró ser más citotóxico en las células U87MG que en las células HeLa. La afinidad selectiva de CTX se confirmó mediante la evaluación de su direccionamiento utilizando anticuerpos monoclonales y un suero policlonal contra la proteína de la superficie celular, actuando como un receptor de la CTX.
The developed self-assembling platform allows the engineering of protein-only nanoparticles (NPs) capable to target and act selectively over cancer cells by means of the interaction with overexpressed receptors. The stability of the spherical NP structures and their adequate size, in combination with the involved targeting peptides, enhance their specificity. Also, the novel incorporation of toxin and venom segments have improved the therapeutic effects of these fully biocompatible materials, without the need of any external carrier or added material, thus fulfilling the newfangled concept for precision medicines that involve self-assembled, self-targeted and efficient vehicle-free recombinant drugs. A modified version of the catalytic ricin A chain, with the ability to diminish the undesired vascular leak syndrome side effects but retaining its natural cytotoxicity, was adapted to the protein platform. The design was developed with the peptide T22 in the N-terminal, which binds CXCR4, and a his-tag in the C-terminal. This was combined with a furin cleavable site fragment in order to release the protein intracellularly, and a KDEL sequence to avoid endoplasmic reticulum secretion. Purified soluble CXCR4-targeted ricin A chain NPs with an average diameter of 11 nm, reached a 100-fold cytotoxic improvement with an IC50 of 13 ± 0.5 x 10 -9 M in HeLa cells. Also, insoluble 400-600 nm inclusion bodies were produced by recombinant methods and purified, with partial cytotoxic results. The receptor-dependent mechanism of T22-mRTA-H6 was verified and evaluated in an acute myeloid leukemia (AML) mouse model by systemic administration through a vein tail injection where an important blockage of the leukemic cells was verified without side systemic or histological toxicity in healthy organs. In a similar way, chlorotoxin (CTX) was also incorporated to the protein platform in order to take advantage of its targeting and therapeutic effect in glioblastoma (GBM), both functions in one peptide. Two versions that target protein Annexin-2 and the matrix metalloproteinase MMP-2 were engineered, namely CTX-GFP-H6 and CTX-KRKRK-GFP-H6. The soluble NPs of an average dimeter of 12 nm were incubated with HeLa cells, overexpressing annexin-2, and in U87MG cells, overexpressing MMP2. Both versions were fully fluorescent but CTX-GFP-H6 presented mild cytotoxic effects, whereas CTX-KRKRK-GFP-H6 showed to be more cytotoxic in U87MG cells than in HeLa cells. The selective affinity of CTX was confirmed by means of evaluating its targeting using a monoclonal antibody and a polyclonal serum against the cell surface protein, acting as a CTX receptor.
Luo, Zhongrui. "In vivo interactions between food availability and nanoparticles in Caenorhabditis elegans." Doctoral thesis, Universitat Autònoma de Barcelona, 2020. http://hdl.handle.net/10803/671182.
Full textDurante las últimas décadas, las nanopartículas (NPs) se han utilizado ampliamente en distintos campos, especialmente en aplicaciones médicas como fármacos, agentes de formación de imágenes y como liberadores de fármacos. Sin embargo, también han planteado dudas respecto a las posibles reacciones adversas sobre la salud humana. Así, se han realizado grandes esfuerzos de investigación en el campo de las ciencias biológicas para elucidar los mecanismos de toxicidad de distintas NPs. En este trabajo de Tesis, hemos dedicado esfuerzos a aplicar el (Caenorhabditis elegans) C. elegans como un organismo modelo robusto y simple para las evaluaciones de toxicidad de NPs. El objetivo general de esta tesis ha sido estudiar la interacción de la comida de estos gusanos con las NPs. En particular, el estudio de las interacciones nano-bio entre nanopartículas de óxido de hierro superparamagnéticas (SPIONs) o AuNPs de 10 nm en C. elegans alimentados o no; así demostrar que este pequeño animal puede utilizarse para estudiar efectos alimentarios. En primer lugar, estudiamos los efectos de la disponibilidad de alimento sobre las toxicidades inducidas por la exposición de SPIONs tras 24 h - exposición aguda - o 72 h - exposición prolongada. Descubrimos que la comida brinda cierta protección a los C. elegans, la cual se determinó midiendo la supervivencia y la reproducción. Los gusanos en la exposición aguda tuvieron una mayor eficiencia de absorción de SPIONs facilitada por la comida en comparación con la condición sin alimento. La utilización de la microespectroscopía infrarroja de Sincrotrón (SR-μFTIR) nos permitió demostrar que la exposición prolongada (24 h versus 4 h) y altas concentraciones de SPIONs (500 µg/mL versus 100 µg/mL) inducen un estrés oxidativo más severo debido a el aumento de la oxidación de lípidos. En segundo lugar, investigamos las consecuencias de la ingesta de comida sobre los gusanos después de 24 h de exposición a AuNP de 10 nm. Se identificó el papel protector de los alimentos en la reducción de efectos tóxicos. Usando SR-μFTIR, encontramos que las AuNPs de pequeño tamaño (10 nm frente a 150 nm) o la exposición prolongada (24 h frente a 4 h) causaron un mayor nivel de oxidación de lípidos que se relacionó con las respuestas contra el estrés oxidativo. Por otro lado, evaluamos preliminarmente la posibilidad de realizar la terapia fototérmica en gusanos que contenian AuNP de 150 nm. Encontramos daños por fotoablación en los puntos de irradiación láser sobre los gusanos, sugiriendo que se podría usar este gusano para evaluar NPs, pero para ello es necesario optimizar la configuración experimental. En la parte final, presentamos algunas colaboraciones donde realizamos experimentos con diferentes nanomateriales como luteína y metal-organic frameworks (MOFs), evaluados empleando C. elegans. Estudiamos las propiedades antioxidantes de la luteína en C. elegans modificados para ser modelos de enfermedades asociadas con el síndrome de Leigh y demostramos la posibilidad de aplicar microscopia de infrarrojo (SR-μFTIR) en estos estudios. Por otro lado, realizamos la evaluación preliminar de toxicidad de MOF, MIL-127 y CS-MIL-127 recubierto de quitosano (CS). Además, investigamos los efectos del recubrimiento de CS en la absorción y excreción por los C. elegans. En resumen, hemos encontrado que la disponibilidad de comida puede disminuir los efectos adversos, parcialmente asociados con el estrés oxidativo, inducidos por SPIONs o AuNPs en C. elegans. Nuestros resultados también sugieren que los C. elegans tienen un gran potencial como modelo de administración oral ya que pueden emplearse para probar diferentes materiales. Además, en combinación con otras técnicas avanzadas, nos pueden ayudar a comprender de forma más general los mecanismos de toxicidad y ampliar el rango de aplicación de las técnicas de ciencia de materiales para la investigación biológica.
During the last decades, nanoparticles (NPs) have been widely used in various fields, especially in medical applications such as drugs, imaging agents, and drug-delivery carriers. However, they also raised public concerns regarding the potential adverse influences on human health. Collective efforts from worldwide researchers in materials and biological science have been invested in investigating the toxicity mechanisms of different NPs. In this thesis, we dedicated major efforts to apply (Caenorhabditis elegans) C. elegans as a robust and simple model organism for toxicity assessments of assorted NPs. The general objective of this thesis was to study effects of food availability on nano-bio interactions between superparamagnetic iron oxide nanoparticles (SPIONs) or 10 nm AuNPs and C. elegans, and prove that this small animal can be used to study alimentary effects. Firstly, we studied the effects of food availability on toxicities induced by exposure to SPIONs after 24 h (acute exposure) or 72 h (prolonged exposure). We found that food provided some protection to C. elegans determined by measuring multiple toxicity endpoints such as survival and reproduction. Worms in the acute exposure condition had a higher uptake efficiency of SPIONS facilitated by food compared with the condition without the addition of food. The utilization of synchrotron Fourier transform infrared microspectroscopy (SR-μFTIR), allowed us to demonstrate that long-exposure (24 h versus 4 h) and high concentrations of SPIONs (500 µg/mL versus 100 µg/mL) induce more severe oxidative stress determined by increased levels of lipid oxidation. Secondly, we investigated food’s influences on worms after 24 h exposure to 10 nm AuNPs. The protective role of food was identified in reducing toxic effects, such as survival and reproduction. Using SR-μFTIR, we found that small-sized AuNPs (10 nm versus 150 nm) or long-exposure (24 h versus 4 h) caused an increased level of lipid oxidation which was related to responses against oxidative stress. On the other hand, we preliminarily evaluated the possibility of performing the photothermal therapy in worms containing 150 nm AuNPs. We found photoablated damages on the laser irradiation spots of worms, suggesting that multiple experimental settings needed to be optimized. At the end of the thesis, also we presented some collaborations where we performed some experiments with different nanomaterials such as lutein and (metal-organic frameworks) MOFs and evaluated them on C. elegans. We studied antioxidative properties of lutein in C. elegans disease models associated with Leigh Syndrome and demonstrated the possibility to apply synchrotron Fourier transform infrared microspectroscopy (SR-μFTIR) on this topic. On the other hand, we performed the preliminary toxicity assessment of MOFs, MIL-127 and chitosan (CS) coated MIL-127 (CS-MIL-127). Additionally, we investigated about effects of the chitosan (CS) coating on C. elegans’ uptake and excretion efficiencies of MIL-127 and CS-MIL-127. We reported the potential of applying C. elegans as an oral administration model of studying metal-organic frameworks’ (MOFs’) in vivo toxicities. In summary, food availability could decrease adverse effects, partially associated with oxidative stress, induce by SPIONs or AuNPs on C. elegans. It also suggested that C. elegans has a great potential of being employed as an oral administration model of testing various materials. Furthermore, combined with other advanced techniques, we could have a more general understanding of the toxicity mechanism and broaden the application range of material science techniques for biological research.
Pantidos, Nikolaos. "Biological synthesis of stable copper nanoparticles." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/29532.
Full textBuchy, Eric. "Conception de bioconjugués squalénisés dotés de propriétés d'auto-assemblage : vers une méthode générale de vectorisation nanoparticulaire." Thesis, Université Paris-Saclay (ComUE), 2015. http://www.theses.fr/2015SACLS267.
Full textSqualenoyl conjugates of semaxanib and sunitinib, two potent antiangiogenic (pyrrolyl)methylidenyl-substituted oxindole multitarget tyrosine kinase inhibitors, were synthesized with a hemiaminal-based pH-sensitive linker. The prodrugs were prepared according to a three-step sequence involving (i) N-alkylation with chloromethoxy-triisopropylsilane; (ii) desilylation; and (iii) acylation with trisnorsqualenic acid. These squalenoyl prodrugs were found to selfassemble into nanoassemblies in aqueous media without the need for any surfactant. The nanosized aggregates were characterized by dynamic light scattering and transmission electron microscopy, and appeared to be stable in water for several days, as determined by particle-size measurement. In vitro biological studies showed that squalenoyl sunitinib nanoassemblies are notably cytotoxic against the human umbilicalvein endothelial cell line (HUVEC), which is involved in the tumor vessel formation
Dzumedzey, Yuliya. "Mobility of manufactured nanoparticles within a natural organic gel." Thesis, Aix-Marseille, 2017. http://www.theses.fr/2017AIXM0159/document.
Full textThe mobility and fate of manufactured nanoparticles (NPs) in the environment drive the exposure behaviour. This study deals with the question on how NPs interact with environmental components, and how this interaction may alter the NPs fate and impact on the biota. We investigated the interaction of variably charged and sized NPs (TiO2 NPs, as analogues of those typically released from sunscreen, and Au NPs as models) with pure polysaccharide YAS34 as analogue of bacterial gels. The release of TiO2 NPs from a typical sunscreen under aqueous aging was first studied. The interaction between NPs and the bacterial polysaccharide was studied (1) in diluted suspension conditions, (2) by deposition on the gel surface as compared to a bare SiO2 mineral collector, and (3) by measuring the NPs transfer through the gel. Favorable and unfavorable conditions for NPs attachment to the polysaccharide were prepared by selecting appropriate pH and NPs coating.Under favorable conditions, the NPs tended to heteroaggregate with the EPS in suspension, leading to their partial sedimentation. On the EPS substrate, the NPs deposition was influenced by the physicochemical conditions. The NPs deposition is driven by electrostatic interactions with the collector and is also affected by the interactions between the neighbouring NPs. Surprisingly, under unfavourable conditions, some weak attractive interactions were again evidenced both in suspension and deposition experiments that we attributed to be dependent on the NP organic coating competing with the EPS.The NPs transfer through the gel was favored under repulsive electrostatic interaction, and affected by the NPs size and by the solution pH
Le, Hong Duc. "Modelling of nanoparticles laden jet from a conveying pipe leakage." Phd thesis, Toulouse, INPT, 2018. http://oatao.univ-toulouse.fr/21454/1/LE_Hong_Duc.pdf.
Full textCampioli, Elisa. "Functional fluorescent organic nanoparticles." Phd thesis, Université Rennes 1, 2013. http://tel.archives-ouvertes.fr/tel-00954407.
Full textNarayanan, Radha. "Shape-Dependent Nanocatalysis and the Effect of Catalysis on the Shape and Size of Colloidal Metal Nanoparticles." Diss., Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/6878.
Full textBooks on the topic "Nanoparticles"
Schmid, Günter, ed. Nanoparticles. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527631544.
Full textSchmid, Gnter, ed. Nanoparticles. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2003. http://dx.doi.org/10.1002/3527602399.
Full textRotello, Vincent, ed. Nanoparticles. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9042-6.
Full textde Mello Donegá, Celso, ed. Nanoparticles. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6.
Full textDe Mello Donega, Celso, ed. Nanoparticles. Cham: Springer Nature Switzerland, 2024. https://doi.org/10.1007/978-3-031-71460-3.
Full textGuet, C., P. Hobza, F. Speigelman, and F. David, eds. Atomic clusters and nanoparticles. Agregats atomiques et nanoparticules. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/3-540-45621-x.
Full textJana, Nikhil Ranjan. Colloidal Nanoparticles. Boca Raton : CRC Press, Taylor & Francis Group, 2018.: CRC Press, 2019. http://dx.doi.org/10.1201/9780429165603.
Full textJoshy, K. S., Thomas Sabu, and Vijay Kumar Thakur, eds. Magnetic Nanoparticles. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1260-2.
Full textPatra, Jayanta Kumar, Leonardo F. Fraceto, Gitishree Das, and Estefânia Vangelie Ramos Campos, eds. Green Nanoparticles. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-39246-8.
Full textBook chapters on the topic "Nanoparticles"
de Mello Donegá, Celso. "The Nanoscience Paradigm: “Size Matters!”." In Nanoparticles, 1–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_1.
Full textHassinen, Antti, José C. Martins, and Zeger Hens. "Solution NMR Toolbox for Colloidal Nanoparticles." In Nanoparticles, 273–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_10.
Full textKoole, Rolf, Esther Groeneveld, Daniel Vanmaekelbergh, Andries Meijerink, and Celso de Mello Donegá. "Size Effects on Semiconductor Nanoparticles." In Nanoparticles, 13–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_2.
Full textZijlstra, Peter, Michel Orrit, and A. Femius Koenderink. "Metal Nanoparticles for Microscopy and Spectroscopy." In Nanoparticles, 53–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_3.
Full textde Jongh, Petra E., and Tamara M. Eggenhuisen. "Nanoporous Materials and Confined Liquids." In Nanoparticles, 99–120. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_4.
Full textEggenhuisen, Tamara M., and Petra E. de Jongh. "Supported Nanoparticles." In Nanoparticles, 121–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_5.
Full textGroeneveld, Esther, and Celso de Mello Donegá. "The Challenge of Colloidal Nanoparticle Synthesis." In Nanoparticles, 145–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_6.
Full textvan Huis, Marijn A., and Heiner Friedrich. "Electron Microscopy Techniques." In Nanoparticles, 191–221. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_7.
Full textLiljeroth, Peter, Bruno Grandidier, Christophe Delerue, and Daniël Vanmaekelbergh. "Scanning Probe Microscopy and Spectroscopy." In Nanoparticles, 223–55. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_8.
Full textBaranov, Pavel G., Nikolai G. Romanov, Celso de Mello Donegá, Sergei B. Orlinskii, and Jan Schmidt. "Electron Paramagnetic Resonance Based Spectroscopic Techniques." In Nanoparticles, 257–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44823-6_9.
Full textConference papers on the topic "Nanoparticles"
Yu, Qun, Chao Zhu, Robert Pfeffer, and Rajesh N. Dave. "Experimental Study on Fluidization Characteristics of Nanoparticles." In ASME 2004 Heat Transfer/Fluids Engineering Summer Conference. ASMEDC, 2004. http://dx.doi.org/10.1115/ht-fed2004-56269.
Full textWang, Jun, and Guodong Xia. "Thermophoresis of Nanoparticles in Dilute Gases." In ASME 2018 5th Joint US-European Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/fedsm2018-83005.
Full textZhang, Martin Y., and Gary J. Cheng. "Nanoscale Size Dependence on Metallic Nanoparticles: Case Study of Titanium Nanoparticles on Pulsed Laser Sintering of Hydroxyapatite/Titanium Nanoparticles." In ASME 2011 International Manufacturing Science and Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/msec2011-50296.
Full textZhu, Youyi, Peng Yu, and Jian Fan. "Study on Nanoparticle Stabilized Emulsions for Chemical Flooding Enhanced Oil Recovery." In International Petroleum Technology Conference. IPTC, 2021. http://dx.doi.org/10.2523/iptc-21456-ms.
Full textKelley, D. F., H. Tu, and K. Mogoyrosi. "Photophysics of GaSe nanoparticles and nanoparticle aggregates." In Optics & Photonics 2005, edited by Clemens Burda and Randy J. Ellingson. SPIE, 2005. http://dx.doi.org/10.1117/12.616960.
Full textYuksel, Anil, Michael Cullinan, and Jayathi Murthy. "Thermal Energy Transport Below the Diffraction Limit in Close-Packed Metal Nanoparticles." In ASME 2017 Heat Transfer Summer Conference. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/ht2017-4968.
Full textMin, Jung Yim, Seok Pil Jang, and Stephen U. S. Choi. "Motion of Nanoparticles in Nanofluids Under an Electric Field." In ASME 2005 International Mechanical Engineering Congress and Exposition. ASMEDC, 2005. http://dx.doi.org/10.1115/imece2005-80139.
Full textKarnik, Rohit, Frank X. Gu, Suman Bose, Pamela Basto, Christopher Cannizzaro, Robert Langer, and Omid C. Farokhzad. "Microfluidic Synthesis of Polymeric Nanoparticles." In ASME 2008 6th International Conference on Nanochannels, Microchannels, and Minichannels. ASMEDC, 2008. http://dx.doi.org/10.1115/icnmm2008-62218.
Full textHeller, Michael J., Dieter Dehlinger, Sadik Esener, and Benjamin Sullivan. "Electric Field Directed Fabrication of Biosensor Devices From Biomolecule Derivatized Nanoparticles." In ASME 2007 2nd Frontiers in Biomedical Devices Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/biomed2007-38093.
Full textLin, Dong, Sergey Suslov, Chang Ye, Yiliang Liao, C. Richard Liu, and Gary J. Cheng. "Nanoparticles Embedding Into Metallic Materials by Laser Direct Irradiation." In ASME 2012 International Manufacturing Science and Engineering Conference collocated with the 40th North American Manufacturing Research Conference and in participation with the International Conference on Tribology Materials and Processing. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/msec2012-7379.
Full textReports on the topic "Nanoparticles"
Venedicto, Melissa, and Cheng-Yu Lai. Facilitated Release of Doxorubicin from Biodegradable Mesoporous Silica Nanoparticles. Florida International University, October 2021. http://dx.doi.org/10.25148/mmeurs.009774.
Full textChumanov, George. Asymmetric Hybrid Nanoparticles. Office of Scientific and Technical Information (OSTI), November 2015. http://dx.doi.org/10.2172/1225813.
Full textVeloso, Rita Carvalho, Catarina Dias, Andrea Resende Souza, Joana Maia, Nuno M. M. Ramos, and João Ventura. Improving the optical properties of finishing coatings for façade systems. Department of the Built Environment, 2023. http://dx.doi.org/10.54337/aau541592743.
Full textBalch, William M., James Vaughn, and Joaquim I. Goes. Nanoparticles and Ocean Optics. Fort Belvoir, VA: Defense Technical Information Center, September 2008. http://dx.doi.org/10.21236/ada533234.
Full textBalch, William M., James Vaughn, and Joaquim I. Goes. Nanoparticles and Ocean Optics. Fort Belvoir, VA: Defense Technical Information Center, January 2008. http://dx.doi.org/10.21236/ada519059.
Full textBalch, William M., James Vaughn, and Joaquim I. Goes. Nanoparticles and Ocean Optics. Fort Belvoir, VA: Defense Technical Information Center, September 2007. http://dx.doi.org/10.21236/ada569308.
Full textChefetz, Benny, Baoshan Xing, and Yona Chen. Interactions of engineered nanoparticles with dissolved organic matter (DOM) and organic contaminants in water. United States Department of Agriculture, January 2013. http://dx.doi.org/10.32747/2013.7699863.bard.
Full textBurgett, Eric, Mohamad Al-Sheikhly, and Christopher Summers. Development of Plasmonically Cloaked Nanoparticles. Office of Scientific and Technical Information (OSTI), May 2015. http://dx.doi.org/10.2172/1253944.
Full textArmstrong, Robert L. Light Control of Fractal Nanoparticles. Fort Belvoir, VA: Defense Technical Information Center, March 2002. http://dx.doi.org/10.21236/ada413632.
Full textDavid, Anand. Bioinspired synthesis of magnetic nanoparticles. Office of Scientific and Technical Information (OSTI), January 2009. http://dx.doi.org/10.2172/967072.
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