Biological applications of magnetic nanoparticles

Magnetically Responsive Microspheres and Other Carriers for the Biophysical Targeting of Antitumor Agents

Widder, K. J., Senyei, A. E., & Ranney, D. F. (1979) · Advances in Pharmacology · doi:10.1016/s1054-3589(08)60246-x · Cited by 193

Degradability of superparamagnetic nanoparticles in a model of intracellular environment: follow-up of magnetic, structural and chemical properties

Lévy, M., Lagarde, F., Maraloiu, V.-A., Blanchin, M.-G., Gendron, F., Wilhelm, C., & Gazeau, F. (2010) · Nanotechnology · doi:10.1088/0957-4484/21/39/395103 · Cited by 193

Lysosomal degradation of the carboxydextran shell of coated superparamagnetic iron oxide nanoparticles and the fate of professional phagocytes

Lunov, O., Syrovets, T., Röcker, C., Tron, K., Ulrich Nienhaus, G., Rasche, V., Mailänder, V., Landfester, K., & Simmet, T. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.08.003 · Cited by 193

Intracellular Nanoparticle Coating Stability Determines Nanoparticle Diagnostics Efficacy and Cell Functionality

Soenen, S. J. H., Himmelreich, U., Nuytten, N., Pisanic, T. R., Ferrari, A., & De Cuyper, M. (2010) · Small · doi:10.1002/smll.201000763 · Cited by 189

Dimercaptosuccinic acid-coated magnetite nanoparticles for magnetically guided in vivo delivery of interferon gamma for cancer immunotherapy

Mejías, R., Pérez-Yagüe, S., Gutiérrez, L., Cabrera, L. I., Spada, R., Acedo, P., Serna, C. J., Lázaro, F. J., Villanueva, Á., Morales, M. D. P., et al. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.01.008 · Cited by 186

Activation of natural killer cells by heat shock protein 70

Multhoff, G. (2009) · International Journal of Hyperthermia · doi:10.1080/02656730902902001 · Cited by 182

Assessing Methods for Blood Cell Cytotoxic Responses to Inorganic Nanoparticles and Nanoparticle Aggregates

Díaz, B., Sánchez‐Espinel, C., Arruebo, M., Faro, J., de Miguel, E., Magadán, S., Yagüe, C., Fernández‐Pacheco, R., Ibarra, M. R., Santamaría, J., et al. (2008) · Small · doi:10.1002/smll.200800199 · Cited by 182

In vitro and in vivo investigations of targeted chemotherapy with magnetic nanoparticles

Alexiou, C., Jurgons, R., Schmid, R., Hilpert, A., Bergemann, C., Parak, F., & Iro, H. (2005) · Journal of Magnetism and Magnetic Materials · doi:10.1016/j.jmmm.2005.02.036 · Cited by 182

Fluorescent Polystyrene–Fe3O4 Composite Nanospheres for In Vivo Imaging and Hyperthermia

Shi, D., Cho, H. S., Chen, Y., Xu, H., Gu, H., Lian, J., Wang, W., Liu, G., Huth, C., Wang, L., et al. (2009) · Advanced Materials · doi:10.1002/adma.200803159 · Cited by 179

Near infrared imaging with nanoparticles

Altınoğlu, E. İ., & Adair, J. H. (2010) · WIREs Nanomedicine and Nanobiotechnology · doi:10.1002/wnan.77 · Cited by 178

In vitro characterization of movement, heating and visualization of magnetic nanoparticles for biomedical applications

Kalambur, V. S., Han, B., Hammer, B. E., Shield, T. W., & Bischof, J. C. (2005) · Nanotechnology · doi:10.1088/0957-4484/16/8/041 · Cited by 175

Controlled Synthesis of Iron Oxide Nanoparticles over a Wide Size Range

Guardia, P., Pérez, N., Labarta, A., & Batlle, X. (2010) · Langmuir · doi:10.1021/la903767e · Cited by 172

Combining Fluorescent Probes and Biofunctional Magnetic Nanoparticles for Rapid Detection of Bacteria in Human Blood

Gao, J., Li, L., Ho, P. ‐., Mak, G. C., Gu, H., & Xu, B. (2006) · Advanced Materials · doi:10.1002/adma.200601058 · Cited by 171

Receptor‐mediated endocytosis of iron‐oxide particles provides efficient labeling of dendritic cells for in vivo MR imaging

Ahrens, E. T., Feili‐Hariri, M., Xu, H., Genove, G., & Morel, P. A. (2003) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10465 · Cited by 168

Targeted Herceptin–dextran iron oxide nanoparticles for noninvasive imaging of HER2/neu receptors using MRI

Chen, T.-J., Cheng, T.-H., Chen, C.-Y., Hsu, S. C. N., Cheng, T.-L., Liu, G.-C., & Wang, Y.-M. (2009) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-008-0445-9 · Cited by 165

Synthesis and in vitro anti-cancer evaluation of tamoxifen-loaded magnetite/PLLA composite nanoparticles

Hu, F. X., Neoh, K. G., & Kang, E. T. (2006) · Biomaterials · doi:10.1016/j.biomaterials.2006.07.014 · Cited by 165

On-chip manipulation of continuous picoliter-volume superparamagnetic droplets using a magnetic force

Zhang, K., Liang, Q., Ma, S., et al. (2009) · Lab on a Chip · doi:10.1039/b906229g · Cited by 164

Addressing the problem of cationic lipid-mediated toxicity: The magnetoliposome model

Soenen, S. J. H., Brisson, A. R., & De Cuyper, M. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2009.03.040 · Cited by 162

Magnetic Resonance Imaging Contrast Agents Based on Iron Oxide Superparamagnetic Ferrofluids

Casula, M. F., Floris, P., Innocenti, C., Lascialfari, A., Marinone, M., Corti, M., Sperling, R. A., Parak, W. J., & Sangregorio, C. (2010) · Chemistry of Materials · doi:10.1021/cm9031557 · Cited by 162

Taking Advantage of Unspecific Interactions to Produce Highly Active Magnetic Nanoparticle−Antibody Conjugates

Puertas, S., Batalla, P., Moros, M., Polo, E., del Pino, P., Guisán, J. M., Grazú, V., & de la Fuente, J. M. (2011) · ACS Nano · doi:10.1021/nn200019s · Cited by 162

Efficient In Vitro Labeling of Human Neural Precursor Cells with Superparamagnetic Iron Oxide Particles: Relevance for In Vivo Cell Tracking

Neri, M., Maderna, C., Cavazzin, C., Deidda-Vigoriti, V., Politi, L. S., Scotti, G., Marzola, P., Sbarbati, A., Vescovi, A. L., & Gritti, A. (2007) · Stem Cells · doi:10.1634/stemcells.2007-0251 · Cited by 160

A Macrophage‐Targeted Theranostic Nanoparticle for Biomedical Applications

McCarthy, J. R., Jaffer, F. A., & Weissleder, R. (2006) · Small · doi:10.1002/smll.200600139 · Cited by 158

Phase I Clinical Evaluation of Citrate-coated Monocrystalline Very Small Superparamagnetic Iron Oxide Particles as a New Contrast Medium for Magnetic Resonance Imaging

Taupitz, M., Wagner, S., Schnorr, J., Kravec, I., Pilgrimm, H., Bergmann-Fritsch, H., & Hamm, B. (2004) · Investigative Radiology · doi:10.1097/01.rli.0000129472.45832.b0 · Cited by 157

Current approaches in dendritic cell generation and future implications for cancer immunotherapy

Tuyaerts, S., Aerts, J. L., Corthals, J., Neyns, B., Heirman, C., Breckpot, K., Thielemans, K., & Bonehill, A. (2007) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-007-0334-z · Cited by 156

MRI detects white matter reorganization after neural progenitor cell treatment of stroke

Jiang, Q., Zhang, Z. G., Ding, G., Silver, B., Zhang, L., Meng, H., Lü, M., Pourabdillah-Nejed-D., S., Wang, L., Savant‐Bhonsale, S., et al. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.05.025 · Cited by 152

Anti-cancer effect of hyperthermia on breast cancer by magnetite nanoparticle-loaded anti-HER2 immunoliposomes

Kikumori, T., Kobayashi, T., Sawaki, M., & Imai, T. (2008) · Breast Cancer Research and Treatment · doi:10.1007/s10549-008-9948-x · Cited by 151

Investigation of neural progenitor cell induced angiogenesis after embolic stroke in rat using MRI

Jiang, Q., Zhang, Z. G., Ding, G., Zhang, L., Ewing, J. R., Wang, L., Zhang, R., Li, L., Lü, M., Meng, H., et al. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.063 · Cited by 151

New Classes of MRI Contrast Agents

Jacques, V., & Desreux, J. F. (2002) · Topics in current chemistry · doi:10.1007/3-540-45733-x_5 · Cited by 150

Monomer-Coated Very Small Superparamagnetic Iron Oxide Particles as Contrast Medium for Magnetic Resonance Imaging

Wagner, S., Schnorr, J., Pilgrimm, H., Hamm, B., & Taupitz, M. (2002) · Investigative Radiology · doi:10.1097/00004424-200204000-00002 · Cited by 145

Preparation and characterization of chitosan–poly(acrylic acid) polymer magnetic microspheres

Wu, Y. F., Guo, J., Yang, W., et al. (2006) · Polymer · doi:10.1016/j.polymer.2006.05.017 · Cited by 144

Polyethyleneimine functionalized iron oxide nanoparticles as agents for DNA delivery and transfection

McBain, S. C., Yiu, H. H. P., Haj, A. J. E., & Dobson, J. (2007) · Journal of Materials Chemistry · doi:10.1039/b617402g · Cited by 143

Thermal dosimetry predictive of efficacy of 111In-ChL6 nanoparticle AMF--induced thermoablative therapy for human breast cancer in mice.

DeNardo, S. J., DeNardo, G. L., Natarajan, A., Miers, L. A., Foreman, A. R., Gruettner, C., Adamson, G. N., & Ivkov, R. (2007) · PubMed · Cited by 143

Electrosteric Enhanced Stability of Functional Sub-10 nm Cerium and Iron Oxide Particles in Cell Culture Medium

Chanteau, B., Fresnais, J., & Berret, J. (2009) · Langmuir · doi:10.1021/la900833v · Cited by 142

Fe3O4/Au Core/Shell Nanoparticles Modified with Ni2+−Nitrilotriacetic Acid Specific to Histidine-Tagged Proteins

Xie, H., Zhen, R., Wang, B., Feng, Y., Chen, P., & Hao, J. (2010) · The Journal of Physical Chemistry C · doi:10.1021/jp910753f · Cited by 141

Intratumoral injection of dendritic cells derived in vitro in patients with metastatic cancer

Triozzi, P. L., Khurram, R., Aldrich, W. A., Walker, M. J., Kim, J. A., & Jaynes, S. (2000) · Cancer · Cited by 141

MR microscopy of magnetically labeled neurospheres transplanted into the Lewis EAE rat brain

Bulte, J. W. M., Ben‐Hur, T., Miller, B. R., et al. (2003) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10511 · Cited by 140

Adsorption and desorption of chemotherapeutic drugs from a magnetically targeted carrier (MTC)

Rudge, S. R., Peterson, C., Vessely, C., Koda, J. E., Stevens, S., & Catterall, L. G. (2001) · Journal of Controlled Release · doi:10.1016/s0168-3659(01)00344-3 · Cited by 139

Magnetic Resonance Tracking of Magnetically Labeled Autologous Bone Marrow CD34 + Cells Transplanted into the Spinal Cord via Lumbar Puncture Technique in Patients with Chronic Spinal Cord Injury: CD34 + Cells' Migration into the Injured Site

Callera, F., & de Melo, C. M. T. P. (2007) · Stem Cells and Development · doi:10.1089/scd.2007.0083 · Cited by 139

Activation of natural killer cells by heat shock protein 70

Multhoff, G. (2002) · International Journal of Hyperthermia · doi:10.1080/0265673021000017109 · Cited by 138

Dual-aptamer-based delivery vehicle of doxorubicin to both PSMA (+) and PSMA (−) prostate cancers

Min, K., Jo, H., Song, K.-M., Cho, M., Chun, Y., Jon, S., Kim, W. J., & Ban, C. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.11.035 · Cited by 137

Migration of dendritic cell based cancer vaccines: in vivo veritas?

Adema, G. J., de Vries, I. J. M., Punt, C. J., & Figdor, C. G. (2005) · Current Opinion in Immunology · doi:10.1016/j.coi.2005.01.004 · Cited by 134

Interactions between Magnetic Nanowires and Living Cells: Uptake, Toxicity, and Degradation

Safi, M., Yan, M., Guedeau‐Boudeville, M., Conjeaud, H., Garnier-Thibaud, V., Boggetto, N., Baeza‐Squiban, A., Niedergang, F., Averbeck, D., & Berret, J. (2011) · ACS Nano · doi:10.1021/nn201121e · Cited by 133

Acute Toxicity of Ferric Oxide and Zinc Oxide Nanoparticles in Rats

Wang, L., Wang, L., Ding, W., & Zhang, F. (2010) · Journal of Nanoscience and Nanotechnology · doi:10.1166/jnn.2010.2483 · Cited by 133

Synthesis and applications of magnetic nanoparticles for biorecognition and point of care medical diagnostics

Sandhu, A., Handa, H., & Abe, M. (2010) · Nanotechnology · doi:10.1088/0957-4484/21/44/442001 · Cited by 131

Multifunctional Magnetic Gold Nanocomposites: Human Epithelial Cancer Detection via Magnetic Resonance Imaging and Localized Synchronous Therapy

Lee, J. Y., Yang, J., Ko, H., Oh, S. J., Kang, J., Son, J., Lee, K., Lee, S. ‐., Yoon, H., Suh, J., et al. (2008) · Advanced Functional Materials · doi:10.1002/adfm.200700482 · Cited by 130

Magnetic-nanoparticle-modified paclitaxel for targeted therapy for prostate cancer

Hua, M., Yang, H., Chuang, C., Tsai, R., Chen, W.-J., Chuang, K., Chang, Y., Chuang, H., & Pang, S. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.05.061 · Cited by 130

Fabrication of Silica Nanoparticles with Both Efficient Fluorescence and Strong Magnetization and Exploration of Their Biological Applications

Mahtab, F., Yu, Y., Lam, J. W. Y., Liu, J., Zhang, B., Lü, P., Zhang, X., & Tang, B. Z. (2011) · Advanced Functional Materials · doi:10.1002/adfm.201002572 · Cited by 130

Smart Multifunctional Nanostructure for Targeted Cancer Chemotherapy and Magnetic Resonance Imaging

Chen, T., Shukoor, M. I., Wang, R., Zhao, Z., Yuan, Q., Bamrungsap, S., Xiong, X., & Tan, W. (2011) · ACS Nano · doi:10.1021/nn202073m · Cited by 129

Sustained release of doxorubicin from zeolite–magnetite nanocomposites prepared by mechanical activation

Arruebo, M., Fernández‐Pacheco, R., Irusta, S., et al. (2006) · Nanotechnology · doi:10.1088/0957-4484/17/16/011 · Cited by 129

Evaluation of systemic chemotherapy with magnetic liposomal doxorubicin and a dipole external electromagnet

Nobuto, H., Sugita, T., Kubo, T., Shimose, S., Yasunaga, Y., Murakami, T., & Ochi, M. (2004) · International Journal of Cancer · doi:10.1002/ijc.20035 · Cited by 126

Size comparison between proteins PEGylated with branched and linear poly(ethylene glycol) molecules

Fee, C. J. (2007) · Biotechnology and Bioengineering · doi:10.1002/bit.21482 · Cited by 126

Lyophilized Paclitaxel Magnetoliposomes as a Potential Drug Delivery System for Breast Carcinoma via Parenteral Administration: In Vitro and in Vivo Studies

Zhang, J., Zhang, Z.-H., Yang, H., Tan, Q., Qin, S.-R., & Qiu, X.-L. (2005) · Pharmaceutical Research · doi:10.1007/s11095-005-2496-8 · Cited by 123

Endothelial delivery of antioxidant enzymes loaded into non-polymeric magnetic nanoparticles

Chorny, M., Hood, E. D., Levy, R. J., & Muzykantov, V. R. (2010) · Journal of Controlled Release · doi:10.1016/j.jconrel.2010.05.003 · Cited by 118

Anticancer effect of hyperthermia on prostate cancer mediated by magnetite cationic liposomes and immune‐response induction in transplanted syngeneic rats

Kawai, N., Itô, A., Nakahara, Y., Futakuchi, M., Shirai, T., Honda, H., Kobayashi, T., & Kohri, K. (2005) · The Prostate · doi:10.1002/pros.20253 · Cited by 116

Multifunctional Nanoparticles for Dual Imaging

Ali, Z., Abbasi, A. Z., Zhang, F., Arosio, P., Lascialfari, A., Casula, M. F., Wenk, A., Kreyling, W. G., Plapper, R., Seidel, M., et al. (2011) · Analytical Chemistry · doi:10.1021/ac103261y · Cited by 115

Using anti-VEGF McAb and magnetic nanoparticles as double-targeting vector for the radioimmunotherapy of liver cancer

Chen, J., Wu, H., Deyan, H., & Xie, C. (2005) · Cancer Letters · doi:10.1016/j.canlet.2005.01.024 · Cited by 114

Magnetic properties of Zn-substituted MnFe2O4 nanoparticles synthesized in polyol as potential heating agents for hyperthermia. Evaluation of their toxicity on Endothelial cells

Beji, Z., Hanini, A., Smiri, L. S., Gavard, J., Kacem, K., Villain, F., Grenèche, J., Chau, F., & Ammar, S. (2010) · Chemistry of Materials · doi:10.1021/cm1001708 · Cited by 114

In vivo magnetic resonance imaging tracks adult neural progenitor cell targeting of brain tumor

Zhang, Z., Jiang, Q., Jiang, F., Ding, G., Zhang, R., Wang, L., Zhang, L., Robin, A. M., Katakowski, M., & Chopp, M. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.05.019 · Cited by 113

Hyperthermia using magnetite cationic liposomes for hamster osteosarcoma

Matsuoka, F., Shinkai, M., Honda, H., Kubo, T., Sugita, T., & Kobayashi, T. (2004) · BioMagnetic Research and Technology · doi:10.1186/1477-044x-2-3 · Cited by 113

Ultrasonically controlled release and targeted delivery of diclofenac sodium via gelatin magnetic microspheres

Muniyandy, S., Bhaskar, K., Maharajan, G., & Pillai, K. S. (2004) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2004.06.023 · Cited by 111

In vivo detection limits of magnetically labeled embryonic stem cells in the rat brain using high-field (17.6 T) magnetic resonance imaging

Stroh, A., Faber, C., Neuberger, T., et al. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.09.014 · Cited by 110

Development of Nanoparticle Libraries for Biosensing

Sun, E. Y., Josephson, L., Kelly, K. A., & Weissleder, R. (2005) · Bioconjugate Chemistry · doi:10.1021/bc050290e · Cited by 109

Dual in vivo magnetic resonance evaluation of magnetically labeled mouse embryonic stem cells and cardiac function at 1.5 t

Arai, T., Kofidis, T., Bulte, J. W. M., de Bruin, J. L., Venook, R. D., Berry, G. J., McConnell, M. V., Quertermous, T., Robbins, R. C., & Yang, P. C.-M. (2005) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20702 · Cited by 108

Magnetic/luminescent core/shell particles synthesized by spray pyrolysis and their application in immunoassays with internal standard

Dosev, D., Nichkova, M. I., Dumas, R. K., Gee, S. J., Hammock, B. D., Liu, K., & Kennedy, I. M. (2007) · Nanotechnology · doi:10.1088/0957-4484/18/5/055102 · Cited by 108

Gene expression profiling reveals early cellular responses to intracellular magnetic labeling with superparamagnetic iron oxide nanoparticles

Kedziorek, D., Muja, N., Walczak, P., Ruíz-Cabello, J., Gilad, A. A., Jie, C., & Bulte, J. W. M. (2010) · Magnetic Resonance in Medicine · doi:10.1002/mrm.22290 · Cited by 106

Tumor selectivity of stealth multi-functionalized superparamagnetic iron oxide nanoparticles

Fan, C., Gao, W., Chen, Z., et al. (2010) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2010.10.038 · Cited by 104

Anticancer effect and immune induction by hyperthermia of malignant melanoma using magnetite cationic liposomes

Suzuki, M., Shinkai, M., Honda, H., & Kobayashi, T. (2003) · Melanoma Research · doi:10.1097/00008390-200304000-00004 · Cited by 103

Hepatocellular Carcinoma in Patients with Chronic Liver Disease: Comparison of SPIO-enhanced MR Imaging and 16–Detector Row CT

Kim, Y. K., Kwak, H. S., Kim, C. S., Chung, G. H., Han, Y. M., & Lee, J. M. (2006) · Radiology · doi:10.1148/radiol.2381042193 · Cited by 103

Pharmacokinetic Characterization in Xenografted Mice of a Series of First-Generation Mimics for HLA-DR Antibody, Lym-1, as Carrier Molecules to Image and Treat Lymphoma

DeNardo, G. L., Natarajan, A., Hok, S., Perkins, J. R., Cosman, M., DeNardo, S. J., Lightstone, F. C., Mirick, G. R., Miers, L. A., & Balhorn, R. (2007) · Journal of Nuclear Medicine · doi:10.2967/jnumed.107.041095 · Cited by 102

Doxorubicin-Loaded Nanoparticles: Increased Efficiency in Murine Hepatic Metastases

Chiannilkulchai, N., Driouich, Z., Benoît, J., PARODI, A. L., & Couvreur, P. (1989) · Selective Cancer Therapeutics · doi:10.1089/sct.1989.5.1 · Cited by 102

Role of Nanoparticle Valency in the Nondestructive Magnetic-Relaxation-Mediated Detection and Magnetic Isolation of Cells in Complex Media

Kaittanis, C., Santra, S., & Pérez, J. M. S. (2009) · Journal of the American Chemical Society · doi:10.1021/ja9041077 · Cited by 101

Magnetic Nanoparticle-Mediated Gene Transfer to Oligodendrocyte Precursor Cell Transplant Populations Is Enhanced by Magnetofection Strategies

Jenkins, S. I., Pickard, M. R., Granger, N. P., & Chari, D. M. (2011) · ACS Nano · doi:10.1021/nn2018717 · Cited by 100

Superparamagnetic Nanoparticles for Effective Delivery of Malaria DNA Vaccine

Al-Deen, F. M. N., Ho, J., Selomulya, C., Ma, C., & Coppel, R. L. (2011) · Langmuir · doi:10.1021/la104479c · Cited by 100

Manipulating the Power of an Additional Phase: A Flower-like Au−Fe3O4 Optical Nanosensor for Imaging Protease Expressions In vivo

Xie, J., Zhang, F., Aronova, M. A., Zhu, L., Lin, X., Quan, Q., Liu, G., Zhang, G., Choi, K. Y., Kim, K., et al. (2011) · ACS Nano · doi:10.1021/nn200161v · Cited by 99

Fluorescent–Magnetic Hybrid Nanoparticles Induce a Dose‐Dependent Increase in Proinflammatory Response in Lung Cells in vitro Correlated with Intracellular Localization

Lehmann, A. D., Parak, W. J., Zhang, F., Ali, Z., Röcker, C., Nienhaus, G. U., Gehr, P., & Rothen‐Rutishauser, B. (2010) · Small · doi:10.1002/smll.200901770 · Cited by 98

Synthesis of Colloidal Cobalt Nanoparticles with Controlled Size and Shapes

Puntes, V., Krishnan, K. M., & Alivisatos, A. P. (2002) · Topics in Catalysis · doi:10.1023/a:1015252904412 · Cited by 97

An Iron Polyolate Complex as a Precursor for the Controlled Synthesis of Monodispersed Iron Oxide Colloids

Niederberger, M., Krumeich, F., Hegetschweiler, Κ., & Nesper, R. (2001) · Chemistry of Materials · doi:10.1021/cm0110472 · Cited by 96

Inorganic Nanoparticles for Multimodal Molecular Imaging

Swierczewska, M., Lee, S., & Chen, X. S. (2011) · Molecular Imaging · doi:10.2310/7290.2011.00001 · Cited by 96

MR imaging of the liver with Resovist: safety, efficacy, and pharmacodynamic properties.

Kopp, A. F., Laniado, M., Dammann, F., et al. (1997) · Radiology · doi:10.1148/radiology.204.3.9280254 · Cited by 95

In vivo magnetic resonance imaging of dendritic cell migration into the draining lymph nodes of mice

Baumjohann, D., Heß, A., Budinský, L., Brune, K., Schuler, G., & Lutz, M. B. (2006) · European Journal of Immunology · doi:10.1002/eji.200535742 · Cited by 93

Bovine Serum Albumin‐Based Magnetic Nanocarrier for MRI Diagnosis and Hyperthermic Therapy: A Potential Theranostic Approach Against Cancer

Franchini, M. C., Baldi, G., Bonacchi, D., Gentili, D., Giudetti, G., Lascialfari, A., Corti, M., Marmorato, P., Ponti, J., Micotti, E., et al. (2009) · Small · doi:10.1002/smll.200901689 · Cited by 93

Attenuation of Mouse Melanoma by A/C Magnetic Field after Delivery of Bi-Magnetic Nanoparticles by Neural Progenitor Cells

Rachakatla, R. S., Balivada, S., Seo, G., Myers, C. B., Wang, H., Samarakoon, T., Dani, R. K., Pyle, M. M., Kroh, F. O., Walker, B., et al. (2010) · ACS Nano · doi:10.1021/nn100870z · Cited by 93

Enzyme‐Responsive Multifunctional Magnetic Nanoparticles for Tumor Intracellular Drug Delivery and Imaging

Yang, Y., Aw, J., Chen, K., Liu, F., Padmanabhan, P., Hou, Y., Cheng, Z., & Xing, B. (2011) · Chemistry - An Asian Journal · doi:10.1002/asia.201000905 · Cited by 93

A contrast agent recognizing activated platelets reveals murine cerebral malaria pathology undetectable by conventional MRI

Mühlen, C. V. Z., Sibson, N. R., Peter, K., Campbell, S. J., Wilainam, P., Grau, G. E., Bode, C., Choudhury, R. P., & Anthony, D. C. (2008) · Journal of Clinical Investigation · doi:10.1172/jci33314 · Cited by 92

Magnetic Capsules for NMR Imaging: Effect of Magnetic Nanoparticles Spatial Distribution and Aggregation

Abbasi, A. Z., Gutiérrez, L., del Mercato, L. L., Herranz, F., Chubykalo‐Fesenko, O., Veintemillas-Verdaguer, S., Parak, W. J., Morales, M. P., González, J. M., Hernando, A., et al. (2011) · The Journal of Physical Chemistry C · doi:10.1021/jp1118234 · Cited by 90

Impact of Mammalian Target of Rapamycin Inhibition on Lymphoid Homing and Tolerogenic Function of Nanoparticle-Labeled Dendritic Cells following Allogeneic Hematopoietic Cell Transplantation

Reichardt, W., Dürr, C., von Elverfeldt, D., Jüttner, E., Gerlach, U. V., Yamada, M., Smith, B., Negrin, R. S., & Zeiser, R. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.7.4770 · Cited by 88

One-step bioengineering of magnetic nanoparticles via a surface diazo transfer/azide–alkyne click reaction sequence

Polito, L., Monti, D., Caneva, E., Delnevo, E., Russo, G., & Prosperi, D. (2008) · Chemical Communications · doi:10.1039/b716113a · Cited by 87

Hybrid Nanoparticles for Magnetic Resonance Imaging of Target‐Specific Viral Gene Delivery

Huh, Y., Lee, E. ‐., Lee, J. ‐., Jun, Y., Kim, P. H., Yun, C., Kim, J. H., Suh, J., & Cheon, J. (2007) · Advanced Materials · doi:10.1002/adma.200701952 · Cited by 87

Sensitive NMR Sensors Detect Antibodies to Influenza

Koh, I., Hong, R., Weissleder, R., & Josephson, L. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200800069 · Cited by 86

Sensitivity of magnetic resonance imaging of dendritic cells for in vivo tracking of cellular cancer vaccines

Verdijk, P., Scheenen, T. W. J., Lesterhuis, W. J., Gambarota, G., Veltien, A. A., Walczak, P., Scharenborg, N. M., Bulte, J. W. M., Punt, C. J. A., Heerschap, A., et al. (2006) · International Journal of Cancer · doi:10.1002/ijc.22385 · Cited by 86

The transfection of multipotent neural precursor/stem cell transplant populations with magnetic nanoparticles

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