TY - JOUR
T1 - Pathogen-mimicking MnO nanoparticles for selective activation of the TLR9 pathway and imaging of cancer cells
AU - Shukoor, Mohammed Ibrahim
AU - Natalio, Filipe
AU - Tahir, Muhammad Nawaz
AU - Wiens, Matthias
AU - Tarantola, Marco
AU - Therese, Helen Annal
AU - Barz, Matthias
AU - Weber, Stefan
AU - Terekhov, Maxim
AU - Schröder, Heinz C.
AU - Müller, Werner E.G.
AU - Janshoff, Andreas
AU - Theato, Patrick
AU - Zentel, Rudolf
AU - Schreiber, Laura Maria
AU - Tremel, Wolfgang
PY - 2009/9/12
Y1 - 2009/9/12
N2 - Here, design of the first pathogen-mimicking metal oxide nanoparticles with the ability to enter cancer cells and to selectively target and activate the TLRf pathway, and with optical and MR imaging capabilities, is reported. The immobilization of ssDNA (CpG ODN 2006) on MnO nanoparticles is performed via the phosphoramidite route using a muitifunlnal poivme. The multifunctional polymer used for the nanoparticle surface modification not only affords a protective organic biocompatible shell but also provides an efficient and convenient means for loading imunostimulatory oligonucleotides. Since fluorescent molecules are amenable to photodetection, a chromophore (Rhodamine) is introduced into the polymer chain to trace the nanoparticles in Caki-1 (human kidney cancer) cells. The ssDNA coupled nanoparticles are used to target Toll-like receptors 9(TLR9) receptors inside the cells and to activate the classical TLR cascade. The presence of TLR9 is demonstrated independently in the Caki-1 cell line by western blottingand immunostaining techniques. The magnetic properties of the MnO core make fiinctionalized MnO nanoparticles potential diagnostic agents for magnetic resonance imaging (MRI) Leb, enabling multimodal detection by a combination of MR and optical imaging methods. The trimodal nanoparticles alow the imaging of cellular trafficking by different means and simultaneously are an effective drug carrier system.
AB - Here, design of the first pathogen-mimicking metal oxide nanoparticles with the ability to enter cancer cells and to selectively target and activate the TLRf pathway, and with optical and MR imaging capabilities, is reported. The immobilization of ssDNA (CpG ODN 2006) on MnO nanoparticles is performed via the phosphoramidite route using a muitifunlnal poivme. The multifunctional polymer used for the nanoparticle surface modification not only affords a protective organic biocompatible shell but also provides an efficient and convenient means for loading imunostimulatory oligonucleotides. Since fluorescent molecules are amenable to photodetection, a chromophore (Rhodamine) is introduced into the polymer chain to trace the nanoparticles in Caki-1 (human kidney cancer) cells. The ssDNA coupled nanoparticles are used to target Toll-like receptors 9(TLR9) receptors inside the cells and to activate the classical TLR cascade. The presence of TLR9 is demonstrated independently in the Caki-1 cell line by western blottingand immunostaining techniques. The magnetic properties of the MnO core make fiinctionalized MnO nanoparticles potential diagnostic agents for magnetic resonance imaging (MRI) Leb, enabling multimodal detection by a combination of MR and optical imaging methods. The trimodal nanoparticles alow the imaging of cellular trafficking by different means and simultaneously are an effective drug carrier system.
UR - https://www.scopus.com/pages/publications/72649090339
U2 - 10.1002/adfm.200900635
DO - 10.1002/adfm.200900635
M3 - Article
AN - SCOPUS:72649090339
SN - 1616-301X
VL - 19
SP - 3717
EP - 3725
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 23
ER -