|1.||Rosenholm, Jessica M: 2 articles (06/2015 - 01/2009)|
|2.||Mamaeva, Veronika: 1 article (06/2015)|
|3.||Näreoja, Tuomas: 1 article (06/2015)|
|4.||Dolenko, Tatiana A: 1 article (06/2015)|
|5.||Prabhakar, Neeraj: 1 article (06/2015)|
|6.||Vlasov, Igor I: 1 article (06/2015)|
|7.||Deguchi, Takahiro: 1 article (06/2015)|
|8.||Burikov, Sergey A: 1 article (06/2015)|
|9.||Şen Karaman, Didem: 1 article (06/2015)|
|10.||Shenderova, Olga A: 1 article (06/2015)|
01/27/2009 - "Mesoporous silica nanoparticles functionalized by surface hyperbranching polymerization of poly(ethylene imine), PEI, were further modified by introducing both fluorescent and targeting moieties, with the aim of specifically targeting cancer cells. "
06/21/2015 - "In this study, the nGOs were organically surface-modified with poly(ethylene glycol)-poly(ethylene imine) (PEG-PEI) copolymers tagged with folic acid as the affinity ligand for cancer cells expressing folate receptors. "
11/01/2013 - "Functionalized SWNTs with polymerised polymeric poly(ethylene imine) was linked NGR (Asn-Gly-Arg) tumor-targeting peptide by DSPE-PEG2000-Maleimide via the maleimide group and sulfhydryl group of cysteine, in the end, doxorubicin (DOX) was attached to SWNT-PEI to obtain a SWNT-PEI/DOX/NGR delivery system. "
12/01/2011 - "Cationic micelles formed from poly(ethylene glycol)-bl-poly(propylene sulfide)-bl-poly(ethylene imine) (PEG-b-PPS-b-PEI) and from mixtures of poly(ethylene glycol)-bl-poly(propylene sulfide) (PEG-b-PPS) with PEG-b-PPS-b-PEI were explored as non-viral vectors for plasmid DNA (pDNA) transfection in a tumor immunotoxicity model. "
02/15/2009 - "We have developed a sensitive electrochemical immunoassay system for the detection of a protein tumor marker, carcinoembryonic antigen (CEA), that is based on a carbon nanoparticle (CNP)/poly(ethylene imine) (PEI)-modified screen-printed graphite electrode (CNP-PEI/SPGE) covered with anti-CEA antibodies. "
09/01/2012 - "In our recent experiments, Small molecular weight cross-linked poly(ethylene imine) by biscarbamate linkage (PEI-Bu) (Mn: 3278, Mw: 4289) can reduce target cell apoptosis induced by polycationic transfection, and has almost the same DNA condensation capability as PEI 25 kDa. PEI-Bu showed significantly higher activity and lower cytotoxicity than PEI 25 kDa in transfecting the anti-inflammatory cytokine interleukin-1 receptor antagonist (IL-1Ra) gene to rat synoviocytes, an optimal target for arthritis treatment. "
|1.||Ethylene Glycol (Monoethylene Glycol)
|2.||Folic Acid (Vitamin M)
|4.||DNA (Deoxyribonucleic Acid)
|5.||Staphylococcal Protein A (A, Protein)
|6.||Silicon Dioxide (Sand)
|8.||Interleukin-1 (Interleukin 1)