Literatura académica sobre el tema "Chitosan nanoparticle"
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Artículos de revistas sobre el tema "Chitosan nanoparticle"
Wang, Cheng, Hong Lin y Yu Yue Chen. "Study on the Preparation of Steady-State Chitosan Nanoparticle as Silk-Fabric Finishing Agent". Advanced Materials Research 175-176 (enero de 2011): 745–49. http://dx.doi.org/10.4028/www.scientific.net/amr.175-176.745.
Texto completoYang, Ming-Hui, Shyng-Shiou Yuan, Ying-Fong Huang, Po-Chiao Lin, Chi-Yu Lu, Tze-Wen Chung y Yu-Chang Tyan. "A Proteomic View to Characterize the Effect of Chitosan Nanoparticle to Hepatic Cells: Is Chitosan Nanoparticle an Enhancer of PI3K/AKT1/mTOR Pathway?" BioMed Research International 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/789591.
Texto completoWang, Cheng, Hong Lin, Yu Yue Chen y Yan Hua Lu. "Preparation and Application of Low Molecular Weight Chitosan Nanoparticle as a Textile Finishing Agent". Advanced Materials Research 796 (septiembre de 2013): 92–97. http://dx.doi.org/10.4028/www.scientific.net/amr.796.92.
Texto completoVerma, Devendra Kumar, Rajdeep Malik, Jagram Meena y Rashmi Rameshwari. "Synthesis, characterization and applications of chitosan based metallic nanoparticles: A review". Journal of Applied and Natural Science 13, n.º 2 (22 de mayo de 2021): 544–51. http://dx.doi.org/10.31018/jans.v13i2.2635.
Texto completoAkmaz, Solmaz, Esra Dilaver Adıgüzel, Muzaffer Yasar y Oray Erguven. "The Effect of Ag Content of the Chitosan-Silver Nanoparticle Composite Material on the Structure and Antibacterial Activity". Advances in Materials Science and Engineering 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/690918.
Texto completoVifta, Rissa Laila y Fania Putri Luhurningtyas. "Nanoparticle from Medinilla speciosa with Various of Encapsulating Agent and Their Antioxidant Activities Using Ferric Reducing Assay". Indonesian Journal of Cancer Chemoprevention 11, n.º 1 (6 de marzo de 2020): 22. http://dx.doi.org/10.14499/indonesianjcanchemoprev11iss1pp22-29.
Texto completoBarbosa, Ana, Sofia Costa Lima y Salette Reis. "Application of pH-Responsive Fucoidan/Chitosan Nanoparticles to Improve Oral Quercetin Delivery". Molecules 24, n.º 2 (18 de enero de 2019): 346. http://dx.doi.org/10.3390/molecules24020346.
Texto completoВалентина Геннадьевна, Матвеева,, Тихонов, Борис Борисович, Стадольникова, Полина Юрьевна, Лисичкин, Даниил Русланович, Манаенков, Олег Викторович y Сульман, Михаил Геннадьевич. "OPTIMIZATION OF CHITOSAN NANOPARTICLES SYNTHESIS CONDITIONS". Вестник Тверского государственного университета. Серия: Химия, n.º 3(49) (28 de octubre de 2022): 13–20. http://dx.doi.org/10.26456/vtchem2022.3.2.
Texto completoWahyuni, S., K. R. P. Wibowo, H. T. Prakoso, M. Bintang y Siswanto. "Chitosan-Ag nanoparticle antifungal activity against Fusarium sp., causal agent of wilt disease on chili". IOP Conference Series: Earth and Environmental Science 948, n.º 1 (1 de diciembre de 2021): 012064. http://dx.doi.org/10.1088/1755-1315/948/1/012064.
Texto completoSmith, Raven A., Rebecca C. Walker, Shani L. Levit y Christina Tang. "Single-Step Self-Assembly and Physical Crosslinking of PEGylated Chitosan Nanoparticles by Tannic Acid". Polymers 11, n.º 5 (27 de abril de 2019): 749. http://dx.doi.org/10.3390/polym11050749.
Texto completoTesis sobre el tema "Chitosan nanoparticle"
Zarate-Triviño, D. G., Acosta E. M. Valenzuela, E. Prokhorov, G. Luna-Bárcenas, Padilla C. Rodríguez y Molina M. A. Franco. "Chitosan-Gold Nanoparticle Composites for Biomedical Application". Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35404.
Texto completoSaner, Brandon. "Physiochemical and Antibacterial Properties of Quaternized Chitosan Nanoparticle-Surfactant Mixtures". University of Toledo / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1525440791263562.
Texto completoPatel, Nimitt G. "Fabrication and characterization of gold nanoparticle reinforced Chitosan nanocomposites for biomedical applications". Thesis, Clarkson University, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3636199.
Texto completoChitosan is a naturally derived polymer, which represents one of the most technologically important classes of active materials with applications in a variety of industrial and biomedical fields. Polymeric materials can be regarded as promising candidates for next generation devices due to their low energy payback time. These devices can be fabricated by high-throughput processing methodologies, such as spin coating, inkjet printing, gravure and flexographic printing onto flexible substrates. However, the extensive applications of polymeric films are still limited because of disadvantages such as poor electromechanical properties, high brittleness with a low strain at break, and sensitivity to water. For certain critical applications the need for modification of physical, mechanical and electrical properties of the polymer is essential. When blends of polymer films with other materials are used, as is commonly the case, device performance directly depends on the nanoscale morphology and phase separation of the blend components. To prepare nanocomposite thin films with the desired functional properties, both the film composition and microstructure have to be thoroughly characterized and controlled.
Chitosan reinforced bio-nanocomposite films with varying concentrations of gold nanoparticles were prepared through a solution casting method. Gold nanoparticles (∼ 32 nm diameter) were synthesized via a citrate reduction method from chloroauric acid and incorporated in the prepared Chitosan solution. Uniform distribution of gold nanoparticles was achieved throughout the chitosan matrix and was confirmed by SEM images. Synthesis outcomes and prepared nanocomposites were characterized using TEM, SAED, SEM, EDX, XRD, UV-Vis, particle size analysis, zeta potential and FT-IR for their physical, morphological and structural properties. Nanoscale mechanical properties of the nanocomposite films were characterized at room temperature, human body temperatures and higher temperatures using instrumented indentation techniques. The obtained films were confirmed to be biocompatible by their ability to support the growth and proliferation of human tissue cells in vitro. Statistical analysis on mechanical properties and biocompatibility results, were conducted. Results revealed significant enhancement on both the mechanical properties and cell adherence and proliferation. The results will enhance our understanding of the effect of nanostructures reinforcement on these important functional polymeric thin films for potential biomedical applications.
Han, Yi. "Development and Evaluation of Mucoadhesive Chitosan Nanoparticle-based Salmonella Vaccine for Oral Delivery in Broiler Birds". The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1587571015936815.
Texto completoPicone, Carolina Siqueira Franco 1983. "Formação de nanopartículas por associação de biopolímeros e surfactantes = Formation of nanoparticles by biopolymer - surfactant association". [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/254194.
Texto completoTexto em português e inglês
Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos
Made available in DSpace on 2018-08-20T12:57:32Z (GMT). No. of bitstreams: 1 Picone_CarolinaSiqueiraFranco_D.pdf: 4074904 bytes, checksum: 1a2779daa118fabb35ba241a8f6bf16f (MD5) Previous issue date: 2012
Resumo: As nano partículas possuem grande potencial para a liberação controlada de bioativos, porém ainda são pouco exploradas na área de alimentos. Neste trabalho foi estudada a formação de nanopartículas a partir da autoagregação de surfactantes, associação surfactante-polissacarídeo e complexação eletrostática entre diferentes polissacarídeos, no caso, quitosana e gelana. A compreensão das interações moleculares responsáveis pela formação das partículas e o conhecimento das variáveis que afetam sua formação permitem predizer e controlar suas propriedades. Tais interações dependem fortemente das características de cada macromolécula, como flexibilidade, estado conformacional e densidade de cargas que são diretamente afetadas pelas condições físico-químicas do meio como pH, força iônica e temperatura. Por isso, este trabalho foi dividido em três etapas. (I) Inicialmente foi avaliado o comportamento em solução dos polissacarídeos utilizados posteriormente para a formação de complexos. Os efeitos do pH e da temperatura nas características reológicas e no estado conformacional de soluções puras de gelana e quitosana foram estudados. A agregação da gelana foi mais sensível às alterações do meio que a quitosana. (II) Na segunda etapa, nanopartículas foram formadas por autoassociação de polissorbatos na presença de quitosana. A influência do comprimento da cauda hidrofóbica do surfactante e do pH do meio nas propriedades das partículas foi estudada por espalhamento de luz, reologia, condutivimetria e microscopia de luz polarizada. O tamanho e estrutura das partículas formadas pelo surfactante de menor cadeia hidrofóbica foram mais favoráveis à associação com a quitosana. O pH do meio (3,0 ou 6,7) não influenciou de maneira significativa as características das partículas. O efeito da concentração de quitosana na estrutura e tamanho de partículas foi analisado. Maiores concentrações levaram a viscosidades mais elevadas, impedindo a agregação das micelas e formando partículas menores. (III) No terceiro estudo, nanopartículas foram obtidas pela complexação eletrostática de gelana e quitosana. Os efeitos da razão de concentração de cada polissacarídeo, do tempo de estocagem a 25 °C e da presença de um surfactante nãoiônico (polissorbato) no tamanho, carga e quantidade de partículas formadas foram avaliados. Devido à menor densidade de carga e flexibilidade da gelana, maior quantidade deste polissacarídeo foi necessária para obtenção de partículas neutras. De forma geral, as partículas apresentaram aumento de tamanho ao longo das primeiras 100 horas após o preparo e não foram observadas mudanças significativas das propriedades das partículas devido à adição de surfactante. O método de preparo das amostras também foi estudado. Partículas preparadas pela mistura das soluções de polissacarídeos em dois passos foram consideravelmente maiores que as preparadas pela mistura em uma única etapa. Este trabalho confirmou a possibilidade de formação de nanopartículas promissoras para a encapsulação de bioativos em alimentos a partir da associação de biopolímeros e surfactantes, cujas propriedades poderiam ser moduladas em função da composição e condições de processo
Abstract: Nanoparticles are promising vehicles for bioactive delivery, but their potential has not been fully explored by the food industry. This work studied the formation of nanoparticles by self-assembly of surfactants, polysaccharide-surfactant association, and electrostatic complexes formed by different polysaccharides, especially chitosan and gellan gum. The knowledge of molecular interactions and the variables that affect particle formation allows predicting and controlling the properties of nanoparticles. These interactions depend on the characteristics of each macromolecule such as conformation, charge density and flexibility, which are affected by the physicol-chemical properties of the solution, such as pH, ionic strength and temperature. This work was divided in three parts: (I) Firstly it was studied the behaviour of each polysaccharide alone. The influence of the pH and temperature on the rheological properties and structural conformation of the pure gellan and chitosan samples was determined. Gellan aggregation was more strongly affected by such variables than chitosan. (II) In the second part, nanoparticles were obtained by polysorbate-chitosan association. The effect of the length of surfactant tail and the solution pH on the particle properties was studied by dynamic light scattering, rheological and conductivity measurements and polarizing microscopy. The size and structure of nanoparticles composed by the shorter surfactant were more appropriated to chitosan assembly. The pH (6.7 or 3.0) did not affect significantly the particle properties. The effects of chitosan concentration on particle structure and size were studied. Greater chitosan concentration led to smaller particles due to the increase in viscosity values which prevented micelles aggregation. (III) In the third study nanoparticles were produced by electrostatic complexation of chitosan and gellan gum. Particle size, charge density, stability and complexes number were evaluated as a function of polysaccharide concentration, chitosan:gellan ratio and the presence of a non-ionic surfactant. Due to the stiffness and low charge density of gellan gum, a greater amount of such polysaccharide was necessary to obtain neutral particles. Overall particles showed an increase in size during 100 hours of storage at 25 °C, but no significant changes on particle properties were observed due to surfactant addition. The methodology of particle preparation was also evaluated. Particles prepared by 2 mixing steps were markedly larger than those prepared by mixing polysaccharides in a single step (all together). This work showed that it is possible to produce nanoparticles with promising application on bioactive delivery by biopolymer-surfactant association, since their properties could be modulated as a function of composition and process conditions
Doutorado
Engenharia de Alimentos
Doutor em Engenharia de Alimentos
Rayasam, Revanth. "Oral delivery of insulin for diabetes therapy : the design, fabrication and characterisation of a modified-chitosan based nanoparticle system". Thesis, Kingston University, 2017. http://eprints.kingston.ac.uk/41955/.
Texto completoMalli, Sophia. "Formulations multifonctionnelles pour le traitement des infections parasitaires cutanéo-muqueuses". Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS043.
Texto completoThis project aims at developing new therapeutic strategies against parasitic muco-cutaneous infections such as urogenital trichomonosis and cutaneous leishmaniasis which still represents a major health problem worldwide.Unfortunately, metronidazole (MTZ) is a first-line systemic treatment for urogenital trichomoniasis that causes resistance and side effects. We have thus developed new strategies by acting on both the pharmacological and the physical mechanisms of Trichomonas vaginalis infection. After a successfull increase of the apparent solubility of MTZ in water using a methylated -cyclodextrin, we formulated it in a thermosensitive and mucoadhesive hydrogel composed of pluronic® F127 and a cationic and mucoadhesive biopolymer, chitosan. This formulation is specifically adapted for topical application providing a control of MTZ release and reduction of its systemic passage through the vaginal mucosa.Then, the ability of the high viscosity hydrogel to immobilize T. vaginalis was investigated by video-microscopy. Monitoring the trajectories of each parasite by multiple particle tracking showed the ability of the hydrogel alone or in combination with chitosan to completely immobilize T. vaginalis and to inhibit parasite attachment to the mucosa. These evaluations were performed on mice experimental model. However, chitosan alone did not allow parasite immobilization and did not show any anti-T. vaginalis activity. In this context, we were inspired by previous works conducted by our team on the development of formulations based on chitosan, and more particularly nanoparticles (NPs) composed of poly(isobutylcyanoacrylates) coated with chitosan. These NPs have their own trichomonacidal activity, even without adding active substances, while NPs without chitosan were inactive. Investigated of the mechanism of the activity showed better internalization of NPs when coated with chitosan. These NPs caused drastic morphological alterations on the parasite membrane. This activity could be due to the electrostatic interaction between negatively charged T. vaginalis surface and cationic chitosan coated NPs.In order to broaden the applications of these NPs to other parasites, we were interested in evaluating the anti-L. major activity of NPs coated or not with chitosan. Indeed, chitosan known for its healing properties could be particularly adapted for this pathology. We thus showed in vitro and in vivo that NPs coated with chitosan had intrinsic anti-L. major activity without adding any drug. In a second step, we decided to design chitosan elongated particles and to evaluate their anti-leishmanial activity. These particles called "platelets" are composed of chitosan hydrophobically-modified with oleic acid and cyclodextrin in water. This strategy could be interesting to improve the interaction of platelets with the L. major membrane, as these parasites had also non-spherical morphology. The histological and immunohistochemical results of skin lesions showed a significant decrease in inflammatory granuloma and a reduction in parasitic load compared with amphotericin B alone, used as a reference.In conclusion, during this thesis, several formulations were developed and showed biological activities by acting on pharmacological and/or physical mechanisms of the parasites
Bissonnette, Caroline. "Biodegradable Polylactide-co-Glycolide-Chitosan Janus Nanoparticles for the Local Delivery of Multifaceted Drug Therapy for Oral Squamous Cell Carcinoma Chemoprevention". The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1590751959128008.
Texto completoYoshida, Jony Takao. "Nanopartículas de quitosana como veículo de vacinação contra a hepatite B via nasal". Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/9/9134/tde-15032013-163603/.
Texto completoThe nasal vaccination is not invasive since its do not require needles for your application and your administration for is easy, thus the immunization via nasal route could be an alternative to intramuscular immunizations. Furthermore, the nasal mucosa has several characteristics like highly vascularized surface area available for absorption of antigen that could elicited the mucosal immune response caused by the competents cell available on the mucosal tissue. Nevertheless, other methods can be employed to improve absorption and availability of antigens to the mucosa, such as the use of nanoparticles of chitosan. Chitosan is a biopolymer product of deacetylation reaction of chitin, that has as main characteristic, the moldability, which enables the production of nanoparticles and its cationic property which allows its binding to proteins and also to the mucosa, which would lead to higher rates of absorption of antigens through the nasal mucosa. Thus, this work investigated the immunogenicity of the administration nanoparticles of chitosan with the surface anti-gen of hepatitis B (HBsAg) via the nasal mucosa in mice, which show levels of IgA in nasal lavages and serum IgG, as well as cytokines such as TNF-α released by RAW 264.7 cells of mice.
Cover, Natasha Faith. "A Novel Device and Nanoparticle-Based Approach for Improving Diagnosis and Treatment of pelvic Inflammatory Disease". Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4020.
Texto completoLibros sobre el tema "Chitosan nanoparticle"
Porous structure and adsorption behaviours of chitosan. Hauppauge, N.Y: Nova Science Publishers, 2010.
Buscar texto completoGupta, Abhishek. Chitosan Nanoparticles. Arcler Education Inc, 2017.
Buscar texto completoGama, Miguel, Paula Pereira, Vera Carvalho y Reinaldo Ramos. Chitosan Nanoparticles for Biomedical Applications. Nova Science Publishers, Inc., 2010.
Buscar texto completoCapítulos de libros sobre el tema "Chitosan nanoparticle"
Lee, Dongwon y Shyam S. Mohapatra. "Chitosan Nanoparticle-Mediated Gene Transfer". En Methods in Molecular Biology, 127–40. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-237-3_8.
Texto completode Oliveira, André Luiz Barros, Francisco Thálysson Tavares Cavalcante, Katerine da Silva Moreira, Paula Jéssyca Morais Lima, Rodolpho Ramilton de Castro Monteiro, Bruna Bandeira Pinheiro, Kimberle Paiva dos Santos y José Cleiton Sousa dos Santos. "Chitosan Nanoparticle: Alternative for Sustainable Agriculture". En Nanomaterials and Nanotechnology, 95–132. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6056-3_4.
Texto completoRevathi, G., S. Elavarasi y K. Saravanan. "Antidiabetic Activity of Drug Loaded Chitosan Nanoparticle". En Drug Development for Cancer and Diabetes, 249–62. Includes bibliographical references and index.: Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780429330490-21.
Texto completoJain, Shardool y Mansoor Amiji. "Target-Specific Chitosan-Based Nanoparticle Systems for Nucleic Acid Delivery". En Chitosan-Based Systems for Biopharmaceuticals, 275–99. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781119962977.ch16.
Texto completoVong, Long Binh, Nhu-Thuy Trinh, Van Toi Vo y Dai-Nghiep Ngo. "Chitosan Oligosaccharide-Based Nanoparticle Delivery Systems for Medical Applications". En Chitooligosaccharides, 157–71. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92806-3_10.
Texto completoMalhotra, Meenakshi, Catherine Tomaro-Duchesneau, Shyamali Saha y Satya Prakash. "Intranasal Delivery of Chitosan–siRNA Nanoparticle Formulation to the Brain". En Methods in Molecular Biology, 233–47. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0363-4_15.
Texto completoAndersen, Morten Østergaard, Kenneth Alan Howard y Jørgen Kjems. "RNAi Using a Chitosan/siRNA Nanoparticle System: In Vitro and In Vivo Applications". En Methods in Molecular Biology™, 77–86. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-295-7_6.
Texto completoAslan, Burcu, Hee Dong Han, Gabriel Lopez-Berestein y Anil K. Sood. "Chitosan Nanoparticles". En Encyclopedia of Nanotechnology, 525–31. Dordrecht: Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-94-017-9780-1_71.
Texto completoPeroulis, Dimitrios, Prashant R. Waghmare, Sushanta K. Mitra, Supone Manakasettharn, J. Ashley Taylor, Tom N. Krupenkin, Wenguang Zhu et al. "Chitosan Nanoparticles". En Encyclopedia of Nanotechnology, 427–33. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-9751-4_71.
Texto completoAkbuga, Julide, Suna Ozbas-Turan y Ceyda Ekentok. "Chitosan Nanoparticles in Gene Delivery". En Percutaneous Penetration Enhancers Chemical Methods in Penetration Enhancement, 337–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-47862-2_22.
Texto completoActas de conferencias sobre el tema "Chitosan nanoparticle"
Musa, Nafisah y Tin Wui Wong. "Nanoparticles-in-soft microagglomerates as oral colon-specific cancer therapeutic vehicle". En 3rd International Congress of Engineering Sciences and Technology. Facultad de Ciencias de la Ingeniería y Tecnología, 2021. http://dx.doi.org/10.37636/recit.cicitec21.1.
Texto completoCetin, Barbaros, Serdar Taze, Mehmet D. Asik y S. Ali Tuncel. "Microfluidic Device for Synthesis of Chitosan Nanoparticles". En ASME 2013 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/fedsm2013-16349.
Texto completoFithriyah, Nurul Hidayati y Erdawati. "Mechanical properties of paper sheets coated with chitosan nanoparticle". En 4TH INTERNATIONAL CONFERENCE ON MATHEMATICS AND NATURAL SCIENCES (ICMNS 2012): Science for Health, Food and Sustainable Energy. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4868781.
Texto completoKim, Song-Bae y Seung-Chan Lee. "Iron Oxide Nanoparticle-Chitosan Composites for Phosphate Removal from Water". En The 3rd World Congress on Recent Advances in Nanotechnology. Avestia Publishing, 2018. http://dx.doi.org/10.11159/icnei18.103.
Texto completo"Synthesis of Aloe Vera Loaded Chitosan Nanoparticle with Ionic Gelling Method". En 2019 Scientific Meeting on Electrical-Electronics & Biomedical Engineering and Computer Science (EBBT). IEEE, 2019. http://dx.doi.org/10.1109/ebbt.2019.8742077.
Texto completo"Antifungal Activities of Chitosan and Nanoparticle Derivatives under Various pH Conditions". En International Conference on Advances in Science, Engineering, Technology and Natural Resources. International Academy of Engineers, 2016. http://dx.doi.org/10.15242/iae.iae1116413.
Texto completoMovahedi, Sara, Farshad Bahramian y Fatemeh Ghorbani-Bidkorbeh. "An experimental and numerical study of microfluidic preparation of chitosan nanoparticle". En 2022 29th National and 7th International Iranian Conference on Biomedical Engineering (ICBME). IEEE, 2022. http://dx.doi.org/10.1109/icbme57741.2022.10052866.
Texto completoJiang, Dahai, Lingegowda S. Mangala, Hongyu Wang, Sherry Wu, Lokesh G. Rao, Cristian Rodriguez-Aguayo, Sunila Pradeep, David E. Volk, Gabriel Lopez-Berestein y Anil K. Sood. "Abstract 4468: Tumor vasculature targeting using cell-specific thioaptamer decorated chitosan nanoparticle". En Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-4468.
Texto completoRozana, R., Y. Yulizar, A. Saefumillah y D. O. B. Apriandanu. "Synthesis, characterization and in vitro release study of efavirenz-loaded chitosan nanoparticle". En PROCEEDINGS OF THE 5TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0007923.
Texto completoWahab, Malik Abdul y E. Yegan Erdem. "Chitosan Coated Iron-Oxide Nanoparticle Synthesis Using a Droplet Based Microfluidic Reactor". En 2019 20th International Conference on Solid-State Sensors, Actuators and Microsystems & Eurosensors XXXIII (TRANSDUCERS & EUROSENSORS XXXIII). IEEE, 2019. http://dx.doi.org/10.1109/transducers.2019.8808426.
Texto completoInformes sobre el tema "Chitosan nanoparticle"
Yoncheva, Krassimira. Benefits and Perspectives of Nanoparticles Based on Chitosan and Sodium Alginate. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, marzo de 2020. http://dx.doi.org/10.7546/crabs.2020.03.01.
Texto completoOliveira, Mariana, Vívian Souza, Guilherme Tavares, Rodrigo Fabri y Ana Carolina Apolônio. Effects of antibiotic-loaded chitosan nanoparticles against resistant bacteria: a systematic review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, junio de 2021. http://dx.doi.org/10.37766/inplasy2021.6.0069.
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