Gadolinium-conjugated dendrimer nanoclusters as a tumor-targeted T1 magnetic resonance imaging contrast agent.
暂无分享,去创建一个
[1] P. Cullis,et al. Liposomal Gd-DTPA: effect of encapsulation on enhancement of hepatoma model by MRI. , 1989, Magnetic resonance imaging.
[2] Walter H Backes,et al. Evaluation of Gd(III)DTPA‐terminated poly(propylene imine) dendrimers as contrast agents for MR imaging , 2006, NMR in biomedicine.
[3] Z. Bhujwalla,et al. PAMAM dendrimer‐based contrast agents for MR imaging of Her‐2/neu receptors by a three‐step pretargeting approach , 2008, Magnetic resonance in medicine.
[4] Chen Chang,et al. Gadolinium(III)-Incorporated Nanosized Mesoporous Silica as Potential Magnetic Resonance Imaging Contrast Agents , 2004 .
[5] R. Weissleder,et al. Method of determining nanoparticle core weight. , 2005, Analytical chemistry.
[6] Donald A. Tomalia,et al. Visualization of Dendrimer Molecules by Transmission Electron Microscopy (TEM): Staining Methods and Cryo-TEM of Vitrified Solutions , 1998 .
[7] Joop A. Peters,et al. Synthesis, characterization, and relaxivity of two linear Gd(DTPA)-polymer conjugates. , 2001, Bioconjugate chemistry.
[8] L. Tei,et al. Paramagnetic Liposomes as Innovative Contrast Agents for Magnetic Resonance (MR) Molecular Imaging Applications , 2008, Chemistry and Biodiversity.
[9] Shelton D Caruthers,et al. Targeted nanoparticles for quantitative imaging of sparse molecular epitopes with MRI , 2004, Magnetic resonance in medicine.
[10] Enzo Terreno,et al. A high relaxivity Gd(III)DOTA-DSPE-based liposomal contrast agent for magnetic resonance imaging. , 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[11] P. Choyke,et al. Synthesis, characterization, and biological evaluation of integrin alphavbeta3-targeted PAMAM dendrimers. , 2008, Molecular pharmaceutics.
[12] T. Meade,et al. Synthesis of multimeric MR contrast agents for cellular imaging. , 2008, Journal of the American Chemical Society.
[13] Weihong Tan,et al. Synthesis and Characterization of Fluorescent, Radio‐Opaque, and Paramagnetic Silica Nanoparticles for Multimodal Bioimaging Applications , 2005 .
[14] Peter Caravan,et al. Influence of molecular parameters and increasing magnetic field strength on relaxivity of gadolinium- and manganese-based T1 contrast agents. , 2009, Contrast media & molecular imaging.
[15] Weili Lin,et al. Hybrid silica nanoparticles for multimodal imaging. , 2007, Angewandte Chemie.
[16] R. Lauffer,et al. Gadolinium(III) Chelates as MRI Contrast Agents: Structure, Dynamics, and Applications. , 1999, Chemical reviews.
[17] A. Tsourkas,et al. Paramagnetic Porous Polymersomes , 2008, Langmuir : the ACS journal of surfaces and colloids.
[18] Thomas J Meade,et al. Bioresponsive, cell-penetrating, and multimeric MR contrast agents. , 2009, Accounts of chemical research.
[19] E. W. Meijer,et al. Dendrimers and magnetic resonance imaging , 2007 .
[20] Hisataka Kobayashi,et al. Nano-sized MRI contrast agents with dendrimer cores. , 2005, Advanced drug delivery reviews.
[21] J. L. Turner,et al. Synthesis of Gadolinium‐Labeled Shell‐Crosslinked Nanoparticles for Magnetic Resonance Imaging Applications , 2005 .
[22] R. D. Bolskar. Gadofullerene MRI contrast agents. , 2008, Nanomedicine.
[23] Marie-France Bellin,et al. MR contrast agents, the old and the new. , 2006, European journal of radiology.
[24] J A Frank,et al. Synthesis and relaxometry of high‐generation (G = 5, 7, 9, and 10) PAMAM dendrimer‐DOTA‐gadolinium chelates , 1999, Journal of magnetic resonance imaging : JMRI.
[25] M. Botta,et al. PAMAM dendrimeric conjugates with a Gd-DOTA phosphinate derivative and their adducts with polyaminoacids: the interplay of global motion, internal rotation, and fast water exchange. , 2006, Bioconjugate chemistry.
[26] F. Shellock,et al. Safety of magnetic resonance imaging contrast agents , 1999, Journal of magnetic resonance imaging : JMRI.