Academic literature on the topic 'Controlled release technology'

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Journal articles on the topic "Controlled release technology"

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Peppas, N. A. "Controlled-release technology: Pharmaceutical applications." Journal of Controlled Release 7, no. 2 (1988): 186. http://dx.doi.org/10.1016/0168-3659(88)90014-4.

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Brannon, M. Lisa. "Controlled release technology: Pharmaceutical applications." Journal of Controlled Release 7, no. 3 (1988): 289. http://dx.doi.org/10.1016/0168-3659(88)90068-5.

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Tabata, Yasuhiko. "Controlled Release Technology to Support Advanced Medicine." Drug Delivery System 31, no. 3 (2016): 219–27. http://dx.doi.org/10.2745/dds.31.219.

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McElnay, J. C. "Pharmaceutical technology. Controlled drug release, vol. 1." Endeavour 12, no. 2 (1988): 95. http://dx.doi.org/10.1016/0160-9327(88)90112-3.

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Agrawala, Praful, and Praveen Tyle. "Pharmaceutical Technology: Controlled Drug Release. Volume 1." Journal of Pharmaceutical Sciences 77, no. 6 (1988): 557–58. http://dx.doi.org/10.1002/jps.2600770622.

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Awad, Atheer, Fabrizio Fina, Sarah Trenfield, et al. "3D Printed Pellets (Miniprintlets): A Novel, Multi-Drug, Controlled Release Platform Technology." Pharmaceutics 11, no. 4 (2019): 148. http://dx.doi.org/10.3390/pharmaceutics11040148.

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Selective laser sintering (SLS) is a single-step three-dimensional printing (3DP) process that can be leveraged to engineer a wide array of drug delivery systems. The aim of this work was to utilise SLS 3DP, for the first time, to produce small oral dosage forms with modified release properties. As such, paracetamol-loaded 3D printed multiparticulates, termed miniprintlets, were fabricated in 1 mm and 2 mm diameters. Despite their large surface area compared with a conventional monolithic tablet, the ethyl cellulose-based miniprintlets exhibited prolonged drug release patterns. The possibility
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Jo, Jun-Ichiro, and Yasuhiko Tabata. "How controlled release technology can aid gene delivery." Expert Opinion on Drug Delivery 12, no. 10 (2015): 1689–701. http://dx.doi.org/10.1517/17425247.2015.1048221.

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Ogueri, Kenneth S., and Sheri L. Shamblin. "Osmotic-controlled release oral tablets: technology and functional insights." Trends in Biotechnology 40, no. 5 (2022): 606–19. http://dx.doi.org/10.1016/j.tibtech.2021.10.001.

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Song, Z. "Chemiluminescence sensor for isoniazid with controlled-reagent-release technology." Talanta 53, no. 6 (2001): 1171–77. http://dx.doi.org/10.1016/s0039-9140(00)00609-3.

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NIZAMI, FARIDA, and YOGENDRA MALVIYA. "RECENT ADVANCEMENT AND CHALLENGES IN BILAYER TABLET TECHNOLOGY: AN OVERVIEW." Current Research in Pharmaceutical Sciences 11, no. 4 (2022): 91–97. http://dx.doi.org/10.24092/crps.2021.110401.

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Bilayer tablets were developed recently for the effective production of controlled release formulations in various quality levels to give a method of successful drug delivery. Over the last three decades, as the cost and complexity of developing novel pharmacological entities have increased and as the therapeutic benefits of controlled drug administration have been recognized, considerable attention has been focused on developing sustained or controlled release drug delivery systems. It is utilized to produce a variety of antihypertensive formulations. Bilayer tablets allow for the predetermin
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Dissertations / Theses on the topic "Controlled release technology"

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Hussey, Jeremy Steven. "Wood in controlled release technology." Thesis, Bangor University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263193.

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Kanga, Yao. "Controlled release of Isothiazoline biocides from industrial minerals." Thesis, University of Birmingham, 2011. http://etheses.bham.ac.uk//id/eprint/1594/.

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This project investigated how various minerals of different surface areas and morphologies can be used to adsorb isothiazoline biocides for controlled-release and antimicrobial purposes. The absorption of the biocides on the mineral powders was achieved by way of using a bench high shear mill (dry process), or combining them to hydrated minerals (wet process). The characterisation of the minerals was achieved by XRF (chemical composition), XRD (crystal composition), SEM (morphology), B.E.T nitrogen (surface area), and Light Scattering (particle size distribution). HPLC was used to determine th
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Christie, Annette Louise. "Synthesis of biodegradable microparticles for controlled active ingredient release." Thesis, University of Warwick, 2017. http://wrap.warwick.ac.uk/103479/.

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This thesis investigates the degradation and release of a fluorescent dye from biodegradable microparticles. Particular attention is given to determining the effect of polymeric properties on the subsequent microparticle degradation and release rate. Chapter 1 reviews the current polymerisation techniques for the synthesis of polyesters and introduces the synthetic procedures and degradability currently attainable for biodegradable microparticles. The concept of ‘smart’ release technology is introduced and the potential for using biodegradable ‘smart’ particles for enhanced agricultural formul
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Sinha, Piyush Mohan. "Nanoengineered implantable devices for controlled drug delivery." Connect to this title online, 2005. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1115138930.

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Thesis (Ph. D.)--Ohio State University, 2005.<br>Title from first page of PDF file. Document formatted into pages; contains xxii, 220 p.; also includes graphics (some col.). Includes bibliographical references (p. 202-220). Available online via OhioLINK's ETD Center.
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Syzov, Vladyslav. "Delivery of a coated bioactive from a rumen controlled-release device." The University of Waikato, 2008. http://hdl.handle.net/10289/2368.

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Ruminants possess a unique digestive system. Using the high metabolic potential of the symbiotic microflora of the rumen, ruminants are capable of digesting plant material and obtaining nutrients and energy from this process. Because of the ruminal fermentation, the most bioactives are not stable in the harsh ruminal environment. Therefore there is a need to improve the bioavailability of a bioactive by protecting it from the ruminal digestion. The formulation of protected bioactive can be delivered in the rumen in a controlled manner and over a long period of time. In this project the degree
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Wang, Hongjuan. "Technology of production of drugs with controlled release in capsules based on nanoporous silicon dioxide." Магістерська робота, Київський національний університет технологій та дизайну, 2021. https://er.knutd.edu.ua/handle/123456789/19265.

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The master's thesis is devoted to study the synthesis technology of mesoporous silicon dioxide with solid and hollow structure based on the self-assemble between surfactants, co-structure directing agents and inorganic silica precursors. Well-defined spherical mesoporous silica displays interesting properties for biomedical applications such as uniform particle size, large surface area and tunable pore diameters and volumes, allowing the incorporation of large amounts of drugs and protecting them from deactivation and degradation processes acting as an excellent nanoplatform for drug delivery.
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Sui, Cong. "Novel encapsulation of water soluble active ingredients to acheive their controlled release in aqueous environment." Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8622/.

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Encapsulation technology has been widely researched and applied to different industry sectors. There are vast examples of encapsulation for controlled release of hydrophilic or hydrophobic ingredients to the target place. However, it is still difficult to encapsulate the small water-soluble salts or molecules, achieving long-term sustained release or even no release in water. Herein, a novel type of organic-inorganic composite solid microsphere, comprised of polystyrene sulfonate and silica was developed here to achieve a sustained release of K+ ions in aqueous environment for over 48 hours. F
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Abu, Awwad Hosam Al-Deen. "Controlled release system for delivery of GET peptide and its application for transcription factor delivery for bone regeneration." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/50996/.

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The repair of bone defects and non-union fractures is a significant challenge for clinicians as it requires tissue replacement. The current graft approaches used to treat these injuries have limitations with regard to quality and availability. This has resulted in research efforts to develop alternative synthetic materials that are able to aid tissue regeneration. These materials usually combined with biological factors to induce cells proliferation and differentiation. Transcription factors can provide specific regulatory effect, however, these transcription factors are very difficult to be d
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Dry, Carolyn. "Design of systems for time delayed activated internal release of chemicals in concrete from porous fibers, aggregates of prills, to improve durability /." This resource online, 1991. http://scholar.lib.vt.edu/theses/available/etd-05222007-091330/.

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Ditto, Andrew. "DNA-LPEI complexes encapsulated in LTP nanospheres as a non-viral gene therapy vector." Akron, OH : University of Akron, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=akron1165596983.

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Thesis (M.S.)--University of Akron, Dept. of Biomedical Engineering, 2006.<br>"December, 2006." Title from electronic thesis title page (viewed 12/31/2008) Advisor, Yang Yun; Committee members, Stephanie Lopina, Steven Schmidt; Department Chair, Daniel Sheffer; Dean of the College, George K. Haritos; Dean of the Graduate School, George R. Newkome. Includes bibliographical references.
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Books on the topic "Controlled release technology"

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Lee, Ping I., and William R. Good, eds. Controlled-Release Technology. American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0348.

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1948-, Lee Ping I., Good William R. 1940-, American Chemical Society. Division of Industrial and Engineering Chemistry., and American Chemical Society Meeting, eds. Controlled-release technology: Pharmaceutical applications. American Chemical Society, 1987.

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Wells, James I. Pharmaceutical Technology. Informa Healthcare, 1991.

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Fan, L. T. Controlled release: A quantitative treatment. Springer-Verlag, 1989.

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Morton, Rosoff, ed. Controlled release of drugs: Polymers and aggregate systems. VCH Publishers, 1989.

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International Symposium on Controlled Release of Bioactive Materials. (18th 1991 Amsterdam, The Netherlands). Proceedings and program of the 18th International Symposium on Controlled Release of Bioactive Materials: July 8-11, 1991, Amsterdam, The Netherlands. Edited by Junginger Hans E, Kellaway Ian W, and Controlled Release Society. Controlled Release Society, 1991.

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International Symposium on Controlled Release of Bioactive Materials. (16th 1989 Chicago, Ill.). Proceedings of the 16th International Symposium on Controlled Release of Bioactive Materials: August 6-9, 1989, Chicago, Illinois, U.S.A. Edited by Janes George, Miller James A, Pearlman Rodney, and Controlled Release Society. Controlled Release Society, 1989.

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International Pharmaceutical Technology Symposium (5th 1990 Ankara, Turkey). New approaches to controlled drug delivery: Minutes of the Fifth International Technology Symposium, Hacettepe University, Ankara, 10 to 13 September 1990 : satellite symposium of the 50th Congress of the FIP. Edited by Hıncal A. Atilla, Kaş H. Süheyla, Şumnu Murat, Hacettepe Üniversitesi, and International Congress of Pharmaceutical Sciences of F.I.P. Editions de Santé, 1990.

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International Symposium on Controlled Release of Bioactive Materials. (17th 1990 Reno, Nevada). Proceedings of the 17th International Symposium on Controlled Release of Bioactive Materials: July 22-25, 1990, Reno, Nevada, U.S.A. Edited by Lee, Vincent H. L., 1951- and Controlled Release Society. Controlled Release Society, 1990.

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International Symposium on Controlled Release of Bioactive Materials. (19th 1992 Orlando, Fla.). Proceedings of the 19th International Symposium on Controlled Release of Bioactive Materials: July 26-31, 1992, Orlando, Florida, U.S.A. Edited by Janes George, Kopeček Jindřich, and Controlled Release Society. Controlled Release Society, 1992.

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Book chapters on the topic "Controlled release technology"

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Thombre, Avinash G., Mary T. am Ende, and Xiao YuShirley Wu. "Controlled Release Technology and Design of Oral Controlled Release Dosage Forms." In Chemical Engineering in the Pharmaceutical Industry. John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470882221.ch37.

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Thombre, Avinash G., Xiao Yu Shirley Wu, and Mary T. am Ende. "CONTROLLED RELEASE TECHNOLOGY AND DESIGN OF ORAL CONTROLLED RELEASE DOSAGE FORMS." In Chemical Engineering in the Pharmaceutical Industry. John Wiley & Sons, Inc., 2019. http://dx.doi.org/10.1002/9781119600800.ch65.

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Borges, Roger, Karen Cristina Kai, and Juliana Marchi. "Biocompatible Glasses for Controlled Release Technology." In Biocompatible Glasses. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-44249-5_12.

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Yam, Kit L., and Xuntao Zhu. "Development of Controlled Release Packaging Technology." In ACS Symposium Series. American Chemical Society, 2014. http://dx.doi.org/10.1021/bk-2014-1162.ch013.

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Rathbone, Michael J., and Christopher R. Burke. "Controlled Release Intravaginal Veterinary Drug Delivery." In Advances in Delivery Science and Technology. Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-4439-8_11.

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Banakar, U. V. "Materials Used in Controlled Release Technology–A Primer." In Advances in Controlled Delivery of Drugs. Routledge, 2021. http://dx.doi.org/10.1201/9781315136837-8.

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Fletcher, John G., Michael J. Rathbone, and Raid G. Alany. "Physicochemical Principles of Controlled Release Veterinary Pharmaceuticals." In Advances in Delivery Science and Technology. Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-4439-8_5.

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Darvari, R., D. L. Wise, V. N. Hasırcı, M. Boroujerdi, Debra J. Trantolo, and Joseph D. Gresser. "Controlled Release Antibiotics for Treatment of Periodontal Disease." In Biomedical Science and Technology. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5349-6_19.

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Tewari, Divya, and Thomas Dürig. "Extrusion: An Enabling Technology for Controlled-Release Hydrophilic Matrix Systems." In Hydrophilic Matrix Tablets for Oral Controlled Release. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1519-4_10.

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Zhang, Xiang, and Mark Cresswell. "Materials for Inorganic Controlled Release Technology." In Inorganic Controlled Release Technology. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-08-099991-3.00001-6.

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Conference papers on the topic "Controlled release technology"

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Marlapalli, Vijayalakshmi, Rajendra Prasad P, Sridevi Velluru, Khairunnisa Nabilah Binti Hj Ruslan, and Rama Rao Karri. "Study on release characteristics of matrix-based zinc sulphate controlled release fertilizers." In 8TH BRUNEI INTERNATIONAL CONFERENCE ON ENGINEERING AND TECHNOLOGY 2021. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0110324.

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Hubatová-Vacková, A., Denisa Lizoňová, A. Pittermannová, V. Tokárová, O. Kašpar, and F. Štěpánek. "Composite alginate microparticles for controlled drug release." In 2nd International Conference on Modern research in Engineering, Technology and Science. GLOBALKS, 2019. http://dx.doi.org/10.33422/2nd.icmets.2019.12.877.

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Rusek, Łukasz. "Technology of obtaining mineral fertilizers with a controlled degree of component release." In 1st International PhD Student’s Conference at the University of Life Sciences in Lublin, Poland: ENVIRONMENT – PLANT – ANIMAL – PRODUCT. Publishing House of The University of Life Sciences in Lublin, 2022. http://dx.doi.org/10.24326/icdsupl1.t048.

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Cui, Yanna, Qingxing Xu, Deping Wang, and Chi-Hwa Wang. "Enhanced Intracellular Delivery and Controlled Drug Release of Magnetic PLGA Nanoparticles Modified with Transferrin." In 5th Asian Particle Technology Symposium. Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-2518-1_374.

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Salleh, N., M. M. Mahat, S. M. Yahaya, and R. Rosmamuhamadani. "Synthesis and characterization of cross-linked zerumbone loaded zeolite Y-gelatin for oral controlled release." In PROCEEDINGS OF ADVANCED MATERIAL, ENGINEERING & TECHNOLOGY. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0023157.

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Thanakorphimol, Kittithat, and Nophawan Paradee. "Fabrication of Transdermal Patch from Freeze-dried Agarose Hydrogel for Electrically Controlled Release." In 2021 18th International Conference on Electrical Engineering/Electronics, Computer, Telecommunications and Information Technology (ECTI-CON). IEEE, 2021. http://dx.doi.org/10.1109/ecti-con51831.2021.9454703.

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Maloney, John M. "An Implantable Microfabricated Drug Delivery System." In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-43186.

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We report on the development of a fully implantable drug delivery system capable of delivering hundreds of individual doses. This product is intended for the controlled release of potent therapeutic compounds that might otherwise require frequent injections. Our system has the following capabilities: • Stable, hermetic storage of therapeutic drugs in solid, liquid, or gel form; • Individual storage of discrete doses for multiple-drug regimens; • Wireless communication with an external controller for device monitoring and therapy modification; • Choice of preprogrammed release or release on com
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Boiarskii, Boris, and Mikhail Sinegovskii. "Application of NDVI and NDRE vegetation indices in the assessment of soybean productivity under nitrogen controlled-release fertilizer." In 2022 VIII International Conference on Information Technology and Nanotechnology (ITNT). IEEE, 2022. http://dx.doi.org/10.1109/itnt55410.2022.9848588.

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Wardhani, Dyah H., Abdullah, Alif N. Azizah, and Muhammad Y. Ananta. "Physicochemical properties of acetylated glucomannan of Amorphophallus onchophillus as excipient of drug controlled release." In THE 2016 CONFERENCE ON FUNDAMENTAL AND APPLIED SCIENCE FOR ADVANCED TECHNOLOGY (CONFAST 2016): Proceeding of ConFAST 2016 Conference Series: International Conference on Physics and Applied Physics Research (ICPR 2016), International Conference on Industrial Biology (ICIBio 2016), and International Conference on Information System and Applied Mathematics (ICIAMath 2016). Author(s), 2016. http://dx.doi.org/10.1063/1.4953964.

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Pankratz, Jennifer, Sabine Schmachtenberg, Nicole Jansen, et al. "Abstract 4048: REAlease® technology: Controlled release of antibody-fluorochrome conjugates for maximal flexibility in flow sorting and fluorescence microscopy applications." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-4048.

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Reports on the topic "Controlled release technology"

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Zohar, Yonathan, Robert Langer, Shimon Hassin, Walton Dickhoff, Abigail Elizur, and Yoav Gothilf. A Novel Technology for the Manipulation of Fish Reproductive Cycles: Controlled Release of Gonadotropin Releasing Hormones. United States Department of Agriculture, 1993. http://dx.doi.org/10.32747/1993.7603811.bard.

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Israel, Alvaro, and John Merrill. Production of Seed Stocks for Sustainable Tank Cultivation of the Red Edible Seaweed Porphyra. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7696527.bard.

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Porphyra species (commonly known as ‘nori’ or ‘purple laver’) are edible red seaweeds rich in proteins, vitamins and other highly valued biogenic compounds. For years Porphyra has been cultured using seeded nets extended in the open sea, and its biomass consumed primarily in the Far East. While demands for international markets have increased steadily at an average of 20% per year, supplies are on the verge and not expected to meet future demands. Alternatively, land-based cultivation of seaweed has become attractive in the mariculture industry since (1) important growth parameters can be cont
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