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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
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
- Kategorien
- Naturwissenschaften Chemie