Academic literature on the topic 'Colloidosomes ; metal shell ; drug delivery'

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Journal articles on the topic "Colloidosomes ; metal shell ; drug delivery"

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Liang, Zuozhong, Zhiyuan Yang, Haitao Yuan, et al. "A protein@metal–organic framework nanocomposite for pH-triggered anticancer drug delivery." Dalton Transactions 47, no. 30 (2018): 10223–28. http://dx.doi.org/10.1039/c8dt01789a.

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Lu, Liangyu, Mengyu Ma, Chengtao Gao, et al. "Metal Organic Framework@Polysilsesequioxane Core/Shell-Structured Nanoplatform for Drug Delivery." Pharmaceutics 12, no. 2 (2020): 98. http://dx.doi.org/10.3390/pharmaceutics12020098.

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Modern pharmaceutics requires novel drug loading platforms with high drug loading capacity, controlled release, high stability, and good biocompacity. Metal–organic frameworks (MOFs) show promising applications in biomedicine owing to their extraordinarily high surface area, tunable pore size, and adjustable internal surface properties. However, MOFs have low stability due to weak coordinate bonding and limited biocompatibility, limiting their bioapplication. In this study, we fabricated MOFs/polysilsesquioxane (PSQ) nanocomposites and utilized them as drug carriers. Amine-functionalized MOF (
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Cong, Hai-Lin, Fei-Fei Jia, Song Wang, Ming-Tao Yu, You-Qing Shen, and Bing Yu. "Core–Shell Upconversion Nanoparticle@Metal–Organic Framework Nanoprobes for Targeting and Drug Delivery." Integrated Ferroelectrics 206, no. 1 (2020): 66–78. http://dx.doi.org/10.1080/10584587.2020.1728627.

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Zhao, Huai-Xin, Quan Zou, Shao-Kai Sun, et al. "Theranostic metal–organic framework core–shell composites for magnetic resonance imaging and drug delivery." Chemical Science 7, no. 8 (2016): 5294–301. http://dx.doi.org/10.1039/c6sc01359g.

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A novel multifunctional MOF-based composite with good biocompatibility, high drug loading capacity, sustained drug release and outstanding MR imaging capability was developed through a simple in situ growth procedure for simultaneous drug delivery and magnetic resonance (MR) imaging.
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Zhao, Linling, Huarong Liu, Fengwei Wang, and Lai Zeng. "Design of yolk–shell Fe3O4@PMAA composite microspheres for adsorption of metal ions and pH-controlled drug delivery." J. Mater. Chem. A 2, no. 19 (2014): 7065–74. http://dx.doi.org/10.1039/c4ta00976b.

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Yolk–shell structured pH-responsive Fe<sub>3</sub>O<sub>4</sub>@PMAA microspheres have been prepared for adsorption of metal ions and drug delivery by combined sol–gel reaction, emulsion polymerization and selective etching methods accompanying hydrolysis of PMMA shells of core–shell–shell Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>@PMMA composite microspheres.
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Porcino, Marianna, Ioanna Christodoulou, Mai Dang Le Vuong, Ruxandra Gref, and Charlotte Martineau-Corcos. "New insights on the supramolecular structure of highly porous core–shell drug nanocarriers using solid-state NMR spectroscopy." RSC Advances 9, no. 56 (2019): 32472–75. http://dx.doi.org/10.1039/c9ra07383c.

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Cai, Mengru, Gongsen Chen, Liuying Qin, et al. "Metal Organic Frameworks as Drug Targeting Delivery Vehicles in the Treatment of Cancer." Pharmaceutics 12, no. 3 (2020): 232. http://dx.doi.org/10.3390/pharmaceutics12030232.

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In recent years, metal organic frameworks (MOFs) have been widely developed as vehicles for the effective delivery of drugs to tumor tissues. Due to the high loading capacity and excellent biocompatibility of MOFs, they provide an unprecedented opportunity for the treatment of cancer. However, drugs which are commonly used to treat cancer often cause side effects in normal tissue accumulation. Therefore, the strategy of drug targeting delivery based on MOFs has excellent research significance. Here, we introduce several intelligent targeted drug delivery systems based on MOFs and their charact
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Klein, Stefanie, Tobias Luchs, Andreas Leng, Luitpold Distel, Winfried Neuhuber, and Andreas Hirsch. "Encapsulation of Hydrophobic Drugs in Shell-by-Shell Coated Nanoparticles for Radio—and Chemotherapy—An In Vitro Study." Bioengineering 7, no. 4 (2020): 126. http://dx.doi.org/10.3390/bioengineering7040126.

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Our research objective was to develop novel drug delivery vehicles consisting of TiO2 and Al2O3 nanoparticles encapsulated by a bilayer shell that allows the reversible embedment of hydrophobic drugs. The first shell is formed by covalent binding of hydrophobic phosphonic acid at the metal oxide surface. The second shell composed of amphiphilic sodium dodecylbenzenesulfonate emerges by self-aggregation driven by hydrophobic interactions between the dodecylbenzene moiety and the hydrophobic first shell. The resulting double layer provides hydrophobic pockets suited for the intake of hydrophobic
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Wang, Daolin, Changyong Gao, Chang Zhou, Zhihua Lin, and Qiang He. "Leukocyte Membrane-Coated Liquid Metal Nanoswimmers for Actively Targeted Delivery and Synergistic Chemophotothermal Therapy." Research 2020 (June 24, 2020): 1–10. http://dx.doi.org/10.34133/2020/3676954.

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We report a leukocyte membrane-coated gallium nanoswimmer (LMGNS) capable of ultrasound-propelled motion, antibiofouling, and cancer cell recognition and targeting. The LMGNS consists of a needle-shaped gallium core encapsulating an anticancer drug and a natural leukocyte membrane shell. Under the propulsion of an ultrasound field, LMGNSs could autonomously move in biological media with a speed up to 108.7 μm s−1. The velocity and motion direction of the LMGNSs can be modulated by regulating the frequency and voltage of the applied ultrasound field. Owing to the leukocyte membrane coating, LMG
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Lin, Caixue, Keke Sun, Cheng Zhang, et al. "Carbon dots embedded metal organic framework @ chitosan core-shell nanoparticles for vitro dual mode imaging and pH-responsive drug delivery." Microporous and Mesoporous Materials 293 (February 2020): 109775. http://dx.doi.org/10.1016/j.micromeso.2019.109775.

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Dissertations / Theses on the topic "Colloidosomes ; metal shell ; drug delivery"

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Sun, Qian. "Aqueous core colloidosomes with a metal shell." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/284921.

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Colloidosomes are microcapsules whose shells consist of colloid particles, which are coagulated by a stabiliser or fused by sintering. In recent years, they have attracted considerable attention because of their potential applications in a range of industries, such as food, bioreactors and medicine. However, traditional particulate polymer shell colloidosomes leak low molecular weight encapsulated materials due to their intrinsic shell permeability, and this problem will limit their applications in pharmaceutical industries. In this thesis, we report aqueous core colloidosomes coated with a si
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