Temporal targeting of tumour cells and neovasculature with a nanoscale delivery system

By Shiladitya Sengupta, David A Eavarone, I. Capila, Ganlin Zhao, N. Watson, T. Kiziltepe, R. Sasisekharan. Nature, 2005

916 citations recorded by the source corpus.

Subfields: Biomedical Engineering, Cancer Research, Cell Biology

View Paper: https://www.semanticscholar.org/paper/98edec4d621afae7972c733cdd7edcad1eb237cc

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In Biomedical Engineering

In Cancer Research

In Cell Biology

Citations in the corpus

Nanoparticle-based combination therapy toward overcoming drug resistance in cancer. (2012, background): “that combines an antiangiogenic factor, combretastatin, with DOX [18].”
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Biosynthesis, characterisation and anti-bacterial effect of plant-mediated silver nanoparticles using Artemisia nilagirica (2013, background): “Studies have shown that the size morphology stability and chemical–physical properties of the metal nanoparticles are strongly influenced by the experimental conditions, the kinetics of the interaction of metal ions with reducing agents, and the adsorption processes of stabilising agents with metal ”
Interactions of nanomaterials and biological systems: implications to personalized nanomedicine (2012, background): “synthesized a biphasic “nanocell” with a lipid layer containing combretastatin and a hydrophobic core containing PLGA-doxorubicin conjugates [193].”
Bio-inspired, bioengineered and biomimetic drug delivery carriers (2011, background): “To co-deliver two antitumour drugs with distinct release kinetics, hybrid lipid and/or polymer 'nanocells' have been devised, which are based on the encapsulation of biodegradable polymer nanoparticles within lipid vesicle”
Antifungal activity of silver nanoparticles synthesized using turnip leaf extract (Brassica rapa L.) against wood rotting pathogens (2014, background): “Moreover, the size, morphology, physical and chemical properties, and stability of the nanoparticles are dependent on the experimental conditions, the interaction of the reducing agent with metal ions, and adsorption of the stabilizing agent onto metal nanoparticles (Knoll and Keilmann 1999; Sengupt”
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Single-step assembly of DOX/ICG loaded lipid--polymer nanoparticles for highly effective chemo-photothermal combination therapy. (2013, positive): “3 It had been reported that the delivery system loaded with a vascular shutdown combretastatin andanapoptosis-inducingdoxorubicin (DOX) significantly suppressed the growth of melanoma and lung carcinoma as compared to either single-agent regimen.(4) The codelivery strategy that utilized siRNA to sil”