Thematische Bibliographien / Stimuli-responsive release

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Auswahl der wissenschaftlichen Literatur zum Thema „Stimuli-responsive release“

Autor: Grafiati

Veröffentlicht am 7. Juni 2025

Zuletzt aktualisiert am 2. August 2025

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Zeitschriftenartikel zum Thema "Stimuli-responsive release"

Okano, Teruo, and Yasuhisa Sakurai. "Stimuli-responsive drug release system." Kobunshi 39, no. 9 (1990): 662–65. http://dx.doi.org/10.1295/kobunshi.39.662.

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Wells, Carlos M., Michael Harris, Landon Choi, Vishnu Priya Murali, Fernanda Delbuque Guerra, and J. Amber Jennings. "Stimuli-Responsive Drug Release from Smart Polymers." Journal of Functional Biomaterials 10, no. 3 (2019): 34. http://dx.doi.org/10.3390/jfb10030034.

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Over the past 10 years, stimuli-responsive polymeric biomaterials have emerged as effective systems for the delivery of therapeutics. Persistent with ongoing efforts to minimize adverse effects, stimuli-responsive biomaterials are designed to release in response to either chemical, physical, or biological triggers. The stimuli-responsiveness of smart biomaterials may improve spatiotemporal specificity of release. The material design may be used to tailor smart polymers to release a drug when particular stimuli are present. Smart biomaterials may use internal or external stimuli as triggering m

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An, Xueqin. "Stimuli-responsive liposome and drug release." SCIENTIA SINICA Chimica 45, no. 4 (2015): 340–49. http://dx.doi.org/10.1360/n032014-00252.

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Peng, Xingxing, Yanfei Liu, Feicheng Peng, et al. "Aptamer-controlled stimuli-responsive drug release." International Journal of Biological Macromolecules 279 (November 2024): 135353. http://dx.doi.org/10.1016/j.ijbiomac.2024.135353.

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Liu, Zhuang, Xiao-Jie Ju, Wei Wang, et al. "Stimuli-Responsive Capsule Membranes for Controlled Release in Pharmaceutical Applications." Current Pharmaceutical Design 23, no. 2 (2017): 295–301. http://dx.doi.org/10.2174/1381612822666161021141429.

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Background: In conventional drug delivery, the drug concentration in the blood raises once the drug taken, and then peaks and declines. Since each drug has a level above which it is toxic and another level below which it is ineffective, the drug concentration in a patient at a particular time depends on compliance with the prescribed routine. Methods: To achieve more effective efficacy and fewer side effects of drugs, the drug carriers with desirable dosing and controllable release property of drugs are highly desired. Stimuli-responsive capsules with smart gating membranes or hydrogel-based m

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Sheng, Yan, Jiaming Hu, Junfeng Shi, and Ly James Lee. "Stimuli-responsive Carriers for Controlled Intracellular Drug Release." Current Medicinal Chemistry 26, no. 13 (2019): 2377–88. http://dx.doi.org/10.2174/0929867324666170830102409.

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Background: Stimuli-responsive carriers are a class of drug delivery systems which can change their physicochemical properties and/or structural conformations in response to specific stimuli. Although passive and active drug targeting has proved to reduce the side effects to normal cells, controlled intracellular drug release should be included in drug carriers to enhance the bioavailability of drugs at the disease site. Methods: This review focuses on several recent advances in the development of stimuli-responsive carriers for spatially and temporally controlled release of therapeutic agents

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Li, Song, Wengang Li, and Niveen M. Khashab. "Stimuli responsive nanomaterials for controlled release applications." Nanotechnology Reviews 1, no. 6 (2012): 493–513. http://dx.doi.org/10.1515/ntrev-2012-0033.

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AbstractThe controlled release of therapeutics has been one of the major challenges for scientists and engineers during the past three decades. Coupled with excellent biocompatibility profiles, various nanomaterials have showed great promise for biomedical applications. Stimuli-responsive nanomaterials guarantee the controlled release of cargo to a given location, at a specific time, and with an accurate amount. In this review, we have combined the major stimuli that are currently used to achieve the ultimate goal of controlled and targeted release by “smart” nanomaterials. The most heavily ex

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Štular, Danaja, Matic Šobak, Mohor Mihelčič, et al. "Proactive Release of Antimicrobial Essential Oil from a “Smart” Cotton Fabric." Coatings 9, no. 4 (2019): 242. http://dx.doi.org/10.3390/coatings9040242.

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Two temperature and pH responsive submicron hydrogels based on poly(N- methylenebisacrylamide), chitosan and β-cyclodextrines (PNCS/CD hydrogel) with varying poly(N-isopropylacrylamide) to chitosan ratios were synthesized according to a simplified procedure, reflecting improved stimuli responsive properties and excellent bio-barrier properties, granted by incorporated chitosan. Hydrogels were applied to cotton-cellulose fabric as active coatings. Subsequently, antimicrobially active savory essential oil (EO) was embedded into the hydrogels in order to develop temperature- and pH-responsive cot

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Malachowski, Kate, Joyce Breger, Hye Rin Kwag, et al. "Stimuli-Responsive Theragrippers for Chemomechanical Controlled Release." Angewandte Chemie 126, no. 31 (2014): 8183–87. http://dx.doi.org/10.1002/ange.201311047.

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Malachowski, Kate, Joyce Breger, Hye Rin Kwag, et al. "Stimuli-Responsive Theragrippers for Chemomechanical Controlled Release." Angewandte Chemie International Edition 53, no. 31 (2014): 8045–49. http://dx.doi.org/10.1002/anie.201311047.

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Dissertationen zum Thema "Stimuli-responsive release"

Cradduck, Emily. "Sonochemically-generated stimuli-responsive polymeric microspheres for controlled release." Thesis, University of Bath, 2018. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.760967.

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Ultrasonic irradiation at the interface between a protein solution and a gas or non-aqueous liquid facilitates the formation of protein-shelled microspheres by a phenomenon of simultaneous emulsification and encapsulation. Sonochemically-generated hollow proteinaceous microspheres have been widely reported in the literature, with a range of current and potential applications including ultrasound contrast agents, drug delivery vehicles and nutrient carriers in the food processing industry. This project builds upon preliminary investigations conducted in the field into the use of synthetic polym

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Zhou, Jun. "Stimuli-responsive microgels for self-assembled crystalline structures and controlled drug release." Thesis, University of North Texas, 2009. https://digital.library.unt.edu/ark:/67531/metadc11001/.

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Tissue response to PNIPAM and HPC nanoparticles has been studied by implantation method. The results suggest that both PNIAPM and HPC nanoparticles possess good biocompatibility and they may serve as a good carrier for the applications of controlled delivery. Rheological properties of dispersions of IPN microgels composed of PNIPAM and PAAc have been studied. It is found that the IPN microgel dispersion can undergo a sol-gel transition at temperature above 33°C. In vivo drug release experiments suggest that the gelation procedure creates a diffusion barrier and thus leads to slow release. An e

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Zhou, Jun Hu Zhibing. "Stimuli-responsive microgels for self-assembled crystalline structures and controlled drug release." [Denton, Tex.] : University of North Texas, 2009. http://digital.library.unt.edu/permalink/meta-dc-11001.

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Giri, Supratim. "Mesoporous silica nanomaterials and magnetic nanoparticles based stimuli-responsive controlled-release delivery systems." [Ames, Iowa : Iowa State University], 2008.

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Chikh, Alard Ibaa. "DEVELOPMENT OF NOVEL MULTI-RESPONSIVE MATERIALS CHARACTERIZED BY POTENTIAL CONTROLLED RELEASE PROPERTIES." Doctoral thesis, Universite Libre de Bruxelles, 2018. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/279147.

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With the emergence of novel and more effective drug therapies, increased importance is being placed upon the methods by which these drugs are being delivered to the body. In conventional drug delivery systems, there is very little control over the release of drug. The effective concentration at the target site can be achieved by intermittent administration of grossly excessive doses, which, often results in constantly, unpredictable variations in plasma concentrations, with the risk of reaching levels below or above the therapeutic range leading to marked side effects. A plethora of formulatio

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Llopis, Lorente Antoni. "Enzyme-functionalized hybrid mesoporous nanodevices for sensing, controlled release and molecular communication." Doctoral thesis, Universitat Politècnica de València, 2019. http://hdl.handle.net/10251/117612.

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[ES] La presente tesis doctoral titulada "Nanodispositivos mesoporosos híbridos funcionalizados con enzimas para detección, liberación controlada y comunicación molecular" se centra en el diseño, preparación, caracterización y evaluación de distintos nanodispositivos híbridos orgánico-inorgánicos utilizando como soporte nanopartículas tipo Janus de oro y sílice mesoporosa, que se equipan con enzimas, especies fluorescentes y puertas moleculares. Como conclusión general, los estudios realizados muestran que la incorporación de enzimas sobre nanopartículas permite introducir funciones de recono

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Sanson, Charles. "Vésicules polymères biorésorbables et stimulables pour des applications en vectorisation." Thesis, Bordeaux 1, 2010. http://www.theses.fr/2010BOR13985/document.

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L’auto-assemblage de copolymères à blocs amphiphiles est un outil puissant de la chimie supramoléculaire pour la conception de nano-objets complexes et fonctionnels. Dans ces travaux de thèse, l’étude approfondie d’un copolymère à blocs « hybride » synthétique-b-peptidique poly(triméthylène carbonate)-b-poly(acide glutamique) pour des applications de vectorisation a été menée. Des morphologies vésiculaires, obtenues par auto-assemblage en voie « co-solvant » et présentant une grande stabilité ainsi qu’un caractère stimulable ont été mises en évidence. Une transition inédite en température, par

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de, Luis Fernández Beatriz. "Development of enzyme-functionalized hybrid mesoporous nanodevices for advanced chemical communication." Doctoral thesis, Universitat Politècnica de València, 2021. http://hdl.handle.net/10251/171506.

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Tesis por compendio<br>[ES] La presente tesis doctoral se centra en el diseño, síntesis y caracterización de varios nanodispositivos híbridos orgánico-inorgánicos, utilizando como soporte nanopartículas de sílice mesoporosa equipadas con enzimas y puertas moleculares, los cuales muestran capacidades comunicativas además de la evaluación de diferentes estrategias de comunicación. El primer capítulo incluye un resumen de diferentes conceptos sobre los que se fundamentan los estudios realizados tales como nanotecnología, materiales de sílice mesoporosa, materiales con puertas moleculares que

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Li, Song. "Stimuli-Responsive Materials for Controlled Release Applications." Diss., 2015. http://hdl.handle.net/10754/552156.

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The controlled release of therapeutics has been one of the major challenges for scientists and engineers during the past three decades. To address this outstanding problem, the design and fabrication of stimuli-responsive materials are pursued to guarantee the controlled release of cargo at a specific time and with an accurate amount. Upon applying different stimuli such as light, magnetic field, heat, pH change, enzymes or redox, functional materials change their physicochemical properties through physical transformation or chemical reactions, allowing the release of payload agents on demand.

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Chia-WeiWang and 王嘉瑋. "Polymeric Micelles with Triple Stimuli-Responsive characteristics for Controlled Drug Release." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/3h6e84.

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Buchteile zum Thema "Stimuli-responsive release"

Hashizume, Mineo, and Kazutoshi Iijima. "Media-Responsive Swelling and Material Release Properties of Polysaccharide Composite Films." In Stimuli-Responsive Interfaces. Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-2463-4_15.

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Trehan, Karan, Muskaan Saini, and Shubham Thakur. "Stimuli-Responsive Material in Controlled Release of Drug." In Engineered Biomaterials. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-6698-1_18.

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Kudaibergenov, S. E., G. S. Tatykhanova, and Zh E. Ibraeva. "Immobilization and Controlled Release of Bioactive Substances from Stimuli-Responsive Hydrogels." In Biodefence. Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-94-007-0217-2_19.

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Du, Xuezhong. "Biomacromolecule-Gated Mesoporous Silica Drug Delivery Systems for Stimuli-Responsive Controlled Release." In Advanced Theranostic Materials. John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118998922.ch3.

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Salve, Rajesh, Pramod Kumar, Kavita R. Gajbhiye, Rajnigandha A. Shende, Bhushan P. Chaudhari, and Virendra Gajbhiye. "Mesoporous silica nanoparticles-based stimuli-triggered drug release systems." In Stimuli-Responsive Nanocarriers. Elsevier, 2022. http://dx.doi.org/10.1016/b978-0-12-824456-2.00007-2.

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Sayed-Pathan, Nida Irfan, Rajesh S. Jadon, Kavita R. Gajbhiye, and Virendra Gajbhiye. "Tailored gold nanoparticles for improved control over drug release." In Stimuli-Responsive Nanocarriers. Elsevier, 2022. http://dx.doi.org/10.1016/b978-0-12-824456-2.00008-4.

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Moudgil, Aliesha, Rajnigandha A. Shende, Anil T. Pawar, Kavita R. Gajbhiye, Virendra Gajbhiye, and Bhushan P. Chaudhari. "Quantum dots based vehicles for controlled drug release in conjunction with bio-imaging." In Stimuli-Responsive Nanocarriers. Elsevier, 2022. http://dx.doi.org/10.1016/b978-0-12-824456-2.00016-3.

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An, Xueqin, and Rijun Gui. "Stimuli-responsive liposome and control release drug." In Nanostructures for Drug Delivery. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-323-46143-6.00028-2.

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Zeybek, Mehmet Can, Egemen Acar, and Gozde Ozaydin-Ince. "Stimuli-Responsive Polymers with Tunable Release Kinetics." In Switchable Bioelectronics. Jenny Stanford Publishing, 2020. http://dx.doi.org/10.1201/9781003056003-3.

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Madane, Mukul P., Prajwal R. Aher, Manoj Somvanshi, et al. "Stimuli responsive polymers used in drug delivery systems." In Targeted Therapies and Drug Delivery Systems: A Multidisciplinary Perspective. Deep Science Publishing, 2025. https://doi.org/10.70593/978-93-7185-674-4_2.

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Smart polymers, frequently referred to as stimuli-responsive polymers that are they have evolved into a unique new material for the design of advanced drug delivery system. These polymers undergo fast, reversible physicochemical change in rejoinder to external impetuses redox potential, and individual biomolecules. Stimuli-responsive polymers can transform to responsive drug carriers that can be triggered using external environmental stimuli for on-site, controlled, and demand release of a drug, cumulative beneficial value while dropping systemic side effects. This chapter describes the numero

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Konferenzberichte zum Thema "Stimuli-responsive release"

Glangchai, Luz Cristal S., Li Shi, and Krishnendu Roy. "Nano-Imprint Fabrication of Injectable, Stimuli-Responsive Drug Delivery Vehicles." In ASME 4th Integrated Nanosystems Conference. ASMEDC, 2005. http://dx.doi.org/10.1115/nano2005-87069.

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Nanofabrication techniques are developed to create well-defined and characterized drug delivery devices that overcome the limitations of current methods. Our approach is to use novel, top-down nano-fabrication technologies, including thermal nano-imprinting and step-and flash imprint lithography (S-FIL), coupled with stimuli-responsive polymer membranes to develop injectable nanocontainers that can release drug only in response to specific physiological signals at specific cellular locations.

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Zhang, Wujie, Kyle Gilstrap, Laying Wu, et al. "Controlled Release and Intracellular Delivery of Small Molecules Using Thermally Responsive Pluronic F127-Chitosan Nanocapsules." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53517.

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Nanoscale particulate systems have been studied as the delivery vehicle of various drugs and therapeutic agents for decades with promising outcomes. Recently, nano-particulate systems that are responsive to one or more environmental stimuli (such as temperature, pH, and electromagnetic field) are attracting increasing attention because they allow drug delivery and release to be done in a more controllable fashion [1]. The thermally (temperature) responsive nanoparticles are of particular interest to many researchers because the temperature controlled release of the encapsulated drug can be con

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Alsmaeil, Ahmed Wasel, Mohamed Amen Hammami, Amr Ismail Abdel-Fattah, Mazin Yousef Kanj, and Emmanuel P. Giannelis. "From Biomedical to Oil Industry: Promising Mesoporous Materials for Oil Field Applications." In SPE Europec featured at 82nd EAGE Conference and Exhibition. SPE, 2021. http://dx.doi.org/10.2118/205175-ms.

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Abstract Developing nanocarriers deliver molecules to targeted locations has received widespread attention in different fields ranging from biomedical to oil and gas industries. Mesoporous Silica Nanoparticles (MSNs), where the pore size diameter ranges from 2-50 nm, have become attractive in many fields including biomedicine. One advantage is the ability to control the size, morphology of the particles, and the internal and external surfaces properties which enable encapsulating molecules of different size and charges. Moreover, it is possible to functionalize the pores and the surface of the

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