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Cancer Nanotheranostics - What Have We Learnd So Far?
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Conniotet al. Nanocarriers for immunecell targetingand tracking FIGURE2 |Examplesofpolymeric, lipid,andmetaland inorganicnanocarriers. liposomesas carriers for antisenseoligonucleotides, as siRNA, in cancer therapy(Tari etal., 1996). Van Broekhoven et al. (2004) have reported a DC-targeting vaccine, based on a liposomal formulation, as an outstanding platformtoinduceahighlyeffectiveimmunityagainsttumorcells (Van Broekhoven et al., 2004). Preclinical studies of liposome- DNAcomplexes have also beendescribed, constituting an effec- tive strategy toelicit anti-tumor immunity(U’renetal., 2006). The phase I clinical trial of a liposomal cancer vaccine for breast, ovarian andprostate cancer has alreadybeen reported. It has been proved that this peptide vaccine, which is intended to elicitmulti-functionalT-cell responses, is safe and immunogenic (Berinsteinetal., 2012). Additionally, liposomeshavebeenstudiedascarriers foralter- native bioorganic and biodegradable contrast agents, as glyco- gen and poly-L-Lysine.With these liposomes, it was possible to develop an in vivomulti-colormagnetic resonance imaging for lymphnodemapping(Chanetal., 2014). Polymericnanoparticles (NPs) Polymeric NPs are submicron-sized polymeric colloidal par- ticles with excellent features as vehicle for the delivery of drugs, biomolecules andgenes (PanyamandLabhasetwar, 2003; MahapatroandSingh,2011). Polymerproperties such as biocompatibility, low toxicity and biodegradability have highlighted polymericNPs as an interest- ing delivery strategy. The chemical structure of the polymers is easilymodified, allowing the development ofmultifunctional engineered systems.Nanoparticle size, shapeandsurfaceproper- ties can also be tailored, as well as the degradation kinetics and mechanicalproperties (Albertsson,2002). PolymericNPs are usually highly stable and can easily entrap and/oradsorbbothhydrophilicandhydrophobicmoleculeswith good efficacy (Gelperina et al., 2005). The drug entrapment protectsmolecules fromdegradation (Singh and Lillard, 2009). Additionally, asnano-sizedpolymericparticles, thesecarriers are easily transported through extra and intracellular barriers. As a result, entrapped agentsmay be delivered site-specifically, for instance in inflamedareasor tumors, after crossing theendothe- lium(ProkopandDavidson,2008;SinghandLillard,2009). Twodifferent types of polymericNPs are usually considered: nanospheresandnanocapsules (Figure3B).Nanospheres consist inapolymericmatrixinwhichthedrugorcargoishomogenously dispersed,whereasnanocapsules arevesicular systems formedby www.frontiersin.org November2014 |Volume2 |Article105 | 76
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Cancer Nanotheranostics What Have We Learnd So Far?
Titel
Cancer Nanotheranostics
Untertitel
What Have We Learnd So Far?
Autoren
João Conde
Pedro Viana Baptista
Jesús M. De La Fuente
Furong Tian
Herausgeber
Frontiers in Chemistry
Datum
2016
Sprache
englisch
Lizenz
CC BY 4.0
ISBN
978-2-88919-776-7
Abmessungen
21.0 x 27.7 cm
Seiten
132
Schlagwörter
Nanomedicine, Nanoparticles, nanomaterials, Cancer, heranostics, Immunotherapy, bioimaging, Drug delivery, Gene Therapy, Phototherapy
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Cancer Nanotheranostics