Auswahl der wissenschaftlichen Literatur zum Thema „On-Demand release“
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Zeitschriftenartikel zum Thema "On-Demand release"
Field, Rachel D., Margaret A. Jakus, Xiaoyu Chen, Kelia A. Human, Xuanhe Zhao, Parag V. Chitnis und Samuel K. Sia. „Ultrasound-responsive hydrogel microcapsules for on-demand drug release“. Journal of the Acoustical Society of America 154, Nr. 4_supplement (01.10.2023): A279. http://dx.doi.org/10.1121/10.0023522.
Der volle Inhalt der QuelleWood, Jonathan. „Coatings release corrosion inhibitors on demand“. Materials Today 8, Nr. 10 (Oktober 2005): 10. http://dx.doi.org/10.1016/s1369-7021(05)71113-5.
Der volle Inhalt der QuelleVakil, Anand Utpal, Maryam Ramezani und Mary Beth B. Monroe. „Magnetically Actuated Shape Memory Polymers for On-Demand Drug Delivery“. Materials 15, Nr. 20 (18.10.2022): 7279. http://dx.doi.org/10.3390/ma15207279.
Der volle Inhalt der QuelleSingh, Baljinder, Kibeom Kim und Myoung-Hwan Park. „On-Demand Drug Delivery Systems Using Nanofibers“. Nanomaterials 11, Nr. 12 (16.12.2021): 3411. http://dx.doi.org/10.3390/nano11123411.
Der volle Inhalt der QuelleGupta, R. K., F. Mirza, M. U. F. Khan und J. Esquivel. „Aluminum containing Na2CrO4: Inhibitor release on demand“. Materials Letters 205 (Oktober 2017): 194–97. http://dx.doi.org/10.1016/j.matlet.2017.06.080.
Der volle Inhalt der QuelleWang, Joseph. „On-Demand Electrochemical Release of Nucleic Acids“. Electroanalysis 13, Nr. 8-9 (Mai 2001): 635–38. http://dx.doi.org/10.1002/1521-4109(200105)13:8/9<635::aid-elan635>3.0.co;2-j.
Der volle Inhalt der QuelleChen, Menglin, Yan-Fang Li und Flemming Besenbacher. „Electrospun Nanofibers-Mediated On-Demand Drug Release“. Advanced Healthcare Materials 3, Nr. 11 (30.05.2014): 1721–32. http://dx.doi.org/10.1002/adhm.201400166.
Der volle Inhalt der QuelleFallahi, Hedieh, Haotian Cha, Hossein Adelnia, Yuchen Dai, Hang Thu Ta, Sharda Yadav, Jun Zhang und Nam-Trung Nguyen. „On-demand deterministic release of particles and cells using stretchable microfluidics“. Nanoscale Horizons 7, Nr. 4 (2022): 414–24. http://dx.doi.org/10.1039/d1nh00679g.
Der volle Inhalt der QuelleEslami, Parisa, Martin Albino, Francesca Scavone, Federica Chiellini, Andrea Morelli, Giovanni Baldi, Laura Cappiello et al. „Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery“. Nanomaterials 12, Nr. 3 (18.01.2022): 303. http://dx.doi.org/10.3390/nano12030303.
Der volle Inhalt der QuelleOnuora, Sarah. „Implanted ‘smart’ cells release biologic drugs on demand“. Nature Reviews Rheumatology 17, Nr. 11 (29.09.2021): 643. http://dx.doi.org/10.1038/s41584-021-00705-z.
Der volle Inhalt der QuelleDissertationen zum Thema "On-Demand release"
Anderson, Stacey N. „Carbon Monoxide on Demand: Light-Induced CO Release of Flavonols“. DigitalCommons@USU, 2018. https://digitalcommons.usu.edu/etd/7388.
Der volle Inhalt der QuelleSinha, Piyush M. „Nanoengineered implantable devices for controlled drug delivery“. The Ohio State University, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=osu1115138930.
Der volle Inhalt der QuelleKovacik, P., M. Soltys und F. Stepanek. „Core-shell Structured Composite Silica Micro- and Nanoparticles with Ability Release a De fined Quantity „on Demand““. Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35571.
Der volle Inhalt der QuelleChiu, Stanley Kai Him. „A hybrid P2P pre-release distribution framework for flash crowd avoidance in P2P video on demand streaming“. Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/4067.
Der volle Inhalt der QuelleSanchez, Velasquez Camilo. „Conception rationnelle d'un revêtement antimicrobien contrôlable basé sur des réseaux de nanofils d'argent : Une étude combinée de la science des matériaux et du marketing“. Electronic Thesis or Diss., Université Grenoble Alpes, 2024. http://www.theses.fr/2024GRALI040.
Der volle Inhalt der QuelleRelease-based antimicrobial coatings have been intensively investigated due to their potential to prevent bacterial infections via contaminated surfaces. However, owing to their uncontrollable burst release profile of antimicrobial payloads, their action may cause systemic toxicity in human cells and the environment, as well as rapid depletion of the antimicrobial pre-loaded compounds until the released quantities drop below bacterial sub-inhibitory concentrations, translating into poor biocidal activity over time. These limitations hinder their widespread application and emphasize the need for engineering strategies to develop novel antimicrobial coatings that incorporate controllable release systems. One way to address these shortcomings is with the development of on-demand triggered release systems. These platforms incorporate a stimulus-responsive material that undergoes morphological changes in response to specific stimuli allowing subsequent controllable release of antimicrobial payloads.This study primarily focuses on developing a comprehensive, step-by-step, rational design of a Joule-heating-triggered on-demand silver release platform based on coated silver nanowire (AgNW) networks. We present, for the first time, the use of these sorts of systems as stimuli-responsive materials, taking advantage of the network degradation pathways via silver atom diffusion from the nanowire surface when subjected to electrical or thermal stress. Here, the release of silver induced by Joule heating serves as an antimicrobial agent for on-demand controlled antimicrobial activity. In addition, we propose the use of a multilayer architecture as a configurational design for AgNW-based antimicrobial coatings with the aim of fabricating a multifunctional antimicrobial platform. This architecture enables the incorporation of a heat-based release trigger and storage capabilities within a unified all-in-one platform. A first demonstration of the concept is presented where a stable AgNW network is used as a heater element, and a sacrificial AgNW network serves as an Ag atom reservoir.Nevertheless, although current advances in nanotechnology open up new opportunities for engineering novel antimicrobial platforms aimed at preventing and inhibiting bacteria growth, nanotechnology-based applications are often perceived by consumers as risky for health and associated with high rates of uncertainty, hindering acceptance and adoption. Concerns about uncontrolled use may lead to negative mental representations and associations among users, shaping their response to such technology. Therefore, there is a need for a deeper understanding of the consumer decision-making process and individual information processing toward nanomaterials-based antimicrobial applications.On this basis, in order to get an in-depth understanding of individuals' behavioural intentions towards nanotechnology-based innovations integrating antimicrobial features, either controllable or not controllable, this work develops an original and comprehensive conceptual framework based on the Technology Acceptance Model (TAM), but integrating more holistic and cognitive considerations and variables. Through this multifaceted model, the study aims to elucidate insight about the interplay of individual mental activity, in terms of mental imagery and memory associations, and the main variables of technology acceptance from TAM (perceived usefulness and perceived ease of use)
Kuan-WenWang und 王冠雯. „Near-Infrared Sensitive Microneedles for On-demand Controlled Release“. Thesis, 2012. http://ndltd.ncl.edu.tw/handle/84349717607950745490.
Der volle Inhalt der Quelle國立成功大學
化學工程學系碩博士班
100
Microneedle (MN) patches, combining the advantages of hypodermic needles and transdermal patches, have been proposed as a new tool for transdermal drug delivery, because of their efficient delivery and lack of pain. Drug release from current available polymeric microneedles mostly depends on the physical properties of polymer; however, little work involves microneedles which can provide “on demand” drug delivery. In this study, a polymeric microneedle patch, which is consisted of biodegradable polymer and photothermal nanoparticles, silica-coated lanthanum hexaboride nanoparticles (LaB6@SiO2 NPs), using near-infrared (NIR) light as a trigger for drug release was reported as a novel transdermal drug delivery device. The skin insertion tests showed that the developed polymeric microneedles were strong enough to insert into the epidermis layer (~150 m) of porcine cadaver skin. After encapsulating LaB6@SiO2 NPs within MNs, the resulting microneedles were shown to have NIR-sensitive property and melt by stimulation with NIR light due to the local heating of the NPs. In vitro triggered release study showed that the drug release from the microneedles can be easily and non-invasively controlled by the adjustment of the irradiation time and frequency of NIR light. The continuous irradiation test demonstrated the encapsulated drugs can be released from the melted microneedles, and the amount of released drug was increased with increasing the irradiation time. The intermittent irradiation test demonstrated the melting of NIR-sensitive MNs exhibit reversible and repeatable heating when exposed to NIR light, and the drug release occurred in a stepwise fashion, where LASER ON induced a steep increase in drug release, and LASER OFF permitted only very little drug from being released over a long period. The animal study demonstrated the feasibility of the NIR-sensitive MNs for in vivo applications. It is expected that the NIR-sensitive microneedles may provide a simple and convenient technology for transdermal delivery of heat-stable drugs (such as DNA vaccine, or anti-cancer drugs etc.) and facilitate the development of drug delivery system.
Yi, Yen-Tsai, und 易延才. „Programmable On-Demand Drug Release Device:An Electro-stimulated Approach“. Thesis, 2012. http://ndltd.ncl.edu.tw/handle/74315425608828124991.
Der volle Inhalt der Quelle國立臺灣大學
化學工程學研究所
100
Drug therapy efficacy depends on therapeutic concentrations of drugs at disease sites. An ideal controlled drug delivery device should safely contain a large quantity of drugs, release little or no drug in the “off ” state, be repeatedly switchable to the “on” state without mechanically disrupting the device, and can actively control release rates. In this thesis, an electro-stimulated membrane-based drug delivery device was developed to release drugs on demand. Drugs over a broad range of molecular weights (300-40000 Da) and different charge properties can be delivered by the same drug delivery approach. Ionic drug molecules were electrically ejected from polyelectrolyte hydrogels into bulk solution in vitro, the response time between electric stimulus and release amounts was fast, and without mechanically disrupting the membrane-based drug delivery device .We showed that the dose of drug delivered across drug delivery device could be tuned by different material of membrane, the strength of applied voltage, and the waveform of applied voltage, allowing for pulsatile drug delivery system of model drug, we could control the release rate at 1 order of magnitude (100~1000 ng / hr) during release processes. The system reported here has great potential for use in biomaterials, tissue engineering, implant technology, and biosensors for biomedical applications.
Chen, Pei-Ying, und 陳佩瑩. „Development of Magnetically-targeted Drug Carriers for On-demand NIR-triggered Drug Release“. Thesis, 2014. http://ndltd.ncl.edu.tw/handle/65877063051141724347.
Der volle Inhalt der Quelle國立清華大學
生醫工程與環境科學系
103
An ideal carrier for chemotherapeutics delivery shall contain features such as cancer cell-targeting capability, low cytotoxicity and efficient killing effect on multiple drug resistant cancer cells. In this study, we proposed a novel nano-sized drug delivery system combining the advantages of: (1) NIR-triggered drug release; (2) magnetically-targeting and (3) magnetic resonance imaging (MRI) contrast. The drug carrier is mainly composed of poly-lactic-co-glycolic acid (PLGA), which is a highly biocompatible, biodegradable and US Food and Drug Administration (FDA)-approved materials for clinical uses. PLGA is widely used for drug delivery applications due to its advantages on protecting drug from loss of activity, reducing drug-associated cytotoxicity and improving drug stability. By utilizing single emulsion method, we have successfully encapsulated doxorubicin (a chemotherapeutic drug), superparamagnetic iron oxide nanoparticles (SPIONs) and gold nanorods (Au NRs) within the hydrophobic core of PLGA nanoparticles (NP). The size and surface potential of the resultant AFP were approximately 200 nm and -24 mV respectively. The prepared DOX@SPIONs/Au NRs/ PLGA nanoparticle(DOX@SAPP)were successfully verified with the following features, including: (1) Hydrophilic nanoparticle surface: the DOX@SAPP were covered with hydrophilic polyethylene glycol (PEG), which helps maintaining particle stability and may extend its in vivo circulation time. (2) Capability of loading of various theranostic materials: The loading contents for doxorubicin, SPIONs were 3.77% and 5.8% respectively. By tuning the feeding amount of dodecane-Au NRs (O.D. value 33, 100 and 300), PLGA nanoparticles with different Au NRs loading content (1.31%, 2.73% and 8.19%) can be prepared. (3) Well colloidal stability: the prepared DOX@SAPP were stable up to 3 days in various mediums such as: water, PBS and 25% FBS DMEM medium. The size of DOX@SAPP was not changed significantly in PBS for 15 days. (4) Magnetically-assisted drug delivery and MRI contrast: the DOX@SAPP exhibits superparamagnetism with the saturation magnetization of 3.04 emu/g. The cellular uptake of DOX@SAPP was greatly enhanced by the presence of external magnetic field. Cell-number dependent T2-weighing MRI was demonstrated from the DOX@SAPP -uptake cancer cells. The DOX@SAPP enters cells via endocytosis which can avoid the “drug pumping out” effect by multiple drug resistant cancer cells. Under the irradiation of NIR, the Au NRs-mediated photothermal effect effectively triggered rapid drug release from DOX@SAPP Finally, the combined photothermal- and chemo- therapeutic effect was successfully demonstrated on astrocytoma tumor cell line (ALTS1C1), human breast cancer cells (MCF7) and its multiple drug resistant strain (ADR-MCF7).
Pitto-Barry, Anaïs, A. Lupan, C. Ellingford, A. A. A. Attia und Nicolas P. E. Barry. „New class of hybrid materials for detection, capture, and "on-demand" release of carbon monoxide“. 2018. http://hdl.handle.net/10454/15942.
Der volle Inhalt der QuelleCarbon monoxide (CO) is both a substance hazardous to health and a side product of a number of industrial processes, such as methanol steam reforming and large-scale oxidation reactions. The separation of CO from nitrogen (N2) in industrial processes is considered to be difficult because of the similarities of their electronic structures, sizes, and physicochemical properties (e.g., boiling points). Carbon monoxide is also a major poison in fuel cells because of its adsorption onto the active sites of the catalysts. It is therefore of the utmost economic importance to discover new materials that enable effective CO capture and release under mild conditions. However, methods to specifically absorb and easily release CO in the presence of contaminants, such as water, nitrogen, carbon dioxide, and oxygen, at ambient temperature are not available. Here, we report the simple and versatile fabrication of a new class of hybrid materials that allows capture and release of carbon monoxide under mild conditions. We found that carborane-containing metal complexes encapsulated in networks made of poly(dimethylsiloxane) react with CO, even when immersed in water, leading to dramatic color and infrared signature changes. Furthermore, we found that the CO can be easily released from the materials by simply dipping the networks into an organic solvent for less than 1 min, at ambient temperature and pressure, which not only offers a straightforward recycling method, but also a new method for the “on-demand” release of carbon monoxide. We illustrated the utilization of the on-demand release of CO from the networks by carrying out a carbonylation reaction on an electron-deficient metal complex that led to the formation of the CO-adduct, with concomitant recycling of the gel. We anticipate that our sponge-like materials and scalable methodology will open up new avenues for the storage, transport, and controlled release of CO, the silent killer and a major industrial poison.
The Royal Society, The Romanian Ministry of Education and Research, The University of Bradford, European Regional Development Fund of the European Union
Research Development Fund Publication Prize Award winner.
Tseng, Ya-Ching, und 曾雅晴. „Reduction- and pH-Sensitive Polymersomes Formed from Dithiomaleimide-Linked AB2-Type Amphiphilic Block Copolymers for On-Demand Drug Release“. Thesis, 2018. http://ndltd.ncl.edu.tw/handle/425pmy.
Der volle Inhalt der QuelleBücher zum Thema "On-Demand release"
Redbooks, IBM. Workspace On-Demand Handbook Release 2.0. Ibm, 1998.
Den vollen Inhalt der Quelle findenNaghib;, Seyed Morteza. Localized Micro/Nanocarriers for Programmed and on-Demand Controlled Drug Release. Bentham Science Publishers, 2022.
Den vollen Inhalt der Quelle findenNaghib, Seyed Morteza, Samin Hoseinpour und Shadi Zarshad. Localized Micro/Nanocarriers for Programmed and on-Demand Controlled Drug Release. Bentham Science Publishers, 2022.
Den vollen Inhalt der Quelle findenNaghib;, Seyed Morteza. Localized Micro/Nanocarriers for Programmed and on-Demand Controlled Drug Release. Bentham Science Publishers, 2022.
Den vollen Inhalt der Quelle findenManaging Your Java Software With IBM Secureway On-Demand Server Release 2.0. Ibm, 1999.
Den vollen Inhalt der Quelle findenSelf-Publishing on Demand: How to Create, Publish and Release Your Next Non-Fiction Book. Jones Media Publishing, 2016.
Den vollen Inhalt der Quelle findenSurdam, David George. An Overview of the Hearings. University of Illinois Press, 2017. http://dx.doi.org/10.5406/illinois/9780252039140.003.0003.
Der volle Inhalt der QuelleBuła, Piotr, und Bogdan Nogalski, Hrsg. The Future of Management. Industry 4.0 and Digitalization. Wydawnictwo Uniwersytetu Jagiellońskiego, 2020. http://dx.doi.org/10.4467/k7123.106/20.20.15521.
Der volle Inhalt der QuelleBuła, Piotr, und Bogdan Nogalski, Hrsg. The Future of Management. Entrepreneurship, Change and Flexibility. Wydawnictwo Uniwersytetu Jagiellońskiego, 2019. http://dx.doi.org/10.4467/k7124.89/20.20.15520.
Der volle Inhalt der QuelleGrewal, J. S. The Second Battle. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199467099.003.0024.
Der volle Inhalt der QuelleBuchteile zum Thema "On-Demand release"
Yoshikawa, Jun-ichi, Kenzo Makino und Akira Furusawa. „On-Demand Release of a Heralded Quantum State from Concatenated Optical Cavities“. In Engineering the Atom-Photon Interaction, 217–40. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-19231-4_8.
Der volle Inhalt der QuelleRiool, Martijn, und Sebastian A. J. Zaat. „Biomaterial-Associated Infection: Pathogenesis and Prevention“. In Urinary Stents, 245–57. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04484-7_20.
Der volle Inhalt der QuelleTurner-Adams, Hana, und Christine Rubie-Davies. „New Zealand: The Experiences of Māori Teachers as an Ethnic Minority in English-Medium Schools“. In To Be a Minority Teacher in a Foreign Culture, 453–69. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-25584-7_29.
Der volle Inhalt der QuelleWendt, Jonas, Astrid Weyand, Boris Barmbold und Matthias Weigold. „Approach for Design of Low Carbon Footprint Paint Shops in the Automotive Industry“. In Lecture Notes in Mechanical Engineering, 490–98. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-28839-5_55.
Der volle Inhalt der QuelleBouacida, Ines. „France’s Hydrogen Strategy: Focusing on Domestic Hydrogen Production to Decarbonise Industry and Mobility“. In Studies in Energy, Resource and Environmental Economics, 67–84. Cham: Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-59515-8_4.
Der volle Inhalt der QuelleNaghib, Seyed Morteza, Samin Hoseinpour und Shadi Zarshad. „Exogeneous-triggered Delivery in Localized Controlled Drug Delivery Systems (LCDDSs)“. In Localized Micro/Nanocarriers for Programmed and On-Demand Controlled Drug Release, 120–51. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815051636122010007.
Der volle Inhalt der QuelleNaghib, Seyed Morteza, Samin Hoseinpour und Shadi Zarshad. „Composites in Localized Controlled Drug Delivery Systems (LCDDSs)“. In Localized Micro/Nanocarriers for Programmed and On-Demand Controlled Drug Release, 93–119. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815051636122010006.
Der volle Inhalt der QuelleHoseinpour, Samin, und Shadi Zarshad. „Introduction to Localized Controlled Drug Delivery Systems (LCDDSs)“. In Localized Micro/Nanocarriers for Programmed and On-Demand Controlled Drug Release, herausgegeben von Seyed Morteza Naghib, 1–19. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815051636122010002.
Der volle Inhalt der QuelleNaghib, Seyed Morteza, Samin Hoseinpour und Shadi Zarshad. „Additive Manufacturing in Developing Localized Controlled Drug Delivery Systems (LCDDSs)“. In Localized Micro/Nanocarriers for Programmed and On-Demand Controlled Drug Release, 211–37. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815051636122010010.
Der volle Inhalt der QuelleNaghib, Seyed Morteza, Samin Hoseinpour und Shadi Zarshad. „Carbon Nanostructures in Localized Controlled Drug Delivery Systems (LCDDSs)“. In Localized Micro/Nanocarriers for Programmed and On-Demand Controlled Drug Release, 20–45. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815051636122010003.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "On-Demand release"
Yao-Joe Yang, Yu-Jie Huang, Hsin-Hung Liao, Tao Wang, Pen-Li Huang, Chii-Wan Lin, Yao-Hong Wang und Shey-shi Lu. „A release-on-demand wireless CMOS drug delivery SoC based on electrothermal activation technique“. In 2009 IEEE International Solid-State Circuits Conference (ISSCC 2009). IEEE, 2009. http://dx.doi.org/10.1109/isscc.2009.4977421.
Der volle Inhalt der QuellePerkins, Jessica L., Salil Desai, Benjamin Harrison und Jagannathan Sankar. „Understanding Release Kinetics of Calcium Alginate Microcapsules Using Drop on Demand Inkjet Printing“. In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-12819.
Der volle Inhalt der QuelleWalter, Ian, Philip E. Paré und Jitesh H. Panchal. „Modeling the Dynamics of Customer Demand to Determine the Optimal Time to Release Product Updates: A Cognitive Approach“. In ASME 2023 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/detc2023-115259.
Der volle Inhalt der QuelleTakatsuka, Shuhei, Takeshi Kubota, Yuta Kurashina und Hiroaki Onoe. „Near Infrared-Triggered On-Demand Adeno-Associated Virus Release From Hydrogel Microbeads For Gene Therapy“. In 2022 IEEE 35th International Conference on Micro Electro Mechanical Systems Conference (MEMS). IEEE, 2022. http://dx.doi.org/10.1109/mems51670.2022.9699702.
Der volle Inhalt der QuelleChiu, Stanley K. H., und Son T. Vuong. „A novel method for flash crowd avoidance in P2P video on demand streaming via pre-release distribution“. In 2008 International Conference on Advanced Technologies for Communications (ATC). IEEE, 2008. http://dx.doi.org/10.1109/atc.2008.4760559.
Der volle Inhalt der QuelleNubli, Haris, Jung Min Sohn und Dongho Jung. „Temperature Reduction on LNG Bunkering Ship Structure Under Accidental Cryogenic Gas Release Using CFD Simulation“. In ASME 2022 41st International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/omae2022-78729.
Der volle Inhalt der QuelleJustin, G. A., Siqiang Zhu, T. R. Nicholson, J. Maskrod, J. Mbugua, M. Chase, June-ho Jung und R. M. L. Mercado. „On-demand controlled release of anti-inflammatory and analgesic drugs from conducting polymer films to aid in wound healing“. In 2012 34th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2012. http://dx.doi.org/10.1109/embc.2012.6346153.
Der volle Inhalt der QuelleStewart, Tiffanie, Emmanuel Stimphil, Rakesh Guduru, Alexandra Rodzinski, Ping Liang, Carolyn Runowicz, Ren-Zhi Cai, Luis Salgueiro, Andrew Schally und Sakhrat Khizroev. „Abstract 1346: Magnetoelectric particles cross blood brain barrier to deliver anti-tumor peptide to glioblastoma cells with on-demand release“. In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-1346.
Der volle Inhalt der QuelleKahl, Torsten, Georg Greifzu, Marion Herrmann, Wolfgang Lippmann und Antonio Hurtado. „Particle Release During Laser Decontamination of Concrete Surfaces“. In 2018 26th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/icone26-81578.
Der volle Inhalt der QuelleRodzinski, Alexandra, Ali Hadjikhani, Tiffanie Stewart, Emmanuel Stimphil, Rakesh Guduru, Ping Liang, Carolyn Runowicz und Sakhrat Khizroev. „Abstract B47: A novel mechanism for field-controlled high-specificity targeted anticancer drug delivery and on-demand release using magnetoelectric nanoparticles“. In Abstracts: Fourth AACR International Conference on Frontiers in Basic Cancer Research; October 23-26, 2015; Philadelphia, PA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.fbcr15-b47.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "On-Demand release"
Dabrovolskas, Audrius. In Search of Film Policy and Film Exhibition Model Based on Mission Economy: the Case of the Baltic Film Industries. Publishing House - Vilnius Business College, Juni 2023. http://dx.doi.org/10.57005/ab.2023.1.2.
Der volle Inhalt der QuelleBaldos, Uris Lantz. Development of GTAP 9 Land Use and Land Cover Data Base for years 2004, 2007 and 2011. GTAP Research Memoranda, August 2017. http://dx.doi.org/10.21642/gtap.rm30.
Der volle Inhalt der QuelleBaldos, Uris Lantz, und Erwin Corong. Development of GTAP 10 Land Use and Land Cover Data Base for years 2004, 2007, 2011 and 2014. GTAP Research Memoranda, November 2020. http://dx.doi.org/10.21642/gtap.rm36.
Der volle Inhalt der QuelleHarris, Jeremy, Paolo Giordano und Matthew Shearer. INTrade: Latin America Trade Trend Estimates: 2012. Inter-American Development Bank, Dezember 2012. http://dx.doi.org/10.18235/0008200.
Der volle Inhalt der QuelleThe underserved middle: defining excluded enterprises in agricultural value chains. Commercial Agriculture for Smallholders and Agribusiness (CASA), 2020. http://dx.doi.org/10.1079/20240191181.
Der volle Inhalt der QuelleThe Competitive Advantage of Nations: A Successful Experience, Realigning the Strategy to Transform the Economic and Social Development of the Basque Country. Universidad de Deusto, 2015. http://dx.doi.org/10.18543/xiqr3861.
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