نتایج جستجو برای: polyamidoamine dendrimer

تعداد نتایج: 2442  

Journal: :Molecular cancer therapeutics 2005
Marina V Backer Timur I Gaynutdinov Vimal Patel Achintya K Bandyopadhyaya B T S Thirumamagal Werner Tjarks Rolf F Barth Kevin Claffey Joseph M Backer

Tumor neovasculature is a potential but, until very recently, unexplored target for boron neutron capture therapy (BNCT) of cancer. In the present report, we describe the construction of a vascular endothelial growth factor (VEGF)-containing bioconjugate that potentially could be used to target up-regulated VEGF receptors (VEGFR), which are overexpressed on tumor neovasculature. A fifth-generat...

Journal: :International Journal of Nanomedicine 2007
Hu Yang Weiyuan John Kao

Spatial control over the distribution and the aggregation of arginine-glycine-aspartate (RGD) peptides at the nanoscale significantly affects cell responses. For example, nanoscale clustering of RGD peptides can induce integrins to cluster, thus triggering complete cell signaling. Dendrimers have a unique, highly branched, nearly spherical and symmetrical structure with low polydispersity, nano...

Journal: :PloS one 2016
Yan Guo Mary A Johnson Zara Mehrabian Manoj K Mishra Rangaramanujam Kannan Neil R Miller Steven L Bernstein

INTRODUCTION Polyamidoamine dendrimer nanoparticles (~ 4 nanometers) are inert polymers that can be linked to biologically active compounds. These dendrimers selectively target and accumulate in inflammatory cells upon systemic administration. Dendrimer-linked compounds enable sustained release of therapeutic compounds directly at the site of damage. The purpose of this study was to determine i...

Journal: :Bioorganic & medicinal chemistry 2012
Keiichi Motoyama Kayoko Hayashida Taishi Higashi Hidetoshi Arima

Nonviral gene delivery suffers from a number of limitations including short transgene expression times and low transfection efficiency. In this study, we examined whether polypseudorotaxanes (PPRXs) of polyethylene glycol (PEG, molecular weight: 2,000)-grafted α-cyclodextrin (α-CyD)/polyamidoamine dendrimer conjugate (PEG-α-CDE) with CyDs have the potential for the novel sustained release syste...

Journal: :Biological & pharmaceutical bulletin 2014
Masanobu Imamura Yukinobu Kodama Norihide Higuchi Kosuke Kanda Hiroo Nakagawa Takahiro Muro Tadahiro Nakamura Takashi Kitahara Hitoshi Sasaki

The purpose of this study was to develop a ternary complex of plasmid DNA (pDNA) electrostatically assembled with polyamidoamine (PAMAM) dendrimer and chondroitin sulfate (CS) for effective and secure gene delivery. PAMAM dendrimers are new cationic polymers that are expected to be used as gene delivery vectors. However, cationic non-viral gene vectors showed cytotoxicity by binding to negative...

Journal: :Chemistry 2014
Stephen M Bromfield Paola Posocco Maurizio Fermeglia Juan Tolosa Ana Herreros-López Sabrina Pricl Julián Rodríguez-López David K Smith

This study investigates transgeden (TGD) dendrimers (polyamidoamine (PAMAM)-type dendrimers modified with rigid polyphenylenevinylene (PPV) cores) and compares their heparin-binding ability with commercially available PAMAM dendrimers. Although the peripheral ligands are near-identical between the two dendrimer families, their heparin binding is very different. At low generation (G1), TGD outpe...

2017
Yoshika Kurokawa Hideko Sone Tin-Tin Win-Shwe Yang Zeng Hiroyuki Kimura Yosuke Koyama Yusuke Yagi Yasuto Matsui Masashi Yamazaki Seishiro Hirano

Dendrimers have been expected as excellent nanodevices for brain medication. An amine-terminated polyamidoamine dendrimer (PD), an unmodified plain type of PD, has the obvious disadvantage of cytotoxicity, but still serves as an attractive molecule because it easily adheres to the cell surface, facilitating easy cellular uptake. Single-photon emission computed tomographic imaging of a mouse fol...

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