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Smart external stimulus-responsive nanocarriers for drug and gene delivery /
The concept of smart drug delivery vehicles involves designing and preparing a nanostructure (or microstructure) that can be loaded with a cargo, this can be a therapeutic drug, a contrast agent for imaging, or a nucleic acid for gene therapy. The nanocarrier serves to protect the cargo from degrada...
| Clasificación: | Libro Electrónico |
|---|---|
| Autores principales: | , , , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
San Rafael [California] (40 Oak Drive, San Rafael, CA, 94903, USA) :
Morgan & Claypool Publishers,
[2015]
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| Colección: | IOP (Series). Release 2.
IOP concise physics. |
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 024 | 7 | |a 10.1088/978-1-6817-4202-1 |2 doi | |
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| 035 | |a (OCoLC)931791841 | ||
| 040 | |a CaBNVSL |b eng |e rda |c CaBNVSL |d CaBNVSL | ||
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| 100 | 1 | |a Karimi, Mahdi |c (Scientist), |e author. | |
| 245 | 1 | 0 | |a Smart external stimulus-responsive nanocarriers for drug and gene delivery / |c Mahdi Karimi, Parham Sahandi Zangabad, Amir Ghasemi and Michael R. Hamblin. |
| 264 | 1 | |a San Rafael [California] (40 Oak Drive, San Rafael, CA, 94903, USA) : |b Morgan & Claypool Publishers, |c [2015] | |
| 264 | 2 | |a Bristol [England] (Temple Circus, Temple Way, Bristol BS1 6HG, UK) : |b IOP Publishing, |c [2015] | |
| 300 | |a 1 online resource (various pagings) : |b illustrations (some color). | ||
| 336 | |a text |2 rdacontent | ||
| 337 | |a electronic |2 isbdmedia | ||
| 338 | |a online resource |2 rdacarrier | ||
| 490 | 1 | |a IOP concise physics, |x 2053-2571 | |
| 490 | 1 | |a [IOP release 2] | |
| 500 | |a "Version: 20151101"--Title page verso. | ||
| 500 | |a "A Morgan & Claypool publication as part of IOP Concise Physics"--Title page verso. | ||
| 504 | |a Includes bibliographical references. | ||
| 505 | 0 | |a Preface -- Acknowledgments -- Author biography -- 1. Introduction | |
| 505 | 8 | |a 2. Light-sensitive nanocarriers -- 2.1. Introduction -- 2.2. Photo-sensitive nanoparticle-based carriers -- 2.3. Drug release via electrostatic assembly/disassembly (reversed surface charge) -- 2.4. Chromophore (or photosensitizer)-activated drug release -- 2.5. Photo-thermal-based drug release -- 2.6. Photo-sensitive caging/uncaging based on photolabile protecting groups -- 2.7. Photo-reduction-triggered drug release | |
| 505 | 8 | |a 3. Temperature-sensitive nanocarriers -- 3.1. Introduction -- 3.2. LCST/UCST behavior -- 3.3. Thermo-responsive nanocarriers -- 3.4. Modulation of phase transition temperature in thermo-responsive nanoparticles -- 3.5. Sustained drug release by hydrophobic hydrogels -- 3.6. Cancer therapy via thermo-responsive nanocarriers -- 3.7. Temperature-responsive gene delivery systems -- 3.8. Thermo-sensitive co-delivery systems for cancer therapy -- 3.9. Temperature in photothermal-responsive micro/nano-systems | |
| 505 | 8 | |a 4. Magnetic-responsive nanocarriers -- 4.1. Introduction -- 4.2. Magnetic-responsive particles for drug delivery -- 4.3. Magnetic-responsive particles for gene delivery | |
| 505 | 8 | |a 5. Ultrasound-responsive nanocarriers -- 5.1. Introduction -- 5.2. Composition and structure of microbubbles -- 5.3. Ultrasound-responsive materials in drug delivery -- 5.4. Ultrasound-responsive materials in gene delivery | |
| 505 | 8 | |a 6. Electrical and mechanical-responsive nanocarriers -- 6.1. Introduction -- 6.2. Electric field-sensitive polymers -- 6.3. Mechanical-responsive nanomaterials -- 7. Nanotoxicology and future scope for smart nanoparticles. | |
| 520 | 3 | |a The concept of smart drug delivery vehicles involves designing and preparing a nanostructure (or microstructure) that can be loaded with a cargo, this can be a therapeutic drug, a contrast agent for imaging, or a nucleic acid for gene therapy. The nanocarrier serves to protect the cargo from degradation by enzymes in the body, to enhance the solubility of insoluble drugs, to extend the circulation half-life, and to enhance its penetration and accumulation at the target site. Importantly, smart nanocarriers can be designed to be responsive to a specific stimulus, so that the cargo is only released or activated when desired. In this volume we cover smart nanocarriers that respond to externally applied stimuli that usually involve application of physical energy. This physical energy can be applied from outside the body and can either cause cargo release, or can activate the nanostructure to be cytotoxic, or both. The stimuli covered include light of various wavelengths (ultraviolet, visible or infrared), temperature (increased or decreased), magnetic fields (used to externally manipulate nanostructures and to activate them), ultrasound, and electrical and mechanical forces. Finally we discuss the issue of nanotoxicology and the future scope of the field. | |
| 521 | |a Biomedical engineers. | ||
| 530 | |a Also available in print. | ||
| 538 | |a Mode of access: World Wide Web. | ||
| 538 | |a System requirements: Adobe Acrobat Reader. | ||
| 545 | |a Mahdi Karimi received his BSc in Medical Laboratory Science from the Iran University of Medical Science (IUMS), in 2005. In 2008, he gained his MSc in Medical Biotechnology from Tabriz University of Medical Science and joined the Tarbiat Modares University as a PhD student in the field of nanobiotechnology. He completed his research in 2013. During his research, in 2012, he affiliated with the laboratory of Professor Michael Hamblin in the Wellman Center for Photomedicine at Massachusetts General Hospital and Harvard Medical School as a researcher visitor, where he contributed to the design and construction of new smart nano-particles for drug/gene delivery. On completion of this study, he joined, as Assistant Professor, the Department of Medical Nanotechnology at IUMS. His current research interests include the design of smart nanoparticles in drug/gene delivery and microfluidic systems. He has established a scientific collaboration between his lab and Professor Michael Hamblin's lab to design new classes of smart nanovehicles in drug/gene delivery systems. Parham Sahandi Zangabad graduated with a BSc from Sahand University of Technology (SUT), Tabriz, Iran, in 2011. He received his MSc in Nanomaterials/Nanotechnology from Sharif University of Technology (SUT), Tehran, Iran. Concurrently, he became the research assistant at the Research Center for Nanostructured and Advanced Materials (RCNAM), SUT, Tehran, Iran. As a BSc and then MSc student he worked on the assessment of microstructural/mechanical properties of friction stir welded pure copper and friction stir processed hybrid TiO2-Al3Ti-MgO/Al nanocomposites. Furthermore, he has done several experiments on synthesis and characterization of sol-gel fabricated ceramic nanocomposite particles. The advent of innovative nanomaterials and nanotechnology interested him in interfacial sciences/technologies and also nanomedicine, including nanoparticle-based drug delivery systems and nanobiosensors. He has now joined Professor Karimi's Nanobiotechnology Research lab in the Iran University of Medical Science, Tehran, Iran, in association with Professor Hamblin from Harvard Medical School, Boston, USA; working on smart micro/nanocarriers applied in therapeutic agent delivery systems employed for diagnosis and therapy of various diseases and disorders such as cancers and malignancies, inflammations, infections, etc. Amir Ghasemi did his BSc at Sharif University of Technology (SUT), the most prestigious technical university in Iran. He joined the polymeric materials research group in 2012, and received his MSc in Materials Engineering from SUT. For his MSc project, he worked on thermoplastic starch (TPS)/cellulose nanofibers (CNF) biocomposites, under the supervision of Professor Bagheri. He synthesized a fully biodegradable nanocomposite, and evaluated the effects of CNF on mechanical and biodegradation of TPS. His research interests lie in the area of mechanical properties of biopolymers and polymer composites, ranging from material design to the performance of the final product. He also works on micro/nano materials, and bio-based polymers as drug carriers under the supervision of Professor Karimi and Professor Hamblin from the Harvard Medical School. He now works at Parsa Polymer Sharif, involved in thermoplastics compounding. He would like to thank Professor Karimi and Professor Hamblin for the opportunity to contribute to this work and most importantly learn about such drug delivery systems. Michael R Hamblin PhD is a principal investigator at the Wellman Center for Photomedicine, Massachusetts General Hospital, an associate professor of dermatology, Harvard Medical School and the affiliated faculty of Harvard-MIT Division of Health Science and Technology. He directs a laboratory of around 12 scientists who work in photodynamic therapy and low-level light therapy. He has published 274 peer-reviewed articles, is associate editor or eight journals and serves on NIH study sections. He has edited ten proceedings volumes, together with four other major textbooks on PDT and photomedicine. In 2011 Dr Hamblin was honored by election as a Fellow of SPIE. | ||
| 588 | 0 | |a Title from PDF title page (viewed on December 1, 2015). | |
| 650 | 0 | |a Nanomedicine. | |
| 650 | 0 | |a Drug delivery systems. | |
| 650 | 0 | |a Gene therapy. | |
| 650 | 1 | 2 | |a Nanomedicine |x methods. |
| 650 | 1 | 2 | |a Drug Delivery Systems. |
| 650 | 1 | 2 | |a Drug Therapy |x methods. |
| 650 | 1 | 2 | |a Gene Therapy |x methods. |
| 650 | 1 | 2 | |a Nanostructures |x therapeutic use. |
| 650 | 7 | |a TECHNOLOGY & ENGINEERING / Biomedical. |2 bicssc | |
| 650 | 7 | |a Biomedical Engineering. |2 bisacsh | |
| 700 | 1 | |a Zangabad, Parham Sahandi, |e author. | |
| 700 | 1 | |a Ghasemi, Amir, |e author. | |
| 700 | 1 | |a Hamblin, Michael R., |e author. | |
| 710 | 2 | |a Morgan & Claypool Publishers, |e publisher. | |
| 710 | 2 | |a Institute of Physics (Great Britain), |e publisher. | |
| 776 | 0 | 8 | |i Print version: |z 9781681741383 |
| 830 | 0 | |a IOP (Series). |p Release 2. | |
| 830 | 0 | |a IOP concise physics. | |
| 856 | 4 | 0 | |u https://iopscience.uam.elogim.com/book/978-1-6817-4202-1 |z Texto completo |