Relevant bibliographies by topics / Colloidal drug delivery systems

Academic literature on the topic 'Colloidal drug delivery systems'

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Published: 18 May 2024

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Journal articles on the topic "Colloidal drug delivery systems"

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Duncan-Hewitt, Wendy C. "Colloidal drug delivery systems." Colloids and Surfaces B: Biointerfaces 5, no. 1-2 (September 1995): 89–90. http://dx.doi.org/10.1016/0927-7765(95)90010-1.

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Brannon-Peppas, Lisa. "Colloidal drug delivery systems." Journal of Controlled Release 37, no. 3 (December 1995): 307–8. http://dx.doi.org/10.1016/0168-3659(95)90003-9.

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Peracchia, Maria Teresa. "Colloidal drug delivery systems." Journal of Controlled Release 35, no. 2-3 (August 1995): 181–82. http://dx.doi.org/10.1016/0168-3659(95)90034-9.

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Beg, Sarwar, Abdus Samad, Iram Nazish, Ruksar Sultana, Mahfoozur Rahman, Md Zaki Ahmad, and Md Akbar. "Colloidal Drug Delivery Systems in Vaccine Delivery." Current Drug Targets 14, no. 1 (December 1, 2012): 123–37. http://dx.doi.org/10.2174/1389450111314010013.

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Beg, Sarwar, Abdus Samad, Iram Nazish, Ruksar Sultana, Mahfoozur Rahman, Md Zaki Ahmad, and Md Akbar. "Colloidal Drug Delivery Systems in Vaccine Delivery." Current Drug Targets 14, no. 1 (January 1, 2013): 123–37. http://dx.doi.org/10.2174/138945013804806523.

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Singh, Sukhbir, Neelam Sharma, Tapan Behl, Bidhan Chandra Sarkar, Hasi Rani Saha, Kanika Garg, Supriya Kamari Singh, et al. "Promising Strategies of Colloidal Drug Delivery-Based Approaches in Psoriasis Management." Pharmaceutics 13, no. 11 (November 22, 2021): 1978. http://dx.doi.org/10.3390/pharmaceutics13111978.

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Psoriasis is a chronic inflammatory autoimmune disorder that moderately affects social and interpersonal relationships. Conventional treatments for psoriasis have certain problems, such as poor drug penetration through the skin, hyper-pigmentation, and a burning sensation on normal and diseased skin. Colloidal drug delivery systems overcome the pitfalls of conventional approaches for psoriasis therapeutics and have improved patient safety parameters, compliance, and superior effectiveness. They also entail reduced toxicity. This comprehensive review’s topics include the pathogenesis of psoriasis, causes and types of psoriasis, conventional treatment alternatives for psoriasis, the need for colloidal drug delivery systems, and recent studies in colloidal drug delivery systems for the treatment of psoriasis. This review briefly describes colloidal drug delivery approaches, such as emulsion systems—i.e., multiple emulsion, microemulsion, and nano-emulsion; vesicular systems—i.e., liposomes, ethosomes, noisomes, and transferosomes; and particulate systems—i.e., solid lipid nanoparticles, solid lipid microparticles, nano-structured lipid carriers, dendrimers, nanocrystals, polymeric nanoparticles, and gold nanoparticles. The review was compiled through an extensive search of the literature through the PubMed, Google Scholar, and ScienceDirect databases. A survey of literature revealed seven formulations based upon emulsion systems, six vesicular drug delivery systems, and fourteen particulate systems reported for antipsoriatic drugs. Based on the literature studies of colloidal approaches for psoriasis management carried out in recent years, it has been concluded that colloidal pharmaceutical formulations could be investigated broadly and have a broad scope for effective management of many skin disorders in the coming decades.
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Mishra, Vijay, Kuldeep Bansal, Asit Verma, Nishika Yadav, Sourav Thakur, Kalvatala Sudhakar, and Jessica Rosenholm. "Solid Lipid Nanoparticles: Emerging Colloidal Nano Drug Delivery Systems." Pharmaceutics 10, no. 4 (October 18, 2018): 191. http://dx.doi.org/10.3390/pharmaceutics10040191.

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Solid lipid nanoparticles (SLNs) are nanocarriers developed as substitute colloidal drug delivery systems parallel to liposomes, lipid emulsions, polymeric nanoparticles, and so forth. Owing to their unique size dependent properties and ability to incorporate drugs, SLNs present an opportunity to build up new therapeutic prototypes for drug delivery and targeting. SLNs hold great potential for attaining the goal of targeted and controlled drug delivery, which currently draws the interest of researchers worldwide. The present review sheds light on different aspects of SLNs including fabrication and characterization techniques, formulation variables, routes of administration, surface modifications, toxicity, and biomedical applications.
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Naeem, Sumaira, Geetha Viswanathan, and Misni Bin Misran. "Liposomes as colloidal nanovehicles: on the road to success in intravenous drug delivery." Reviews in Chemical Engineering 34, no. 3 (April 25, 2018): 365–83. http://dx.doi.org/10.1515/revce-2016-0018.

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AbstractThe advancement of research in colloidal systems has led to the increased application of this technology in more effective and targeted drug delivery. Nanotechnology enables control over functionality parameters and allows innovations in biodegradable, biocompatible, and stimuli-responsive delivery systems. The first closed bilayer phospholipid system, the liposome system, has been making steady progress over five decades of extensive research and has been efficient in achieving many desirable parameters such as remote drug loading, size-controlling measures, longer circulation half-lives, and triggered release. Liposome-mediated drug delivery has been successful in overcoming obstacles to cellular and tissue uptake of drugs with improved biodistributionin vitroandin vivo. These colloidal nanovehicles have moved on from a mere concept to clinical applications in various drug delivery systems for antifungal, antibiotic, and anticancer drugs.
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Swamy, P. V., Ch Sucharitha, and G. Surendra Babu. "A REVIEW ON PRONIOSOMES: A PRO-COLLOIDAL PARTICULATE DRUG CARRIER." International Journal of Research in Ayurveda and Pharmacy 11, no. 6 (December 30, 2020): 119–30. http://dx.doi.org/10.7897/2277-4343.1106198.

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Colloidal particulate carrier systems are the systems which carry particulates in a nanometre size. These systems are substantially effective for transportation and distribution of variety of loaded drugs to desired site and increase efficacy and decrease toxicity, to provide therapeutic activity in a controlled manner for a prolonged period of time. One such new emerging colloidal systems is proniosomes which has capacity to improve the bioavailability and also permeation of drugs across the stratum corneum to provide a controlled release action and reduce toxic effects associated with drugs. These are the dry formulations of water-soluble non-ionic surfactant coated carrier systems which immediately on hydration form niosomes. They have the capacity to overcome the various problems associated with niosomes and liposomes, like instability, transportation, distribution, storage and dosing. They offer versatile drug delivery concept for both hydrophilic and hydrophobic drugs. They have the capacity to deliver drugs effectively through different routes at specific site to achieve controlled release action. This review concentrates on preparation, characterization, components, structure, types, evaluation parameters, proniosomes in drug delivery and targeting, toxicities associated with proniosomes, proniosomes versus niosomes, clinical applications, mechanism of vesicle formation in proniosomes and future trends associated with it. Also, drug delivery via different routes, such as oral, parenteral, topical and transdermal, ocular, vaginal, mucosal, pulmonary and intranasal were discussed.
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Krishna Sailaja, Abbaraju, and Ganparaju Vaishnavi. "Overall Review On Permeation Enhancers in Drug Delivery Systems." Archives of Medical Case Reports and Case Study 4, no. 3 (July 21, 2021): 01–04. http://dx.doi.org/10.31579/2692-9392/051.

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60%-70% Several drugs can be administered orally as liquids, capsules, tablets, or chewable tablets because the oral route is the most convenient, safest and less expensive. The important challenge in the oral drug delivery is the growth of novel approaches to approve absorption of poorly permeable drugs across the intestinal permeability. The Biopharmaceutics Classification System (BCS) categorized based on their solubility and permeability. The BCS Class III, Class IV with low permeability across the biological membranes with low bioavailability. While these drugs are pharmacologically effective, poor absorption due to low permeability becomes the rate-limiting step to improve oral bioavailability. Various approaches for improving the permeability include physical, chemical, colloidal carriers and other methods such as prodrugs, permeation enhancers, ion-pairing, nanoencapsulation and combination/hybridization of one or more traditional approaches to improve drug permeability for better absorption. Among many advantages over other routes of administration 3 crucial ones are avoiding metabolism in liver, minimal negative effects and increased bioavailability.This article discusses the commonly various strategiesand various approaches for improving the permeability of BCS Class III and Class IVdrugs to enhance bioavailability.
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Dissertations / Theses on the topic "Colloidal drug delivery systems"

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Castro-Lopez, Vanessa. "Colloidal microgels as (trans)dermal drug delivery systems." Thesis, University of Greenwich, 2005. http://gala.gre.ac.uk/6230/.

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In this study microgels have been used as novel drug carriers (i.e. a novel controlled drug delivery system) for either dermal or transdermal delivery. The experiments conducted in this project were, firstly, to investigate the uptake and release of model compounds with different physico-chemical properties (i.e. solubility and logKoct/w) to and from two colloidal gel systems. Secondly, the permeation of model compounds across a model skin membrane (silicone membrane), and human epidermis was investigated. The first part of the project was to co-synthesise temperature-sensitive colloidal microgels particles based on a co-polymer of poly(N-isopropylacrylamide) (90%)-co-butyl acrylate (10%) (NIPAM/BA) (90/10)(w/w)%, in the presence of and in the absence of ibuprofen (IBU), methyl paraben (MP), and propyl paraben (PP), by a surfactant-free emulsion polymerisation (SFEP) in water. Physico-chemical properties of the microgels were determined using different techniques including photon correlation spectroscopy (PCS), transmission electron microscopy (TEM), nuclear magnetic resonance (NMR spectroscopy), and turbidimetric analysis (UV-vis). The uptake and release of the model compounds to and from colloidal microgel particles was controlled by the solubility and logKoct/w of the drugs. Their subsequent permeation across a model silicone membrane and human skin, were investigated over a range of temperatures (292 K – 313 K). The transport rate of IBU and, PP from poly(NIPAM) microgel is significantly reduced by two and one order of magnitude, respectively, compared with the transport rate of saturated solutions. A huge reduction in the flux indicates that the microgel retards permeation of the drug across both membranes, and hence the microgel can be considered as a permeation retarder. However, fluxes of MP from poly(NIPAM) microgel are equivalents to fluxes of saturated solutions of MP. There is a clear correlation between the solubility and logKoct/w value of the drugs and the flux value for the microgels, incorporating the drugs, across both types of membranes. In the second part of the work, a co-polymer of poly(NIPAM) (85%) co-butyl acrylate (10%) co-methacrylic acid (5%) (NIPAM/BA/MAA) (85/10/5) microgel was synthesised and investigated as a potential pH and temperature sensitive transdermal delivery device. Three compounds having different logKoct/w and solubilities were incorporated into the microgel, namely: salicylamide (SA), methyl paraben and propyl paraben.
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Tison, Christopher Kirby. "Programmable, isothermal disassembly of DNA-linked colloidal particles." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/28189.

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Thesis (M. S.)--Materials Science and Engineering, Georgia Institute of Technology, 2009.
Committee Chair: Milam, Valeria; Committee Member: Boyan, Barbara; Committee Member: Li, Mo; Committee Member: McDevitt, Todd; Committee Member: Sandhage, Ken.
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Fiebrig, Immo. "Solution studies on the mucoadhesive potential of various polymers for use in gastrointestinal drug delivery systems." Thesis, University of Nottingham, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307747.

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Dennis, Andrew C. "Studies of some molecular reorganisations in the solid state and in colloidal media by vibrational spectroscopy." Thesis, Queen's University Belfast, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.322846.

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Karmakar, Gourab. "Physicochemical investigation on Nanostructural Lipid Carriers." Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2855.

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Corvari, Susan Jane. "The implications of physical stability on orally administered colloidal drug delivery systems and cyclosporin A absorption /." Ann Arbor, Mich. : UMI, 1992. http://www.gbv.de/dms/bs/toc/016076850.pdf.

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Swami, Salesh N., University of Western Sydney, of Science Technology and Environment College, and of Science Food and Horticulture School. "Radiation synthesis of polymeric hydrogels for swelling-controlled drug release studies." THESIS_CSTE_SFH_Swami_S.xml, 2004. http://handle.uws.edu.au:8081/1959.7/698.

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Hydrogels are three dimensional networks of hydrophilic homopolymers or copolymers generally covalently or ionically crosslinked. They interact with aqueous media by swelling to some equilibrium value by retaining the aqueous media in their structures. This study concerns the investigation of the swelling and the controlled drug release behaviour of hydrogels synthesized via the photopolymerisation process. The study of hydrogels in this project was oriented towards their biomedical applications as controlled drug delivery devices. It is a known fact that the complete conversion of monomers to polymers may not be achieved in the polymerisation process thus there is always a certain component of unreacted toxic monomers still remained in the polymer matrix. These monomers have the tendency to leach out of the polymer matrices when the polymers are in contact with an aqueous medium thus rendering the hydrogel to be nonbiocompatable. The polymers synthesized in this work were washed thoroughly in milli-Q-water and then evaluated in vitro for any possible toxic effect on human keratinocyte (HaCaT)v cells using a 3-[4,5-dimethylthiazol-2-yl]-2,5-diaphenyl tetrazolium bromide (MTT) cell proliferation assay. The cytotoxicity results indicated that the hydrogels understudy sustained and allowed a positive growth of the HaCat cells in the duration of the cytotoxicity experiment, thus proving to be satisfactorily compatible.
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Blackburn, William H. "Microgel bioconjugates for targeted delivery to cancer cells." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/31792.

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Thesis (Ph.D)--Chemistry and Biochemistry, Georgia Institute of Technology, 2009.
Committee Chair: Lyon, L. Andrew; Committee Member: Barry, Bridgette; Committee Member: Fahrni, Christoph J.; Committee Member: Hud, Nicholas V.; Committee Member: Le Doux, Joseph M. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Tuesca, Anthony D. Lowman Anthony M. "Synthesis, characterization, and application of polyethylene glycol modified insulin for oral delivery using complexation hydrogels /." Philadelphia, Pa. : Drexel University, 2008. http://hdl.handle.net/1860/2715.

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Swami, Salesh N. "Radiation synthesis of polymeric hydrogels for swelling-controlled drug release studies." Thesis, View thesis, 2004. http://handle.uws.edu.au:8081/1959.7/698.

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Hydrogels are three dimensional networks of hydrophilic homopolymers or copolymers generally covalently or ionically crosslinked. They interact with aqueous media by swelling to some equilibrium value by retaining the aqueous media in their structures. This study concerns the investigation of the swelling and the controlled drug release behaviour of hydrogels synthesized via the photopolymerisation process. The study of hydrogels in this project was oriented towards their biomedical applications as controlled drug delivery devices. It is a known fact that the complete conversion of monomers to polymers may not be achieved in the polymerisation process thus there is always a certain component of unreacted toxic monomers still remained in the polymer matrix. These monomers have the tendency to leach out of the polymer matrices when the polymers are in contact with an aqueous medium thus rendering the hydrogel to be nonbiocompatable. The polymers synthesized in this work were washed thoroughly in milli-Q-water and then evaluated in vitro for any possible toxic effect on human keratinocyte (HaCaT)v cells using a 3-[4,5-dimethylthiazol-2-yl]-2,5-diaphenyl tetrazolium bromide (MTT) cell proliferation assay. The cytotoxicity results indicated that the hydrogels understudy sustained and allowed a positive growth of the HaCat cells in the duration of the cytotoxicity experiment, thus proving to be satisfactorily compatible.
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Books on the topic "Colloidal drug delivery systems"

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1948-, Kreuter Jörg, ed. Colloidal drug delivery systems. New York: M. Dekker, 1994.

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Monzer, Fanun, ed. Colloids in drug delivery. Boca Raton: Taylor & Francis, 2010.

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Müller, Rainer H. Colloidal carriers for controlled drug delivery and targeting. Boca Raton: CRC Press, 1990.

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Müller, Rainer H. Colloidal carriers for controlled drug delivery and targeting: Modification, characterization, and in vivo distribution. Stuttgart: Wissenschaftliche Verlagsgesellschaft, 1991.

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Park, Kinam. Biodegradable hydrogels for drug delivery. Lancaster, PA: Technomic Pub., 1993.

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Arias, José L. Drug targeting by magnetically responsive colloids. Hauppauge, N.Y: Nova Science, 2010.

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T, Nylander, and Lindman Björn 1942-, eds. Lipids and polymer-lipid systems. Berlin: Springer, 2002.

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Teruo, Okano, ed. Biorelated polymers and gels: Controlled release and applications in biomedical engineering. San Diego: Academic Press, 1998.

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Ranade, Vasant V. Drug delivery systems. 3rd ed. Boca Raton: CRC Press, 2011.

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Jain, Kewal K., ed. Drug Delivery Systems. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-210-6.

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Book chapters on the topic "Colloidal drug delivery systems"

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Ascenso, Andreia, Sandra Simões, Joana Marto, Helena Margarida Ribeiro, and António José Almeida. "Colloidal Disperse Systems: Microemulsions and Nanoemulsions." In Nanocarriers for Drug Delivery, 73–81. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63389-9_4.

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Parmar, Komal, and Jayvadan K. Patel. "Colloidal Carrier Systems for Transscleral Drug Delivery." In Drug Delivery for the Retina and Posterior Segment Disease, 229–39. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-95807-1_13.

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Gurny, R. "Controlled Drug Delivery with Colloidal Polymeric Systems." In Polymeric Biomaterials, 195–211. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4390-2_12.

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Rosaria Lauro, Maria, Teresa Musumeci, Francesca Sansone, Giovanni Puglisi, and Rosario Pignatello. "Polymeric Colloidal Carriers for Natural Polyphenolic Compounds." In Novel Drug Delivery Systems for Phytoconstituents, 261–82. Boca Raton : Taylor & Francis, 2020. | “A CRC title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa plc.”: CRC Press, 2019. http://dx.doi.org/10.1201/9781351057639-13.

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Prokop, Ales, Evgenii Kozlov, Gianluca Carlesso, and Jeffrey M. Davidson. "Hydrogel-Based Colloidal Polymeric System for Protein and Drug Delivery: Physical and Chemical Characterization, Permeability Control and Applications." In Filled Elastomers Drug Delivery Systems, 119–73. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45362-8_3.

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Rivera Gil, Pilar, Moritz Nazarenus, and Wolfgang J. Parak. "Composite Colloidal Nanosystems for Targeted Delivery and Sensing1." In Bioinspired and Biomimetic Polymer Systems for Drug and Gene Delivery, 61–84. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527672752.ch3.

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Brenner, Nancy J., Christine Fioravanti, and H. Donald Burns. "Application of Nuclear Imaging to Drug Delivery Evaluation and Development: A Review of Radiolabeled, Injectable, Colloidal Systems of Delivery." In Nuclear Imaging in Drug Discovery, Development, and Approval, 283–300. Boston, MA: Birkhäuser Boston, 1993. http://dx.doi.org/10.1007/978-1-4684-6808-3_15.

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Kommareddy, Sushma, and Mansoor Amiji. "Targeted Drug Delivery to Tumor Cells Using Colloidal Carriers." In Cellular Drug Delivery, 181–215. Totowa, NJ: Humana Press, 2004. http://dx.doi.org/10.1007/978-1-59259-745-1_11.

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Gupta, Deepak. "Colloidal Carriers in Ophthalmic Drug Delivery." In Nano-Biomaterials For Ophthalmic Drug Delivery, 321–49. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29346-2_15.

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Holowka, Eric P., and Sujata K. Bhatia. "Controlled-Release Systems." In Drug Delivery, 7–62. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1998-7_2.

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Conference papers on the topic "Colloidal drug delivery systems"

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Popova, O. S. "Nanoparticles as a transport system for corvacrol compounds." In SPbVetScience. FSBEI HE St. Petersburg SUVM, 2023. http://dx.doi.org/10.52419/3006-2023-8-64-67.

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Colloidal delivery systems, including microencapsulation and nanotechnology, are promising approaches in pharmacology. We have used liposomes to deliver systems containing Corvacrol and assessed the promise of liposomal agents for solving major problems in drug pharmacokinetics.
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Zheng, Zhuoyuan, Akash Singh, and Yumeng Li. "Molecular Dynamic Simulation Study on Soy Protein As Drug Delivery Vehicle." In ASME 2020 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/imece2020-23590.

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Abstract Protein-based drug carriers are promising candidates for efficient drug delivery among the available potential colloidal carrier systems, due to their low cytotoxicity, abundance, renewability, diverse functional groups and interactions, and high drug loading capacity, etc. In this study, molecular dynamics (MD) simulations are performed to study the mechanisms of 11S molecule of soy protein as drug delivery vehicle to attach allyl isothiocyanate (AITC) and doxorubicin (DOX) drugs. The intermolecular interactions between protein and drugs are investigated; and the loading capacities of the protein molecules are calculated and compared with experiments. It is found that, for the AITC system, both nonpolar and polar residues of protein have the ability to adsorb AITCs; particularly, the polar residues serve as the primary active sites for the stable attachment of the drug molecules through the electrostatic (dipole-dipole) interactions. For the DOX system, however, the main driving force become the π-π stacking (the van der Waals interactions) among the aromatic rings of DOX and protein. In addition to pristine protein, different denaturation processes are found to be able to increase the exposure of active sites, therefore, enhance the loading efficiency of the protein carriers.
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Wang, Xiaoliang, Hongchen Gu, and Xinyuan Zhu. "A Novel Remote Controllable Drug Delivery System Triggered by Heating From Magnetic Nanoparticles." In ASME 2009 Second International Conference on Micro/Nanoscale Heat and Mass Transfer. ASMEDC, 2009. http://dx.doi.org/10.1115/mnhmt2009-18052.

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Target drug delivery is one of the core issues in modern medicine. Although both thermo-sensitive and magnetic drug vehicles have been developed for this purpose, reliable drug targeting is yet to achieve, because it’s hard to control local temperature in body for thermo-sensitive drugs, and it’s also difficult to control the colloidal sizes of magnetic vehicles to meet the requirements for both long-time circulation and magnetic responsibility. Here we present a new technology to solve these two problems. The drug (taxel) was combined with hyper-branched thermo-sensitive polymer and magnetic nanoparticles. Magnetic responsibility of the complex can be remotely controlled by applying an alternating magnetic field. The untreated complexes were stable in dispersion, while after exposing to the alternating magnetic filed for 5 minutes, the complexes were destabilized and deposited from dispersion quickly. Unlike the commonly used water bath, the technology present here can heat up the drug vehicles remotely from outside, which must have great potentials in the applications of magnetic or thermo-sensitive drug delivery.
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Vasile, Georgiana, Andreea Țigău, Alina Popescu, Rodica Roxana Constantinescu, and Laura Chirilă. "Hydrogels-Based Textile Materials for Treatment of First-Degree Burn Injuries." In The 9th International Conference on Advanced Materials and Systems. INCDTP - Leather and Footwear Research Institute (ICPI), Bucharest, Romania, 2022. http://dx.doi.org/10.24264/icams-2022.ii.28.

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Hydrogels based on collagen and xanthan have found various applications as drug delivery carriers. The main strategy is to combine the traditional perspective of using essential oils with polymeric hydrogels in order to develop a potential dressing that provides wound healing for first-degree burn injuries. In this regard, the present study is aimed to develop textile materials with potential for use in the treatment of first-degree burn injuries by approaching the hydrogels based on xanthan gum and collagen as polymeric matrix loaded with essential oils (cinnamon essential oil, tea tree essential oil), propolis (hydroglyceric extract or with content of colloidal silver) and drugs (chlorhexidine, ciprofloxacin). A total of six experimental variants of hydrogels were synthesized and then were applied by padding method on a plain weave textile structure from 100% cotton. The functionalized textile materials were characterized by morphological and antibacterial point of view. The textile materials treated materials with all synthesized hydrogels based on xanthan and collagen as polymeric matrices have antibacterial activity against S. aureus and E. coli test strains, the highest inhibition zone was provided by the samples loaded with ciprofloxacin (MUP3 and MUP4 code).
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Mahadevan, T. S., M. Milosevic, M. Kojic, F. Hussain, N. Kojic, M. Ferrari, and A. Ziemys. "Nanoparticle Transport Through Boundaries of Nanoporous Structures." In ASME 2012 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/imece2012-85775.

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In transport phenomena involving colloidal nanoparticle (NP) suspensions in complex environments, the inter particle interactions play an important role especially when the sizes of the confining environments approaches the particle sizes. Specific examples of such systems are encountered in NP transport through nanochannels used in drug delivery and nanofluidic cooling[1–5]. In ionic colloidal suspensions like the ones encountered in the above applications, the NPs acquire characteristic surface charges which results in a surface potential and a double layer of co- and counter-ions from the solution. DLVO theory predicts the interaction energy resulting from the double layer to be [6]:(1)Wr=64πkBTRρ∞γ2κ2exp-κr where r is the separation between NP surfaces, and R is the radius of the NP, ρ∞ is the concentration of ions in the suspension, κ−1 is the Debye screening length (characteristic size of the double layer) and kB and T are the Boltzmann constant and the temperature. As κ−1 approaches the size range of the particles, the interactions amongst the particles may span several times the particle size and contributes to particle diffusion.
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Yeo, Leslie Y., and James R. Friend. "Fast Inertial Microfluidic Actuation and Manipulation Using Surface Acoustic Waves." In ASME 2010 8th International Conference on Nanochannels, Microchannels, and Minichannels collocated with 3rd Joint US-European Fluids Engineering Summer Meeting. ASMEDC, 2010. http://dx.doi.org/10.1115/fedsm-icnmm2010-30181.

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Though uncommon in most microfluidic systems due to the dominance of viscous and capillary stresses, it is possible to drive microscale fluid flows with considerable inertia using surface acoustic waves (SAWs), which are nanometer order amplitude electro-elastic waves that can be generated on a piezoelectric substrate. Due to the confinement of the acoustic energy to a thin localized region along the substrate surface and its subsequent leakage into the body of liquid with which the substrate comes into contact, SAWs are an extremely efficient mechanism for driving fast microfluidics. We demonstrate that it is possible to generate a variety of efficient microfluidic flows using the SAW. For example, the SAWs can be exploited to pump liquids in microchannels or to translate free droplets typically one or two orders of magnitude faster than conventional electroosmotic or electrowetting technology. In addition, it is possible to drive strong microcentrifugation for micromixing and bioparticle concentration or separation. In the latter, rich and complex colloidal pattern formation dynamics have also been observed. At large input powers, the SAW is a powerful means for the generation of jets and atomized aerosol droplets through rapid destabilization of the parent drop interface. In the former, slender liquid jets that persist up to centimeters in length can be generated without requiring nozzles or orifices. In the latter, a monodispersed distribution of 1–10 micron diameter aerosol droplets is obtained, which can be exploited for drug delivery and encapsulation, nanoparticle synthesis, and template-free polymer array patterning.
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Ray, Aniruddha, Shuoran Li, Tatiana Segura, and Aydogan Ozcan. "Monitoring of nanoparticle degradation using holographic on-chip microscopy for drug delivery applications (Conference Presentation)." In Colloidal Nanoparticles for Biomedical Applications XIII, edited by Xing-Jie Liang, Wolfgang J. Parak, and Marek Osiński. SPIE, 2018. http://dx.doi.org/10.1117/12.2290520.

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Lombardo, Domenico. "Smart Nanocarriers and Drug Delivery: Soft Interaction and Colloidal Stability in Complex Biological Media." In The 5th World Congress on New Technologies. Avestia Publishing, 2019. http://dx.doi.org/10.11159/icbb19.01.

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George, Ashline, and Jerin Cyriac. "Nano particle based drug delivery systems." In 2017 Third International Conference on Advances in Electrical, Electronics, Information, Communication and Bio-Informatics (AEEICB). IEEE, 2017. http://dx.doi.org/10.1109/aeeicb.2017.7972386.

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Chen, Michael. "Nanotechnologies for Advanced Drug Delivery Systems." In The 5th World Congress on New Technologies. Avestia Publishing, 2019. http://dx.doi.org/10.11159/icbb19.02.

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Reports on the topic "Colloidal drug delivery systems"

1

Zarabi, Bahar, and Hamid Ghandehari. Magnetic Resonance Imaging of Polymeric Drug Delivery Systems in Breast Cancer Solid Tumors. Fort Belvoir, VA: Defense Technical Information Center, July 2005. http://dx.doi.org/10.21236/ada439254.

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Popova, Teodora, Borislav Tzankov, Christina Voycheva, Krassimira Yoncheva, and Nikolai Lambov. Development of Advanced Drug Delivery Systems with Bicalutamide Based on Mesoporous Silica Particles. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, December 2019. http://dx.doi.org/10.7546/crabs.2019.12.08.

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Zarabi, Bahar, and Hamid Ghandehari. Magnetic Resonance Imaging of Polymeric Drug Delivery Systems in Breast Cancer Solid Tumors. Fort Belvoir, VA: Defense Technical Information Center, July 2006. http://dx.doi.org/10.21236/ada469974.

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Zarabi, Bahar. Magnetic Resonance Imaging of Polymeric Drug Delivery Systems in Breast Cancer Solid Tumors. Fort Belvoir, VA: Defense Technical Information Center, December 2007. http://dx.doi.org/10.21236/ada480781.

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Dżaman, Karolina, and Katarzyna Czerwaty. Extracellular Vesicle-Based Drug Delivery Systems for Head and Neck Squamous Cell Carcinoma: A Systematic Review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, April 2023. http://dx.doi.org/10.37766/inplasy2023.4.0021.

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Review question / Objective: This systematic review aims to identify studies investigating the membrane vesicle-based drug de-livery systems (DDS) for HNSCC and define the potential of extracellular vesicles (EVs) in the treatment of this disease according to the current state of knowledge. Condition being studied: Head and neck squamous cell carcinoma (HNSCC), which is ranked the sixth most common malignancy worldwide, originates in the epithelium of the oral and nasal cavities, pharynx, and larynx. The treatment of HNSCC remains a challenge and requires the involvement of a multidisciplinary team. Currently available methods of treatment, such as surgery, radiotherapy, and chemotherapy, cause significant dysfunctions and toxicity, which highlights the necessity to explore new therapeutic options. One-third of patients treated with intended curative surgery and adjuvant therapy experience local or regional recurrence and/or distant metastasis.
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